bioRxivMicrobiologyPreprint
HIV-1 hijacks the cell extracellular matrix to spread collectively and efficiently between T lymphocytes
C. Inizan, M. Caillet, A. Desrames, P. Bomme, A. MALLET, K. Bourdic, O. Lambotte, F. Boufassa, M. Mesel-Lemoine, F. Tangy, G. Pancino, H. Mouquet, t. Lagache, A. C. Dufour, J.-C. Olivo-Marin, F. A. Rey, A. Saez-Cirion, M.-I. Thoulouze
Abstract
Collective transmission via structures containing several virions has recently emerged as a highly efficient mode of viral spread. Here, we demonstrate that HIV-1 spreads between T lymphocytes in the form of viral particles colonies that are concentrated and sheltered in an extracellular matrix (ECM) lattice enabling their collective transmission upon cell contacts. Intrinsically, ECM-clustered viruses infect T lymphocytes more efficiently than individual viral particles. They preserve HIV-1 transmission from antiretroviral treatment (ArT) and potent broadly neutralizing antibodies. We also show that collagen induced by HIV-1 infection controls the clustering of virions and their collective spread, thereby enhancing infectivity. CD4+ T cells from HIV-1-infected patients produce and transmit ECM-virus clusters, supporting that they could be involved in vivo. This study provides new insights into modes of HIV-1 transmission and identifies a novel fundamental role for collagen in this process. HIV-1 spread via ECM-virus clusters may have important implications for viral dissemination and persistence, including during therapy.
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