4.0 Article

Characterization of HIV Risk Behaviors and Clusters Using HIV-Transmission Cluster Engine Among a Cohort of Persons Living with HIV in Washington, DC

Journal

AIDS RESEARCH AND HUMAN RETROVIRUSES
Volume 37, Issue 9, Pages 706-715

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/aid.2021.0031

Keywords

HIV; molecular epidemiology; HIV clusters; HIV-TRACE; District of Columbia

Funding

  1. DC Cohort Study [U01 AI69503-03S2, 1R24AI152598-01]
  2. Women's Interagency Study for HIV [410722_GR410708]
  3. DC CFAR pilot award
  4. NIH-NIAID R01 [AI135992]
  5. 2015 HIV Phylodynamics Supplement award from the DC CFAR
  6. NIH [AI117970]
  7. NIH: NIAID
  8. NIH: NCI
  9. NIH: NICHD
  10. NIH: NHLBI
  11. NIH: NIDA
  12. NIH: NIMH
  13. NIH: NIA
  14. NIH: FIC
  15. NIH: NIGMS
  16. NIH: NIDDK
  17. NIH: OAR

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Molecular epidemiology is utilized as a tool to combat the HIV epidemic in the United States, combining clinical and behavioral data with HIV sequence information to identify transmission clusters and associated factors. These insights aid in enhancing local efforts to interrupt transmission and prevent new infections.
Molecular epidemiology (ME) is one tool used to end the HIV epidemic in the United States. We combined clinical and behavioral data with HIV sequence data to identify any overlap in clusters generated from different sequence datasets; to characterize HIV transmission clusters; and to identify correlates of clustering among people living with HIV (PLWH) in Washington, District of Columbia (DC). First, Sanger sequences from DC Cohort participants, a longitudinal HIV study, were combined with next-generation sequences (NGS) from participants in a ME substudy to identify clusters. Next, demographic and self-reported behavioral data from ME substudy participants were used to identify risks of secondary transmission. Finally, we combined NGS from ME substudy participants with Sanger sequences in the DC Molecular HIV Surveillance database to identify clusters. Cluster analyses used HIV-Transmission Cluster Engine to identify linked pairs of sequences (defined as distance <= 1.5%). Twenty-eight clusters of >= 3 sequences (size range: 3-12) representing 108 (3%) participants were identified. None of the five largest clusters (size range: 5-12) included newly diagnosed PLWH. Thirty-four percent of ME substudy participants (n = 213) reported condomless sex during their last sexual encounter and 14% reported a Syphilis diagnosis in the past year. Seven transmission clusters (size range: 2-19) were identified in the final analysis, each containing at least one ME substudy participant. Substudy participants in clusters from the third analysis were present in clusters from the first analysis. Combining HIV sequence, clinical and behavioral data provided insights into HIV transmission that may not be identified using traditional epidemiological methods alone. Specifically, the sexual risk behaviors and STI diagnoses reported in the substudy survey may not have been disclosed during Partner Services activities and the survey data complemented clinical data to fully characterize transmission clusters. These findings can be used to enhance local efforts to interrupt transmission and avert new infections.

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