Ultrafast Evolution and Loss of CRISPRs Following a Host Shift in a Novel Wildlife Pathogen, Mycoplasma gallisepticum

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Ultrafast Evolution and Loss of CRISPRs Following a Host Shift in a Novel Wildlife Pathogen, Mycoplasma gallisepticum

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dc.contributor.author Balenger, Susan
dc.contributor.author Bonneaud, Camille
dc.contributor.author Ferguson-Noel, Naola
dc.contributor.author Rodrigo, Allen
dc.contributor.author Delaney, Nigel F.
dc.contributor.author Marx, Christopher J
dc.contributor.author Hill, Geoffrey E.
dc.contributor.author Tsai, Peter Tzu-shin
dc.contributor.author Edwards, Scott V.
dc.date.accessioned 2012-04-03T17:43:30Z
dc.date.issued 2012
dc.identifier.citation Delaney, Nigel F., Susan Balenger, Camille Bonneaud, Christopher J. Marx, Geoffrey E. Hill, Naola Ferguson-Noel, Peter Tsai, Allen Rodrigo, and Scott V. Edwards. 2012. Ultrafast evolution and loss of CRISPRs following a host shift in a novel wildlife pathogen, Mycoplasma gallisepticum. PLoS Genetics 8(2): e1002511. en_US
dc.identifier.issn 1553-7390 en_US
dc.identifier.uri http://nrs.harvard.edu/urn-3:HUL.InstRepos:8497448
dc.description.abstract Measureable rates of genome evolution are well documented in human pathogens but are less well understood in bacterial pathogens in the wild, particularly during and after host switches. \(Mycoplasma\) \(gallisepticum\) (MG) is a pathogenic bacterium that has evolved predominantly in poultry and recently jumped to wild house finches \((Carpodacus\) \(mexicanus\)), a common North American songbird. For the first time we characterize the genome and measure rates of genome evolution in House Finch isolates of MG, as well as in poultry outgroups. Using whole-genome sequences of 12 House Finch isolates across a 13-year serial sample and an additional four newly sequenced poultry strains, we estimate a nucleotide diversity in House Finch isolates of only \(\sim2\%\) of ancestral poultry strains and a nucleotide substitution rate of \(0.8−1.2\times10^{−5}\) per site per year both in poultry and in House Finches, an exceptionally fast rate rivaling some of the highest estimates reported thus far for bacteria. We also found high diversity and complete turnover of CRISPR arrays in poultry MG strains prior to the switch to the House Finch host, but after the invasion of House Finches there is progressive loss of CRISPR repeat diversity, and recruitment of novel CRISPR repeats ceases. Recent (2007) House Finch MG strains retain only \(\sim50\%\) of the CRISPR repertoire founding (1994–95) strains and have lost the CRISPR–associated genes required for CRISPR function. Our results suggest that genome evolution in bacterial pathogens of wild birds can be extremely rapid and in this case is accompanied by apparent functional loss of CRISPRs. en_US
dc.description.sponsorship Organismic and Evolutionary Biology en_US
dc.language.iso en_US en_US
dc.publisher Public Library of Science en_US
dc.relation.isversionof doi:10.1371/journal.pgen.1002511 en_US
dc.relation.hasversion http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276549/pdf/ en_US
dash.license OAP
dc.subject biology en_US
dc.subject evolutionary biology en_US
dc.subject microbiology en_US
dc.subject population biology en_US
dc.subject zoology en_US
dc.title Ultrafast Evolution and Loss of CRISPRs Following a Host Shift in a Novel Wildlife Pathogen, Mycoplasma gallisepticum en_US
dc.type Journal Article en_US
dc.description.version Version of Record en_US
dc.relation.journal PLoS Genetics en_US
dash.depositing.author Edwards, Scott V.
dc.date.available 2012-04-03T17:43:30Z

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  • FAS Scholarly Articles [7501]
    Peer reviewed scholarly articles from the Faculty of Arts and Sciences of Harvard University

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