Human Immunodeficiency Virus Type 1 Group M Protease in Cameroon: Genetic Diversity and Protease Inhibitor Mutational Features

Author:

Fonjungo Peter N.1,Mpoudi Eitel N.2,Torimiro Judith N.2,Alemnji George A.2,Eno Laura T.2,Lyonga Esther J.2,Nkengasong John N.34,Lal Renu B.5,Rayfield Mark1,Kalish Marcia L.1,Folks Thomas M.1,Pieniazek Danuta1

Affiliation:

1. HIV and Retrovirology Branch

2. Hôpital Militaire de Yaoundé, Yaoundé, Cameroon

3. Division of HIV/AIDS Prevention, National Center for HIV, STD, and TB Prevention, Centers for Disease ControlPrevention, Atlanta, Georgia

4. Projet RETRO-CI, Abidjan, Côte d'Ivoire

5. HIV Immunology and Diagnostics Branch, Division of AIDS, STD, and TB Laboratory Research, National Center for Infectious Diseases

Abstract

ABSTRACT To establish a baseline for monitoring resistance to protease inhibitors (PIs) and examining the efficacy of their use among persons in Cameroon infected with human immunodeficiency virus type 1 (HIV-1), we analyzed genetic variability and PI resistance-associated substitutions in PCR-amplified protease (PR) sequences in strains isolated from 110 HIV-1-infected, drug-naïve Cameroonians. Of the 110 strains, 85 were classified into six HIV-1 PR subtypes, A ( n = 1), B ( n = 1), F ( n = 4), G ( n = 7), H ( n = 1), and J ( n = 7), and a circulating recombinant form, CRF02-AG ( n = 64). PR genes from the remaining 25 (23%) specimens were unclassifiable, whereas 2% (7 of 301) unclassifiable PR sequences were reported for a global collection. Two major PI resistance-associated mutations, 20M and 24I, were detected in strains from only two specimens, whereas secondary mutations were found in strains from all samples except one strain of subtype B and two strains of CRF02-AG. The secondary mutations showed the typical PI resistance-associated pattern for non-subtype B viruses in both classifiable and unclassifiable PR genes, with 36I being the predominant (99%) mutation, followed by 63P (18%), 20R (15%), 77I (13%), and 10I or 10V (11%). Of these mutations, dual and triple PI resistance-associated substitutions were found in 38% of all the Cameroonian strains. Compared with classifiable PR sequences, unclassifiable sequences had significantly more dual and triple substitutions (64% versus 30%; P = 0.004). Phenotypic and clinical evaluations are needed to estimate whether PI resistance during antiretroviral drug treatment occurs more rapidly in individuals infected with HIV-1 strains harboring multiple PI resistance-associated substitutions. This information may be important for determination of appropriate drug therapies for HIV-1-infected persons in Cameroon, where more than one-third of HIV-1 strains were found to carry dual and triple minor PI resistance-associated mutations.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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