| Literature DB >> 26045430 |
Angela Kling1, Peer Lukat2, Deepak V Almeida3, Armin Bauer4, Evelyne Fontaine5, Sylvie Sordello5, Nestor Zaburannyi1, Jennifer Herrmann1, Silke C Wenzel1, Claudia König4, Nicole C Ammerman3, María Belén Barrio5, Kai Borchers4, Florence Bordon-Pallier6, Mark Brönstrup7, Gilles Courtemanche5, Martin Gerlitz4, Michel Geslin5, Peter Hammann8, Dirk W Heinz9, Holger Hoffmann4, Sylvie Klieber10, Markus Kohlmann4, Michael Kurz4, Christine Lair5, Hans Matter4, Eric Nuermberger11, Sandeep Tyagi11, Laurent Fraisse5, Jacques H Grosset3, Sophie Lagrange5, Rolf Müller12.
Abstract
The discovery of Streptomyces-produced streptomycin founded the age of tuberculosis therapy. Despite the subsequent development of a curative regimen for this disease, tuberculosis remains a worldwide problem, and the emergence of multidrug-resistant Mycobacterium tuberculosis has prioritized the need for new drugs. Here we show that new optimized derivatives from Streptomyces-derived griselimycin are highly active against M. tuberculosis, both in vitro and in vivo, by inhibiting the DNA polymerase sliding clamp DnaN. We discovered that resistance to griselimycins, occurring at very low frequency, is associated with amplification of a chromosomal segment containing dnaN, as well as the ori site. Our results demonstrate that griselimycins have high translational potential for tuberculosis treatment, validate DnaN as an antimicrobial target, and capture the process of antibiotic pressure-induced gene amplification.Entities:
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Year: 2015 PMID: 26045430 DOI: 10.1126/science.aaa4690
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728