Abstract

Transfusion-transmissible infections including HIV-1 continue to pose major risks for unsafe blood transfusions due to both window phase infections and divergent viruses that may not be detected by donor screening assays. Given the recent emergence of several HIV-1 circulating recombinant forms (CRFs) in high-risk populations in the Southeast Asia region, we investigated the genetic diversity of HIV-1 among the blood donors in Kuala Lumpur, Malaysia. A total of 211 HIV-positive plasma samples detected among 730,188 donations to the National Blood Centre between 2013 and 2014 were provided (90.5% male, median age: 27.0 years old). Recent or long-term infection status at the time of donation was determined using a limiting antigen avidity enzyme immunoassay (LAg-Avidity EIA). HIV-1 gag-pol genes were amplified and sequenced from residual plasma for 149 cases followed by genotype determination using phylogenetic and recombination analyses. Transmitted antiretroviral resistance mutations were not observed among the blood donors, among which 22.7% were classified as recent or incident infections. Major circulating HIV-1 genotypes determined by neighbour-joining phylogenetic inference included CRF01_AE at 40.9% (61/149), CRF33_01B at 21.5% (32/149), and subtype B at 10.1% (15/149). Newly-described CRFs including CRF54_01B circulated at 4.0%, CRF74_01B at 2.0%, and CRF53_01B and CRF48_01B at 0.7% each. Interestingly, unique HIV-1 genotypes including African subtype G (8.7%), CRF45_cpx (1.3%), CRF02_AG (0.7%) and CRF07_BC (0.7%) from China were detected for the first time in the country. A cluster of subtype G sequences formed a distinct founder sub-lineage within the African strains. In addition, 8.7% (13/149) of HIV-infected donors had unique recombinant forms (URFs) including CRF01_AE/B' (4.7%), B'/C (2.7%) and B'/G (1.3%) recombinants. Detailed analysis identified similar recombinant structures with shared parental strains among the B'/C and B'/G URFs, some of which were sequenced from recently infected individuals, indicating the possible emergence and on-going spread of foreign clades of CRF candidates among the local population. The findings demonstrate extensive molecular complexity of HIV-1 among the infected blood donors in Malaysia, driven in part by the increased spread of recently described CRFs and multiple introductions of previously unreported genotypes from highly prevalent countries.

Highlights

  • In 2014, an estimated 37 million people were living with human immunodeficiency virus-1 (HIV-1) and within the same year, a total of 2 million people were newly diagnosed with HIV1 [1]

  • The study population comprised of 211 adults who donated blood at the National Blood Centre of Kuala Lumpur (NBCKL) between 2013 and 2014

  • We hereby report a molecular epidemiological surveillance analysis of HIV-1 strains among a subset of HIV-1 infected blood donors recruited in Kuala Lumpur between 2013 and 2014, using a set of phylogenetic and recombination analysis methods

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Summary

Introduction

In 2014, an estimated 37 million people were living with human immunodeficiency virus-1 (HIV-1) and within the same year, a total of 2 million people were newly diagnosed with HIV1 [1]. Incidence assays were primarily developed to enable estimation of HIV-1 incidence (defined as the number of new infections during a period of time) in a population [6,7], they identify recentlyacquired (incident) infections in a cross-sectional sample of population. This allows for epidemiological and molecular analyses of the characteristics of recently transmitted HIV-1 infections, enabling more accurate monitoring of the HIV-1 epidemic, providing a reliable measure of the impact of preventive measures aimed at reducing HIV-1 transmission, especially in high-risk populations [8]

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