Identification of genes required for <i>Mycobacterium abscessus</i> growth in vivo with a prominent role of the ESX-4 locus

Laura Laencina(Inserm), Violaine Dubois(Inserm), Vincent Le Moigne(Inserm), Albertus Viljoen(Centre National de la Recherche Scientifique), Laleh Majlessi(Institut Pasteur), Justin R. Pritchard(Harvard University), Audrey Bernut(Centre National de la Recherche Scientifique), Laura Piel(Inserm), Anne-Laure Roux(Inserm), Jean-Louis Gaillard(Inserm), Bérengère Lombard(Institut Curie), Damarys Loew(Institut Curie), Eric J. Rubin(Harvard University), Roland Brosch(Institut Pasteur), Laurent Kremer(Centre National de la Recherche Scientifique), Jean‐Louis Herrmann(Inserm), Fabienne Girard‐Misguich(Inserm)
Proceedings of the National Academy of Sciences
January 17, 2018
Cited by 140

Abstract

Significance The coevolution of mycobacteria and amoebae seems to have contributed to shaping the virulence of nontuberculous mycobacteria in macrophages. We identified a pool of genes essential for the intracellular survival of Mycobacterium abscessus inside amoebae and macrophages and discovered a hot spot of transposon insertions within the orthologous ESX-4 T7SS locus. We generated a mutant with the deletion of a structural key ESX component, EccB 4 . We demonstrate rupture of the phagosomal membrane only in the presence of an intact eccB 4 gene. These results suggest an unanticipated role of ESX-4 T7SS in governing the intracellular behavior of a mycobacterium. Because M. abscessus lacks ESX-1, it is tempting to speculate that ESX-4 operates as a surrogate for ESX-1 in M. tuberculosis .


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