Abstract

Washington, D.C., has 2.5% HIV prevalence, 3.9% among African Americans. Antiretrovirals are the cornerstone for treatment and prevention. Monitoring changes in transmitted drug resistance (TDR) is critical for effective HIV care. HIV genotype data for individuals enrolled in research studies in metropolitan Washington, D.C., were used to identify TDR using the World Health Organization mutation list[1]. HIV phylogenies were reconstructed using maximum likelihood and Bayesian methods. HIV transmission clusters were supported by 1000 bootstrap values >0.70 and posterior probability >0.95 of having a common ancestor. Among 710 individuals enrolled in 1994-2013, the median age was 38.6 years, 46.2% were female, and 53.3% were African-American. TDR was 22.5% among 566 treatment naïve individuals; 15.8% had NRTI resistance, 9.8% had NNRTI resistance, and 4.2% had PI resistance. Single class TDR was 10.0%, 5.1%, 1.6% to NRTIs, NNRTIs, and PIs. Dual TDR to PI and NRTI was seen in 1.6%, NRTI and NNRTI in 3.4%, and triple class TDR in 0.9%. The most common NRTI-associated TDR mutations were L215Y/F/D/S (7.0%), D67N/G/E (5.0%), M41L (4.6%), K70R (4.5%), and M184V (3.9%); NNRTI-associated mutation was K103N/S (7.1%); and PI-associated mutation was L90M (2.0%). TDR frequency decreased from 1994-2006 (27.1%) to 2007-2013 (19.4%) (p=0.02). Only 6/79 (7.6%) individuals within transmission clusters had evidence of TDR.We identified high prevalence of TDR among HIV-infected individuals in metropolitan Washington, D.C., regardless of gender. Active surveillance for TDR is needed to guide antiretroviral usage and analyses of risk group contributions to HIV transmission and resistance.

View details for DOI 10.1093/cid/ciw382

View details for PubMedID 27307507