| Literature DB >> 21349992 |
Anne Jolivet-Gougeon1, Bela Kovacs2, Sandrine Le Gall-David1, Hervé Le Bars1, Latifa Bousarghin1, Martine Bonnaure-Mallet1, Bernard Lobel3, François Guillé3, Claude-James Soussy4, Peter Tenke2.
Abstract
Heritable hypermutation in bacteria is mainly due to alterations in the methyl-directed mismatch repair (MMR) system. MMR-deficient strains have been described from several bacterial species, and all of the strains exhibit increased mutation frequency and recombination, which are important mechanisms for acquired drug resistance in bacteria. Antibiotics select for drug-resistant strains and refine resistance determinants on plasmids, thus stimulating DNA recombination via the MMR system. Antibiotics can also act as indirect promoters of antibiotic resistance by inducing the SOS system and certain error-prone DNA polymerases. These alterations have clinical consequences in that efficacious treatment of bacterial infections requires high doses of antibiotics and/or a combination of different classes of antimicrobial agents. There are currently few new drugs with low endogenous resistance potential, and the development of such drugs merits further research.Entities:
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Year: 2011 PMID: 21349992 DOI: 10.1099/jmm.0.024083-0
Source DB: PubMed Journal: J Med Microbiol ISSN: 0022-2615 Impact factor: 2.472