Literature DB >> 33137698

A highly rifampicin resistant Mycobacterium tuberculosis strain emerging in Southern Brazil.

Maria Lucia Rossetti1, Pedro Eduardo Almeida da Silva2, Richard Steiner Salvato3, Ana Júlia Reis2, Sun Hee Schiefelbein4, Andrea von Groll5, Regina Bones Barcellos6, Raquel Maschmann7, Leonardo Souza Esteves8, Fernanda Spies7, Rubia Raubach Trespach5, Elis Regina Dalla Costa8, Hermes Luís Neubauer de Amorim9.   

Abstract

Here we described phenotypical, molecular and epidemiological features of a highly rifampicin-resistant Mycobacterium tuberculosis strain emerging in Southern Brazil, that carries an uncommon insertion of 12 nucleotides at the codon 435 in the rpoB gene. Employing a whole-genome sequencing-based study on drug-resistant Mycobacterium tuberculosis strains, we identified this emergent strain in 16 (9.19%) from 174 rifampicin-resistant clinical strains, all of them belonging to LAM RD115 sublineage. Nine of these 16 strains were available to minimum inhibitory concentration determination and for all of them was found a high rifampicin-resistance level (≥to 32 mg/L). This high resistance level could be explained by structural changes into the RIF binding site of RNA polymerase caused by the insertions, and consequent low-affinity interaction with rifampicin complex confirmed through protein modeling and molecular docking simulations. Epidemiological investigation showed that most of the individuals (56.25%) infected by the studied strains were prison inmate individuals or that spent some time in prison. The phylogenomic approach revealed that strains carrying on insertion belonged to same genomic cluster, evidencing a communal transmission chain involving inmate individuals and community. We stress the importance of tuberculosis genomic surveillance and introduction of measures to interrupt Mycobacterium tuberculosis transmission chain in this region.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Mycobacterium tuberculosis; Resistance; Rifampicin; Transmission; Whole genome sequencing

Year:  2020        PMID: 33137698     DOI: 10.1016/j.tube.2020.102015

Source DB:  PubMed          Journal:  Tuberculosis (Edinb)        ISSN: 1472-9792            Impact factor:   3.131


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