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Cyclic di-GMP regulates Mycobacterium tuberculosis resistance to ethionamide.


ABSTRACT: Tuberculosis is still on the top of infectious diseases list on both mobility and mortality, especially due to drug-resistance of Mycobacterium tuberculosis (M.tb). Ethionamide (ETH) is one of effective second line anti-TB drugs, a synthetic compound similar to isoniazid (INH) structurally, with existing severe problem of ETH resistance. ETH is a prodrug, which is activated by Etha inside M.tb, and etha is transcriptionally repressed by Ethr. We found that c-di-GMP could bind Ethr, enhanced the binding of Ethr to the promoter of etha, and then repressed the transcription of etha, thus caused resistance of M.tb to ETH. Through docking analysis and in vitro validation, we identified that c-di-GMP binds 3 amino acids of Ethr, i.e., Q125, R181 and E190, while the first 2 were the major binding sites. Homology analysis showed that Ethr was highly conservative among mycobacteria. Further docking analysis showed that c-di-GMP preferentially bound proteins of TetR family at the junction hole of symmetric dimer or tetramer proteins. Our results suggest a possible drug-resistance mechanism of ETH through the regulation of Ethr by c-di-GMP.

SUBMITTER: Zhang HN 

PROVIDER: S-EPMC5517500 | biostudies-literature | 2017 Jul

REPOSITORIES: biostudies-literature

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Cyclic di-GMP regulates Mycobacterium tuberculosis resistance to ethionamide.

Zhang Hai-Nan HN   Xu Zhao-Wei ZW   Jiang He-Wei HW   Wu Fan-Lin FL   He Xiang X   Liu Yin Y   Guo Shu-Juan SJ   Li Yang Y   Bi Li-Jun LJ   Deng Jiao-Yu JY   Zhang Xian-En XE   Tao Sheng-Ce SC  

Scientific reports 20170719 1


Tuberculosis is still on the top of infectious diseases list on both mobility and mortality, especially due to drug-resistance of Mycobacterium tuberculosis (M.tb). Ethionamide (ETH) is one of effective second line anti-TB drugs, a synthetic compound similar to isoniazid (INH) structurally, with existing severe problem of ETH resistance. ETH is a prodrug, which is activated by Etha inside M.tb, and etha is transcriptionally repressed by Ethr. We found that c-di-GMP could bind Ethr, enhanced the  ...[more]

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