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Clinical isolates of Mycobacterium tuberculosis in four European hospitals are uniformly susceptible to benzothiazinones.


ABSTRACT: The new antitubercular drug candidate 2-[2-S-methyl-1,4-dioxa-8-azaspiro[4.5]dec-8-yl]-8-nitro-6-(trifluoromethyl)-4H-1,3-benzothiazin-4-one (BTZ043) targets the DprE1 (Rv3790) subunit of the enzyme decaprenylphosphoryl-beta-d-ribose 2'-epimerase. To monitor the potential development of benzothiazinone (BTZ) resistance, a total of 240 sensitive and multidrug-resistant Mycobacterium tuberculosis clinical isolates from four European hospitals were surveyed for the presence of mutations in the dprE1 gene and for BTZ susceptibility. All 240 strains were susceptible, thus establishing the baseline prior to the introduction of BTZ043 in clinical trials.

SUBMITTER: Pasca MR 

PROVIDER: S-EPMC2849388 | biostudies-literature | 2010 Apr

REPOSITORIES: biostudies-literature

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Clinical isolates of Mycobacterium tuberculosis in four European hospitals are uniformly susceptible to benzothiazinones.

Pasca Maria Rosalia MR   Degiacomi Giulia G   Ribeiro Ana Luisa de Jesus Lopes AL   Zara Francesca F   De Mori Patrizia P   Heym Beate B   Mirrione Maurizio M   Brerra Roberto R   Pagani Laura L   Pucillo Leopoldo L   Troupioti Panajota P   Makarov Vadim V   Cole Stewart T ST   Riccardi Giovanna G  

Antimicrobial agents and chemotherapy 20100119 4


The new antitubercular drug candidate 2-[2-S-methyl-1,4-dioxa-8-azaspiro[4.5]dec-8-yl]-8-nitro-6-(trifluoromethyl)-4H-1,3-benzothiazin-4-one (BTZ043) targets the DprE1 (Rv3790) subunit of the enzyme decaprenylphosphoryl-beta-d-ribose 2'-epimerase. To monitor the potential development of benzothiazinone (BTZ) resistance, a total of 240 sensitive and multidrug-resistant Mycobacterium tuberculosis clinical isolates from four European hospitals were surveyed for the presence of mutations in the dprE  ...[more]

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