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DOI 10.1016/j.meegid.2016.09.019

Медицинская библиотека · Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2016

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

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Аннотация

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.

Для цитирования: 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. VNTR diversity in Yersinia pestis isolates from an animal challenge study reveals the potential for in vitro mutations during laboratory cultivation.. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases. 2016. DOI: 10.1016/j.meegid.2016.09.019.

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