Transmission of highly virulent CXCR4 tropic HIV-1 through the mucosal route in an individual with a wild-type CCR5 genotype

Author:

Song Hongshuo1,Marichannegowda Manukumar1,Setua Saini1,Bose Meera,Sanders-Buell Eric2,King David3,Zemil Michelle4,Wieczorek Lindsay4,Diaz-Mendez Felisa1,Chomont Nicolas5ORCID,Thomas Rasmi4,Francisco Leilani4,Eller Leigh Anne4,Polonis Victoria4,Tovanabutra Sodsai6ORCID,Tagaya Yutaka1,Michael Nelson7,Robb Merlin8

Affiliation:

1. University of Maryland School of Medicine, Baltimore

2. Henry M Jackson Foundation

3. The Henry M. Jackson Foundation for the Advancement of Military Medicine

4. U.S. Military HIV Research Program, Walter Reed Army Institute of Research

5. Université de Montréal, Department of Microbiology, Infectiology and Immunology

6. MHRP-HJF

7. Center for Infectious Diseases Research, Walter Reed Army Institute of Research

8. U.S. Military HIV Research Program, Walter Reed Army Institute of Research; The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc

Abstract

Abstract Nearly all transmitted/founder (T/F) HIV-1 are CCR5 (R5)-tropic. While previous evidence suggested that CXCR4 (X4)-tropic HIV-1 are transmissible, detection was not at the earliest stages of acute infection. Here, we identified an X4-tropic T/F HIV-1 in a participant in acute infection cohort. Coreceptor assays demonstrated that this T/F virus is strictly CXCR4 tropic. The participant experienced significantly faster CD4 depletion compared with R5 virus infected participants in the same cohort. Naïve and central memory CD4 subsets declined faster than effector and transitional memory subsets. All CD4 subsets, including naïve, were productively infected. Increased CD4+ T cell activation was observed over time. This X4-tropic T/F virus is resistant to broadly neutralizing antibodies (bNAbs) targeting V1/V2 and V3 regions. These findings demonstrate that X4-tropic HIV-1 is transmissible through the mucosal route in people with the wild-type CCR5 genotype and have implications for understanding the transmissibility and immunopathogenesis of X4-tropic HIV-1.

Publisher

Research Square Platform LLC

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