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research article

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

Pasca, Maria Rosalia
•
Degiacomi, Giulia
•
Ribeiro, Ana Luisa de Jesus Lopes
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2010
Antimicrobial agents and chemotherapy

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.

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Type
research article
DOI
10.1128/AAC.01676-09
Web of Science ID

WOS:000275662700030

PubMed ID

20086151

Author(s)
Pasca, Maria Rosalia
Degiacomi, Giulia
Ribeiro, Ana Luisa de Jesus Lopes
Zara, Francesca
De Mori, Patrizia
Heym, Beate
Mirrione, Maurizio
Brerra, Roberto
Pagani, Laura
Pucillo, Leopoldo
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Date Issued

2010

Published in
Antimicrobial agents and chemotherapy
Volume

54

Issue

4

Start page

1616

End page

8

Subjects

Resistance

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
UPCOL  
Available on Infoscience
September 7, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/53079
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