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Combining Phylogenetic and Network Approaches to Identify HIV-1 Transmission Links in San Mateo County, California
The HIV epidemic in San Mateo County is sustained by multiple overlapping risk groups and is an important hub for HIV transmission in northern California. Limited access to care has led historically to delayed clinical presentation, higher rates of opportunistic infections, and an increased prevalen...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292275/ https://www.ncbi.nlm.nih.gov/pubmed/30574123 http://dx.doi.org/10.3389/fmicb.2018.02799 |
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author | Dalai, Sudeb C. Junqueira, Dennis Maletich Wilkinson, Eduan Mehra, Renee Kosakovsky Pond, Sergei L. Levy, Vivian Israelski, Dennis de Oliveira, Tulio Katzenstein, David |
author_facet | Dalai, Sudeb C. Junqueira, Dennis Maletich Wilkinson, Eduan Mehra, Renee Kosakovsky Pond, Sergei L. Levy, Vivian Israelski, Dennis de Oliveira, Tulio Katzenstein, David |
author_sort | Dalai, Sudeb C. |
collection | PubMed |
description | The HIV epidemic in San Mateo County is sustained by multiple overlapping risk groups and is an important hub for HIV transmission in northern California. Limited access to care has led historically to delayed clinical presentation, higher rates of opportunistic infections, and an increased prevalence of antiretroviral drug resistance. The virologic and clinical consequences of treatment within these multiple ethnic and behavioral groups are poorly understood, highlighting the need for efficient surveillance strategies that are able to elucidate transmission networks and drug resistance patterns. We obtained sequence data from a group of 316 HIV-positive individuals in the San Mateo AIDS Program over a 14-year period and integrated epidemiologic, phylogenetic, and network approaches to characterize transmission clusters, risk factors and drug resistance. Drug resistance mutations were identified using the Stanford HIV Drug Resistance Database. A maximum likelihood tree was inferred in RAxML and subjected to clustering analysis in Cluster Picker. Network analysis using pairwise genetic distances was performed in HIV-TRACE. Participants were primarily male (60%), white Hispanics and non-Hispanics (32%) and African American (20.6%). The most frequent behavior risk factor was male-male sex (33.5%), followed by heterosexual (23.4%) and injection drug use (9.5%). Nearly all sequences were subtype B (96%) with subtypes A, C, and CRF01_AE also observed. Sequences from 65% of participants had at least one drug resistance mutation. Clustered transmissions included a higher number of women when compared to non-clustered individuals and were more likely to include heterosexual or people who inject drugs (PWID). Detailed analysis of the largest network (N = 47) suggested that PWID played a central role in overall transmission of HIV-1 as well as bridging men who have sex with men (MSM) transmission with heterosexual/PWID among primarily African American men. Combined phylogenetic and network analysis of HIV sequence data identified several overlapping risk factors in the epidemic, including MSM, heterosexual and PWID transmission with a disproportionate impact on African Americans and a high prevalence of drug resistance. |
format | Online Article Text |
id | pubmed-6292275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62922752018-12-20 Combining Phylogenetic and Network Approaches to Identify HIV-1 Transmission Links in San Mateo County, California Dalai, Sudeb C. Junqueira, Dennis Maletich Wilkinson, Eduan Mehra, Renee Kosakovsky Pond, Sergei L. Levy, Vivian Israelski, Dennis de Oliveira, Tulio Katzenstein, David Front Microbiol Microbiology The HIV epidemic in San Mateo County is sustained by multiple overlapping risk groups and is an important hub for HIV transmission in northern California. Limited access to care has led historically to delayed clinical presentation, higher rates of opportunistic infections, and an increased prevalence of antiretroviral drug resistance. The virologic and clinical consequences of treatment within these multiple ethnic and behavioral groups are poorly understood, highlighting the need for efficient surveillance strategies that are able to elucidate transmission networks and drug resistance patterns. We obtained sequence data from a group of 316 HIV-positive individuals in the San Mateo AIDS Program over a 14-year period and integrated epidemiologic, phylogenetic, and network approaches to characterize transmission clusters, risk factors and drug resistance. Drug resistance mutations were identified using the Stanford HIV Drug Resistance Database. A maximum likelihood tree was inferred in RAxML and subjected to clustering analysis in Cluster Picker. Network analysis using pairwise genetic distances was performed in HIV-TRACE. Participants were primarily male (60%), white Hispanics and non-Hispanics (32%) and African American (20.6%). The most frequent behavior risk factor was male-male sex (33.5%), followed by heterosexual (23.4%) and injection drug use (9.5%). Nearly all sequences were subtype B (96%) with subtypes A, C, and CRF01_AE also observed. Sequences from 65% of participants had at least one drug resistance mutation. Clustered transmissions included a higher number of women when compared to non-clustered individuals and were more likely to include heterosexual or people who inject drugs (PWID). Detailed analysis of the largest network (N = 47) suggested that PWID played a central role in overall transmission of HIV-1 as well as bridging men who have sex with men (MSM) transmission with heterosexual/PWID among primarily African American men. Combined phylogenetic and network analysis of HIV sequence data identified several overlapping risk factors in the epidemic, including MSM, heterosexual and PWID transmission with a disproportionate impact on African Americans and a high prevalence of drug resistance. Frontiers Media S.A. 2018-12-06 /pmc/articles/PMC6292275/ /pubmed/30574123 http://dx.doi.org/10.3389/fmicb.2018.02799 Text en Copyright © 2018 Dalai, Junqueira, Wilkinson, Mehra, Kosakovsky Pond, Levy, Israelski, de Oliveira and Katzenstein. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Dalai, Sudeb C. Junqueira, Dennis Maletich Wilkinson, Eduan Mehra, Renee Kosakovsky Pond, Sergei L. Levy, Vivian Israelski, Dennis de Oliveira, Tulio Katzenstein, David Combining Phylogenetic and Network Approaches to Identify HIV-1 Transmission Links in San Mateo County, California |
title | Combining Phylogenetic and Network Approaches to Identify HIV-1 Transmission Links in San Mateo County, California |
title_full | Combining Phylogenetic and Network Approaches to Identify HIV-1 Transmission Links in San Mateo County, California |
title_fullStr | Combining Phylogenetic and Network Approaches to Identify HIV-1 Transmission Links in San Mateo County, California |
title_full_unstemmed | Combining Phylogenetic and Network Approaches to Identify HIV-1 Transmission Links in San Mateo County, California |
title_short | Combining Phylogenetic and Network Approaches to Identify HIV-1 Transmission Links in San Mateo County, California |
title_sort | combining phylogenetic and network approaches to identify hiv-1 transmission links in san mateo county, california |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292275/ https://www.ncbi.nlm.nih.gov/pubmed/30574123 http://dx.doi.org/10.3389/fmicb.2018.02799 |
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