Resistance to Second-Generation HIV-1 Maturation Inhibitors

Author:

Urano Emiko1,Timilsina Uddhav2,Kaplan Justin A.1,Ablan Sherimay1,Ghimire Dibya2,Pham Phuong1,Kuruppu Nishani1,Mandt Rebecca1,Durell Stewart R.3,Nitz Theodore J.4,Martin David E.4,Wild Carl T.4,Gaur Ritu2,Freed Eric O.1

Affiliation:

1. Virus-Cell Interaction Section, HIV Dynamics and Replication Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, USA

2. Faculty of Life Sciences and Biotechnology, South Asian University, New Delhi, India

3. Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA

4. DFH Pharma, Gaithersburg, Maryland, USA

Abstract

HIV-1 maturation inhibitors are a class of small-molecule compounds that block a late step in the viral protease-mediated processing of the Gag polyprotein precursor, the viral protein responsible for the formation of virus particles. The first-in-class HIV-1 maturation inhibitor bevirimat was highly effective in blocking HIV-1 replication, but its activity was compromised by naturally occurring sequence polymorphisms within Gag. Recently developed bevirimat analogs, referred to as “second-generation” maturation inhibitors, overcome this issue. To understand more about how these second-generation compounds block HIV-1 maturation, here we selected for HIV-1 mutants that are resistant to these compounds. Selections were performed in the context of two different subtypes of HIV-1. We identified a small set of mutations at highly conserved positions within the capsid and spacer peptide 1 domains of Gag that confer resistance. Identification and analysis of these maturation inhibitor-resistant mutants provide insights into the mechanisms of resistance to these compounds.

Funder

Department of Biotechnology, India

HHS | NIH | National Cancer Institute

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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