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Letter
Nature 450, 1079-1081 (13 December 2007) | doi:10.1038/nature06350; Received 9 July 2007; Accepted 4 October 2007; Published online 2 December 2007
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Postdoctoral Fellow
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Post-doctoral Research Associate
- Royal Veterinary College
- Hertfordshire AL9 7TA United Kingdom
Coevolution with viruses drives the evolution of bacterial mutation rates
Csaba Pal1,2, María D. Maciá3, Antonio Oliver3, Ira Schachar1 & Angus Buckling1
- Department of Zoology, University of Oxford, Oxford OX1 3PS, UK
- Institute of Biochemistry, Biological Research Center, Temesvári krt. 62. Szeged, H-6701, Hungary
- Servicio de Microbiologia and Unidad de Investigación, Hospital Son Dureta, Instituto Universitario de Investigación en Ciencias de la Salud (IUNICS), 07014, Palma de Mallorca, Spain
Correspondence to: Csaba Pal1,2Angus Buckling1 Correspondence and requests for materials should be addressed to A.B. (Email: angus.buckling@zoo.ox.ac.uk) or C.P. (Email: cpal@ramet.elte.hu).
Abstract
Bacteria with greatly elevated mutation rates (mutators) are frequently found in natural1, 2, 3 and laboratory4, 5 populations, and are often associated with clinical infections6, 7. Although mutators may increase adaptability to novel environmental conditions, they are also prone to the accumulation of deleterious mutations. The long-term maintenance of high bacterial mutation rates is therefore likely to be driven by rapidly changing selection pressures8, 9, 10, 11, 12, 13, 14, in addition to the possible slow transition rate by point mutation from mutators to non-mutators15. One of the most likely causes of rapidly changing selection pressures is antagonistic coevolution with parasites16, 17. Here we show whether coevolution with viral parasites could drive the evolution of bacterial mutation rates in laboratory populations of the bacterium Pseudomonas fluorescens18. After fewer than 200 bacterial generations, 25% of the populations coevolving with phages had evolved 10- to 100-fold increases in mutation rates owing to mutations in mismatch-repair genes; no populations evolving in the absence of phages showed any significant change in mutation rate. Furthermore, mutator populations had a higher probability of driving their phage populations extinct, strongly suggesting that mutators have an advantage against phages in the coevolutionary arms race. Given their ubiquity, bacteriophages may play an important role in the evolution of bacterial mutation rates.
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