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Transglutaminase type 2 plays a key role in the pathogenesis of Mycobacterium tuberculosis infection
Author(s) -
Palucci I.,
Matic I.,
Falasca L.,
Minerva M.,
Maulucci G.,
De Spirito M.,
Petruccioli E.,
Goletti D.,
Rossin F.,
Piacentini M.,
Delogu G.
Publication year - 2018
Publication title -
journal of internal medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.625
H-Index - 160
eISSN - 1365-2796
pISSN - 0954-6820
DOI - 10.1111/joim.12714
Subject(s) - autophagy , tissue transglutaminase , mycobacterium tuberculosis , pathogenesis , macrophage , microbiology and biotechnology , phagosome , biology , intracellular , medicine , tuberculosis , virology , immunology , phagocytosis , in vitro , enzyme , biochemistry , pathology , apoptosis
Abstract Background Mycobacterium tuberculosis ( MTB ) , the aetiological agent of tuberculosis ( TB ), is capable of interfering with the phagosome maturation pathway, by inhibiting phagosome–lysosome fusion and the autophagic process to ensure survival and replication in macrophages. Thus, it has been proposed that the modulation of autophagy may represent a therapeutic approach to reduce MTB viability by enhancing its clearance. Objective The aim of this study was to investigate whether transglutaminase type 2 ( TG 2) is involved in the pathogenesis of MTB . Results We have shown that either genetic or pharmacological inhibition of TG 2 leads to a marked reduction in MTB replicative capacity. Infection of TG 2 knockout mice demonstrated that TG 2 is required for MTB intracellular survival in macrophages and host tissues. The same inhibitory effect can be reproduced in vitro using Z‐ DON , a specific inhibitor of the transamidating activity of TG 2. Massive cell death observed in macrophages that properly express TG 2 is hampered by the absence of the enzyme and can be largely reduced by the treatment of wild‐type macrophages with the TG 2 inhibitor. Our data suggest that reduced MTB replication in cells lacking TG 2 is due to the impairment of LC 3/autophagy homeostasis. Finally, we have shown that treatment of MTB ‐infected murine and human primary macrophages with cystamine, a TG 2 inhibitor already tested in clinical studies, causes a reduction in intracellular colony‐forming units in human macrophages similar to that achieved by the anti‐ TB drug capreomycin. Conclusion These results suggest that inhibition of TG 2 activity is a potential novel approach for the treatment of TB .