Hostname: page-component-78c5997874-xbtfd Total loading time: 0 Render date: 2024-11-15T09:22:42.517Z Has data issue: false hasContentIssue false

One Health: parasites and beyond

Published online by Cambridge University Press:  30 August 2016

DAMER P. BLAKE*
Affiliation:
Department of Pathology and Pathogen Biology, Royal Veterinary College, North Mymms, Hertfordshire, UK
MARTHA BETSON*
Affiliation:
School of Veterinary Medicine, University of Surrey, Guildford, Surrey, UK
*
*Corresponding author: Department of Pathology and Pathogen Biology, Royal Veterinary College, North Mymms, Hertfordshire, UK and School of Veterinary Medicine, University of Surrey, Guildford, Surrey, UK. E-mail: [email protected]; [email protected]
*Corresponding author: Department of Pathology and Pathogen Biology, Royal Veterinary College, North Mymms, Hertfordshire, UK and School of Veterinary Medicine, University of Surrey, Guildford, Surrey, UK. E-mail: [email protected]; [email protected]

Extract

The field of parasitism is broad, encompassing relationships between organisms where one benefits at the expense of another. Traditionally the discipline focuses on eukaryotes, with the study of bacteria and viruses complementary but distinct. Nonetheless, parasites vary in size and complexity from single celled protozoa, to enormous plants like those in the genus Rafflesia. Lifecycles range from obligate intracellular to extensive exoparasitism. Examples of parasites include high-profile medical and zoonotic pathogens such as Plasmodium, veterinary pathogens of wild and captive animals and many of the agents which cause neglected tropical diseases, stretching to parasites which infect plants and other parasites (e.g. Kikuchi et al. 2011; Hotez et al. 2014; Blake et al. 2015; Hemingway, 2015; Meekums et al. 2015; Sandlund et al. 2015). The breadth of parasitology has been matched by the variety of ways in which parasites are studied, drawing upon biological, chemical, molecular, epidemiological and other expertise. Despite such breadth bridging between disciplines has commonly been problematic, regardless of extensive encouragement from government agencies, peer audiences and funding bodies promoting multidisciplinary research. Now, progress in understanding and collaboration can benefit from establishment of the One Health concept (Zinsstag et al. 2012; Stark et al. 2015). One Health draws upon biological, environmental, medical, veterinary and social science disciplines in order to improve human, animal and environmental health, although it remains tantalizingly difficult to engage many relevant parties. For infectious diseases traditional divides have been exacerbated as the importance of wildlife reservoirs, climate change, food production systems and socio-economic diversity have been recognized but often not addressed in a multidisciplinary manner. In response the 2015 Autumn Symposium organized by the British Society for Parasitology (BSP; https://www.bsp.uk.net/home/) was focused on One Health, running under the title ‘One Health: parasites and beyond…’. The meeting, held at the Royal Veterinary College (RVC) in Camden, London from September 14th to 15th, drew upon a blend of specialist parasitology reinforced with additional complementary expertise. Scientists, advocates, policy makers and industry representatives were invited to present at the meeting, promoting and developing One Health understanding with relevance to parasitology. The decision to widen the scope of the meeting to non-parasitological, but informative topics, is reflected in the diversity of the articles included in this special issue. A key feature of the meeting was encouragement of early career scientists, with more than 35% of the delegates registered as students and 25 posters.

Type
Special Issue Review
Copyright
Copyright © Cambridge University Press 2016 

INTRODUCTION

The field of parasitism is broad, encompassing relationships between organisms where one benefits at the expense of another. Traditionally the discipline focuses on eukaryotes, with the study of bacteria and viruses complementary but distinct. Nonetheless, parasites vary in size and complexity from single celled protozoa, to enormous plants like those in the genus Rafflesia. Lifecycles range from obligate intracellular to extensive exoparasitism. Examples of parasites include high-profile medical and zoonotic pathogens such as Plasmodium, veterinary pathogens of wild and captive animals and many of the agents which cause neglected tropical diseases, stretching to parasites which infect plants and other parasites (e.g. Kikuchi et al. Reference Kikuchi, Cotton, Dalzell, Hasegawa, Kanzaki, McVeigh, Takanashi, Tsai, Assefa, Cock, Otto, Hunt, Reid, Sanchez-Flores, Tsuchihara, Yokoi, Larsson, Miwa, Maule, Sahashi, Jones and Berriman2011; Hotez et al. Reference Hotez, Alvarado, Basanez, Bolliger, Bourne, Boussinesq, Brooker, Brown, Buckle, Budke, Carabin, Coffeng, Fevre, Furst, Halasa, Jasrasaria, Johns, Keiser, King, Lozano, Murdoch, O'Hanlon, Pion, Pullan, Ramaiah, Roberts, Shepard, Smith, Stolk, Undurraga, Utzinger, Wang, Murray and Naghavi2014; Blake et al. Reference Blake, Clark, Macdonald, Thenmozhi, Kundu, Garg, Jatau, Ayoade, Kawahara, Moftah, Reid, Adebambo, Alvarez Zapata, Srinivasa Rao, Thangaraj, Banerjee, Dhinakar-Raj, Raman and Tomley2015; Hemingway, Reference Hemingway2015; Meekums et al. Reference Meekums, Hawash, Sparks, Oviedo, Sandoval, Chico, Stothard, Cooper, Nejsum and Betson2015; Sandlund et al. Reference Sandlund, Nilsen, Male, Grotmol, Kongshaug and Dalvin2015). The breadth of parasitology has been matched by the variety of ways in which parasites are studied, drawing upon biological, chemical, molecular, epidemiological and other expertise. Despite such breadth bridging between disciplines has commonly been problematic, regardless of extensive encouragement from government agencies, peer audiences and funding bodies promoting multidisciplinary research. Now, progress in understanding and collaboration can benefit from establishment of the One Health concept (Zinsstag et al. Reference Zinsstag, Meisser, Schelling, Bonfoh and Tanner2012; Stark et al. Reference Stark, Arroyo Kuribrena, Dauphin, Vokaty, Ward, Wieland and Lindberg2015). One Health draws upon biological, environmental, medical, veterinary and social science disciplines in order to improve human, animal and environmental health, although it remains tantalizingly difficult to engage many relevant parties. For infectious diseases traditional divides have been exacerbated as the importance of wildlife reservoirs, climate change, food production systems and socio-economic diversity have been recognized but often not addressed in a multidisciplinary manner. In response the 2015 Autumn Symposium organized by the British Society for Parasitology (BSP; https://www.bsp.uk.net/home/) was focused on One Health, running under the title ‘One Health: parasites and beyond…’. The meeting, held at the Royal Veterinary College (RVC) in Camden, London from September 14th to 15th, drew upon a blend of specialist parasitology reinforced with additional complementary expertise. Scientists, advocates, policy makers and industry representatives were invited to present at the meeting, promoting and developing One Health understanding with relevance to parasitology. The decision to widen the scope of the meeting to non-parasitological, but informative topics, is reflected in the diversity of the articles included in this special issue. A key feature of the meeting was encouragement of early career scientists, with more than 35% of the delegates registered as students and 25 posters.

ONE HEALTH?

There is no formal definition of One Health but at its core is the promotion of animal, human and environmental health through cross-disciplinary working. Taking a historical perspective, this concept is far from new. Until formal veterinary training was established in the 18th century, human health practitioners often treated animals (Currier & Steele, Reference Currier and Steele2011). In the 19th century, the German physician and statesman Rudolf Virchow coined the term ‘zoonosis’ and stated that ‘between animal and human medicine there are no dividing lines – nor should there be’ (Kahn et al. Reference Kahn, Kaplan and Steele2007). However, in the 20th century there was an ever increasing separation between human and veterinary medicine. It was only in the second half of this century that the close relationship between humans, animals and public health was again recognized through the work of the Canadian epidemiologist Calvin Schwabe (Schwabe, Reference Schwabe1984), where he formalized the concept of ‘One Medicine’ – a general medicine of human and animals.

The emergence of a number of zoonotic viruses with pandemic potential in the early 2000s led to a recognition of the need for greater collaboration across disciplines including human and veterinary medicine, wildlife biology, environmental science, anthropology, economics and sociology to prevent infectious disease emergence and spread (Gibbs, Reference Gibbs2014). At a meeting of the Wildlife Conservation Society in 2004, the term ‘One World-One Health’ was introduced to encompass medicine and ecosystem health, and the Manhattan principles were established promoting a holistic approach to preventing disease emergence and spread, and maintaining ecosystem integrity (Calistri et al. Reference Calistri, Iannetti, Danzetta, Narcisi, Cito, Sabatino, Bruno, Sauro, Atzeni, Carvelli and Giovannini2013). Since then, the One Health approach has gathered significant momentum, receiving official endorsement from the European Commission, the World Bank, World Health Organization (WHO), Food and Agriculture Organization of the United Nations (FAO) and the World Organization for Animal Health (OIE), among others (http://www.onehealthglobal.net).

Current definitions of ‘One Health’ abound. The Food and Agricultural Organization describes it as ‘A collaborative, international, cross-sectoral, multidisciplinary mechanism to address threats and reduce risks of detrimental infectious diseases at the animal–human–ecosystem interface’ (http://www.fao.org/ag/againfo/home/en/news_archive/2010_one-health.html), whereas the American Veterinary Medical Association takes a broader approach: ‘the collaborative efforts of multiple disciplines working locally, nationally and globally to attain optimal health for people, animals and our environment’ (https:// www.avma.org/KB/Resources/Reference/Pages/One-Health94.aspx). The One Health Initiative definition follows in a similar vein, describing One Health as ‘a worldwide strategy for expanding interdisciplinary collaborations and communications in all aspects of health care for humans, animals and the environment’ (http://www.onehealthinitiative.com/about.php). In contrast, Zinsstag et al. proposed an operational definition of One Health focusing on the added value in terms of human and animal health or cost savings or environmental and social benefits that can be achieved through professionals from different disciplines working together (Zinsstag et al. Reference Zinsstag, Meisser, Schelling, Bonfoh and Tanner2012). It has been suggested that the flexibility of the One Health concept is part of its success as it can be adapted to suit the missions of different organizations (Gibbs, Reference Gibbs2014).

One confusing aspect of the varying definitions of One Health is the apparently interchangeable use of the words ‘multidisciplinary’ and ‘interdisciplinary’. These terms actually have different definitions with ‘multidisciplinary’ referring to projects involving experts from different disciplines who remain within their area of expertise over the course of the project. Interpretation and integration of results from different disciplines often occurs only at the end of the project. In contrast, in ‘interdisciplinary’ projects, experts from various fields collaborate closely throughout the course of the project, integrating and synthesizing ideas and methodologies from different disciplines with the potential to generate new research questions and approaches (Eigenbrode et al. Reference Eigenbrode, O'Rourke, Wulfhorst, Althoff, Goldberg, Merrill, Morse, Nielsen-Pincus, Stephens, Winowiecki and Bosque-Perez2007; Moore et al. Reference Moore, Dilmore and Robinson2011; Conrad et al. Reference Conrad, Meek and Dumit2013). Going beyond interdisciplinarity, a ‘transdisciplinary’ approach cuts across disciplines where project participants use a common conceptual framework integrating theories and methods of different disciplines to address a shared problem. Participation of community members and key stakeholders in developing the conceptual framework and shared approach is an important aspect of transdisciplinary projects (Min et al. Reference Min, Allen-Scott and Buntain2013; Allen-Scott et al. Reference Allen-Scott, Buntain, Hatfield, Meisser and Thomas2015). It has been argued that the One Health approach is transdisciplinary by its very nature (Mazet et al. Reference Mazet, Clifford, Coppolillo, Deolalikar, Erickson and Kazwala2009) and certainly the application of transdisciplinarity to One Health projects has great potential (Min, Reference Min, Allen-Scott and Buntain2013).

THE BRITISH SOCIETY FOR PARASITOLOGY AUTUMN SYMPOSIUM, 2015

This special issue contains a series of invited reviews drawn from the BSP Autumn Symposium. The first, provided by Pete Kingsley and Emma Taylor, introduces the concept of ‘One Health’ and considers what the term actually means (Kingsley & Taylor, Reference Kingsley and Taylor2016). An enormous volume of activity has been advertised as One Health; some merely rebranding existing pursuits, others pushing at fundamental boundaries and genuinely creating new connections. The control of African trypanosomiasis provides an historic example of One Health in action, even before the birth of the term. The authors highlight the importance of improved information and fairer approaches, expanding the remit of assessments beyond individual-specific medical, veterinary or environmental concerns. Assessing not only the impact of pathogens and interventions, but also the intrinsic value of human and animal welfare, food safety, security, and the environment, provides a natural entrée to the paper presented by Rushton and Bruce in this issue (Rushton & Bruce, Reference Rushton and Bruce2016). The need for flexibility is emphasized, with views evolving as more information becomes available or situations change.

Building on an understanding of One Health it becomes clear that assessing losses caused by parasitic disease, even if we incorporate the direct cost of controlling the disease, fails to reveal the true impact. For human pathogens disability adjusted life years (DALYs) have been developed to provide a single measure of total disease burden, presented as the number of years lost as a consequence of ill-health, disability or early death (Fernandez Martin et al. Reference Fernandez Martin, Pereira Candel and Torres Cantero1995). Despite creation of the DALYs measure the true cost of many diseases of humans remains underestimated, with the inaccuracy magnified for zoonotic diseases where veterinary costs are commonly poorly defined. Further, difficulty quantifying indirect costs such as resources used or lost, impact on services and other social or environmental factors adds yet more uncertainty. In their paper presented here, Johnathan Rushton and Mieghan Bruce assess the approaches, which might be taken to identify One Health variables and include them in a quantifiable metric (Rushton & Bruce, Reference Rushton and Bruce2016). Taking avian coccidiosis caused by the protozoan Eimeria species as an example, the authors begin to explore application of quantifiable One Health cost matrices. The cost attributed to coccidiosis may be as high as $3 billion per annum, although estimates vary by tenfold or greater (Blake & Tomley, Reference Blake and Tomley2014). Indicators of environmental and social impact are suggested for inclusion in forthcoming quantitative analysis.

There have been increasing reports of emerging infectious diseases (EIDs) over the past few decades. EIDs include new diseases caused by novel pathogens, such as the highly publicized emergence of severe acute respiratory syndrome (SARS) in China in 2002, and existing diseases which spread into new areas, as exemplified by the recent outbreak of Ebola virus disease in West Africa. In their review, Bryony Jones, Martha Betson and Dirk Pfeiffer (Jones et al. Reference Jones, Betson and Pfeiffer2016) contend that anthropogenic changes to the global ecosystem are drivers of disease emergence and identify important eco-social processes, which may play a role including human population growth, urbanization, increasing mobility and connectedness, inequality, increasing consumption, habitat destruction, biodiversity loss and climate change. They go on to illustrate the impact of human activity on emergence of infectious diseases using examples from different continents. Finally, given the complexity and connectedness of the eco-social processes, which can drive disease emergence and spread, the authors argue that management of disease threats requires a systems-based One Health approach, citing appropriate theoretical frameworks which could be adopted.

In a more practical offering Rachel Chalmers and colleagues recommend development and agreement of a standardized genotyping approach for Cryptosporidium diagnosis, surveillance and outbreak investigation (Chalmers et al. Reference Chalmers, Robinson, Hotchkiss, Alexander, May, Gilray, Connelly and Hadfield2016). Cryptosporidium parvum is a major cause of livestock and zoonotic cryptosporidiosis. Morphological approaches are limited to genus-level identification, as indicated by the relatively recent differentiation of species such as C. parvum and Cryptosporidium hominis with molecular and epidemiological support (Abrahamsen et al. Reference Abrahamsen, Templeton, Enomoto, Abrahante, Zhu, Lancto, Deng, Liu, Widmer, Tzipori, Buck, Xu, Bankier, Dear, Konfortov, Spriggs, Iyer, Anantharaman, Aravind and Kapur2004; Xu et al. Reference Xu, Widmer, Wang, Ozaki, Alves, Serrano, Puiu, Manque, Akiyoshi, Mackey, Pearson, Dear, Bankier, Peterson, Abrahamsen, Kapur, Tzipori and Buck2004). Sequence analysis of targets including the 18S ribosomal DNA and glycoprotein 60 (gp60) were widely employed and offer value for money (Cardona et al. Reference Cardona, Carabin, Goni, Arriola, Robinson, Fernandez-Crespo, Clavel, Chalmers and Carmena2011; Chalmers et al. Reference Chalmers, Smith, Hadfield, Elwin and Giles2011). Greater detail has been achieved using multi-locus sequence typing, although the relative cost is greater (Ramo et al. Reference Ramo, Quilez, Del Cacho and Sanchez-Acedo2014). Recent protocols which support whole-genome sequencing of Cryptosporidium isolated directly from fecal samples may well replace these tools in time (Hadfield et al. Reference Hadfield, Pachebat, Swain, Robinson, Cameron, Alexander, Hegarty, Elwin and Chalmers2015), but at present cost-effective, robust and reproducible assays are urgently required to facilitate comparison of results between studies and laboratories. Currently, variable number of tandem repeat (VNTR) and associated variation in polymerase chain reaction (PCR) amplicon size, offer a reasonable solution. In the work presented, Chalmers et al. compare a panel of nine VNTR-based markers across multiple samples assessed in three different laboratories. They found some loci to present unexpectedly complex repeat units, weakening their value to routine analysis, and take a significant step towards standardization of tools for molecular C. parvum genotyping. At this time it is clear that additional markers are still required as the research community drives towards a consistent nomenclature for these parasites.

Stepping back in time, Piers Mitchell's article demonstrates how a combination of parasitology, anthropology and historical research can provide insights into human infection and disease in the previous generations (Mitchell, Reference Mitchell2016). He focuses on the Roman Empire and investigates whether ‘Romanization’ altered the balance of parasitic infection in people living in Europe and the Mediterranean region. Interestingly, despite substantial improvements in hygiene and sanitation during this period, gastrointestinal parasites such as Trichuris and Ascaris infections were widespread and fish tapeworm and ectoparasites such as lice and fleas were also present. The author discusses these findings in relation to what is known about the Roman diet and farming and bathing practices. He also reflects on what Roman physicians believed about intestinal worms and how to treat them. This article provides an excellent illustration of how different complementary disciplines can be successfully integrated to address a research question.

The neglected tropical diseases and neglected zoonotic diseases have received increasing attention over the past few years and new goals have been set for control and elimination at a regional and global level (WHO, 2012). One such neglected zoonosis is Taenia solium taeniosis/cysticercosis (TSTC), which the World Health Organization (WHO) considers to be an eradicable disease and has decided to target for elimination in certain endemic countries (WHO, 2015). In their article, Maria Vang Johansen and colleagues reflect on why no endemic country has managed to eliminate T. solium (Johansen et al. Reference Johansen, Trevisan, Gabriel, Magnussen and Braae2016). They identify a number of factors including an inadequate understanding of social factors, which influence transmission and the fact that neither the medical nor veterinary services want to take responsibility for control. The authors then describe a theoretical model of T. solium transmission in an endemic area and use this model to predict the effect of various intervention strategies on taeniosis in humans and cystercercosis in pigs. Based on model simulations, an integrated One Health approach combining interventions in humans and pigs would be able to reduce disease significantly in both species. However, this approach does not appear to be sufficient to achieve elimination of TSTC, thus highlighting the need to set realistic targets for control, before aiming for elimination.

Over the last decade the relevance of animal reservoirs to the (re)emergence of infectious agents has become well defined (Morens et al. Reference Morens, Folkers and Fauci2004). Protozoan parasites have been highlighted as posing a particular risk in contrast to helminths (Taylor et al. Reference Taylor, Latham and Woolhouse2001), possibly a consequence of the latter's greater complexity, longer generation time and size. Nonetheless, novel helminths have been described. Hybrid and/or introgressed Fasciola derived from Fasciola hepatica and Fasciola gigantica have been described across much of Asia with relevance to veterinary and human health (Le et al. Reference Le, De, Agatsuma, Thi Nguyen, Nguyen, McManus and Blair2008). Similarly, hybridization and/or introgression between Schistosoma species have been well documented in recent years and now reviewed here by Elsa Leger and Joanne Webster. The authors review multiple examples of hybridization between Schistosoma species, which traditionally infect humans, livestock, and humans and livestock. Intriguingly, reports of hybrid schistosomes date back many decades with multiple examples from the 1950s and 1960s (Leger and Webster, Reference Leger and Webster2016). The authors describe the ways in which hybrid schistosomes have been defined, including egg morphology and several molecular approaches, before focusing on possible drivers towards hybridization such as human interventions like dam construction and changes to farming which impact on the snail intermediate host, as well as the selection imposed by mass drug administration. The emergence of novel parasite genotypes with expanded host ranges and/or altered pathogenicity bears obvious significance to human and veterinary medicine, once again posing problems in the assessment of cost and development of effective control(s).

Zoonotic parasites are a global concern as demonstrated in Celia Holland's article (Holland, Reference Holland2015). This review provides a comprehensive overview of the latest research into the biology, epidemiology and public health impact of the roundworm Toxocara and highlights the important gaps, which exist in our understanding of this cosmopolitan parasite. The author describes the multiple manifestations of toxocariasis in humans, while stressing the difficulties of diagnosing this disease and of linking exposure to clinical presentation. The important role which vets can play, both in treatment of infected animals and in education of pet owners and the general public about the importance of Toxocara as a zoonotic infection, is discussed. The review draws attention to our poor understanding of the relative contribution of paratenic hosts and environmental contamination with fox, dog and cat feces to Toxocara transmission and illustrates how mathematical modelling approaches can shed light on this question. Finally, the author proposes a One Health framework for research into this enigmatic parasite.

In the final paper of this special issue, Shazia Hosein and colleagues review the current understanding of adaptive and innate immune responses against Leishmania infection in dogs. The outcome of infection by many Leishmania species is strongly influenced by the nature of the initial immune response. Induction of a predominantly Th1-type immune response, featuring CD4+ T cell expansion and elevated interferon gamma (IFNγ) production, commonly associates with a positive outcome as the host controls the infection. Contrastingly, induction of a Th2-type immune response correlates with susceptibility to infection, with interleukin (IL)-4 a key determining factor (Hosein et al. Reference Hosein, Blake and Solano-Gallego2016). The authors provide a thorough, organ-by-organ summary of immune responses induced during Leishmania infection in dogs, before discussing the small number of anti-Leishmania vaccines currently available for dogs in some markets.

Concluding remarks

The necessity of combining medical, veterinary and environmental strands in order to improve opportunities to resolve global health concerns coalesced into the One Health concept more than ten years ago as an evolution from One Medicine (Zinsstag et al. Reference Zinsstag, Meisser, Schelling, Bonfoh and Tanner2012). Nonetheless, despite the rapid proliferation of peer reviewed manuscripts within the One Health remit effective integration remains a challenge. In a recent systematic review, social network analysis of interdisciplinarity in One Health publications revealed three distinct, albeit overlapping communities representing ecologists, veterinarians and a diverse assembly of population biologists, mathematicians, epidemiologists and experts in human health (Manlove et al. Reference Manlove, Walker, Craft, Huyvaert, Joseph, Miller, Nol, Patyk, O'Brien, Walsh and Cross2016). Recognition of these persistent gaps, as well as the resultant opportunities, has prompted establishment of One Health educational openings in many institutions and societies such as the British Society for Parasitology. Improved interactions between academia and other stakeholders, including medicine, animal production, health and food user groups, can fast track global development and implementation of innovative science, and promote dissemination of key outputs. Examples include assessment and development of integrated pathogen monitoring, evaluation and control strategies, as well as development of novel research proposals supported by access to new research partners.

ACKNOWLEDGEMENTS

The BSP and organizers of the 2015 Autumn Symposium would like to acknowledge the kind support provided by Merck Animal Health and Ceva as meeting sponsors. Institutional support provided by the Royal Veterinary College, London School of Hygiene & Tropical Medicine and London International Development Centre was also much appreciated as an integral part of the meetings success.

FINANCIAL SUPPORT

This research received no specific grant from any funding agency, commercial or not-for-profit sectors.

References

REFERENCES

Abrahamsen, M. S., Templeton, T. J., Enomoto, S., Abrahante, J. E., Zhu, G., Lancto, C. A., Deng, M., Liu, C., Widmer, G., Tzipori, S., Buck, G. A., Xu, P., Bankier, A. T., Dear, P. H., Konfortov, B. A., Spriggs, H. F., Iyer, L., Anantharaman, V., Aravind, L. and Kapur, V. (2004). Complete genome sequence of the apicomplexan, Cryptosporidium parvum . Science 304, 441445.CrossRefGoogle ScholarPubMed
Allen-Scott, L. K., Buntain, B., Hatfield, J. M., Meisser, A. and Thomas, C. J. (2015). Academic institutions and One Health: building capacity for transdisciplinary research approaches to address complex health issues at the animal–human–ecosystem interface. Academic Medicine 90, 866871.CrossRefGoogle ScholarPubMed
Blake, D. P. and Tomley, F. M. (2014). Securing poultry production from the ever-present Eimeria challenge. Trends in Parasitology 30, 1219.CrossRefGoogle ScholarPubMed
Blake, D. P., Clark, E. L., Macdonald, S. E., Thenmozhi, V., Kundu, K., Garg, R., Jatau, I. D., Ayoade, S., Kawahara, F., Moftah, A., Reid, A. J., Adebambo, A. O., Alvarez Zapata, R., Srinivasa Rao, A. S., Thangaraj, K., Banerjee, P. S., Dhinakar-Raj, G., Raman, M. and Tomley, F. M. (2015). Population, genetic, and antigenic diversity of the apicomplexan Eimeria tenella and their relevance to vaccine development. Proceedings of the National Academy of Sciences of the United States of America 112, E5343E5350.Google ScholarPubMed
Calistri, P., Iannetti, S., Danzetta, M. L., Narcisi, V., Cito, F., Sabatino, D. D., Bruno, R., Sauro, F., Atzeni, M., Carvelli, A. and Giovannini, A. (2013). The components of ‘One World – One Health’ approach. Transboundary and Emerging Diseases 60 (Suppl. 2), 413.CrossRefGoogle ScholarPubMed
Cardona, G. A., Carabin, H., Goni, P., Arriola, L., Robinson, G., Fernandez-Crespo, J. C., Clavel, A., Chalmers, R. M. and Carmena, D. (2011). Identification and molecular characterization of Cryptosporidium and Giardia in children and cattle populations from the province of Alava, North of Spain. The Science of the Total Environment 412–413, 101108.CrossRefGoogle ScholarPubMed
Chalmers, R. M., Smith, R. P., Hadfield, S. J., Elwin, K. and Giles, M. (2011). Zoonotic linkage and variation in Cryptosporidium parvum from patients in the United Kingdom. Parasitology Research 108, 13211325.CrossRefGoogle ScholarPubMed
Chalmers, R. M., Robinson, G., Hotchkiss, E., Alexander, C., May, S., Gilray, J., Connelly, L. and Hadfield, S. J. (2016). Suitability of loci for multiple-locus variable-number of tandem-repeats analysis of Cryptosporidium parvum for inter-laboratory surveillance and outbreak investigations. Parasitology 143, 00–00.Google Scholar
Conrad, P. A., Meek, L. A. and Dumit, J. (2013). Operationalizing a One Health approach to global health challenges. Comparative Immunology Microbiology and Infectious Diseases 36, 211216.CrossRefGoogle ScholarPubMed
Currier, R. W. and Steele, J. H. (2011). One Health-One Medicine: unifying human and animal medicine within an evolutionary paradigm. Annals of the New York Academy of Sciences 1230, 411.CrossRefGoogle ScholarPubMed
Eigenbrode, S. D., O'Rourke, M., Wulfhorst, J. D., Althoff, D. M., Goldberg, C. S., Merrill, K., Morse, W., Nielsen-Pincus, M., Stephens, J., Winowiecki, L. and Bosque-Perez, N. A. (2007). Employing philosophical dialogue in collaborative science. Bioscience 57, 5564.CrossRefGoogle Scholar
Fernandez Martin, J., Pereira Candel, J. and Torres Cantero, A. (1995). An agenda to debate: the World Bank report investing in health. Revista Espanola de Salud Publica 69, 385391.Google ScholarPubMed
Gibbs, E. P. (2014). The evolution of One Health: a decade of progress and challenges for the future. Veterinary Record 174, 8591.CrossRefGoogle ScholarPubMed
Hadfield, S. J., Pachebat, J. A., Swain, M. T., Robinson, G., Cameron, S. J., Alexander, J., Hegarty, M. J., Elwin, K. and Chalmers, R. M. (2015). Generation of whole genome sequences of new Cryptosporidium hominis and Cryptosporidium parvum isolates directly from stool samples. BMC Genomics 16, 650.CrossRefGoogle ScholarPubMed
Hemingway, J. (2015). Malaria: fifteen years of interventions. Nature 526, 198199.CrossRefGoogle ScholarPubMed
Holland, C. V. (2015). Knowledge gaps in the epidemiology of Toxocara: the enigma remains. Parasitology 143, 00–00.Google Scholar
Hosein, S., Blake, D. P. and Solano-Gallego, L. (2016). Insights on adaptive and innate immunity in canine leishmaniosis. Parasitology 121. Published online 20 April 2016. doi: 10.1017/S003118201600055X.Google ScholarPubMed
Hotez, P. J., Alvarado, M., Basanez, M. G., Bolliger, I., Bourne, R., Boussinesq, M., Brooker, S. J., Brown, A. S., Buckle, G., Budke, C. M., Carabin, H., Coffeng, L. E., Fevre, E. M., Furst, T., Halasa, Y. A., Jasrasaria, R., Johns, N. E., Keiser, J., King, C. H., Lozano, R., Murdoch, M. E., O'Hanlon, S., Pion, S. D., Pullan, R. L., Ramaiah, K. D., Roberts, T., Shepard, D. S., Smith, J. L., Stolk, W. A., Undurraga, E. A., Utzinger, J., Wang, M., Murray, C. J. and Naghavi, M. (2014). The global burden of disease study 2010: interpretation and implications for the neglected tropical diseases. PLoS Neglected Tropical Diseases 8, e2865.CrossRefGoogle ScholarPubMed
Johansen, M. V., Trevisan, C., Gabriel, S., Magnussen, P. and Braae, U. C. (2016). Are we ready for Taenia solium cysticercosis elimination in sub-Saharan Africa? Parasitology 143, 00–00.Google Scholar
Jones, B. A., Betson, M. and Pfeiffer, D. U. (2016). Eco-social processes influencing infectious disease emergence and spread. Parasitology, 143, 00–00.Google Scholar
Kahn, L. H., Kaplan, B. and Steele, J. H. (2007). Confronting zoonoses through closer collaboration between medicine and veterinary medicine (as ‘one medicine’). Veterinaria Italiana 43, 519.Google ScholarPubMed
Kikuchi, T., Cotton, J. A., Dalzell, J. J., Hasegawa, K., Kanzaki, N., McVeigh, P., Takanashi, T., Tsai, I. J., Assefa, S. A., Cock, P. J., Otto, T. D., Hunt, M., Reid, A. J., Sanchez-Flores, A., Tsuchihara, K., Yokoi, T., Larsson, M. C., Miwa, J., Maule, A. G., Sahashi, N., Jones, J. T. and Berriman, M. (2011). Genomic insights into the origin of parasitism in the emerging plant pathogen Bursaphelenchus xylophilus . PLoS Pathogens 7, e1002219.CrossRefGoogle ScholarPubMed
Kingsley, P. and Taylor, E. M. (2016). One Health: competing perspectives in an emerging field. Parasitology 143, 00–00.Google Scholar
Le, T. H., De, N. V., Agatsuma, T., Thi Nguyen, T. G., Nguyen, Q. D., McManus, D. P. and Blair, D. (2008). Human fascioliasis and the presence of hybrid/introgressed forms of Fasciola hepatica and Fasciola gigantica in Vietnam. International Journal for Parasitology 38, 725730.CrossRefGoogle ScholarPubMed
Leger, E. and Webster, J. P. (2016). Hybridizations within the genus Schistosoma: implications for evolution, epidemiology and control. Parasitology, 143, 00–00.Google Scholar
Manlove, K. R., Walker, J. G., Craft, M. E., Huyvaert, K. P., Joseph, M. B., Miller, R. S., Nol, P., Patyk, K. A., O'Brien, D., Walsh, D. P. and Cross, P. C. (2016). “One Health” or Three? publication silos among the One Health Disciplines. PLoS Biology 14, e1002448. doi: 10.1371/journal.pbio.1002448.CrossRefGoogle ScholarPubMed
Mazet, J. A. K., Clifford, D. L., Coppolillo, P. B., Deolalikar, A. B., Erickson, J. D. and Kazwala, R. R. (2009). A “One Health” approach to address emerging zoonoses: the HALI project in Tanzania. Plos Medicine 6. doi: ARTN e100019010.1371/journal.pmed.1000190.CrossRefGoogle Scholar
Meekums, H., Hawash, M. B., Sparks, A. M., Oviedo, Y., Sandoval, C., Chico, M. E., Stothard, J. R., Cooper, P. J., Nejsum, P. and Betson, M. (2015). A genetic analysis of Trichuris trichiura and Trichuris suis from Ecuador. Parasit Vectors 8, 168.CrossRefGoogle ScholarPubMed
Min, B., Allen-Scott, L. K. and Buntain, B. (2013). Transdisciplinary research for complex One Health issues: a scoping review of key concepts. Preventive Veterinary Medicine 112, 222229.CrossRefGoogle ScholarPubMed
Mitchell, P. D. (2016). Human parasites in the Roman World: health consequences of conquering an empire. Parasitology 143, 00–00.Google Scholar
Moore, D. W., Dilmore, T. C. and Robinson, G. F. W. B. (2011). Advancing knowledge and research: developing a doctoral program in clinical and translational science. Cts – Clinical and Translational Science 4, 359362.CrossRefGoogle ScholarPubMed
Morens, D. M., Folkers, G. K. and Fauci, A. S. (2004). The challenge of emerging and re-emerging infectious diseases. Nature 430, 242249.CrossRefGoogle ScholarPubMed
Ramo, A., Quilez, J., Del Cacho, E. and Sanchez-Acedo, C. (2014). Optimization of a fragment size analysis tool for identification of Cryptosporidium species and Gp60 alleles infecting domestic ruminants. Veterinary Parasitology 205, 466471.CrossRefGoogle ScholarPubMed
Rushton, J. and Bruce, M. (2016). Using a One Health approach to assess the impact of parasitic disease in livestock: how does it add value? Parasitology 143, 00–00.Google Scholar
Sandlund, L., Nilsen, F., Male, R., Grotmol, S., Kongshaug, H. and Dalvin, S. (2015). Molecular characterisation of the salmon louse, Lepeophtheirus salmonis salmonis (Kroyer, 1837), ecdysone receptor with emphasis on functional studies of female reproduction. International Journal for Parasitology 45, 175185.CrossRefGoogle ScholarPubMed
Schwabe, C. (1984). Veterinary Medicine and Human Health, 3rd Edn. Baltimore, USA, Williams & Wilkins.Google Scholar
Stark, K. D., Arroyo Kuribrena, M., Dauphin, G., Vokaty, S., Ward, M. P., Wieland, B. and Lindberg, A. (2015). One Health surveillance – more than a buzz word? Preventive Veterinary Medicine 120, 124130.CrossRefGoogle ScholarPubMed
Taylor, L. H., Latham, S. M. and Woolhouse, M. E. (2001). Risk factors for human disease emergence. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 356, 983989.CrossRefGoogle ScholarPubMed
WHO (2012). Accelerating work to overcome the global impact of neglected tropical diseases. A roadmap for implementation. http://www.who.int/neglected_diseases/NTD_RoadMap_2012_Fullversion.pdf Google Scholar
WHO (2015). Assembling a framework for intensified control of taeniasis and neurocysticercosis caused by Taenia solium. Report of an informal consultation. http://apps.who.int/iris/bitstream/10665/153237/1/9789241508452_eng.pdf Google Scholar
Xu, P., Widmer, G., Wang, Y., Ozaki, L. S., Alves, J. M., Serrano, M. G., Puiu, D., Manque, P., Akiyoshi, D., Mackey, A. J., Pearson, W. R., Dear, P. H., Bankier, A. T., Peterson, D. L., Abrahamsen, M. S., Kapur, V., Tzipori, S. and Buck, G. A. (2004). The genome of Cryptosporidium hominis . Nature 431, 11071112.CrossRefGoogle ScholarPubMed
Zinsstag, J., Meisser, A., Schelling, E., Bonfoh, B. and Tanner, M. (2012). From ‘two medicines’ to ‘One Health’ and beyond. Onderstepoort Journal of Veterinary Research 79, 492.CrossRefGoogle ScholarPubMed