Detection and Identification ofYersinia pestisby Polymerase Chain Reaction (PCR) Using Multiplex Primers
Author:
Affiliation:
1. Department of Bacteriology; National Institute of Health; Shinjuku-ku Tokyo 162 Japan
2. Center for Infection of Imported Foods and Infectious Disease; Yokohama Kanagawa 236 Japan
Publisher
Wiley
Subject
Virology,Immunology,Microbiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1348-0421.1996.tb01140.x/fullpdf
Reference15 articles.
1. Yops of pathogenic Yersinia spp.;Bliska,1994
2. The genus Yersinia: Biochemistry and genetics of virulence;Brubaker;Curr. Top. Microbiol. Immunol.,1972
3. Plasmid in Yersinia pestis;Ferber;Infect. Immun.,1981
4. Nucleotide sequence of the Yersinia pestis gene encoding F1 antigen and the primary structure of the protein. Putative T and B cell epitopes;Galyov;FEBS Lett.,1990
5. New method for plague surveillance using polymerase chain reaction to detect Yersinia pestis in fleas;Hinnebusch;J. Clin. Microbiol.,1993
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