High HIV diversity, recombination, and superinfection revealed in a large outbreak among persons who inject drugs in Kentucky and Ohio, USA

Author:

Switzer William M1ORCID,Shankar Anupama1,Jia Hongwei1,Knyazev Sergey12ORCID,Ambrosio Frank1,Kelly Reagan13,Zheng HaoQiang1,Campbell Ellsworth M1,Cintron Roxana1,Pan Yi1,Saduvala Neeraja4,Panneer Nivedha1,Richman Rhiannon5,Singh Manny B6,Thoroughman Douglas A67,Blau Erin F68,Khalil George M1,Lyss Sheryl156910,Heneine Walid1

Affiliation:

1. Division of HIV Prevention, CDC , 1600 Clifton Rd, Atlanta, GA 30329, USA

2. Oak Ridge Institute for Science and Education , 1299 Bethel Valley Rd, Oak Ridge, TN 37830, USA

3. General Dynamics Information Technology , 3150 Fairview Park Dr, Falls Church, VA 22042, USA

4. SeKON , 2801 Buford Hwy NE, Suite 280, Brookhaven, GA 30329, USA

5. HIV Surveillance Program, Bureau of HIV/STI/Viral Hepatitis, Ohio Department of Health , 246 North High Street, Colombus, OH 43215, USA

6. Division of Epidemiology and Health Planning , Kentucky Department for Public Health, Frankfort, KY 40621, USA

7. ORR/Division of State and Local Readiness/Field Services Branch/CEFO Program, CDC , 1600 Clifton Rd, Atlanta, GA 30329, USA

8. Epidemic Intelligence Service, CDC , 1600 Clifton Rd, Atlanta, GA 30329, USA

9. Hamilton County Public Health , 250 William Howard Taft Rd, Cincinnati, OH 45219, USA

10. Northern Kentucky Health Department , 8001 Veterans Memorial Drive, Florence, KY 41042, USA

Abstract

Abstract We investigated transmission dynamics of a large human immunodeficiency virus (HIV) outbreak among persons who inject drugs (PWID) in KY and OH during 2017–20 by using detailed phylogenetic, network, recombination, and cluster dating analyses. Using polymerase (pol) sequences from 193 people associated with the investigation, we document high HIV-1 diversity, including Subtype B (44.6 per cent); numerous circulating recombinant forms (CRFs) including CRF02_AG (2.5 per cent) and CRF02_AG-like (21.8 per cent); and many unique recombinant forms composed of CRFs with major subtypes and sub-subtypes [CRF02_AG/B (24.3 per cent), B/CRF02_AG/B (0.5 per cent), and A6/D/B (6.4 per cent)]. Cluster analysis of sequences using a 1.5 per cent genetic distance identified thirteen clusters, including a seventy-five-member cluster composed of CRF02_AG-like and CRF02_AG/B, an eighteen-member CRF02_AG/B cluster, Subtype B clusters of sizes ranging from two to twenty-three, and a nine-member A6/D and A6/D/B cluster. Recombination and phylogenetic analyses identified CRF02_AG/B variants with ten unique breakpoints likely originating from Subtype B and CRF02_AG-like viruses in the largest clusters. The addition of contact tracing results from OH to the genetic networks identified linkage between persons with Subtype B, CRF02_AG, and CRF02_AG/B sequences in the clusters supporting de novo recombinant generation. Superinfection prevalence was 13.3 per cent (8/60) in persons with multiple specimens and included infection with B and CRF02_AG; B and CRF02_AG/B; or B and A6/D/B. In addition to the presence of multiple, distinct molecular clusters associated with this outbreak, cluster dating inferred transmission associated with the largest molecular cluster occurred as early as 2006, with high transmission rates during 2017–8 in certain other molecular clusters. This outbreak among PWID in KY and OH was likely driven by rapid transmission of multiple HIV-1 variants including de novo viral recombinants from circulating viruses within the community. Our findings documenting the high HIV-1 transmission rate and clustering through partner services and molecular clusters emphasize the importance of leveraging multiple different data sources and analyses, including those from disease intervention specialist investigations, to better understand outbreak dynamics and interrupt HIV spread.

Publisher

Oxford University Press (OUP)

Reference57 articles.

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