Different region analysis for genotyping Yersinia pestis isolates from China

DFR (different region) analysis has been developed for typing Yesinia pestis in our previous study, and in this study, we extended this method by using 23 DFRs to investigate 909 Chinese Y. pestis strains for validating DFR-based genotyping method and better understanding adaptive microevolution of...

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Veröffentlicht in:PloS one 2008-05, Vol.3 (5), p.e2166-e2166
Hauptverfasser: Li, Yanjun, Dai, Erhei, Cui, Yujun, Li, Min, Zhang, Yujiang, Wu, Mingshou, Zhou, Dongsheng, Guo, Zhaobiao, Dai, Xiang, Cui, Baizhong, Qi, Zhizhen, Wang, Zuyun, Wang, Hu, Dong, Xingqi, Song, Zhizhong, Zhai, Junhui, Song, Yajun, Yang, Ruifu
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Sprache:eng
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Zusammenfassung:DFR (different region) analysis has been developed for typing Yesinia pestis in our previous study, and in this study, we extended this method by using 23 DFRs to investigate 909 Chinese Y. pestis strains for validating DFR-based genotyping method and better understanding adaptive microevolution of Y. pestis. On the basis of PCR and Bionumerics data analysis, 909 Y. pestis strains were genotyped into 32 genomovars according to their DFR profiles. New terms, Major genomovar and Minor genomovar, were coined for illustrating evolutionary relationship between Y. pestis strains from different plague foci and different hosts. In silico DFR profiling of the completed or draft genomes shed lights on the evolutionary scenario of Y. pestis from Y. pseudotuberculosis. Notably, several sequenced Y. pestis strains share the same DFR profiles with Chinese strains, providing data for revealing the global plague foci expansion. Distribution of Y. pestis genomovars is plague focus-specific. Microevolution of biovar Orientalis was deduced according to DFR profiles. DFR analysis turns to be an efficient and inexpensive method to portrait the genome plasticity of Y. pestis based on horizontal gene transfer (HGT). DFR analysis can also be used as a tool in comparative and evolutionary genomic research for other bacteria with similar genome plasticity.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0002166