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Mycobacterium tuberculosis Inhibits RAB7 Recruitment to Selectively Modulate Autophagy Flux in Macrophages

Chandra, Pallavi and Ghanwat, Swapnil and Matta, Sumit Kumar and Yadav, Swati Seth and Mehta, Mansi and Siddiqui, Zaved and Singh, Amit and Kumar, Dhiraj (2015) Mycobacterium tuberculosis Inhibits RAB7 Recruitment to Selectively Modulate Autophagy Flux in Macrophages. In: SCIENTIFIC REPORTS, 5 .

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Official URL: http://dx.doi.org/10.1038/srep16320

Abstract

Here we report a novel regulatory mechanism for autophagy-mediated degradation of Mycobacterium tuberculosis (Mtb) and specific strategy exploited by the virulent Mtb to evade it. We show while both avirulent (H37Ra) and virulent (H37Rv) mycobacteria could readily localize to autophagosomes, their maturation into autolysosomes (flux) was significantly inhibited by the latter strain. The inhibition of autophagy flux by the virulent strain was highly selective, as it did not perturb the basal autophagy flux in the macrophages. Selective inhibition of flux of Mtb-containing autophagosomes required virulence regulators PhoP and ESAT-6. We show that the maturation of Mtb-containing autophagosomes into autolysosomes required recruitment of the late endosome marker RAB7, forming the intermediate compartment amphisomes. Virulent Mtb selectively evaded their targeting to the amphisomes. Thus we report a crosstalk between autophagy and phagosome maturation pathway and highlight the adaptability of Mtb, manifested by selective regulation of autophagy flux.

Item Type: Journal Article
Publication: SCIENTIFIC REPORTS
Publisher: NATURE PUBLISHING GROUP
Additional Information: Copyright for this article belongs to the NATURE PUBLISHING GROUP, MACMILLAN BUILDING, 4 CRINAN ST, LONDON N1 9XW, ENGLAND
Department/Centre: Division of Biological Sciences > Microbiology & Cell Biology
Date Deposited: 02 Dec 2015 08:26
Last Modified: 02 Dec 2015 08:26
URI: http://eprints.iisc.ac.in/id/eprint/52836

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