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Accumulation of mutants in "aging" bacterial colonies is due to growth under selection, not stress-induced mutagenesis
Uppsala University, Disciplinary Domain of Science and Technology, Biology, Department of Cell and Molecular Biology, Microbiology.
University of California, Davis.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Biochemistry and Microbiology.
2008 (English)In: Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, E-ISSN 1091-6490, Vol. 105, no 33, 11863-11868 p.Article in journal (Refereed) Published
Abstract [en]

Several bacterial systems show behavior interpreted as evidence for stress-induced mutagenesis (adaptive mutation), a postulated process by which nongrowing cells temporarily increase their general mutation rate. Theoretical considerations suggest that periodic stress-induced general mutagenesis would not be advantageous in the long term, due to the high cost of deleterious mutations. Alternative explanations have been tested for very few of the systems used as evidence for stress-induced mutation. In one prominent system, mutants resistant to rifampicin (RifR; rpoB; RNA polymerase) accumulate in cell populations that “age” on solid medium with little net growth. Mutant accumulation was initially attributed to stress-induced general mutagenesis in nongrowing cells. Evidence is presented that these RifR mutants accumulate because they grow faster than parent cells during the aging period. Direct tests revealed no increase in the frequency of other mutant types during the aging period.

Place, publisher, year, edition, pages
2008. Vol. 105, no 33, 11863-11868 p.
Keyword [en]
Stress-induced mutagenesis, selection, adaptive mutation, aging, rpoB, rpoS
National Category
Natural Sciences
Research subject
Microbiology
Identifiers
URN: urn:nbn:se:uu:diva-172388DOI: 10.1073/pnas.0804739105OAI: oai:DiVA.org:uu-172388DiVA: diva2:514516
Available from: 2012-04-10 Created: 2012-04-10 Last updated: 2017-12-07Bibliographically approved

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Wrande, MarieHughes, Diarmaid
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