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Comparison of 16S rDNA analysis and rep-PCR genomic fingerprinting for molecular identification of Yersinia pseudotuberculosis

Authors
Kim, WonyongSong, Mi-OkSong, WonkeunKim, Ki-JungChung, Sang-InChoi, Chul-SoonPark, Yong-Ha
Issue Date
Mar-2003
Publisher
KLUWER ACADEMIC PUBL
Keywords
16S rDNA; genus Yersinia; rep-PCR genomic fingerprinting; Yersinia pestis; Yersinia pseudotuberculosis
Citation
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, v.83, no.2, pp 125 - 133
Pages
9
Journal Title
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY
Volume
83
Number
2
Start Page
125
End Page
133
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/25045
DOI
10.1023/A:1023301924932
ISSN
0003-6072
1572-9699
Abstract
16S rDNA sequence analysis and repetitive element sequence-based PCR (rep-PCR) genomic fingerprinting were evaluated on 11 type strains of the genus Yersinia and 17 recognized serotype strains of Y. pseudotuberculosis to investigate their genetic relatedness and to establish the value of techniques for the identification of Y. pseudotuberculosis. A phylogenetic tree constructed from 16S rDNA sequences showed that the type strains of Yersinia species formed distinct clusters with the exception of Y. pestis and Y. pseudotuberculosis. Moreover, Y. pestis NCTC 5923(T) was found to be closely related to Y. pseudotuberculosis serotypes 1b, 3, and 7. Dendrograms generated from REP-PCR, and ERIC-PCR data revealed that members of the genus Yersinia differed from each other with the degree of similarity 62% and 58%, respectively. However, the BOX-PCR results showed that Y. pestis 5923(T) clustered with the Y. pseudotuberculosis group with a degree of similarity 74%. According to these findings, 16S rDNA sequence analysis was unable to reliably discriminate Y. pseudotuberculosis from Y. pestis. However, REP-PCR and especially ERIC-PCR provided an effective means of differentiating between members of the taxa.
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