Hostname: page-component-586b7cd67f-gb8f7 Total loading time: 0 Render date: 2024-11-27T18:16:37.116Z Has data issue: false hasContentIssue false

Using molecular network analysis to understand current HIV-1 transmission characteristics in an inland area of Yunnan, China

Published online by Cambridge University Press:  18 July 2023

Rui Cao
Affiliation:
School of Public Health, Kunming Medical University, Kunming, China
Shouxiong Lei
Affiliation:
Division for AIDS/STD Control and Prevention, Zhaotong Center for Disease Control and Prevention, Zhaotong, China
Huichao Chen
Affiliation:
Institute for AIDS/STD Control and Prevention, Yunnan Center for Disease Control and Prevention, Kunming, China
Yanling Ma
Affiliation:
Institute for AIDS/STD Control and Prevention, Yunnan Center for Disease Control and Prevention, Kunming, China
Jie Dai
Affiliation:
Institute for AIDS/STD Control and Prevention, Yunnan Center for Disease Control and Prevention, Kunming, China
Lijuan Dong
Affiliation:
Institute for AIDS/STD Control and Prevention, Yunnan Center for Disease Control and Prevention, Kunming, China
Xiaomei Jin
Affiliation:
Institute for AIDS/STD Control and Prevention, Yunnan Center for Disease Control and Prevention, Kunming, China
Min Yang
Affiliation:
Institute for AIDS/STD Control and Prevention, Yunnan Center for Disease Control and Prevention, Kunming, China
Pengyan Sun
Affiliation:
Institute for AIDS/STD Control and Prevention, Yunnan Center for Disease Control and Prevention, Kunming, China
Yawen Wang
Affiliation:
School of Public Health, Kunming Medical University, Kunming, China
Yuying Zhang
Affiliation:
School of Public Health, Kunming Medical University, Kunming, China
Manhong Jia*
Affiliation:
Institute for AIDS/STD Control and Prevention, Yunnan Center for Disease Control and Prevention, Kunming, China
Min Chen*
Affiliation:
Health Laboratory Center, Yunnan Center for Disease Control and Prevention, Kunming, China
*
Corresponding authors: Min Chen and Manhong Jia; Emails: [email protected]; [email protected]
Corresponding authors: Min Chen and Manhong Jia; Emails: [email protected]; [email protected]
Rights & Permissions [Opens in a new window]

Abstract

HIV-1 molecular surveillance provides a new approach to explore transmission risks and targeted interventions. From January to June 2021, 663 newly reported HIV-1 cases were recruited in Zhaotong City, Yunnan Province, China. The distribution characteristics of HIV-1 subtypes and HIV-1 molecular network were analysed. Of 542 successfully subtyped samples, 12 HIV-1 strains were identified. The main strains were CRF08_BC (47.0%, 255/542), CRF01_AE (17.0%, 92/542), CRF07_BC (17.0%, 92/542), URFs (8.7%, 47/542), and CRF85_BC (6.5%, 35/542). CRF08_BC was commonly detected among Zhaotong natives, illiterates, and non-farmers and was mostly detected in Zhaoyang County. CRF01_AE was frequently detected among married and homosexual individuals and mostly detected in Weixin and Zhenxiong counties. Among the 516 pol sequences, 187 (36.2%) were clustered. Zhaotong natives, individuals aged ≥60 years, and illiterate individuals were more likely to be found in the network. Assortativity analysis showed that individuals were more likely to be genetically associated when stratified by age, education level, occupation, and reporting area. The genetic diversity of HIV-1 reflects the complexity of local HIV epidemics. Molecular network analyses revealed the subpopulations to focus on and the characteristics of the risk networks. The results will help optimise local prevention and control strategies.

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

Since the recognition of acquired immune deficiency syndrome (AIDS) in 1981 and the discovery of human immunodeficiency virus (HIV) in 1983, the HIV epidemic has remained a major public health problem worldwide [Reference Hemelaar1]. According to the UNAIDS data [2], by the end of 2021, 38.4 million people were living with HIV globally. In 2021, 1.5 million people were newly infected with HIV and 650,000 people died from AIDS-related illnesses. Meanwhile, the rapid replication rate, error-prone reverse transcription, and frequent genetic recombination make HIV highly variable [Reference Hemelaar, Elangovan, Yun, Dickson-Tetteh, Fleminger, Kirtley, Williams, Gouws-Williams and Ghys3, Reference Hemelaar, Loganathan, Elangovan, Yun, Dickson-Tetteh and Kirtley4], hindering the development of biomedical approaches for prevention and treatment [Reference Korber, Hraber, Wagh and Hahn5, Reference Haynes, Wiehe, Borrow, Saunders, Korber, Wagh, McMichael, Kelsoe, Hahn, Alt and Shaw6].

The transmission of HIV/AIDS is complex and influenced by a variety of social and biological factors. Social discrimination and privacy issues make it difficult to trace the sources of infection and effectively stop transmission. Therefore, the accurate identification of HIV transmission is the first step in public health interventions [Reference Frieden, das-Douglas, Kellerman and Henning7]. Even with the 90–90–90 strategy for HIV/AIDS control and prevention, the key measures are to identify populations at high risk of HIV transmission and to prioritise resources for treatment and prevention [8]. In recent years, the use of HIV-1 molecular network analysis has increased [Reference Han, Zhao, An, Zhong and Shang9Reference Poon, Gustafson, Daly, Zerr, Demlow, Wong, Woods, Hogg, Krajden, Moore, Kendall, Montaner and Harrigan12]. Phylogenetic analysis, genetic distance analysis, and a combination of both methods are used to identify HIV-1 molecular networks [Reference Han, Zhao, An, Zhong and Shang9, 13]. In the phylogenetic tree approach, a cluster is identified as a molecular network if its node support value is within a specified range. The gene distance method uses a specific gene distance threshold between sequences to determine the molecular network [14]. As the genetic distance is related to the evolution of the virus, it can reflect the proximity of the time of transmission [14]. Thus, some HIV-1 molecular network studies using phylogenies have also added a genetic distance component. In practice, the choice of methods depends on the characteristics of the data and research objectives. Transmission networks can be further inferred from molecular networks when combined with epidemiological information, providing a basis for risk assessment [Reference Xia, Wertheim, Braunstein, Misra, Udeagu and Torian15Reference McLaughlin, Sereda, Oliveira, Barrios, Brumme, Brumme, Montaner and Joy18]. In addition to retrospective analysis, real-time molecular surveillance provides a tool for identifying and responding to rapid HIV transmission in communities, which can slow or even prevent HIV outbreaks [Reference Poon, Gustafson, Daly, Zerr, Demlow, Wong, Woods, Hogg, Krajden, Moore, Kendall, Montaner and Harrigan12]. Consequently, real-time detection and response to HIV clusters are considered a key strategy for ending the HIV epidemic [Reference Fauci, Redfield, Sigounas, Weahkee and Giroir11].

Yunnan Province is located in southwest China bordering Myanmar, Laos, and Vietnam. Because of its proximity to the Golden Triangle, HIV entered Yunnan through drug traffic. In 1989, HIV epidemics were first reported among intravenous drug users in the western border area of Yunnan [Reference Lu, Jia, Ma, Yang, Chen, Ho, Jiang and Zhang19]. After that, the HIV epidemic developed rapidly, and Yunnan became one of the areas hardest hit by HIV/AIDS in China. After 2006, heterosexual contact replaced intravenous drug use as the predominant mode of transmission in Yunnan [Reference Jia, Luo, Ma, Wang, Smith, Mei, Lu, Lu, Fu, Zhang, Wu and Lu20]. According to a series of retrospective molecular epidemiological studies, the major HIV-1 strains circulating in China are associated with Yunnan Province [Reference Lu, Jia, Ma, Yang, Chen, Ho, Jiang and Zhang19, Reference Meng, Xin, Zhong, Zhang, Abubakar, Li, Liu, Zhang and Xu21Reference Li, He, Wang, Xing, Li, Yang, Wang, Takebe and Shao23]. For example, CRF07_BC and CRF08_BC were generated by the recombination of subtypes B and C in Yunnan and were transmitted to other parts of China [Reference Feng, Takebe, Wei, He, Hsi, Li, Xing, Ruan, Yang, Li, Wei, Li and Shao22]. In addition, Yunnan has become a genetic reservoir for HIV-1, and to date, more than 17 circulating recombinant forms (CRFs) have been identified in Yunnan.

Although the HIV-1 epidemic started in border areas, it gradually spread inland. Zhaotong City, which covers 11 counties with a population of 501.4 million, is located in the northeastern part of Yunnan Province, bordering Sichuan Province to the northwest and Guizhou Province to the east and is an important gateway to Sichuan and Guizhou provinces. By the end of 2020, the cumulative number of people living with HIV/AIDS (PLWHA) in Zhaotong City was 7,805, of which 7,188 (92.1%) were receiving antiretroviral therapy (ART). In 2020, the number of newly reported infections in Zhaotong City ranked third in Yunnan Province. Meanwhile, heterosexual transmission has continued to increase. In particular, more than 30% of cases were detected late, with CD4+T lymphocyte counts below 200 cells/μl. This suggests that the local HIV epidemic is still complex and that the risk of transmission remains. To control the HIV-1 epidemic, it is necessary to understand its transmission characteristics and risk networks. In combination with the 90–90–90 strategy, effective detection and intervention measures should be developed. To this end, a molecular epidemiological study combined with social network analysis was conducted in Zhaotong City.

Methods

Study participants and sample collection

From January to June 2021, 671 HIV/AIDS cases were newly reported in Zhaotong City, of which 663 (98.8%) were recruited for this study. The inclusion criteria were as follows: (1) AIDS patients aged 15 years and above and (2) those willing to participate in the survey and sign an informed consent form. This study was approved by the Research Ethics Review Committee of the Yunnan Center for Disease Control and Prevention (YNCDC-ER-202108). Written informed consent was provided by adults and legal guardians. All methods were performed in accordance with relevant guidelines and regulations.

Amplification and sequencing of HIV-1 gene fragments

HIV-1 viral RNA was extracted from 140 μl of plasma using a QIAamp Viral RNA Kit (Qiagen, Germany). The gag (HXB2:781–1861), pol (HXB2:2147–3462), and env (HXB2:7002–7541) genes were amplified by nested polymerase chain reaction (PCR). The first round of PCR amplification was performed using the One Step RNA PCR Kit (Takara, Dalian, China), and the second round of amplification was performed using 2 × Taq PCR MasterMix (Tiangen, Beijing, China). The primers and procedures used for nested PCR were described previously [Reference Zhang, Dai, Li, Ma, Chen, Dong, Jin, Yang, Zeng, Sun, Hu and Chen24]. Amplified products were sent to SinoGenoMax Co. (Beijing, China) for Sanger sequencing with ABI 3730XL.

Sequence analysis

Sequences were assembled using Sequencher 5.1 (Gene Codes, Ann Arbor, MI). The BioEdit software (version 7.0) was used for sequence alignment and cleaning. Neighbour-joining phylogenetic trees were constructed using the Kimura 2-parameter model with 1000 bootstrap replicates in MEGA-X. Subtype reference alignments were downloaded from HIV databases (www.hiv.lanl.gov), which includes four genomes for each subtype and CRF. Sequences with unclear subtyping were further analysed using the REGA HIV subtyping tool (http://dbpartners.stanford.edu:8080/RegaSubtyping/stanford-hiv/typingtool/) and the Recombination Identification Program (RIP, https://www.hiv.lanl.gov/content/sequence/RIP/RIP.html). The final subtyping result for each sample was based on at least any two segments of gag, pol, and env genes (Supplementary Table S1).

Spatial analysis

The distributions of major HIV-1 strains are presented using dot density maps. The percentage of a given HIV strain is shown as the number of dots, with one dot representing 0.03% of the total number of subtyped cases. Global Moran’s I was calculated to determine the global spatial autocorrelation of HIV-1 strains, which varies between −1 and 1. Moran’s I > 0 indicates spatial clustering, and Moran’s I < 0 indicates spatial dispersal. If the global Moran’s I was significant, the local Moran’s I was calculated. Local Moran’s I > 0 and Z ≥ 1.96 indicate positive spatial correlations (high–high and low–low clusters). Local Moran’s I < 0 and Z ≤ −1.96 indicate negative spatial correlations (high–low and low–high clusters). Data on administrative boundaries were downloaded from the National Catalogue Service for Geographic Information (https://www.webmap.cn; accessed on November 11, 2022). Spatial analysis was performed using GeoDa 1.20 and QGIS 3.28.

Construction and analysis of HIV-1 molecular network

HIV-1 molecular clusters were investigated using phylogenetic analysis combined with genetic distance analysis. A maximum likelihood (ML) phylogenetic tree was constructed with 516 pol sequences using FastTree software with the generalised time-reversible model. The reliability of nodes was assessed using the Shimodaira–Hasegawa (SH) test with 1000 resamples, from which transmission clusters were extracted using Cluster Picker software [Reference Ragonnet-Cronin, Hodcroft, Hué, Fearnhill, Delpech, Brown and Lycett25]. To select the optimal genetic distance, the pairwise genetic distance was varied from 0.5 to 5.0%, with an interval of 0.5% when the node support threshold was set at ≥90%. As shown in Supplementary Figure S1, the growth rate of the number of clusters decreased significantly when the genetic distance was >2.5%. Therefore, a genetic distance of 2.5% was selected. The HIV-1 molecular network was visualised using the igraph R package.

The assortativity coefficient measures the degree of homophyly of a network based on a given node attribute [Reference Newman26]. The assortativity coefficient ranges from −1.0 to 1.0. When the assortativity coefficient is greater than zero, individuals in the same category tend to cluster. Individuals from different categories tend to cluster when the assortativity coefficient is less than 0. When the assortativity coefficient is zero, the category does not influence individual clustering. In this study, the assortativity coefficient was calculated using R package igraph. For each category, a null expectation was generated by randomly permuting trait labels across the static network 1000 times and recalculating assortativity [Reference Ragonnet-Cronin, Benbow, Hayford, Poortinga, Ma, Forgione, Sheng, Hu, Torian and Wertheim27].

Sequence data

The sequences obtained in this study were submitted to NCBI GenBank under accession numbers OP979115-OP980539.

Statistical analysis

Statistical analysis was conducted using SPSS software (version 19.0; SPSS Inc. Chicago, IL). Categorical variables were compared using the $ {\chi}^2 $ test. Factors of interest were analysed using logistic regression analysis. All tests were two-tailed, and a p value <0.05 was considered statistically significant.

Results

Demographic characteristics of the participants

From January to June 2021, 663 newly diagnosed HIV-1 cases were recruited from Zhaotong City. From the plasma samples, 495 gag, 516 pol, and 414 env sequences were obtained. After phylogenetic analysis (Supplementary Figures S2S4), 542 samples were subtyped. Reasons for some sequences not successfully amplified included poor conditions for storing and transporting samples, or low viral loads. There were no significant differences in the demographic characteristics between samples with and without genotypes (Supplementary Table S2).

Of the 542 participants, 91.7% (497/542) were from Zhaotong, 1.3% (7/542) were from other cities in Yunnan Province, and 7.0% (38/542) were from other provinces. The median age was 50 (range, 17–83) years. The proportion of males and females was 72.3% (392/542) and 27.7% (150/542), respectively. In total, 91.7% (497/542) of the participants were of Han ethnicity. Those with a primary education were the most common, accounting for 60.3% (327/542). The majority of the participants were married, accounting for 52.8% (286/542). Farming was the main occupation, accounting for 83.0% (450/542) of the sample. Heterosexual transmission was the predominant mode of transmission, accounting for 98.3% (533/542) of the cases.

HIV-1 genotypes detected in the participants

Twelve HIV-1 strains were detected in the 542 participants. CRF08_BC was the predominant strain (47.0%, 255/542), followed by CRF01_AE (17.0%, 92/542), CRF07_BC (17.0%, 92/542), URFs (8.7%, 47/542), CRF85_BC (6.4%, 35/542), CRF125_0107 (1.8%, 10/542), Subtype B (0.5%, 3/542), Subtype C (0.4%, 2/542), CRF55_01B (0.4%, 2/542), CRF64_BC (0.4%, 2/542), CRF101_01B (0.2%, 1/542), and CRF118_BC (0.2%, 1/542). URFs included BC recombinants (48.9%, 23/47), CRF01_AE/C (19.1%, 9/47), CRF08_BC/CRF07_BC (12.8%, 6/47), CRF01_AE/BC (6.4%, 3/47), CRF01_AE/CRF08_BC (4.3%, 2/47), CRF85_BC/CRF08_BC (4.3%, 2/47), CRF01_AE/ CRF07_BC (2.1%, 1/47), and CRF01_AE/B (2.1%, 1/47).

Demographic characteristics of HIV-1 genotypes

The demographic characteristics of the main HIV-1 genotypes were analysed (Supplementary Table S3 and Table 1). Multivariate logistic analysis showed that CRF08_BC was more likely to be detected among the Zhaotong natives (odds ratio (OR) (95% confidence interval (CI)):2.801 (1.279–6.132)), illiterate (OR (95% CI):4.311 (1.463–12.703)), and non-farmers (OR (95% CI):2.603(1.496–4.528)). CRF01_AE was more likely to be detected in married persons (OR (95% CI):1.983(1.136–3.463)) and those infected through non-heterosexual contact (OR (95% CI):6.573(1.334–32.391)). The distribution of CRF07_BC, URFs, and CRF85_BC showed no significant demographic characteristics.

Table 1. Demographic characteristics associated with HIV-1 genotypes (multivariate analysis)

Spatial autocorrelation analysis of HIV-1 genotypes

As shown in Figure 1, CRF01_AE was mainly distributed in the eastern region, and CRF08_BC was mainly distributed in the southeastern region. CRF85_BC was mainly distributed in three counties bordering Sichuan Province in the north.

Figure 1. Spatial distribution of the major HIV-1 genotypes in Zhaotong City. The dot density maps for CRF01_AE, CRF07_BC, CRF08_BC, CRF85_BC, and URFs. One dot represented 0.03% of the total subtyped cases. According to the local spatial autocorrelation analysis, the areas outlined in blue are the high–high aggregation area. Administrative boundary data were downloaded from the National Catalogue Service for Geographic Information (https://www.webmap.cn). The map content approval number: ZhaotongS(2022)6.

Global spatial autocorrelation analysis of key HIV-1 strains at the county level showed that CRF07_BC (Moran’s I = −0.507, Z = −1.217, p = 0.224), CRF85_BC (Moran’s I = 0.306, Z = 1.192, p = 0.233), and URFs (Moran’s I = −0.180, Z = −0.385, p = 0.700) tended to be randomly distributed. However, CRF01_AE (Moran’s I = 0.768, Z = 2.903, p = 0.004) and CRF08_BC (Moran’s I = 0.272, Z = 2.013, p = 0.044) showed non-random positive correlation distributions, suggesting a tendency towards spatial clustering. Local spatial autocorrelation analysis showed that the high–high cluster area of CRF01_AE was located in Weixin and Zhenxiong counties and that of CRF08_BC was located in Zhaoyang County (Figure 1).

HIV-1 molecular network analysis

To explore HIV-1 transmission characteristics in the local area, an HIV-1 molecular network was constructed. Among the 516 pol sequences, 187 (36.2%) were detected in 61 clusters, with a genetic distance threshold of 2.5%. Cluster sizes ranged from 2 to 12, with 35 (57.4%) having a cluster size of two. The median pairwise genetic distance was 0.0067 substitutions/site (interquartile range: 0.0033–0.0100 substitutions/site). Of the 187 nodes, 141 (75.4%) had one link and 46 (24.6%) had two or more links (Figure 2).

Figure 2. Characteristics of the HIV-1 molecular network in Zhaotong City. (a) Distribution of genetic transmission clusters by cluster size. (b) Distribution of sequence pairs by genetic distance. (c) Distribution of nodes in clusters by links.

Factors associated with joining the network were analysed using logistic regression (Table 2). Multivariate analysis showed that the Zhaotong natives (OR (95% CI):2.574 (1.014–6.534)), those aged 60 years and older (OR (95% CI):6.081 (1.560–23.699)), married (OR (95% CI):2.206 (1.100–4.425)), and illiterate (OR (95% CI):4.681 (1.155–18.962)) were more likely to be found in the network.

Table 2. Associated demographic factors of the individuals clustering in the HIV-1 molecular network

To further investigate the common features of the transmission clusters, the assortativity coefficient (ra) of the demographic characteristics was analysed (Figure 3). The results showed that individuals in the same age group (ra = 0.166, p < 0.05), with a similar educational level (ra = 0.108, p < 0.05), with the same occupation (ra = 0.400, p < 0.05), and reported in the same county (ra = 0.695, p < 0.05) were more likely to be genetically linked.

Figure 3. Assortativity analysis of the linked individuals in the HIV-1 molecular network in Zhaotong City. (a) Left panel: HIV-1 molecular clusters coded by age group. Right panel: assortativity analysed by age group. (b) Left panel: HIV-1 molecular clusters coded by educational level. Right panel: assortativity analysed by education level. (c) Left panel: HIV-1 molecular clusters coded by occupation. Right panel: assortativity analysed by occupation. (d) Left panel: HIV-1 molecular clusters coded by report area. Right panel: assortativity analysed by report area. The grey dotted line represents the 5% significance level. The pink vertical line represents the corresponding assortativity.

Discussion

In this study, a cross-sectional HIV-1 molecular epidemiological survey was conducted in Zhaotong City, an area severely affected by HIV-1 in Yunnan Province, which revealed the demographic and spatial distributions of HIV-1 genotypes in the local area. HIV-1 molecular network analysis revealed the characteristics and risks of HIV-1 transmission.

The dominant HIV-1 strains circulating in China originate mainly in Yunnan Province [Reference Lu, Jia, Ma, Yang, Chen, Ho, Jiang and Zhang19]. CRF01_AE was first introduced into Yunnan from Thailand [Reference Cheng, Zhang, Capizzi, Young and Mastro28]. CRF07_BC and CRF08_BC are considered to be formed in Yunnan Province [Reference Tee, Pybus, Li, Han, Shang, Kamarulzaman and Takebe29]. Similar to other parts of Yunnan Province [Reference Chen, Ma, Chen, Dai, Luo, Yang, Dong, Jin, Yang, Yang, Song, Song and Jia30], CRF08_BC, CRF07_BC, and CRF01_AE were also the predominant strains in Zhaotong City. According to a national HIV-1 molecular epidemiology survey, CRF07_BC was the most prevalent strain in China [Reference He, Xing, Ruan, Hong, Cheng, Hu, Xin, Wei, Feng, Hsi, Takebe and Shao31, Reference Ge, Feng, Zhang, Rashid, Zaongo, Li, Yu, Lv, Sun, Liang, Xing, Sönnerborg, Ma and Shao32]. In the neighbouring provinces of Sichuan and Guizhou, CRF07_BC was the predominant HIV-1 genotype [Reference Zhou, Liang, Li, Zhang, Li, Ye, Yuan and Su33, Reference Sun, Xing, Li, Cheng, Zhang, Shen and He34]. However, CRF08_BC was the most prevalent strain in Yunnan, which appears to be a feature of the HIV-1 epidemic in Yunnan Province. In this study, the demographic analysis showed that CRF08_BC was most likely to be found in individuals whose household registration address was Zhaotong City, illiterate, and those with occupations other than farming. Individuals with other occupations included workers, clerks, civil servants, students, and service workers, which widened the social range of HIV transmission. Meanwhile, CRF08_BC showed a tendency for spatial clustering, with a high–high cluster area detected in Zhaoyang County, the capital city of Zhaotong City, suggesting that CRF08_BC had the characteristics of an endemic epidemic. However, CRF07_BC did not exhibit significant demographic or spatial distribution characteristics.

Initially, CRF01_AE was found mainly in FSWs in Yunnan Province [Reference Zhang, Lu, Ba, Liu, Yang, Jia, Wang, Fang, Shi, Yan, Chang, Zhang, Ho and Chen35]. Therefore, it was thought to be transmitted through heterosexual contact. With the increase in CRF08_BC in heterosexual transmission, the proportion of CRF01_AE in heterosexual transmission remained low [Reference Chen, Ma, Chen, Dai, Luo, Yang, Dong, Jin, Yang, Yang, Song, Song and Jia30]. In this study, CRF01_AE was most likely found in married individuals, who may represent a specific subgroup of heterosexual transmission. With the increase in homosexual transmission, CRF01_AE has been reported to be one of the predominant strains in men who have sex with men [Reference Chen, Ma, Chen, Dai, Dong, Yang, Li, Luo, Zhang, Jin, Yang, AKL, Jia and Song36]. This study also found that the proportion of CRF01_AE was higher in homosexual transmissions. In terms of spatial distribution, the cluster of CRF01_AE was detected in the eastern region of Zhaotong City, including Zhenxiong and Weixin counties. These two counties border Luzhou City in Sichuan Province, where CRF01_AE is the predominant strain [Reference Zhou, Liang, Li, Zhang, Li, Ye, Yuan and Su33]. This suggests that interregional transmission may occur.

Owing to a prolonged epidemic, HIV-1 genetic recombination is a universal phenomenon in Yunnan Province, including the high frequency of URFs and the emergence of novel CRFs, which have contributed to the diversity of HIV-1 genetics. In this study, the proportion of URFs ranked fourth. Although BC recombination was dominant, some second-generation recombination also occurred from the dominant CRFs. Among the six novel CRFs detected in this study, four (CRF64_BC, CRF101_ 01 B, CRF118_BC, and CRF125_0107) were identified for the first time in Yunnan Province. One of the three near-full-length sequences used for the nomenclature of CRF101_ 01 B originated from Zhaotong City [Reference Zhang, Feng, Gao, Zhang, Miao, Dong and Xia37]. CRF125_0107 was recently identified among heterosexuals in Zhaotong City [Reference Xiao, Feng, Gao, Yang, Liu, He, Li, Zhang, Dong and Xia38]. This study confirms the local transmission of these two CRFs. The other two (CRF55_01B and CRF85_BC) were first detected in other provinces. CRF55_01B was considered the first CRFs circulating mainly among MSM [Reference Han, An, Zhang, Cai, Chen, Takebe and Shang39], but is now found in the heterosexual contact population. CRF85_BC was first identified among heterosexuals in Yibin City, Sichuan Province, and remains the most prevalent strain in Yibin [Reference Zhou, Liang, Li, Zhang, Li, Ye, Yuan and Su33, Reference Su, Wei, Yang, Zeng, Hu, Yuan, Feng, Ruan, Qin and Liang40]. Although the global spatial autocorrelation analysis of CRF85_BC showed no statistical difference, it appeared that CRF85_BC was mainly distributed in the three counties (Shuifu, Yanjin, and Weixin) bordering Yibin, suggesting cross-regional transmission of this CRF.

In this study, a basic molecular network was constructed with newly reported HIV cases. Compared with individuals from other provinces, Zhaotong natives were more likely to be found in the network, suggesting that the network was localised and that the epidemic was endemic. Compared to unmarried individuals, married individuals were more likely to be found in the network. The proportion of commercial heterosexual contacts was higher among unmarried individuals (42.3%, 33/78) than among married individuals (30.5%, 85/279). Meanwhile, 11.5% of the married respondents had marital transmission. The data showed that the proportion of individuals detected in networks with commercial heterosexual contact (30.7%, 51/166) was lower than the proportion of those with non-marital non-commercial heterosexual contact (39.2%, 121/309) and those transmitting between spouses (43.8%, 14/32), probably because commercial heterosexual behaviour was relatively covert and infection tracing was not easy to trace. This may explain why married people are more likely to be found in networks, but further investigation is needed. In addition, spousal notification and positive prevention measures need to be strengthened.

Zhaotong City is an underdeveloped area in Yunnan Province, and the education level of its population is low. Low literacy leads to low awareness of HIV/AIDS [Reference Haque, Hossain, Chowdhury and Uddin41]. Among the participants, 78.9% had a primary school education or lower. As the level of education decreased, the proportion of people in networks increased, especially among illiterates. In recent years, the age of people newly diagnosed with HIV infection in China has gradually increased. In this study, more than half of the reported HIV-infected individuals were older than 50 years. In addition, people aged ≥60 years were more likely to be detected in networks than in other age groups. This suggests that older people are a large high-risk group in the transmission network. In fact, the proportion of illiterate people increased with age (trend χ 2 = 24.064, p < 0.001) and was the highest among those aged 60 years and older (29.6%, 29/98). A low level of education leads to a lack of knowledge about AIDS in older age groups, which increases the incidence of HIV-related high-risk sexual behaviour [Reference Gao and Lu42]. Meanwhile, high-risk behaviours in this subpopulation were as complex as in any other age group, including commercial heterosexual contact (36.7%, 36/98), non-commercial heterosexual contact (54.1%, 53/98), and transmission between spouses or fixed sexual partners (7.1%, 7/98). Therefore, targeted intervention and counselling services for older adults should be developed and made available in the community.

As the methodology evolves, molecular networks are increasingly combined with social networks to estimate the transmission characteristics [Reference Wertheim, Kosakovsky Pond, Forgione, Mehta, Murrell, Shah, Smith, Scheffler and Torian43, Reference Kostaki, Nikolopoulos, Pavlitina, Williams, Magiorkinis, Schneider, Skaathun, Morgan, Psichogiou, Daikos, Sypsa, Smyrnov, Korobchuk, Malliori, Hatzakis, Friedman and Paraskevis44]. Some statistical methods from social network analysis have also been applied to molecular network analysis, including individual- and network-level metrics [Reference Jiang, Feng and Shao45]. In this study, a network-level indicator, assortativity, was attempted. Assortativity assesses whether nodes with the same attributes tend to connect with one another. If assortativity is positive, people with the same characteristics tend to come together in social networks. In this study, the assortativity of reporting areas was higher, suggesting that HIV-1 cases from each county tended to cluster separately. Therefore, it is necessary to develop preventive strategies and policies based on the characteristics of different countries. Meanwhile, cases with the same age, education level, and occupation tended to cluster separately and formed different subpopulations. Thus, it may be more effective to implement interventions according to the characteristics of subpopulations, such as developing core prevention and control knowledge points for subpopulations and implementing peer education and counselling.

In the context of a long-term HIV-1 epidemic, this study used a cross-sectional HIV-1 molecular epidemiological study to reveal the complicated epidemic characteristics of HIV-1 in Zhaotong City. Multiple HIV-1 strains co-circulate in the local area, among which CRF01_AE and CRF08_BC show a unique population and spatial distribution. In particular, HIV-1 molecular network analysis provides an opportunity for an in-depth analysis of transmission characteristics and potential risks by constructing individual transmission correlations. The analysis suggested that some subpopulations were at a specific risk and should be targeted, such as infections in the elderly, illiterate, and married. People with some of the same characteristics tended to be genetically linked, suggesting that holistic interventions may be effective. In short, this study provides clues and directions for further targeted detection and intervention.

Supplementary material

The supplementary material for this article can be found at http://doi.org/10.1017/S0950268823001140.

Data availability statement

The datasets used and/or analysed in the current study are available upon request from the corresponding author.

Acknowledgements

We acknowledge the staff of the local Centers for Disease Control and Prevention for their assistance with the sample collection.

Author contribution

Conceptualisation: M.C., M.J., Y.M.; Data curation: M.C., H.C.; Formal analysis: R.C., Y.M., M.C.; Funding acquisition: M.C., M.J.; Investigation: R.C., S.L., H.C., Y.M., J.D., L.D., X.J., M.Y., P.S., Y.W., Y.Z., M.J., M.C.; Project administration: H.C., J.D.; Resources: S.L.; Supervision: M.J.; Writing – original draft: R.C., M.C; Writing – review and editing: R.C., S.L., H.C., Y.M., J.D., L.D., X.J., M.Y., P.S., Y.W., Y.Z., M.J., M.C.

Financial support

This work was supported by the National Natural Science Foundation of China (82160635), Cultivating Plan Program for the Leader in Science and Technology of Yunnan Province (2019HB053), and Rejuvenating Yunnan Talents Support Plan (Special Project for Famous Doctor). The funders had no role in the study design, data collection and analysis, interpretation of data, or preparation of the manuscript.

Competing interest

The authors declare no conflict of interest.

Ethical standard

This study was approved by the Research Ethics Review Committee of the Yunnan Center for Disease Control and Prevention (YNCDC-ER-202108). All methods were performed in accordance with relevant guidelines and regulations. Written informed consent was obtained from the adults themselves and adolescents by their legal guardians.

Footnotes

These authors contributed equally to this work.

References

Hemelaar, J (2012) The origin and diversity of the HIV-1 pandemic. Trends in Molecular Medicine 18(3), 182192.CrossRefGoogle ScholarPubMed
UNAIDS. Executive Summary-In Danger: UNAIDS Global AIDS Update 2022. Available at https://www.unaids.org/en/resources/documents/2022/in-danger-global-aids-update-summary (accessed 21 December 2022).Google Scholar
Hemelaar, J, Elangovan, R, Yun, J, Dickson-Tetteh, L, Fleminger, I, Kirtley, S, Williams, B, Gouws-Williams, E and Ghys, PD (2019) Global and regional molecular epidemiology of HIV-1, 1990–2015: A systematic review, global survey, and trend analysis. Infectious Diseases 19(2), 143155.Google ScholarPubMed
Hemelaar, J, Loganathan, S, Elangovan, R, Yun, J, Dickson-Tetteh, L, Kirtley, S and WHO-UNAIDS Network for HIV Isolation and Characterization (2020) Country level diversity of the HIV-1 pandemic between 1990 and 2015. Journal of Virology 95(2), e01580-20.CrossRefGoogle ScholarPubMed
Korber, B, Hraber, P, Wagh, K and Hahn, BH (2017) Polyvalent vaccine approaches to combat HIV-1 diversity. Immunological Reviews 275(1), 230244.CrossRefGoogle ScholarPubMed
Haynes, BF, Wiehe, K, Borrow, P, Saunders, KO, Korber, B, Wagh, K, McMichael, AJ, Kelsoe, G, Hahn, BH, Alt, F and Shaw, GM (2023) Strategies for HIV-1 vaccines that induce broadly neutralizing antibodies. Nature Reviews Immunology 23, 142158.CrossRefGoogle ScholarPubMed
Frieden, TR, das-Douglas, M, Kellerman, SE and Henning, KJ (2005) Applying public health principles to the HIV epidemic. The New England Journal of Medicine 353(22), 23972402.CrossRefGoogle Scholar
UNAIDS. 90–90-90: An ambitious treatment target to help end the AIDS epidemic. Available at https://www.aidsdatahub.org/sites/default/files/resource/90-90-90-ambitious-treatment-target-help-end-aids-epidemic.pdfGeneva (accessed October 2014).Google Scholar
Han, X, Zhao, B, An, M, Zhong, P and Shang, H (2020) Molecular network-based intervention brings us closer to ending the HIV pandemic. Frontiers of Medicine 14(2), 136148.CrossRefGoogle ScholarPubMed
Oster, AM, Lyss, SB, McClung, RP, Watson, M, Panneer, N, Hernandez, AL, Buchacz, K, Robilotto, SE, Curran, KG, Hassan, R, Ocfemia, MCB, Linley, L, Perez, SM, Phillip, SA Jr and France, AM (2021) HIV cluster and outbreak detection and response: The science and experience. American Journal of Preventive Medicine 61(5 Suppl 1), S130S142.CrossRefGoogle ScholarPubMed
Fauci, AS, Redfield, RR, Sigounas, G, Weahkee, MD and Giroir, BP (2019) Ending the HIV epidemic: A plan for the United States. Journal of the American Medical Association 321(9), 844845.CrossRefGoogle Scholar
Poon, AF, Gustafson, R, Daly, P, Zerr, L, Demlow, SE, Wong, J, Woods, CK, Hogg, RS, Krajden, M, Moore, D, Kendall, P, Montaner, JSG and Harrigan, PR (2016) Near real-time monitoring of HIV transmission hotspots from routine HIV genotyping: An implementation case study. The Lancet HIV 3(5), e231e238.CrossRefGoogle ScholarPubMed
Chian Center for Disease Control and Prevention (2021) Technical Guideline for HIV Transmission Networks Monitoring and Intervention.Google Scholar
National Center for HIV/AIDS, Viral Hepatitis, STD and TB Prevention; Division of HIV/AIDS Prevention (2018) Detecting and Responding to HIV Transmission Clusters: A Guide for Health Department. Available at https://www.cdc.gov/hiv/pdf/funding/announcements/ps18-1802/CDC-HIV-PS18-1802-AttachmentE-Detecting-Investigating-and-Responding-to-HIV-Transmission-Clusters.pdf (accessed 12 December 2018).Google Scholar
Xia, Q, Wertheim, JO, Braunstein, SL, Misra, K, Udeagu, CC and Torian, LV (2020) Use of molecular HIV surveillance data and predictive modeling to prioritize persons for transmission-reduction interventions. AIDS 34(3), 459467.CrossRefGoogle ScholarPubMed
Arantes, I, Bello, G, Darcissac, E, Lacoste, V and Nacher, M (2021) Using phylogenetic surveillance and epidemiological data to understand the HIV-1 transmission dynamics in French Guiana. AIDS 35(6), 979984.CrossRefGoogle ScholarPubMed
Billock, RM, Powers, KA, Pasquale, DK, Samoff, E, Mobley, VL, Miller, WC, Eron, JJ and Dennis, AM (2019) Prediction of HIV transmission cluster growth with statewide surveillance data. Journal of Acquired Immune Deficiency Syndromes 80(2), 152159.CrossRefGoogle ScholarPubMed
McLaughlin, A, Sereda, P, Oliveira, N, Barrios, R, Brumme, CJ, Brumme, ZL, Montaner, JSG and Joy, JB (2019) Detection of HIV transmission hotspots in British Columbia, Canada: A novel framework for the prioritization and allocation of treatment and prevention resources. eBioMedicine 48, 405413.CrossRefGoogle Scholar
Lu, L, Jia, M, Ma, Y, Yang, L, Chen, Z, Ho, DD, Jiang, Y and Zhang, L (2008) The changing face of HIV in China. Nature 455(7213), 609611.CrossRefGoogle ScholarPubMed
Jia, M, Luo, H, Ma, Y, Wang, N, Smith, K, Mei, J, Lu, R, Lu, J, Fu, L, Zhang, Q, Wu, Z and Lu, L (2010) The HIV epidemic in Yunnan Province, China, 1989–2007. Journal of Acquired Immune Deficiency Syndromes 53(Suppl 1), S34S40.CrossRefGoogle Scholar
Meng, Z, Xin, R, Zhong, P, Zhang, C, Abubakar, YF, Li, J, Liu, W, Zhang, X and Xu, J (2012) A new migration map of HIV-1 CRF07_BC in China: Analysis of sequences from 12 provinces over a decade. PLoS One 7(12), e52373.CrossRefGoogle Scholar
Feng, Y, Takebe, Y, Wei, H, He, X, Hsi, JH, Li, Z, Xing, H, Ruan, Y, Yang, Y, Li, F, Wei, J, Li, X and Shao, Y (2016) Geographic origin and evolutionary history of China’s two predominant HIV-1 circulating recombinant forms, CRF07_BC and CRF08_BC. Scientific Reports 6, 19279.CrossRefGoogle ScholarPubMed
Li, Z, He, X, Wang, Z, Xing, H, Li, F, Yang, Y, Wang, Q, Takebe, Y and Shao, Y (2012) Tracing the origin and history of HIV-1 subtype B’ epidemic in China by near full-length genome analyses. AIDS 26(7), 877884.CrossRefGoogle Scholar
Zhang, Y, Dai, J, Li, Z, Ma, Y, Chen, H, Dong, L, Jin, X, Yang, M, Zeng, Z, Sun, P, Hu, A and Chen, M (2022) Using molecular network analysis to explore the characteristics of HIV-1 transmission in a China-Myanmar border area. PLoS One 17(5), e0268143.CrossRefGoogle Scholar
Ragonnet-Cronin, M, Hodcroft, E, Hué, S, Fearnhill, E, Delpech, V, Brown, AJ and Lycett, S (2013) Automated analysis of phylogenetic clusters. BMC Bioinformatics 14, 317.CrossRefGoogle ScholarPubMed
Newman, ME (2003) Mixing patterns in networks. Physical Review E-Statistical, Nonlinear, and Soft Matter Physics 67(2 Pt 2), 026126.CrossRefGoogle ScholarPubMed
Ragonnet-Cronin, M, Benbow, N, Hayford, C, Poortinga, K, Ma, F, Forgione, LA, Sheng, Z, Hu, YW, Torian, LV and Wertheim, JO (2021) Sorting by race/ethnicity across HIV genetic transmission networks in three major metropolitan areas in the United States. AIDS Research and Human Retroviruses 37(10), 784792.CrossRefGoogle Scholar
Cheng, H, Zhang, J, Capizzi, J, Young, NL and Mastro, TD (1994) HIV-1 subtype E in Yunnan, China. The Lancet 344(8927), 953954.CrossRefGoogle ScholarPubMed
Tee, KK, Pybus, OG, Li, XJ, Han, X, Shang, H, Kamarulzaman, A and Takebe, Y (2008) Temporal and spatial dynamics of human immunodeficiency virus type 1 circulating recombinant forms 08_BC and 07_BC in Asia. Journal of Virology 82(18), 92069215.CrossRefGoogle ScholarPubMed
Chen, M, Ma, Y, Chen, H, Dai, J, Luo, H, Yang, C, Dong, L, Jin, X, Yang, M, Yang, L, Song, L, Song, Z and Jia, M (2019) Spatial clusters of HIV-1 genotypes in a recently infected population in Yunnan, China. BMC Infectious Diseases 19(1), 669.CrossRefGoogle Scholar
He, X, Xing, H, Ruan, Y, Hong, K, Cheng, C, Hu, Y, Xin, R, Wei, J, Feng, Y, Hsi, JH, Takebe, Y and Shao, Y (2012) A comprehensive mapping of HIV-1 genotypes in various risk groups and regions across China based on a Nationwide molecular epidemiologic survey. PLoS One 7(10), e47289.CrossRefGoogle ScholarPubMed
Ge, Z, Feng, Y, Zhang, H, Rashid, A, Zaongo, SD, Li, K, Yu, Y, Lv, B, Sun, J, Liang, Y, Xing, H, Sönnerborg, A, Ma, P and Shao, Y (2021) HIV-1 CRF07_BC transmission dynamics in China: Two decades of national molecular surveillance. Emerging Microbes & Infections 10(1), 19191930.CrossRefGoogle Scholar
Zhou, C, Liang, S, Li, Y, Zhang, Y, Li, L, Ye, L, Yuan, D and Su, L (2022) Characterization of HIV-1 molecular epidemiology and transmitted drug-resistance in newly diagnosed HIV-infected patients in Sichuan, China. BMC Infectious Diseases 22(1), 602.CrossRefGoogle ScholarPubMed
Sun, XG, Xing, H, Li, ZJ, Cheng, CL, Zhang, XH, Shen, LM and He, X (2011) Distribution of HIV-1 subtype and its relationship with HIV/AIDS epidemic in Guizhou province. Chinese Journal of Epidemiology 32(7), 689692.Google ScholarPubMed
Zhang, Y, Lu, L, Ba, L, Liu, L, Yang, L, Jia, M, Wang, H, Fang, Q, Shi, Y, Yan, W, Chang, G, Zhang, L, Ho, DD and Chen, Z (2006) Dominance of HIV-1 subtype CRF01_AE in sexually acquired cases leads to a new epidemic in Yunnan province of China. PLoS Medicine 3(11), e443.CrossRefGoogle ScholarPubMed
Chen, M, Ma, Y, Chen, H, Dai, J, Dong, L, Yang, C, Li, Y, Luo, H, Zhang, R, Jin, X, Yang, L, AKL, Cheung, Jia, M and Song, Z (2018) HIV-1 genetic transmission networks among men who have sex with men in Kunming, China. PLoS One 13(4), e0196548.CrossRefGoogle ScholarPubMed
Zhang, C, Feng, Y, Gao, L, Zhang, M, Miao, J, Dong, X and Xia, X (2019) Genetic characterization and recombinant history of a novel HIV-1 circulating recombinant form (CRF101_01B) identified in Yunnan, China. Infection, Genetics and Evolution 73, 109112.CrossRefGoogle ScholarPubMed
Xiao, M, Feng, Y, Gao, L, Yang, C, Liu, J, He, M, Li, J, Zhang, M, Dong, X and Xia, X (2022) Characterization of a newly emerging HIV-1 second-generation recombinant form (CRF125_0107) among heterosexuals in Yunnan, China. Journal of Infection 84(6), e112e115.CrossRefGoogle ScholarPubMed
Han, X, An, M, Zhang, W, Cai, W, Chen, X, Takebe, Y and Shang, H (2013) Genome sequences of a novel HIV-1 circulating recombinant form, CRF55_01B, identified in China. Genome Announcements 1(1), e00050-12.Google ScholarPubMed
Su, L, Wei, D, Yang, H, Zeng, Y, Hu, Y, Yuan, D, Feng, L, Ruan, Y, Qin, G and Liang, S (2016) Identification of a novel HIV-1 circulating recombinant form (CRF85_BC) in Sichuan, China. AIDS Research and Human Retroviruses 32(9), 895899.CrossRefGoogle ScholarPubMed
Haque, MA, Hossain, MSN, Chowdhury, MAB and Uddin, MJ (2018) Factors associated with knowledge and awareness of HIV/AIDS among married women in Bangladesh: Evidence from a nationally representative survey. Journal of Social Aspects of HIV/AIDS 15(1), 121127.CrossRefGoogle ScholarPubMed
Gao, Y and Lu, H (2020) Review of infuencing factors of high-risk sexual behaviors among elderly people. Chinese Journal Of AIDS and STDs 26(4), 452454+354.Google Scholar
Wertheim, JO, Kosakovsky Pond, SL, Forgione, LA, Mehta, SR, Murrell, B, Shah, S, Smith, DM, Scheffler, K and Torian, LV (2017) Social and genetic networks of HIV-1 transmission in new York City. PLoS Pathogens 13(1), e1006000.CrossRefGoogle ScholarPubMed
Kostaki, EG, Nikolopoulos, GK, Pavlitina, E, Williams, L, Magiorkinis, G, Schneider, J, Skaathun, B, Morgan, E, Psichogiou, M, Daikos, GL, Sypsa, V, Smyrnov, P, Korobchuk, A, Malliori, M, Hatzakis, A, Friedman, SR and Paraskevis, D (2018) Molecular analysis of human immunodeficiency virus type 1 (HIV-1)-infected individuals in a network-based intervention (transmission reduction intervention project): Phylogenetics identify HIV-1-infected individuals with social links. The Journal of Infectious Diseases 218(5), 707715.CrossRefGoogle Scholar
Jiang, H, Feng, Y and Shao, Y (2022) Progress in research of HIV transmission network analysis methods and metrics. Chinese Journal of Epidemiology 43(1), 123127.Google ScholarPubMed
Figure 0

Table 1. Demographic characteristics associated with HIV-1 genotypes (multivariate analysis)

Figure 1

Figure 1. Spatial distribution of the major HIV-1 genotypes in Zhaotong City. The dot density maps for CRF01_AE, CRF07_BC, CRF08_BC, CRF85_BC, and URFs. One dot represented 0.03% of the total subtyped cases. According to the local spatial autocorrelation analysis, the areas outlined in blue are the high–high aggregation area. Administrative boundary data were downloaded from the National Catalogue Service for Geographic Information (https://www.webmap.cn). The map content approval number: ZhaotongS(2022)6.

Figure 2

Figure 2. Characteristics of the HIV-1 molecular network in Zhaotong City. (a) Distribution of genetic transmission clusters by cluster size. (b) Distribution of sequence pairs by genetic distance. (c) Distribution of nodes in clusters by links.

Figure 3

Table 2. Associated demographic factors of the individuals clustering in the HIV-1 molecular network

Figure 4

Figure 3. Assortativity analysis of the linked individuals in the HIV-1 molecular network in Zhaotong City. (a) Left panel: HIV-1 molecular clusters coded by age group. Right panel: assortativity analysed by age group. (b) Left panel: HIV-1 molecular clusters coded by educational level. Right panel: assortativity analysed by education level. (c) Left panel: HIV-1 molecular clusters coded by occupation. Right panel: assortativity analysed by occupation. (d) Left panel: HIV-1 molecular clusters coded by report area. Right panel: assortativity analysed by report area. The grey dotted line represents the 5% significance level. The pink vertical line represents the corresponding assortativity.

Supplementary material: File

Cao et al. supplementary material
Download undefined(File)
File 1.2 MB