Abstract

Introduction: Transmitted drug-resistance mutations (TDRM) may hamper successful anti-HIV-1 therapy and impact future control of the HIV-1 epidemic. Recently infected, therapy-naïve individuals are best suited for surveillance of such TDRM. In this study, TDRM, detected by next-generation sequencing (NGS) were compared to those identified by Sanger-based population sequencing (SBS) in recently infected HIV-1 patients.Methods: Historical samples from 80 recently infected HIV-1 patients, diagnosed between 2000 and 2014, were analysed by MiSeq (NGS) and ABI (SBS). DeepChek-HIV (ABL) was used for interpretation of the results.Results: Most patients were males (80%); Men who have sex with men (MSM) was the major transmission group (58.8%). Overall, TDRM were detected in 31.3% of patients by NGS and 8.8% by SBS, with SBS TDRM restricted to persons infected with subtype B. All SBS-detected TDRM were identified by NGS. The prevalence of TDRM impacting protease inhibitors (PI), nucleoside reverse transcriptase inhibitors (NRTI) and non-nucleoside reverse transcriptase inhibitors (NNRTI) was 11.3, 26.2 7.5%, respectively, in NGS analyses and 0, 3.8 and 5%, respectively, in SBS analyses. More patients with NGS and SBS TDRM were identified in 2008–2014 (37.2% or 13.9%, respectively) compared to 2000–2007 (24.3% or 2.7%, respectively), and a significantly greater number of these patients had multiple NGS TDRM. The most abundant, albeit, minor-frequency RT TDRM, were the K65R and D67N, while K103N, M184V and T215S were high-frequency mutations. Minor TDRM did not become a major variant in later samples and did not hinder successful treatment.Conclusions: NGS can replace SBS for mutation detection and allows for the detection of low-frequency TDRM not identified by SBS. Although rates of TDRM in Israel continued to increase from 2000 to 2014, minor TDRM did not become major species. The need for ongoing surveillance of low-frequency TDRM should be revisited in a larger study.

Highlights

  • Transmitted drug-resistance mutations (TDRM) may hamper successful anti-HIV-1 therapy and impact future control of the HIV-1 epidemic

  • Characterization of study population Between January 2000 and December 2014, 5830 HIV-1infected persons were identified by the National HIV Reference Laboratory (NHRL) in Israel, 4.1% (236/5830) of whom were diagnosed during seroconversion

  • Patients bearing next-generation sequencing (NGS)-identified TDRM had significantly lower HIV-1 viral load, a higher number of non-synonymous reverse transcriptase (RT) mutations and significantly lower mean prevalence of such mutations in the viral pool, most of which were below a prevalence of 5%. These results suggest that compared to HIV-1-infected persons without TDRM, patients with NGSidentified TDRM have a diverse population of high and low frequency viral variants, some of which are probably less fit compared to wild type

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Summary

Introduction

Transmitted drug-resistance mutations (TDRM) may hamper successful anti-HIV-1 therapy and impact future control of the HIV-1 epidemic. Therapy-naïve individuals are best suited for surveillance of such TDRM. TDRM, detected by next-generation sequencing (NGS) were compared to those identified by Sanger-based population sequencing (SBS) in recently infected HIV-1 patients. The prevalence of TDRM impacting protease inhibitors (PI), nucleoside reverse transcriptase inhibitors (NRTI) and non-nucleoside reverse transcriptase inhibitors (NNRTI) was 11.3, 26.2 7.5%, respectively, in NGS analyses and 0, 3.8 and 5%, respectively, in SBS analyses. Transmitted drug-resistance mutations (TDRM) challenge HIV-1 treatment of therapy-naïve individuals. They reduce therapeutic options, increase the risk for treatment failure and maintain onward transmission of drug resistance [1]. Prevalence of nucleoside RT inhibitors (NRTI), non-nucleoside RT inhibitors (NNRTI) and protease inhibitors (PI) TDRM in 2008–2010 in this subgroup of patients was 4.7, 3.8 and 2.4%, respectively, compared to 4.4, 2.9

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