Near Real-Time Identification of Recent Human Immunodeficiency Virus Transmissions, Transmitted Drug Resistance Mutations, and Transmission Networks by Multiplexed Primer ID–Next-Generation Sequencing in North Carolina

Author:

Zhou Shuntai1ORCID,Sizemore Sabrina1,Moeser Matt1,Zimmerman Scott2,Samoff Erika2,Mobley Victoria2,Frost Simon3,Cressman Andy1,Clark Michael1,Skelly Tara1,Kelkar Hemant1,Veluvolu Umadevi1,Jones Corbin1,Eron Joseph1,Cohen Myron1,Nelson Julie A E1,Swanstrom Ronald1,Dennis Ann M1

Affiliation:

1. University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA

2. North Carolina Department of Health and Human Services, Raleigh, North Carolina, USA

3. University of Cambridge, Cambridge, United Kingdom

Abstract

Abstract Background The identification of recent human immunodeficiency virus (HIV) 1 infections among people with new HIV diagnoses is important to both tailoring and assessing the impact of HIV-1 prevention strategies. Methods We developed a multiplexed Primer ID–next-generation sequencing approach to identify recent infections by measuring the intrahost viral diversity over multiple regions of the HIV-1 genome, in addition to detecting drug resistance mutations (DRMs) and phylogenetically linked clusters. We summarize the field implementation of this all-in-one platform among persons with newly diagnosed HIV-1 by the North Carolina State Laboratory of Public Health in 2018. Results Overall, recent infection was identified in 94 (35%) of 268 patients with new HIV diagnoses. People <30 years old, and people who inject drugs were more likely to have diagnoses of recent infection. The reverse-transcriptase region K103N was the most commonly detected DRM (prevalence, approximately 15%). We found a total of 28 clusters, and persons with recent infection were more likely to be cluster members than were those with chronic infections (P = .03). Conclusions We demonstrate the rapid identification of recent infection and pretreatment DRMs coupled with cluster analysis that will allow prioritization of linkage to care, treatment, and prevention interventions to those at highest risk of onward transmission.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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