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An investigation of the seasonal relationships between meteorological factors, water quality, and sporadic cases of Legionnaires’ disease in Washington, DC

Published online by Cambridge University Press:  15 May 2023

Alexander Kirpich*
Affiliation:
Department of Population Health Sciences, School of Public Health, Georgia State University, Atlanta, GA, USA
Aleksandr Shishkin
Affiliation:
Department of Population Health Sciences, School of Public Health, Georgia State University, Atlanta, GA, USA
Pema Lhewa
Affiliation:
Department of Population Health Sciences, School of Public Health, Georgia State University, Atlanta, GA, USA
Chen Yang
Affiliation:
Department of Biostatistics, Harvard T.H. Chan School of Public Health, Harvard University, Boston, MA, USA
Michael E. von Fricken
Affiliation:
Department of Global and Community Health, College of Public Health, George Mason University, Fairfax, VA, USA
Michael H. Norris
Affiliation:
Department of Geography, University of Florida, Gainesville, FL, USA Emerging Pathogens Institute, University of Florida, Gainesville, FL, USA
Thomas A. Weppelmann
Affiliation:
Department of Internal Medicine, University of South Florida, Tampa, FL, USA
*
Corresponding author: Alexander Kirpich; Email: [email protected]
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Abstract

Since the discovery of Legionnaires’ disease (LD), limited progress has been made in understanding the epidemiology of sporadic cases of LD. Outbreaks have confirmed that air conditioning and potable water systems can be sources of community-acquired LD. However, studying the association between water quality and LD incidence has been challenging due to the heterogeneity of water systems across large geographic areas. Furthermore, although seasonal trends in incidence have been linked to increased rainfall and temperatures, the large geographic units have posed similar difficulties. To address this issue, a retrospective ecological study was conducted in Washington, DC, from 2001 to 2019. The study identified aseasonal pattern of LD incidence, with the majority of cases occurring between June and December, peaking in August, October, and November. Increased temperature was found to be associated with LD incidence. In surface water, higher concentrations of manganese, iron, and strontium were positively associated with LD, while aluminum and orthophosphate showed a negative association. Intreatment plant water, higher concentrations of total organic carbon, aluminum, barium, and chlorine were positively associated with LD, while strontium, zinc, and orthophosphate showed a negative association. The results for orthophosphates and turbidity were inconclusive, indicating the need for further research.

Type
Original Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2023. Published by Cambridge University Press

Introduction

Originally discovered in 1976 at a convention of the American Legion in Philadelphia, legionellosis is caused by either pneumonic or non-pneumonic infections with Gram-negative Legionella spp. [Reference Fraser, Tsai, Orenstein, Parkin, Beecham, Sharrar, Harris, Mallison, Martin, McDade, Shepard and Brachman1]. Unlike the localised outbreak of 1976, which led to its discovery, the majority of LD cases are acquired within communities where corresponding common point source(s) are not always properly identified. Those sources may include human-created environments such as air conditioning systems, fountains, wastewater, ice/ice machines, room humidifiers, mist machines, etc., as well as natural reservoirs such as surface water, groundwater, and rainwater [Reference Marston2,Reference van Heijnsbergen, Schalk, Euser, Brandsema, den Boer and de Roda Husman3]. In particular, Legionella spp. was isolated from a wide range of environments including rivers, lakes, puddles, and moist soil, as well as from municipal water distribution systems, hospital water supplies, and hotel water supplies [Reference Fields, Benson and Besser4Reference Lapierre, Nazarian, Zhu, Wroblewski, Saylors, Passaretti, Hughes, Tran, Lin, Kornblum, Morrison, Mercante, Fitzhenry, Weiss, Raphael, Varma, Zucker, Rakeman and Musser6].

For example within the natural reservoirs and aquatic environments, Legionella pneumophila is found in either biofilms or within their natural protozoan predators. As a result, their location within biofilms and intracellular niches leads to higher resistance to sterilising chemicals and environmental pressures [Reference Abdel-Nour, Duncan, Low and Guyard7Reference Sciuto, Laganà, Filice, Scalese, Libertino, Corso, Faro and Coniglio11]. For example, Legionella pneumophila that persist in amoebae have higher nutrient uptake, increased aquatic fitness, and an increased ability to infect mammalian cells [Reference Fields, Benson and Besser4]. The associations of the meteorological factors with LD cases have been studied and confirmed multiple times [Reference Pampaka, Gómez-Barroso, López-Perea, Carmona and Portero12]. Within human-created environments, Legionella spp. has been found in various water supply systems, including water towers [Reference Ragull, Garcia-Nuñez, Pedro-Botet, Sopena, Esteve, Montenegro and Sabrià9,Reference Fitzhenry, Weiss, Cimini, Balter, Boyd, Alleyne, Stewart, McIntosh, Econome, Lin, Rubinstein, Passaretti, Kidney, Lapierre, Kass and Varma1316]. In these environments, Legionella spp. Are known to replicate within protozoan hosts and persist in biofilms [Reference Mondino, Schmidt, Rolando, Escoll, Gomez-Valero and Buchrieser17Reference Newton, Ang, van Driel and Hartland19].

The potential amplification of Legionella spp. in municipal water may pose a serious public health risk. This happens because human infection most commonly occurs due to inhaling Legionella-containing aerosols from contaminated water sources [Reference Mondino, Schmidt, Rolando, Escoll, Gomez-Valero and Buchrieser17], while direct human-to-human transmission is known to be rare [Reference Correia, Ferreira, Borges, Nunes, Gomes, Capucho, Gonçalves, Antunes, Almeida, Mendes, Guerreiro, Sampaio, Vieira, Machado, Simões, Gonçalves and Gomes20]. After inhalation by humans, it can be engulfed by macrophages in the alveolar parts of the lungs. The bacteria replicate within the macrophages and can cause a severe type of pneumonia known as Legionnaires’ disease [Reference Mondino, Schmidt, Rolando, Escoll, Gomez-Valero and Buchrieser17,Reference Albert-Weissenberger, Cazalet and Buchrieser21]. Individuals at higher risk for developing Legionnaires’ disease are older individuals $ (\ge 50 $ years) who have predisposing risk factors, such as smoking habits, chronic cardiovascular or respiratory disease, diabetes, alcoholism, and immunosuppression [Reference Mondino, Schmidt, Rolando, Escoll, Gomez-Valero and Buchrieser17,Reference Phin, Parry-Ford, Harrison, Stagg, Zhang, Kumar, Lortholary, Zumla and Abubakar22,23]. In the United States, during the past twenty years (i.e., 2000 and onwards), there has been a continuous and steady increase in LD cases. In particular, in 2018, more than a five-fold increase in LD cases per 100,000 was documented in comparison to the early 2000s [Reference Cassell, Davis and Berkelman24,Reference Garrison, Kunz, Cooley, Moore, Lucas, Schrag, Sarisky and Whitney25].

At the same time, the incidence of LD cases has not been spatially uniform. For example, geographic heterogeneity was observed in the early 2000s when a large increase in LD was observed in the Mid-Atlantic Region [Reference Neil and Berkelman26]. Multiple causes have been hypothesised, such as the increasing median age of Americans raising the proportion of the elderly population, better diagnostic tests, more effective surveillance, and increased testing of pneumonia patients for severe acute respiratory syndrome (SARS) infections in early 2003. Those explanations, however, failed to explain much of the temporal or geographic variations in the incidence at that time [Reference Hicks, Rose, Fields, Drees, Engel, Jenkins, Rouse, Blythe, Khalifah, Feikin and Whitney27].

Historically, due to the relatively low frequency of reported LD cases in small administrative units, previous epidemiological analyses relied on aggregates of cases at the regional level (i.e., the large geographic area) [Reference Pampaka, Gómez-Barroso, López-Perea, Carmona and Portero12,Reference Hicks, Rose, Fields, Drees, Engel, Jenkins, Rouse, Blythe, Khalifah, Feikin and Whitney27Reference Fisman, Lim, Wellenius, Johnson, Britz, Gaskins, Maher, Mittleman, Victor Spain, Haas and Newbern32]. Studies addressing the association of LD cases with municipal water quality and climate have the potential to be unreliable and are challenging to conduct due to case aggregation over administrative units and corresponding heterogeneity in water sources and climatic environments over specified large geographic areas [Reference Pampaka, Gómez-Barroso, López-Perea, Carmona and Portero12,Reference Simmering, Polgreen, Hornick, Sewell and Polgreen33,Reference Beauté, Sandin, Uldum, Rota, Brandsema, Giesecke and Sparén34].

To overcome the challenge of large geographic units, the discrete municipality of Washington, DC, was selected for this retrospective ecological study from 2001 to 2019 because of the following reasons: i) it is located in the Northeastern Mid-Atlantic region which had a history of outbreaks earlier; ii) it is geographically homogenous and is located within the same climatic region (i.e., humid subtropical climate) with precise meteorological data; iii) it has had only a single source of municipal water drawn from the Potomac River, and, most importantly; iv) it has maintained detailed water quality records of both surface water and water processed by treatment plants. As a result, those detailed data records make this LD incidence study possible on a more precise and very detailed scale.

In summary, this study aimed i) to ascertain if changes in municipal or surface water component concentrations were associated with the increase in sporadic cases of LD and ii) to ascertain whether meteorological factors and climatic changes [Reference Pampaka, Gómez-Barroso, López-Perea, Carmona and Portero12] as well as monthly seasonality were associated with the increase in sporadic cases of LD.

Methods

Incidence, meteorological, and water quality data sources

LD (Legionnaires’ disease) is a reportable disease in the United States [Reference Van Kenhove, Dinne, Janssens and Laverge35]. Weekly counts of Legionnaires’ disease cases in Washington, DC, from January 2001 to December 2019 were obtained from the Centers for Disease Control and Prevention (CDC) Notifiable Infectious Disease Data Tables [36]. In particular, the CDC reports include cases which are clinically compatible and have laboratory-confirmed infections [37]. This includes both Legionnaires’ disease, which is typically characterised by fever with pneumonia, as well as Pontiac fever, which only has mild clinical symptoms without pneumonia. Water quality measurements were obtained from the United States Army Corps of Engineers (USACE) Water Analysis Reports [38]. The measurements included records for both the untreated surface water of the Potomac River and the treated water from two facilities (Dalecarlia and McMillan Treatment Plants) that serve as Washington, DC, treatment sources. The monthly records from January 2001 to December 2019 analyzed in this study include multiple organic and inorganic measurements available monthly. The majority of studied water components have previously been studied in relation to health and selected because of that reason. The surface water measurements include pH, concentrations of nitrate [Reference Pennino, Leibowitz, Compton, Hill and Sabo39Reference Bruning-Fann and Kaneene43], orthophosphate [Reference Hashim, Ewadh, Muhsin, Zubaidi, Kot, Muradov, Aljefery and al-Khaddar44Reference Pflüger-Grau and Görke48], manganese, strontium [Reference Li, Zhang, Yu, Hu, Zeng, Liu, Wang, Deng, Li, Liu, Zeng and Mei49], barium [Reference Kravchenko, Darrah, Miller, Lyerly and Vengosh50Reference Rohaim, Gong, Li, Rui, Blachowicz and Roux55], nickel, total organic carbon [Reference Falkinham, Norton and LeChevallier56], turbidity [Reference Falkinham, Norton and LeChevallier56Reference Valster, Wullings, van den Berg and van der Kooij59], aluminium [Reference Rhoads, Bradley, Mantha, Buttling, Keane, Pruden and Edwards60Reference Krewski, Yokel, Nieboer, Borchelt, Cohen, Harry, Kacew, Lindsay, Mahfouz and Rondeau63], zinc [Reference Rhoads, Bradley, Mantha, Buttling, Keane, Pruden and Edwards60], and iron. The treated water measurements include pH, concentrations of nitrate [Reference Pennino, Leibowitz, Compton, Hill and Sabo39Reference Bruning-Fann and Kaneene43], orthophosphate [Reference Hashim, Ewadh, Muhsin, Zubaidi, Kot, Muradov, Aljefery and al-Khaddar44Reference Pflüger-Grau and Görke48], manganese, strontium [Reference Li, Zhang, Yu, Hu, Zeng, Liu, Wang, Deng, Li, Liu, Zeng and Mei49], barium [Reference Kravchenko, Darrah, Miller, Lyerly and Vengosh50Reference Rohaim, Gong, Li, Rui, Blachowicz and Roux55], nickel, total organic carbon, turbidity [Reference Falkinham, Norton and LeChevallier56Reference Valster, Wullings, van den Berg and van der Kooij59], aluminium [Reference Rhoads, Bradley, Mantha, Buttling, Keane, Pruden and Edwards60Reference Krewski, Yokel, Nieboer, Borchelt, Cohen, Harry, Kacew, Lindsay, Mahfouz and Rondeau63], total coliform [Reference Nadakavukaren64], heterotrophic plate count (HPC), zinc [Reference Rhoads, Bradley, Mantha, Buttling, Keane, Pruden and Edwards60], iron, and chlorine [Reference Fish, Reeves-McLaren, Husband and Boxall65Reference Xu, Huang, Shi, Dong, Yuan and Nguyen68]. Meteorological data were obtained from the National Oceanographic and Atmospheric Association (NOAA) in the form of the Global Summary of the Day (GSOD) generated reports. Since the Ronald Reagan International Airport monitoring station (WBAN ID: 72405013743) is directly adjacent to Washington, DC, the data from that station [69,70] were used for the analysis. In particular, the obtained meteorological daily measurements included total precipitation (i.e., rain and/or melted snow) in inches (in), WDSP – mean wind speed (WDSP) in knots (knots), and average temperature in Fahrenheit (°F). The GSOD measurements were available daily for the entire studied period from January 2001 to December 2019.

Data processing

The available data were thoroughly checked and minor discrepancies were fixed before the analysis. In particular, those weeks that had no reporting of LD (i.e., coded as ‘-’ symbol which denotes ‘No reported cases’ and as the symbol ‘N’ which denotes ‘Not reportable’ cases) received zero counts. The reported weekly counts (from 1 to 52) within each year were cumulative and therefore non-decreasing from week to week. Those cumulative counts were used to compute the corresponding weekly increments for each week. For the year 2008, the presumably cumulative (and non-decreasing) counts decreased from 7 to 3 from week 20 to week 21 [71,72], and counts started to be non-decreasing again from 3. Since no explanation was available for this 7 to 3 move, the increase from week 20 to 21 was assumed to be 0, and cumulative counting proceeded further within 2008 starting from 3 in week 21, so that those weekly increments were properly counted. For the year 2012, the last reported week was 23 [73] and the cumulative reporting stopped afterwards until the end of the year. Those non-reported weekly values from week 24 were coded as 0. For water treatment facilities, if the measurement was available for both plants, then the average was taken as the final measurement, while if the measurement was available for one plant only (i.e., due to plant repairs or missing data), then that value was taken as the final measurement. The averaged values for each compound for the two plants were taken since i) the measurements between the plants varied only slightly [38] and ii) there was no way to detect which of the reported cases used the water from which plant so the averages were used as proxies. The values of not detected (‘ND’) reported for treatment plants for the compounds were coded as 0. The final sets of considered water measurement variables together with the corresponding units were summarised in Supplementary Tables S1 (river water) and S2 (treatment plant water). The meteorological measurements from the weather station were converted to the International System of Units (also known as the SI system) during the study period, which resulted in temperature being converted to degrees in Celsius (C), WDSP being converted to metres per second (m/s), and precipitation being converted to centimetres (cm). In the end, all the data were processed to be on the same time scale across all datasets. In particular, the weekly case counts were aggregated monthly, the daily meteorological measurements were averaged monthly for temperature and wind speed, and summed monthly for precipitation.

Statistical analysis

In total, three different sets of potential predictors were considered for the statistical modelling of LD cases. Those sets of predictors were selected since for the majority of them, their relationship and association with Legionella spp. or LD cases have previously been considered or studied. The first set included meteorological factors (temperature, precipitation, and WDSP) [Reference Pampaka, Gómez-Barroso, López-Perea, Carmona and Portero12], together with the categorical variable month to account for seasonality, as the set of predictors. The second set included meteorological factors (temperature, precipitation, and WDSP) [Reference Pampaka, Gómez-Barroso, López-Perea, Carmona and Portero12] and surface water characteristics such as pH, concentrations of nitrate, orthophosphate, manganese, strontium, barium, nickel, total organic carbon, turbidity, aluminium, zinc, and iron as predictors. The third set included meteorological factors (temperature, precipitation, and WDSP) [Reference Pampaka, Gómez-Barroso, López-Perea, Carmona and Portero12] and treatment plant water characteristics such as pH, concentrations of nitrate, orthophosphate, manganese, strontium, barium, nickel, total organic carbon, turbidity, aluminium, total coliform, heterotrophic plate count (HPC), zinc, iron, and chlorine as predictors.

The Poisson and negative binomial generalised linear modelling frameworks were used for the preliminary analysis [Reference McCullagh and Nelder7476]. Those models were determined to be insufficient in capturing the data variability for the given data due to excess zero counts. To address that concern, hurdle versions of Poisson and negative binomial models were used [Reference Zeileis, Kleiber and Jackman77]. In the hurdle model, there are two components: the binary hurdle component, which accounts for excessive zeroes in the distribution (i.e., it models zeroes vs. non-zeroes) with the logit link; and the truncated Poisson (or negative binomial) distribution, which is used for the remaining counts starting from one (i.e., omitting zero) with the log link. Both components have the same set of predictors, but the coefficient estimates for those predictors are different. Those components are subsequently referred to as the logit component or the hurdle component of the model and the log component or the counts component of the model, respectively. The interpretation of the model coefficients is performed accordingly, that is, for the logit component, they are identical to the logistic regression for zero vs non-zero counts, while for the log component, they are the same as for the Poisson or negative binomial model with a log link but restricted to non-zero counts, within the model. The logit component fit is identical for both models, while the log component fits may differ since the negative binomial model provides more flexible fits than the Poisson model [Reference Zeileis, Kleiber and Jackman77]. The interpretation of the model’s coefficients is provided in terms of the estimated odds for the logit component and in terms of the expected increases or decreases in counts based on the multipliers which are made from the exponentiated values of the estimated predictor coefficients for the log component. Since the month is a categorical variable, the first month (January) is used as the baseline (i.e., the reference for the other months) during the model-fitting process due to the structure of the model. As a result, there is no estimate for January in the model fit output. All data processing, statistical analyses, and figures were produced in R programming language [78] and RStudio [79], while package pscl [80] was used for the hurdle model fitting. The source code files together with the processed datasets were made publicly available on GitHub and can be downloaded [Reference Kirpich81].

Results

Summary of cases

The raw summaries of case counts for each month over time are provided in Figure 1a. The same raw counts are summarised as box and whisker plots both monthly across all studied years (Figure 1b) and yearly across all months within each year (Figure 1c). Based on panels a, b, and c of Figure 1, large heterogeneity of counts was observed with the majority of cases happening from August to November, while the largest number of cases was observed in the early 2000s and in 2019.

Figure 1. The visualisation of the case counts for each studied month (panel a) is reported together with the box and whisker plots both monthly across all studied years (panel b) and yearly across all months within each year (panel c).

If the entire set of raw case counts is desired, it is presented in Table 1 for all months and for all studied years. The total number of months was 228, while the number of months with any reported LD cases was 71. The total number of cases during those months was 215. The total number of months without any reported cases was 157.

Table 1. Monthly reports of Legionnaires’ disease cases for Washington, DC, from January 2001 until December 2019

The inspection of Table 1 and Figure 1 reveals the annual seasonality of cases, with almost no cases in the first quarter of the year during the colder winter months and most of the cases in the third and fourth quarters (late summer and early fall). The summaries of cases for each month across all studied years are provided in Table 2. In particular, the median value for all (except November) months was 0, while for November it was 1, and the 75% percentile values across all months were between 0 and 3. The largest observed number of cases during any month was 42 in October. The monthly summaries also indicate the rarity of the LD incidence. There were no records found regarding the excessive counts of October 2019 or any earlier counts that were linked to any single outbreak [82], and so the counts were analyzed in a routine way with the rest of the data.

Table 2. Monthly summaries of Legionnaires’ disease cases with the corresponding quantiles across studied years for Washington, DC, from January 2001 until December 2019

The analogous summaries for each year summarised across all months within that year are provided in Table 3. In particular, the median value varied from 0 to 1 across all years, while the 75% percentile values varied from 0 to 3.25 across all years. The largest observed number of cases during the year was 33 in 2006. Those summaries also indicate the rarity of the LD incidence.

Table 3. Annual summaries of Legionnaires’ disease cases with the corresponding quantiles across all months within each year for Washington, DC, from January 2001 until December 2019

The other useful summaries are the pairwise relationships between the considered predictors of interest and for the logit and log components of the model are summarised in Figure 2 for meteorological factors and in Supplementary Figures S1S28 for the studied water components.

Figure 2. The visualisation of the LD case counts for each studied month (panel a) reported together with the environmental predictors such as average temperature (panel b), total precipitation (panel c), and the average wind speed (panel d). The corresponding pairwise relationships for the pairwise logit components (panels e, g, and i) and log components (panels f, h, and j) are also provided. For the logit components (panels e, g, and i), the logistic regression probability fits of zero vs non-zero counts based on the corresponding predictors are displayed in dark orange (Binomial Fit). For the log components (panels f, h, and j), the linear model fits of log non-zero counts based on the corresponding predictor are displayed in dark orange (LM Fit).

More precisely, since the model has two components (logit for zero vs non-zero counts and log for the non-zero counts), the corresponding pairwise relationships between each predictor and the transformed case counts can be illustrated visually. Such relationships are presented for meteorological factors (temperature, precipitation, and wind speed) in Figure 2 panels e, g, and i for the logit component and in panels f, h, and j for the log component. The raw data for the LD case counts and the meteorological predictors are presented in panels a–d. The analogous figures for the river predicting compounds and for the treatment plant water predicting compounds are presented in panels c and d of Supplementary Figures S1S28 along with the raw data in panels a and b. In summary, the binomial fits in the presented figures visualise the logit (hurdle) component relationships of the data and the model and the log (counts) component relationships of the data and the model, respectively.

The detailed summaries of the monthly predictor’s ranges for all investigated parameters for the river (surface) water model are presented in Tables 4 and 5, while the detailed summaries of the monthly predictor’s ranges of all investigated parameters for the treatment plant water model are presented in Tables 6 and 7. The 2.4% to 97.6% quantiles contain 95% of the observed values for a given predictor and summarise the corresponding range of the predictor’s values. The 50% percentile represents the median value for a given predictor.

Table 4. The summary statistics over all months from January 2001 until December 2019 for the predictors used in the surface water model together with the corresponding measurement units

Table 5. The summary statistics over all months from January 2001 until December 2019 for the predictors used in the surface water model together with the corresponding measurement units

Table 6. The summary statistics over all months from January 2001 until December 2019 for the predictors used in the treatment plant water model together with the corresponding measurement units

Table 7. The summary statistics over all months from January 2001 until December 2019 for the predictors used in the treatment plant water model together with the corresponding measurement units

If the same summaries are desired individually for each year and are summarised for all months within that year and for each month summarised across all studied years, they are available as separate tables in the Supplementary material in the form of individual files for each year and month, respectively.

Initial analysis: Meteorological factors and seasonality with LD incidence

The complete model outputs for the hurdle Poisson and hurdle negative binomial models for the association of LD incidence with temperature (°C), precipitation (cm), wind speed (m/s), and monthly seasonality (for each month in relation to the baseline month of January) are presented in the Supplementary Files S1 and S2. Only statistically significant results $ (p<0.1 $ ) are summarised in this section, while the entire model outputs are provided in the Supplementary material.

For the logit component (which is identical for the two models), the baseline odds of having non-zero counts versus zero counts for zero values of all other predictors was estimated to be 0.004 $ (p=0.03 $ ), confirming the rarity of the Legionnaires’ disease in general. The meteorological factors were not significant for the presence of any counts vs zero counts, while the last three months of the year had increased odds of LD incidence in comparison to the baseline month of January. More precisely, the odds of LD case presence were estimated to be 18.719 times $ (p=0.09 $ ) higher for October, 34.377 times $ (p=0.009 $ ) higher for November, and 8.168 times $ (p=0.079 $ ) higher for December, than the baseline month of January.

For the log component, results differed for the Poisson model and for the negative binomial model. For the negative binomial model, no statistically significant associations were detected. For the Poisson model, given the counts are positive for every temperature unit increase (C), the estimated increase in case counts is 1.181 times  $ (p<0.008 $ ) higher than without such an increase in temperature. In a similar way, given the counts are positive, there is an estimated decrease in case counts for being in March 0.186 times $ (p=0.048 $ ) lower, in April 0.105 times $ (p=0.035 $ ) lower, in May 0.027 times $ (p=0.005 $ ) lower, in June 0.021 times $ (p=0.010 $ ) lower, in July by 0.016 times $ (p=0.010 $ ) lower, in August 0.039 times $ (p=0.036 $ ) lower and in September by 0.061 times $ (p=0.035 $ ) lower in comparison to the baseline month of January.

Within the single -paragraph summary of the meteorological factors and the seasonality models, there are indications that the months of October, November, and December were estimated to be positively associated with any presence of LD cases vs no cases in relation to the baseline month of January. Also, given that cases are present, there are indications that the increase in the number of cases is associated with the increase in temperature, while the decrease in the number of cases is expected in the months of March, April, May, June, July, August, and September.

Surface water analysis: Meteorological factors and water with LD incidence

The complete model outputs for the hurdle Poisson and hurdle negative binomial models for the association of LD incidence with temperature (°C), precipitation (cm), wind speed (m/s), pH, nitrate (ppm), orthophosphate (ppm), manganese (ppb), strontium (ppb), barium (ppb), nickel (ppb), total organic carbon (ppb), turbidity (NTU), aluminium (ppb), zinc (ppb), and iron (ppb) are presented in the Supplementary Files S3 and S4. Only statistically significant results $ (p<0.1 $ ) are summarised in this section, while the entire model outputs are provided in the Supplementary material.

For the logit component (which is identical for the two models), the meteorological factors were not significant for the presence of any counts vs zero counts.

For the logit component (which is identical for the two models), some statistically significant associations were identified for the river water components (manganese, aluminium, and iron). In particular, the odds of LD cases presence for manganese were estimated to be 1.015 times $ (p=0.008 $ ) higher, for aluminium were estimated to be 0.994 times $ (p=0.06 $ ) lower, and for iron were estimated to be 1.003 times $ (p=0.079 $ ) higher for the corresponding unit increase in the mentioned compounds. The corresponding predictor’s units and ranges are summarised in Tables 4 and 5.

For the log component, the meteorological factors results differed for the Poisson model and for the negative binomial model. For the Poisson model given the counts are positive for every temperature unit increase (°C), the expected decrease in case counts is estimated to be 0.965 times $ (p=0.075 $ ), while for every wind speed unit increase (m/s), the expected decrease in case counts is estimated to be 0.540 times $ (p=0.023 $ ). For the negative binomial model given the counts are positive only for every wind speed unit increase (m/s), the expected decrease in case counts is estimated to be 0.310 times $ (p=0.043 $ ).

For the log component, different statistically significant associations for the Poisson and for the negative binomial were also identified for the river water components. For the Poisson model given the counts are positive for every orthophosphate unit increase (ppm), the expected decrease in case counts is estimated to be 0.071 times $ (p=0.013 $ ), for every strontium unit increase (ppb) the expected increase in case counts is estimated to be 1.009 times $ (p=0.010 $ ), while for every aluminium unit increase (ppb) the expected decrease in case counts is estimated to be 0.998 times $ (p<0.001 $ ). No stable estimate was produced for the iron component by the Poisson model. For the negative binomial model given the counts are positive only for every orthophosphate unit increase (ppm), the expected decrease in case counts is estimated to be 0.024 times $ (p=0.079 $ ).

Within the single-paragraph summary of the meteorological factors and the surface water components models, there are indications that an increase in the concentration of manganese and iron is positively associated and of aluminium is negatively associated with the presence of LD cases in any amounts. Also given that cases are present for the meteorological factors, there are indications that a further increase in the number of cases is associated with the decrease of temperature and wind speed. For the river water compounds, given that cases are present, the increase in concentrations of orthophosphate, and aluminium are associated with the decrease in the number of cases, while the increase in the concentration of strontium is associated with the increase in the number of cases.

Treatment plants water: Meteorological factors and water with LD incidence

The complete model outputs for the hurdle Poisson and hurdle negative binomial models for the association of LD incidence with temperature (°C), precipitation (cm), wind speed (m/s), pH, nitrate (ppm), orthophosphate (ppm), manganese (ppb), strontium (ppb), barium (ppb), nickel (ppb), total organic carbon (ppb), turbidity (NTU), aluminium (ppb), total coliform-positive (MPN/100mL), heterotrophic plate count (CFU/mL), Zinc (ppb), Iron (ppb), Chlorine (ppm) are presented in the Supplementary Files S5 and S6. Only statistically significant results $ (p<0.1 $ ) are summarised in this section, while the entire model outputs are provided in the Supplementary material.

For the logit component (which is identical for the two models), the baseline odds of having non-zero counts versus zero counts for zero values of all predictors was estimated to be <0.001 $ (p=0.087 $ ) confirming the rarity of Legionnaires’ disease in general. In the meantime, for the logit component, no meteorological factors were statistically significant for the presence of any counts vs zero counts.

For the logit component (which is identical for the two models), some statistically significant associations were identified for the treatment plant water components (strontium, total organic carbon, turbidity, aluminium, zinc and chlorine). In particular, the odds of LD cases presence for strontium were estimated to be 0.978 times $ (p=0.015 $ ) lower, for total organic carbon were estimated to be 5.250 times $ (p=0.032 $ ) higher, for turbidity were estimated to be ~4.77 x 1026 times $ (p<0.001 $ ) higher, for aluminium were estimated to be 1.013 times $ (p=0.090 $ ) higher, for zinc were estimated to be 0.664 times $ (p=0.041 $ ) lower, and for chlorine were estimated to be 2100.687 times $ (p=0.018 $ ) higher for the corresponding unit increase in the mentioned compounds. The corresponding predictor’s units and ranges are summarised in Tables 6 and 7.

For the log component, the meteorological factors results were similar for the Poisson model and for the negative binomial model with no statistically significant associations.

For the log component, different statistically significant associations for the Poisson and for the negative binomial were also identified for the treatment plant components. For the Poisson model, given the counts are positive for every nitrate unit increase (ppm), the expected decrease in case counts is estimated to be 0.513 times $ (p=0.076 $ ); for every orthophosphate unit increase (ppm), the expected decrease in case counts is estimated to be 0.736 times $ (p=0.035 $ ); for every barium unit increase (ppb), the expected increase in case counts is estimated to be 1.103 times $ (p=0.042 $ ); for every turbidity unit increase (NTU), the expected decrease in case counts is estimated to be <0.001 times $ (p<0.001 $ ); while for every chlorine unit increase (ppm), the expected increase in case counts is estimated to be 4962.582 times $ (p=0.003 $ ). For the negative binomial model, given the counts are positive for every orthophosphate unit increase (ppm), the expected decrease in case counts is estimated to be 0.690 times $ (p=0.080 $ ); for every turbidity unit increase (NTU), the expected decrease in case counts is estimated to be <0.001 times $ (p=0.002 $ ); while for every chlorine unit increase (ppm), the expected increase in case counts is estimated to be 10572.286 times $ (p=0.010 $ ).

In summary of the meteorological factors and the treatment plant water models, no meteorological factors for either logit component or log component of any of the models were statistically significant for the presence of any case counts or increase in case counts. There were indications, however, that the increase in concentrations of total organic carbon, turbidity, aluminium, and chlorine is positively associated with the presence of LD cases in any amounts, while the increase in concentration of strontium and zinc is negatively associated with the presence of LD cases in any amounts. For the treatment plant water quality measurements, given that cases are present, the increase in concentrations of barium and chlorine is associated with the increase in the number of cases, while the increase in the concentration of nitrate, orthophosphate, and turbidity is associated with the decrease in the number of cases.

Discussion

Raw data summaries

The annual seasonality of LD cases identified in the present study partially corroborates the earlier CDC observations that the highest annual frequency of cases occurs around the late summer and early fall [83]. In particular, when specific months were investigated (Table 2), the largest monthly averages and the total monthly counts (across all years) were observed from July to November. This was confirmed in the meteorological factors and the seasonality models where the months of October, November, and December were statistically significant and associated with the presence of LD cases in any amount. At the same time, the observed seasonality has not been consistent from year to year (Table 3), when the largest numbers of cases were reported from 2003 to 2006 and from 2017 to 2019 and no cases were reported during 2013 and 2014. Within a given year, the most frequent monthly presence was observed during 2006 when cases were reported in eight months during the year, with the most cases during the last two quarters. We hypothesise that the inconsistencies in predictions from year to year are linked to the sparsity of LD outbreaks during some years.

Incidence data reporting quality

While there can be multiple explanations for the observed heterogeneity, among the most obvious ones is the potential underreporting. In particular, the symptoms of Legionnaires’ disease are not specific, that is, it presents as a range of clinical manifestations and symptoms which may cause misdiagnosis of the pathogen and subsequent undercounting of LD cases [Reference Schofield and Trent84Reference Como, Moffa, Bhanot, Min, Cole, Kuzyck and Walsh87]. More specifically, the myriad of symptoms associated with LD such as pneumonia, hyponatremia, hypophosphatemia, increased liver enzyme levels, acute mental status changes, headache, diarrhoea, early onset of pleuritic pain, diarrhoea, and fever with multisystem disease including rhabdomyolysis with renal failure can contribute to the difficulty of a differential diagnosis by medical practitioners [Reference Phin, Parry-Ford, Harrison, Stagg, Zhang, Kumar, Lortholary, Zumla and Abubakar22,Reference Chahin and Opal88]. The CDC reports, which were used for the analysis, include all clinically compatible and laboratory-confirmed cases [37]. Therefore, the cases can either be Legionnaires’ disease with pneumonia or Pontiac fever, which only has mild clinical symptoms. While underreporting of some level is expected for both disease manifestations, the Pontiac fever infections are hypothesised to have much smaller testing rates and to comprise only a small fraction of all reported cases, if any. This is expected to happen as more severe infections are more likely to be investigated thoroughly and clinically tested. There is no way, however, from the available CDC reporting data to distinguish between the two.

At the same time, for LD infection, the time to detection is critical, especially for high-risk populations. Nowadays several methods can be used to detect LD, including serological and antibody-based assays, bacterial culture, urinary antigen tests, and real-time PCR. Within this set of available tests, not all of them may always have the desired sensitivity, which varies by method [Reference Cunha, Burillo and Bouza89]. For example, serology tests as well as the urinary antigen tests for LD infections have different issues [Reference Den Boer and Yzerman90]. Recently PCR-based methods have become more common and are now regarded as the best molecular method for detection because they offer specificity, sensitivity, and desired speed [Reference Mondino, Schmidt, Rolando, Escoll, Gomez-Valero and Buchrieser17,Reference Phin, Parry-Ford, Harrison, Stagg, Zhang, Kumar, Lortholary, Zumla and Abubakar22].

The Notifiable Infectious Disease Data Tables [36], which were used for the analysis, had some data discrepancies for 2008 and 2012, which were discussed earlier. It is also important to point out that based on the available data, it is not possible to completely exclude potential travel-associated LD. In particular, cases reported in the Disease Data Tables [36] for Washington, DC, may have consumed water or spent time outside Washington, DC, due to frequent commutes and domestic or international travels. The sparsity of data (Tables 13) and the low counts for each individual month can be a source of instability for the model’s fits and the corresponding estimates. In particular, the estimates for iron concentrations were unstable (Supplementary Files S3).

Meteorological factors and seasonality with LD incidence

There was an agreement between the empirical observations of the reported LD in any amount in the last three months of a given year and the statistical significance of the corresponding estimates. There has been a notable difference between the meteorological factors and seasonality model results for the Poisson and for the negative binomial models, given that cases are present for a few months in the middle of the year. In particular, given that cases are present, the months of March through September had negative statistically significant associations in comparison to the reference January month for the Poisson version of the hurdle model. Importantly, given that cases are present, the increase in temperature was positively associated with the increase in LD cases for a Poisson model. This can be explained mathematically by the fact that the Poisson hurdle model is more restrictive and less versatile than the corresponding negative binomial analogue. Overall, the meteorological and seasonality models confirmed the presence of monthly seasonality for cases as well as an indication of positive associations with the temperature increase and the corresponding LD incidence, given the cases are detected.

Aside from pronounced monthly seasonal patterns of LD incidence, the identified association of higher temperatures with an increase in incidence has biologically plausible explanations. In particular, elevated water temperatures have been known to increase the occurrence of L. pneumophila and a range of its thermophilic host organisms [Reference Fields, Benson and Besser4]. Since the trophozoite forms of the free-living amoebae that support intracellular replication of L. pneumophila have a growth optimum between 20 and 50 °C and the L. pneumophila virulence regulator csrA, which allows for intracellular replication, is only expressed above 25 °C, it is likely that the pathogen density in the aquatic environment is highest during the warm summer months [Reference Ohno, Kato, Sakamoto, Kimura and Yamaguchi91]. It is also plausible that resources are more available due to decreases in microbial diversity and abundance within the aquatic community during warmer temperatures, which allow for higher nutrient availability that supports the growth of protozoa containing intracellular L. pneumophila [Reference Kuiper, Wullings, Akkermans, Beumer and van der Kooij92,Reference Shafi, Kamili, Shah, Parray and Bandh93]. In a similar way the potential decrease in microbial diversity in treated water due to an increase in chlorine levels may lead to higher nutrient availability. This availability of nutrients could increase the presence of L. pneumophila and lead to the corresponding observed increase in incidence.

Even though precipitation has been previously demonstrated to alter the distribution of various host organisms for L. pneumophila in the aquatic environment and has the potential to simultaneously increase both organic and inorganic nutrients that lead to the proliferation of L. pneumophila in surface water [Reference Schalk, Docters van Leeuwen, Lodder, de Man, Euser, den Boer and de Roda Husman94,Reference Wallace, Burton, Hefner and DeWitt95], such association with the precipitation level was not identified from the data. More specifically, there were no direct indications from the data that the increased monthly precipitation has been associated with an increase in LD cases.

Meteorological factors and surface water with LD incidence

Despite the fact that surface water conditions such as compound concentrations were expected to be closely related to air temperature, total precipitation, and wind speed, no such associations were identified between the presence of any LD cases and those meteorological conditions within the combined model for the two. Surprisingly, there were indications that increases in the concentration of manganese and iron were positively associated and for aluminium negatively associated with the presence of LD cases in any amounts. Even more surprisingly, given that cases are present, there are indications that a further increase in the number of cases is associated with the decrease in temperature values and in wind speed, which was counterintuitive. For the river water compounds, given that cases are present, the increases in concentration of orthophosphate and aluminium are associated with the decrease in the number of cases, while the increases in the concentration of strontium are associated with the increase in the number of cases. Among the associations identified, given that cases are present, the strongest effect per compound unit increase was observed for the orthophosphate. No effect was observed just for the presence of LD cases. This finding is a bit counterintuitive, since phosphate can be a limiting factor that plays a role in buffering effect and as an essential nutrient for the growth and replication of bacteria in the natural environment, and when supplemented into drinking water, it can lead to a rapid increase in the concentration of heterotrophic bacteria [Reference Miettinen, Vartiainen and Martikainen96]. After closer inspection (Supplementary Figure S7), the orthophosphate concentrations only had non-negative values starting from July 2004 up to January 2009. This time period is roughly within the ‘spiked’ period for cases (Figure 1 and Table 3), but the number of years with multiple LD case reports empirically looks to be longer (i.e., 2004 to 2009). We hypothesise that the non-negative orthophosphate concentration (i.e., presence of such) was only for a short subset of months (52 out of 228, Supplementary Figure S7), which could make the corresponding statistical estimates unstable. More research is recommended on the topic since there are direct lab indications that orthophosphates in drinking water promote L. pneumophila growth [Reference Jereb, Eržen, Oder and Poljšak97]. In particular, considering that L. pneumophila multiplies inside heterotrophic organisms [Reference Tyndall and Domingue98], its concentration is likely the highest in surface water when the availability of total organic carbon and concentrations of heterotrophic bacteria is maximised during the late summer and early fall [Reference Lau and Ashbolt99]. Also, inorganic phosphates can be key factors in metabolism and have been previously found to increase both the proliferation of bacteria and the species diversity within biofilms growing in simulated distribution systems, even in the presence of a disinfectant residual [Reference Jang, Choi, Ro and Ka100,Reference Yao, Elling, Jones, Nomosatryo, Long, Crowe, Antoniewicz, Hinrichs and Maresca101]. Due to the relative abundance of organic carbon in the surface waters of the Potomac River, phosphate is likely the limiting nutrient for bacterial growth in the surface water, which is dramatically increased during treatment, whereas organic carbon is actually reduced [Reference Sathasivan, Ohgaki, Yamamoto and Kamiko102]. Either way, it is worth emphasising that the utilised predictors were measured in the surface river water, and even if such growth of L. pneumophila was or was not present, the linkage with the reported LD incidence may be dubious. People do not drink or otherwise consume river water directly.

From previous findings, there have been indications that changes in manganese concentrations are associated with the increase in the proliferation of L. pneumophila in hot water systems [Reference Bargellini, Marchesi, Righi, Ferrari, Cencetti, Borella and Rovesti103], while more research was recommended on the topic. Also, there has been evidence that the fluctuations in manganese concentrations that were associated with rainfall and water temperature could be the result of increased infiltration of soil containing manganese into the surface water during rainfall events, the higher solubility of manganese with increases in water temperature, or the increase in humic acid concentration from decaying organic matter washed into the river by rainfall [Reference Wang, Li, Wang, Zhou, Fu and Li104]. The identified positive statistically significant associations between the increase in the concentration of manganese in surface (river) water and the increased odds of reporting any LD cases agree with those findings of the proliferation of L. pneumophila under such conditions. Also, given that cases are present, no such associations were detected for the counts (i.e., log component) of the model. This may be in part due to the relative sparsity of non-zero counts for most months (157 counts total presented in 71 months out of 228) and the inability to detect the statistically significant effect on the quantity with such a sample.

From the considered models, there were indications that high concentrations of aluminium were associated with the decrease in LD counts for both models (Poisson and negative binomial) and both components, that is, the logit component (any LD cases presence) and log component (changes in counts).

The other significant factors were the positive association with strontium for the logit component (any LD cases presence) for the Poisson model. It is worth noting that the estimates for iron were unstable for the Poisson-only version of the model, so the corresponding results should be interpreted with caution.

Meteorological factors and treatment plant water with LD incidence

For the meteorological factors and the treatment plant water models, no meteorological factors for either logit component or log components of any of the models were statistically significant for the presence of any counts or increase in counts. Such findings are expected since after processing water characteristics are changing and the effect of the meteorological factors becomes more limited.

The other compounds whose increase in concentration was associated with a statistically significant change in LD incidence and LD counts included total organic carbon, turbidity, aluminium, chlorine, strontium, zinc, barium, nitrate, and orthophosphate.

In particular, though some of the changes in surface water quality can be explained by natural phenomena and (potential) weather and climatic changes, the presence of phosphates in the finished water has a more direct link to treatment practices. More specifically, during November 2000, the District of Columbia Water and Sewer Authority (DC Water or DCWASA) switched the primary disinfectant from free chlorine (Cl2) to chloramine (NH2Cl) by the addition of ammonia during the water treatment process [105]. It was not until 2002 that public health officials noticed elevated blood lead levels in DC children, leading to the discovery that the switch to chloramines had altered the chemistry of the municipal water, resulting in the leaching of lead from the service lines joining the distribution system to individual houses [Reference Jean Brown, Raymond, Homa, Kennedy and Sinks106]. To reduce the lead concentrations and prevent corrosion of the distribution system, supplementation of the finished water with 2 to 4 ppm of zinc orthophosphate was started in mid-2004 [Reference Guidotti, Calhoun, Davies-Cole, Knuckles, Stokes, Glymph, Lum, Moses, Goldsmith and Ragain107]. Though it had been later documented that phosphate addition can lead to higher concentrations of bacteria in finished water and has previously been implicated in an outbreak of LD, it was uncertain what effect this would have on water quality [Reference Appenzeller, Batté, Mathieu, Block, Lahoussine, Cavard and Gatel108,Reference Crespí and Ferra109]. Also, phosphates in the finished water can inhibit copper-silver ionisation systems that are commonly used by both nursing homes and hospital facilities as a secondary disinfection technique to protect immunocompromised individuals from water-borne nosocomial infections [Reference Edwards, Hidmi and Gladwell110Reference Triantafyllidou, Lytle, Muhlen and Swertfeger112]. The precise scope of use of such copper-silver ionisation systems throughout Washington, DC, is unknown.

While the heterotrophic plate count predictor was not significant in both models, the turbidity parameter was highly significant in both models, which indicated associations of water turbidity concentration with LD incidence (Supplementary Figure S27). This water turbidity parameter should be amongst the focuses of potential future studies. The other important components identified from the analysis were chlorine presence and total organic carbon, which were both associated with LD incidence and require more focus in the future.

Conclusions

The findings from this study support previous work identifying the seasonality of LD incidence. The majority of cases during the study period were observed in the month of June to December. The three months with the largest total numbers reported were August, October, and November. After accounting for seasonality and for the presence of LD cases, temperature increase was determined to be statistically significant in predicting the increase in the number of cases.

For the surface water, there were indications that an increase in concentration of manganese and iron was positively associated and of aluminium was negatively associated with the presence of LD cases in any amounts. Also, given that cases were present for the meteorological factors, there were indications that a further increase in the number of cases was associated with the decrease in temperature and wind speed. For the river water compounds, given that cases were present, the increase in concentrations of orthophosphate and aluminium was associated with the decrease in the number of cases, while the increase in the concentration of strontium was associated with the increase in the number of cases.

For the treatment plant water, there were indications that the increase in concentrations of total organic carbon, turbidity, aluminium, and chlorine was positively associated with the presence of LD cases in any amounts, while the increase in the concentration of strontium and zinc was negatively associated with the presence of LD cases in any amounts. For the treatment plant water compounds, given that cases were present, the increase in concentrations of barium and chlorine was associated with the increase in the number of cases, while the increase in the concentration of nitrate, orthophosphate, and turbidity was associated with the decrease in the number of cases.

More research is recommended on the relationships between the concentrations of phosphates and turbidity in drinking water and their relations to the LD incidence. Also, further research is recommended on the changes in concentrations of water compounds which are identified as statistically significant in this study based on the meteorological factors which could affect them. Understanding these relationships can contribute to raising people’s prevention awareness during peak times and calling for government and public health scientists’ attention to water quality, therefore reducing future LD outbreaks within the United States.

Supplementary material

The supplementary material for this article can be found at https://doi.org/10.1017/S0950268823000651.

Data availability statement

The entire analysis was performed in R programming language and the source code together with the analyzed data were made publicly available on GitHub and can be downloaded [Reference Kirpich81].

Author contribution

Conceptualisation, Methodology, Investigation, Data Curation and Analysis, Statistical Modelling, Code Writing, Writing (Original Draft), Writing (Review and Editing), Supervision, Project administration: A.K.; Investigation, Literature Review, Data Curation, Writing (Original Draft), Writing (Review and Editing): A.S.; Investigation, Literature Review, Data Curation, Writing (Original Draft), Writing (Review and Editing): P.L.; Investigation, Literature Review, Data Curation, Writing (Original Draft), Writing (Review and Editing): C.Y.; Conceptualisation, Methodology: M.E.V.F.; Conceptualisation, Methodology, Writing (Original Draft): M.N.; Conceptualisation, Methodology, Investigation, Data Curation and Analysis, Statistical Modelling, Code Writing, Writing (Original Draft), Writing (Review and Editing): T.A.W.

Financial support

No funding has been received for this project.

Competing interest

The authors declare none.

Footnotes

A.S., P.L., and C.Y. contributed equally to this work.

References

Fraser, DW, Tsai, TR, Orenstein, W, Parkin, WE, Beecham, HJ, Sharrar, RG, Harris, J, Mallison, GF, Martin, SM, McDade, JE, Shepard, CC, Brachman, PS and the Field Investigation Team (1977) Legionnaires’ disease: Description of an epidemic of pneumonia. The New England Journal of Medicine 297, 11891197.CrossRefGoogle ScholarPubMed
Marston, BJ (1994) Surveillance for legionnaires’ disease. Archives of Internal Medicine American Medical Association (AMA) 154, 2417.CrossRefGoogle ScholarPubMed
van Heijnsbergen, E, Schalk, JAC, Euser, SM, Brandsema, PS, den Boer, JW and de Roda Husman, AM (2015) Confirmed and potential sources of Legionella reviewed. Environmental Science & Technology 49, 47974815.CrossRefGoogle ScholarPubMed
Fields, BS, Benson, RF and Besser, RE (2002) Legionella and Legionnaires’ disease: 25 years of investigation. Clinical Microbiology Reviews 15, 506526.CrossRefGoogle ScholarPubMed
Atlas, RM (1999) Legionella: From environmental habitats to disease pathology, detection and control. Environmental Microbiology 1, 283293.CrossRefGoogle ScholarPubMed
Lapierre, P, Nazarian, E, Zhu, Y, Wroblewski, D, Saylors, A, Passaretti, T, Hughes, S, Tran, A, Lin, Y, Kornblum, J, Morrison, SS, Mercante, JW, Fitzhenry, R, Weiss, D, Raphael, BH, Varma, JK, Zucker, HA, Rakeman, JL and Musser, KA (2017) Legionnaires’ disease outbreak caused by endemic strain of Legionella pneumophila, New York, New York, USA, 2015, Emerging Infectious Diseases 23, 17841791.CrossRefGoogle ScholarPubMed
Abdel-Nour, M, Duncan, C, Low, D and Guyard, C (2013) Biofilms: The stronghold of Legionella pneumophila. International Journal of Molecular Science 14, 21660CrossRefGoogle ScholarPubMed
Oguma, K, Katayama, H and Ohgaki, S (2004) Photoreactivation of Legionella pneumophila after inactivation by low- or medium-pressure ultraviolet lamp. Water Research 38, 27572763.CrossRefGoogle ScholarPubMed
Ragull, S, Garcia-Nuñez, M, Pedro-Botet, ML, Sopena, N, Esteve, M, Montenegro, R and Sabrià, M (2007) Legionella pneumophila in cooling towers: Fluctuations in counts, determination of genetic variability by pulsed-field gel electrophoresis (PFGE), and persistence of PFGE patterns. Applied and Environmental Microbiology 73, 53825384.CrossRefGoogle ScholarPubMed
Ensminger, AW (2016) Legionella pneumophila, armed to the hilt: Justifying the largest arsenal of effectors in the bacterial world. Current Opinion in Microbiology 29, 7480.CrossRefGoogle Scholar
Sciuto, EL, Laganà, P, Filice, S, Scalese, S, Libertino, S, Corso, D, Faro, G and Coniglio, MA (2021) Environmental management of Legionella in domestic water systems: Consolidated and innovative approaches for disinfection methods and risk assessment. Microorganisms 577.CrossRefGoogle ScholarPubMed
Pampaka, D, Gómez-Barroso, D, López-Perea, N, Carmona, R and Portero, RC (2022) Meteorological conditions and Legionnaires’ disease sporadic cases – A systematic review. Environmental Research Academic Press 214, 114080.Google ScholarPubMed
Fitzhenry, R, Weiss, D, Cimini, D, Balter, S, Boyd, C, Alleyne, L, Stewart, R, McIntosh, N, Econome, A, Lin, Y, Rubinstein, I, Passaretti, T, Kidney, A, Lapierre, P, Kass, D and Varma, JK (2017) Legionnaires’ disease outbreaks and cooling towers, New York City, New York, USA. Emerging Infectious Diseases 23, 1769CrossRefGoogle ScholarPubMed
Horng, Y-T, Soo, P-C, Shen, B-J, Hung, Y-L, Lo, K-Y, Su, H-P, Wei, J-R, Hsieh, S-C, Hsueh, P-R and Lai, H-C (2006) Development of an improved PCR–ICT hybrid assay for direct detection of Legionellae and Legionella pneumophila from cooling tower water specimens. Water Research 40, 22212229.CrossRefGoogle ScholarPubMed
Miyamoto, H, Yamamoto, H, Arima, K, Fujii, J, Maruta, K, Izu, K, Shiomori, T and Yoshida, S (1997) Development of a new seminested PCR method for detection of Legionella species and its application to surveillance of Legionellae in hospital cooling tower water. Applied and Environmental Microbiology 63, 24892494.CrossRefGoogle ScholarPubMed
The Science of the Total Environment (2017) A discussion about public health, lead and Legionella pneumophila in drinking water supplies in the United States. Elsevier, pp. 590–591: 843852.Google Scholar
Mondino, S, Schmidt, S, Rolando, M, Escoll, P, Gomez-Valero, L and Buchrieser, C (2020) Legionnaires’ disease: State of the art knowledge of pathogenesis mechanisms of Legionella. Annual Review of Pathology 15, 439466.CrossRefGoogle ScholarPubMed
Abu Khweek, A and Amer, AO (2018) Factors mediating environmental biofilm formation by Legionella pneumophila. Frontiers in Cellular and Infection Microbiology 8, 38.CrossRefGoogle ScholarPubMed
Newton, HJ, Ang, DKY, van Driel, IR and Hartland, EL (2010) Molecular pathogenesis of infections caused by Legionella pneumophila. Clinical Microbiology Reviews 23, 274298.CrossRefGoogle ScholarPubMed
Correia, AM, Ferreira, JS, Borges, V, Nunes, A, Gomes, B, Capucho, R, Gonçalves, J, Antunes, DM, Almeida, S, Mendes, A, Guerreiro, M, Sampaio, DA, Vieira, L, Machado, J, Simões, MJ, Gonçalves, P and Gomes, JP (2016) Probable person-to-person transmission of legionnaires’ disease. The New England Journal of Medicine 374, 497498.CrossRefGoogle ScholarPubMed
Albert-Weissenberger, C, Cazalet, C and Buchrieser, C (2007) Legionella pneumophila – A human pathogen that co-evolved with fresh water protozoa. Cellular and Molecular Life Sciences: CMLS 64, 432448.CrossRefGoogle ScholarPubMed
Phin, N, Parry-Ford, F, Harrison, T, Stagg, HR, Zhang, N, Kumar, K, Lortholary, O, Zumla, A and Abubakar, I (2014) Epidemiology and clinical management of Legionnaires’ disease. The Lancet Infectious Diseases 14, 10111021.CrossRefGoogle ScholarPubMed
EPA (1999) Legionella: Human Health Criteria Document EPA-822-R-99-001. EPA Washington, DC. Available at https://nepis.epa.gov/ (accessed 24 September 2021).Google Scholar
Cassell, K, Davis, JL and Berkelman, R (2021) Legionnaires’ disease in the time of COVID-19. Pneumonia 13, 13.CrossRefGoogle ScholarPubMed
Garrison, LE, Kunz, JM, Cooley, LA, Moore, MR, Lucas, C, Schrag, S, Sarisky, J and Whitney, CG (2016) Vital signs: Deficiencies in environmental control identified in outbreaks of legionnaires’ disease — North America, 2000–2014. MMWR. Morbidity and Mortality Weekly Report, 576584.CrossRefGoogle Scholar
Neil, K and Berkelman, R (2008) Increasing incidence of legionellosis in the United States, 1990–2005: Changing epidemiologic trends. Clinical Infectious Diseases 47, 591599.CrossRefGoogle ScholarPubMed
Hicks, LA, Rose, CE Jr, Fields, BS, Drees, ML, Engel, JP, Jenkins, PR, Rouse, BS, Blythe, D, Khalifah, AP, Feikin, DR and Whitney, CG (2007) Increased rainfall is associated with increased risk for legionellosis. Epidemiology and Infection 135, 811817.CrossRefGoogle ScholarPubMed
Joseph, CA, Ricketts, KD, Yadav, R, Patel, S, European Working Group for Legionella Infections (2010) Travel-associated legionnaires disease in Europe in 2009. Euro Surveillance: Bulletin Europeen sur les Maladies Transmissibles (European Communicable Disease Bulletin ) 15, 19683.Google ScholarPubMed
Ricketts, KD, Charlett, A, Gelb, D, Lane, C, Lee, JV and Joseph, CA (2009) Weather patterns and legionnaires’ disease: A meteorological study. Epidemiology and Infection 137, 10031012.CrossRefGoogle ScholarPubMed
Karagiannis, I, Brandsema, P and van der Sande, M (2009) Warm, wet weather associated with increased legionnaires’ disease incidence in the Netherlands. Epidemiology and Infection 137, 181187.CrossRefGoogle ScholarPubMed
Garcia-Vidal, C, Labori, M, Viasus, D, Simonetti, A, Garcia-Somoza, D, Dorca, J, Gudiol, F and Carratalà, J (2013) Rainfall is a risk factor for sporadic cases of Legionella pneumophila pneumonia. PLoS One 8, e61036.CrossRefGoogle ScholarPubMed
Fisman, DN, Lim, S, Wellenius, GA, Johnson, C, Britz, P, Gaskins, M, Maher, J, Mittleman, MA, Victor Spain, C, Haas, CN and Newbern, C (2005) It’s not the heat, it’s the humidity: Wet weather increases legionellosis risk in the greater Philadelphia metropolitan area. The Journal of Infectious Diseases 192, 20662073.CrossRefGoogle Scholar
Simmering, JE, Polgreen, LA, Hornick, DB, Sewell, DK and Polgreen, PM (2017) Weather-dependent risk for legionnaires’ disease, United States. Emerging Infectious Diseases 23, 1843.CrossRefGoogle ScholarPubMed
Beauté, J, Sandin, S, Uldum, SA, Rota, MC, Brandsema, P, Giesecke, J and Sparén, P (2017) Short-term effects of atmospheric pressure, temperature, and rainfall on notification rate of community-acquired Legionnaires’ disease in four European countries – CORRIGENDUM. Epidemiology and Infection 33193319.CrossRefGoogle ScholarPubMed
Van Kenhove, E, Dinne, K, Janssens, A and Laverge, J (2019) Overview and comparison of Legionella regulations worldwide. American Journal of Infection Control 47, 968978.CrossRefGoogle ScholarPubMed
The Centers for Disease Control and Prevention – Notifiable Infectious Disease Tables (2021). Avaible at https://www.cdc.gov/nndss/data-statistics/infectious-tables/index.html (accessed 9 December 2021).Google Scholar
The Centers for Disease Control and Prevention – Legionellosis (2021). Available at https://ndc.services.cdc.gov/conditions/legionellosis/ (accessed 30 March 2023).Google Scholar
USACE (2021) United States Army Corps of Engineers – Water Analysis Reports. Available at https://www.nab.usace.army.mil/Missions/Washington-Aqueduct/Water-Quality/ (accessed 24 September 2021).Google Scholar
Pennino, MJ, Leibowitz, SG, Compton, JE, Hill, RA and Sabo, RD (2020) Patterns and predictions of drinking water nitrate violations across the conterminous United States. Science of the Total Environment 137661.CrossRefGoogle ScholarPubMed
Fan, AM and Steinberg, VE (1996) Health implications of nitrate and nitrite in drinking water: An update on methemoglobinemia occurrence and reproductive and developmental toxicity. Regulatory Toxicology and Pharmacology 3543.CrossRefGoogle ScholarPubMed
McCarthy, CM (1987) Utilization of nitrate or nitrite as single nitrogen source by Mycobacterium avium. Journal of Clinical Microbiology 263267.CrossRefGoogle ScholarPubMed
Wheeler, DC, Nolan, BT, Flory, AR, DellaValle, CT and Ward, MH (2015) Modeling groundwater nitrate concentrations in private wells in Iowa. The Science of the Total Environment 536, 481488.CrossRefGoogle ScholarPubMed
Bruning-Fann, CS and Kaneene, JB (1993) The effects of nitrate, nitrite and N-nitroso compounds on human health: A review. Veterinary and Human Toxicology 35, 521538.Google ScholarPubMed
Hashim, KS, Ewadh, HM, Muhsin, AA, Zubaidi, SL, Kot, P, Muradov, M, Aljefery, M and al-Khaddar, R (2021) Phosphate removal from water using bottom ash: Adsorption performance, coexisting anions and modelling studies. Water Science and Technology: a Journal of the International Association on Water Pollution Research 83, 7789.CrossRefGoogle ScholarPubMed
Ortiz-Roque, CM and Hazen, TC (1987) Abundance and distribution of Legionellaceae in Puerto Rican waters. Applied and Environmental Microbiology 22312236.CrossRefGoogle ScholarPubMed
Kawakami, N and Fujisaki, S (2018) Undecaprenyl phosphate metabolism in Gram-negative and Gram-positive bacteria. Bioscience, Biotechnology, and Biochemistry 940946.CrossRefGoogle ScholarPubMed
Matsuura, M (2013) Structural modifications of bacterial Lipopolysaccharide that facilitate Gram-negative bacteria evasion of host innate immunity. Frontiers in Immunology.CrossRefGoogle ScholarPubMed
Pflüger-Grau, K and Görke, B(2010) Regulatory roles of the bacterial nitrogen-related phosphotransferase system. Trends in Microbiology 205214.CrossRefGoogle ScholarPubMed
Li, Y, Zhang, Y, Yu, M, Hu, L, Zeng, T, Liu, L, Wang, L, Deng, L, Li, X, Liu, P, Zeng, D and Mei, S (2022) Biological monitoring and health assessment of 21 metal(loid)s in children and adolescents in Liuzhou City, Southwest China. Environmental Science and Pollution Research International 29, 1868918701.CrossRefGoogle ScholarPubMed
Kravchenko, J, Darrah, TH, Miller, RK, Lyerly, HK and Vengosh, A (2014) A review of the health impacts of barium from natural and anthropogenic exposure. Environmental Geochemistry and Health 36, 797814.CrossRefGoogle ScholarPubMed
Peana, M, Medici, S, Dadar, M, Zoroddu, MA, Pelucelli, A, Chasapis, CT and Bjørklund, G (2021) Environmental barium: Potential exposure and health-hazards. Archives of Toxicology 95, 26052612.CrossRefGoogle ScholarPubMed
Zhang, X, Wu, Q, Gao, S, Wang, Z and He, S (2021) Distribution, source, water quality and health risk assessment of dissolved heavy metals in major rivers in Wuhan, China. PeerJ 9, e11853.CrossRefGoogle ScholarPubMed
National Toxicology Program (U.S.), National Institutes of Health (U.S.) (1994) NTP technical report on the toxicology and carcinogenesis studies of barium chloride dihydrate in F344/N rats and B6C3F1 mice (drinking water studies).Google Scholar
Williams, CEDPL, Dallas, CE and Williams, PL (2001) Barium: Rationale for a new oral reference dose. Journal of Toxicology and Environmental Health, Part B 395429.CrossRefGoogle Scholar
Rohaim, A, Gong, LD, Li, J, Rui, H, Blachowicz, L and Roux, B (2020) Open and closed structures of a barium-blocked potassium channel. Journal of Molecular Biology 47834798.CrossRefGoogle ScholarPubMed
Falkinham, JO, Norton, CD and LeChevallier, MW (2001) Factors influencing numbers of Mycobacterium avium, Mycobacterium intracellulare, and other Mycobacteria in drinking water distribution systems. Applied and Environmental Microbiology 67, 12251231.CrossRefGoogle ScholarPubMed
Mac Kenzie, WR, Hoxie, NJ, Proctor, ME, Gradus, MS, Blair, KA, Peterson, DE, Kazmierczak, JJ, Addiss, DG, Fox, KR, Rose, JB and Davis, JP (1994) A massive outbreak in Milwaukee of cryptosporidium infection transmitted through the public water supply. The New England Journal of Medicine 331, 161167.CrossRefGoogle ScholarPubMed
Falkinham, JO. Current epidemiologic trends of the nontuberculous mycobacteria (NTM). Current environmental health reports 2016; 3: 161167.CrossRefGoogle ScholarPubMed
Valster, RM, Wullings, BA, van den Berg, R and van der Kooij, D (2011) Relationships between free-living protozoa, cultivable Legionella spp., and water quality characteristics in three drinking water supplies in the Caribbean. Applied and Environmental Microbiology 73217328.CrossRefGoogle ScholarPubMed
Rhoads, WJ, Bradley, TN, Mantha, A, Buttling, L, Keane, T, Pruden, A and Edwards, MA (2020) Residential water heater cleaning and occurrence of Legionella in Flint, MI. Water Research 171, 115439.CrossRefGoogle ScholarPubMed
United States Environmental Protection Agency (2015) Secondary drinking water standards: Guidance for nuisance chemicals. Published online: 2 September 2015.Google Scholar
World Health Organization (2003) Aluminum in Drinking Water. Website. Available at http://www.who.int/water_sanitation_health/dwq/chemicals/en/aluminium.pdf (accessed 2022).Google Scholar
Krewski, D, Yokel, RA, Nieboer, E, Borchelt, D, Cohen, J, Harry, J, Kacew, S, Lindsay, J, Mahfouz, AM and Rondeau, V (2007) Human health risk assessment for aluminium, aluminium oxide, and aluminium hydroxide. Journal of Toxicology and Environmental Health. Part B, Critical Reviews 10(Suppl 1), 1269.CrossRefGoogle ScholarPubMed
Nadakavukaren, A (1995) Our Global Environment: A Health Perspective.Google Scholar
Fish, KE, Reeves-McLaren, N, Husband, S and Boxall, J (2020) Unchartered waters: The unintended impacts of residual chlorine on water quality and biofilms. NPJ Biofilms and Microbiomes 6, 34.CrossRefGoogle ScholarPubMed
Solomon, ET, Robele, S, Kloos, H and Mengistie, B (2020) Effect of household water treatment with chlorine on diarrhea among children under the age of five years in rural areas of Dire Dawa, eastern Ethiopia: A cluster randomized controlled trial. Infectious Diseases of Poverty 9, 64.CrossRefGoogle ScholarPubMed
Zhou, X, Ahmad, JI, van der Hoek, JP and Zhang, K (2020) Thermal energy recovery from chlorinated drinking water distribution systems: Effect on chlorine and microbial water and biofilm characteristics. Environmental Research, 109655.CrossRefGoogle ScholarPubMed
Xu, J, Huang, C, Shi, X, Dong, S, Yuan, B and Nguyen, TH (2018 ) Role of drinking water biofilms on residual chlorine decay and trihalomethane formation: An experimental and modeling study. Science of The Total Environment 516525.CrossRefGoogle ScholarPubMed
NOAA (2013) National Oceanographic and Atmospheric Association. Global Summary of the Day (GSOD) 72405013743. Available at https://www.ncei.noaa.gov/access/search/data-search/global-summary-of-the-day (accessed 24 September 2021).Google Scholar
National Centers For Environmental Information. Global Surface Summary Of Day Data (GSOD) - ReadMe. Available at https://www.ncei.noaa.gov/data/global-summary-of-the-day/doc/readme.txt (accessed 18 February 2022).Google Scholar
cdc.gov. TABLE II. (Part 3) Provisional cases of selected notifiable diseases, United States, week ending May 17, 2008 (WEEK 20)*. Available at (https://wonder.cdc.gov/nndss/nndss_weekly_tables_1995_2014.asp?mmwr_year=2008&mmwr_week=20&mmwr_table=2C&request=Submit (accessed 25 October 2022).Google Scholar
cdc.gov. TABLE II. (Part 3) Provisional cases of selected notifiable diseases, United States, week ending May 24, 2008 (WEEK 21)*. Available at https://wonder.cdc.gov/nndss/nndss_weekly_tables_1995_2014.asp?mmwr_year=2008&mmwr_week=21&mmwr_table=2C&request=Submit (accessed 25 October 2022).Google Scholar
cdc.gov. TABLE II. (Part 6) Provisional cases of selected notifiable diseases, United States, week ending June 16, 2012 (WEEK 24)*. Available at https://wonder.cdc.gov/nndss/nndss_weekly_tables_1995_2014.asp?mmwr_year=2012&mmwr_week=24&mmwr_table=2F&request=Submit (accessed 24 October 2022).Google Scholar
McCullagh, P and Nelder, JA (1989) Generalized Linear Models, 2nd Edn. Boston, MA: CRC Press.CrossRefGoogle Scholar
McCullagh, P (2019) Generalized Linear Models. Routledge.CrossRefGoogle Scholar
Package ‘MASS’ in R. Available at https://cran.r-project.org/web/packages/MASS/MASS.pdf (accessed 9 December 2021).Google Scholar
Zeileis, A, Kleiber, C and Jackman, S (2008) Regression models for count data in R. Journal of Statistical Software Foundation for Open Access Statistics 27, 125.Google Scholar
The R Project for Statistical Computing . Availabe at https://www.r-project.org/ (accessed 9 December 2021).Google Scholar
RStudio . (https://www.rstudio.com/ (accessed 9 December 2021).Google Scholar
Comprehensive R Archive Network (CRAN) (2015) pscl: Political Science Computational Laboratory. Available at https://CRAN.R-project.org/package=pscl (accessed 19 October 2022).Google Scholar
Kirpich, A (2022) GitHub – akirpich-ap/legionella-dc. GitHub. Availabe at https://github.com/akirpich-ap/legionella-dc (accessed 21 March 2022).Google Scholar
HC Info (2015) The Most Recent Legionnaires’ Disease Outbreaks. Availabe at https://hcinfo.com/about/outbreaks/recent/ (accessed 25 October 2022).Google Scholar
CDC. Legionellosis Case Reports from 2000-2009. Available at http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6032a3.htm?s_cid=mm6032a3_w (accessed 24 September 2021).Google Scholar
Schofield, R and Trent, RJ (2010) Swine flu: False-positive rapid flu swab with resulting misdiagnosis of a case of Legionella pneumonia. BMJ Case Reports. doi:10.1136/bcr.12.2009.2519.CrossRefGoogle ScholarPubMed
Stone, W, Louw, TM, Gakingo, GK, Nieuwoudt, MJ and Booysen, MJ (2019) A potential source of undiagnosed Legionellosis: Legionella growth in domestic water heating systems in South Africa. Energy for Sustainable Development 48, 130138.CrossRefGoogle Scholar
Musso, D and Raoult, D (1997) Serological cross-reactions between Coxiella burnetii and Legionella micdadei. Clinical and Diagnostic Laboratory Immunology 4, 208212.CrossRefGoogle ScholarPubMed
Como, J, Moffa, MA, Bhanot, N, Min, Z, Cole, KS, Kuzyck, J and Walsh, TL (2019) Potential false-positive urine Legionella enzyme immunoassay test results. European Journal of Clinical Microbiology & Infectious Diseases 38, 13771382.CrossRefGoogle ScholarPubMed
Chahin, A and Opal, SM (2017) Severe pneumonia caused by Legionella pneumophila: Differential diagnosis and therapeutic considerations. Infectious Disease Clinics of North America 31, 111121.CrossRefGoogle ScholarPubMed
Cunha, BA, Burillo, A and Bouza, E (2016) Legionnaires’ disease. The Lancet 387, 376385.CrossRefGoogle ScholarPubMed
Den Boer, JW and Yzerman, EPF (2004) Diagnosis of Legionella infection in Legionnaires’ disease. European Journal of Clinical Microbiology & Infectious Diseases 23, 871878.Google ScholarPubMed
Ohno, A, Kato, N, Sakamoto, R, Kimura, S and Yamaguchi, K (2008) Temperature-dependent parasitic relationship between Legionella pneumophila and a free-living amoeba (Acanthamoeba castellanii). Applied and Environmental Microbiology 74, 45854588.CrossRefGoogle Scholar
Kuiper, MW, Wullings, BA, Akkermans, ADL, Beumer, RR and van der Kooij, D (2004) Intracellular proliferation of Legionella pneumophila in Hartmannella vermiformis in aquatic biofilms grown on plasticized polyvinyl chloride. Applied and Environmental Microbiology 70, 68266833.CrossRefGoogle ScholarPubMed
Shafi, S, Kamili, AN, Shah, MA, Parray, JA and Bandh, SA (2017) Aquatic bacterial diversity: Magnitude, dynamics, and controlling factors. Microbial Pathogenesis 104, 3947.CrossRefGoogle ScholarPubMed
Schalk, JAC, Docters van Leeuwen, AE, Lodder, WJ, de Man, H, Euser, S, den Boer, JW and de Roda Husman, AM (2012) Isolation of Legionella pneumophila from pluvial floods by amoebal coculture. Applied and Environmental Microbiology 78, 45194521.CrossRefGoogle ScholarPubMed
Wallace, CB, Burton, MG, Hefner, SG and DeWitt, TA (2013) Effect of preceding rainfall on sediment, nutrients, and bacteria in runoff from biosolids and mineral fertilizer applied to a hayfield in a mountainous region. Agricultural Water Management 130, 113118.CrossRefGoogle Scholar
Miettinen, IT, Vartiainen, T and Martikainen, PJ (1997) Phosphorus and bacterial growth in drinking water. Applied and Environmental Microbiology 63, 32423245.CrossRefGoogle ScholarPubMed
Jereb, G, Eržen, I, Oder, M and Poljšak, B (2022) Phosphate drinking water softeners promote Legionella growth. Journal of Water and Health 20, 10841090.CrossRefGoogle ScholarPubMed
Tyndall, RL and Domingue, EL (1982) Cocultivation of Legionella pneumophila and free-living amoebae. Applied and Environmental Microbiology 44, 954959.CrossRefGoogle ScholarPubMed
Lau, HY and Ashbolt, NJ (2009) The role of biofilms and protozoa in Legionella pathogenesis: Implications for drinking water. Journal of Applied Microbiology 107, 368378.CrossRefGoogle ScholarPubMed
Jang, H-J, Choi, YJ, Ro, HM and Ka, JO (2012) Effects of phosphate addition on biofilm bacterial communities and water quality in annular reactors equipped with stainless steel and ductile cast iron pipes. Journal of Microbiology 50, 1728.CrossRefGoogle ScholarPubMed
Yao, M, Elling, FJ, Jones, CA, Nomosatryo, S, Long, CP, Crowe, SA, Antoniewicz, MR, Hinrichs, KU and Maresca, JA (2016) Heterotrophic bacteria from an extremely phosphate-poor lake have conditionally reduced phosphorus demand and utilize diverse sources of phosphorus. Environmental Microbiology Reports 18, 656667.Google ScholarPubMed
Sathasivan, A, Ohgaki, S, Yamamoto, K and Kamiko, N (1997) Role of inorganic phosphorus in controlling regrowth in water distribution system. Water Science and Technology 3744.CrossRefGoogle Scholar
Bargellini, A, Marchesi, I, Righi, E, Ferrari, A, Cencetti, S, Borella, P and Rovesti, S (2011) Parameters predictive of Legionella contamination in hot water systems: Association with trace elements and heterotrophic plate counts. Water Research 45, 23152321.CrossRefGoogle ScholarPubMed
Wang, J, Li, A, Wang, Q, Zhou, Y, Fu, L and Li, Y (2010) Assessment of the manganese content of the drinking water source in Yancheng, China. Journal of Hazardous Materials 182, 259265.CrossRefGoogle ScholarPubMed
DCWASA, DC Water (2003) District of Columbia – Water and Sewer Authority – 2003 Water Quality Report. Available at https://www.dcwater.com/content/2003-water-quality-report (accessed 24 September 2021).Google Scholar
Jean Brown, M, Raymond, J, Homa, D, Kennedy, C and Sinks, T (2011) Association between children’s blood lead levels, lead service lines, and water disinfection, Washington, DC, 1998–2006. Environmental Research 111, 6774.CrossRefGoogle Scholar
Guidotti, TL, Calhoun, T, Davies-Cole, JO, Knuckles, ME, Stokes, L, Glymph, C, Lum, G, Moses, MS, Goldsmith, DF and Ragain, L (2007) Elevated lead in drinking water in Washington, DC, 2003–2004: The public health response. Environmental Health Perspectives 115, 695701.CrossRefGoogle ScholarPubMed
Appenzeller, BM, Batté, M, Mathieu, L, Block, JC, Lahoussine, V, Cavard, J and Gatel, D (2001) Effect of adding phosphate to drinking water on bacterial growth in slightly and highly corroded pipes. Water Research 35, 11001105.CrossRefGoogle ScholarPubMed
Crespí, S and Ferra, J. (1997) Outbreak of Legionellosis in a tourist complex in Lanzarote concomitant with a treatment of the water system with megadoses of polyphosphates. Water Science and Technology 307309.CrossRefGoogle Scholar
Edwards, M, Hidmi, L and Gladwell, D (2002) Phosphate inhibition of soluble copper corrosion by-product release. Corrosion Science Elsevier BV 44, 10571071.CrossRefGoogle Scholar
Stüken, A, Haverkamp, THA, Dirven, HAAM, Gilfillan, GD, Leithaug, M and Lund, V (2018) Microbial community composition of tap water and biofilms treated with or without copper-silver ionization. Environmental Science & Technology 52, 33543364.CrossRefGoogle ScholarPubMed
Triantafyllidou, S, Lytle, D, Muhlen, C and Swertfeger, J (2016) Copper-silver ionization at a US hospital: Interaction of treated drinking water with plumbing materials, aesthetics and other considerations. Water research Pergamon 102, 110.CrossRefGoogle Scholar
Figure 0

Figure 1. The visualisation of the case counts for each studied month (panel a) is reported together with the box and whisker plots both monthly across all studied years (panel b) and yearly across all months within each year (panel c).

Figure 1

Table 1. Monthly reports of Legionnaires’ disease cases for Washington, DC, from January 2001 until December 2019

Figure 2

Table 2. Monthly summaries of Legionnaires’ disease cases with the corresponding quantiles across studied years for Washington, DC, from January 2001 until December 2019

Figure 3

Table 3. Annual summaries of Legionnaires’ disease cases with the corresponding quantiles across all months within each year for Washington, DC, from January 2001 until December 2019

Figure 4

Figure 2. The visualisation of the LD case counts for each studied month (panel a) reported together with the environmental predictors such as average temperature (panel b), total precipitation (panel c), and the average wind speed (panel d). The corresponding pairwise relationships for the pairwise logit components (panels e, g, and i) and log components (panels f, h, and j) are also provided. For the logit components (panels e, g, and i), the logistic regression probability fits of zero vs non-zero counts based on the corresponding predictors are displayed in dark orange (Binomial Fit). For the log components (panels f, h, and j), the linear model fits of log non-zero counts based on the corresponding predictor are displayed in dark orange (LM Fit).

Figure 5

Table 4. The summary statistics over all months from January 2001 until December 2019 for the predictors used in the surface water model together with the corresponding measurement units

Figure 6

Table 5. The summary statistics over all months from January 2001 until December 2019 for the predictors used in the surface water model together with the corresponding measurement units

Figure 7

Table 6. The summary statistics over all months from January 2001 until December 2019 for the predictors used in the treatment plant water model together with the corresponding measurement units

Figure 8

Table 7. The summary statistics over all months from January 2001 until December 2019 for the predictors used in the treatment plant water model together with the corresponding measurement units

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