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VNTR diversity in Yersinia pestis isolates from an animal challenge study reveals the potential for in vitro mutations during laboratory cultivation.
Vogler, Amy J; Nottingham, Roxanne; Busch, Joseph D; Sahl, Jason W; Shuey, Megan M; Foster, Jeffrey T; Schupp, James M; Smith, Susan R; Rocke, Tonie E; Keim, Paul; Wagner, David M.
Affiliation
  • Vogler AJ; Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, AZ, United States.
  • Nottingham R; Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, AZ, United States.
  • Busch JD; Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, AZ, United States.
  • Sahl JW; Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, AZ, United States.
  • Shuey MM; Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, AZ, United States; Department of Medicine, Vanderbilt University, School of Medicine, Nashville, TN, United States.
  • Foster JT; Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, AZ, United States; Department of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH, United States.
  • Schupp JM; Translational Genomics Research Institute North, Flagstaff, AZ, United States.
  • Smith SR; US Geological Survey, National Wildlife Health Center, Madison, WI, United States.
  • Rocke TE; US Geological Survey, National Wildlife Health Center, Madison, WI, United States.
  • Keim P; Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, AZ, United States; Translational Genomics Research Institute North, Flagstaff, AZ, United States.
  • Wagner DM; Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, AZ, United States. Electronic address: Dave.Wagner@nau.edu.
Infect Genet Evol ; 45: 297-302, 2016 11.
Article in En | MEDLINE | ID: mdl-27664903
Underlying mutation rates and other evolutionary forces shape the population structure of bacteria in nature. Although easily overlooked, similar forces are at work in the laboratory and may influence observed mutations. Here, we investigated tissue samples and Yersinia pestis isolates from a rodent laboratory challenge with strain CO92 using whole genome sequencing and multi-locus variable-number tandem repeat (VNTR) analysis (MLVA). We identified six VNTR mutations that were found to have occurred in vitro during laboratory cultivation rather than in vivo during the rodent challenge. In contrast, no single nucleotide polymorphism (SNP) mutations were observed, either in vivo or in vitro. These results were consistent with previously published mutation rates and the calculated number of Y. pestis generations that occurred during the in vitro versus the in vivo portions of the experiment. When genotyping disease outbreaks, the potential for in vitro mutations should be considered, particularly when highly variable genetic markers such as VNTRs are used.
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Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plague / Yersinia pestis / DNA, Bacterial / Minisatellite Repeats / Evolution, Molecular / Mutation Type of study: Prognostic_studies Limits: Animals Language: En Journal: Infect Genet Evol Journal subject: BIOLOGIA / DOENCAS TRANSMISSIVEIS / GENETICA Year: 2016 Document type: Article Affiliation country: United States Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plague / Yersinia pestis / DNA, Bacterial / Minisatellite Repeats / Evolution, Molecular / Mutation Type of study: Prognostic_studies Limits: Animals Language: En Journal: Infect Genet Evol Journal subject: BIOLOGIA / DOENCAS TRANSMISSIVEIS / GENETICA Year: 2016 Document type: Article Affiliation country: United States Country of publication: Netherlands