MptpB inhibitor improves the action of antibiotics against mycobacterium tuberculosis and nontuberculous mycobacterium avium infections

Rodríguez-Fernández, Pablo and Botella, Laure and Cavet, Jennifer S. and Domínguez, Jose and Gutierrez, Maximiliano G. and Suckling, Colin J. and Scott, Fraser J. and Tabernero, Lydia (2024) MptpB inhibitor improves the action of antibiotics against mycobacterium tuberculosis and nontuberculous mycobacterium avium infections. ACS Infectious Diseases, 10 (1). 170–183. (https://doi.org/10.1021/acsinfecdis.3c00446)

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Abstract

ABSTRACT: Treatment of Mycobacterium tuberculosis and Mycobacterium avium infections requires multiple drugs for long time periods. Mycobacterium protein-tyrosine-phosphatase B (MptpB) is a key M. tuberculosis virulence factor that subverts host antimicrobial activity to promote intracellular survival. Inhibition of MptpB reduces the infection burden in vivo and offers new opportunities to improve current treatments. Here, we demonstrate that M. avium produces an MptpB orthologue and that the MptpB inhibitor C13 reduces the M. avium infection burden in macrophages. Combining C13 with the antibiotics rifampicin or bedaquiline showed an additive effect, reducing intracellular infection of both M. tuberculosis and M. avium by 50%, compared to monotreatment with antibiotics alone. This additive effect was not observed with pretomanid. Combining C13 with the minor groove-binding compounds S-MGB-362 and S-MGB-363 also reduced the M. tuberculosis intracellular burden. Similar additive effects of C13 and antibiotics were confirmed in vivo using Galleria mellonella infections. We demonstrate that the reduced mycobacterial burden in macrophages observed with C13 treatments is due to the increased trafficking to lysosomes.

ORCID iDs

Rodríguez-Fernández, Pablo, Botella, Laure, Cavet, Jennifer S., Domínguez, Jose, Gutierrez, Maximiliano G., Suckling, Colin J., Scott, Fraser J. ORCID logoORCID: https://orcid.org/0000-0003-0229-3698 and Tabernero, Lydia;