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PMID: 12676866 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Expression of heterologous O-antigen in Yersinia pestis KIM does not affect virulence by the intravenous route.

Journal of medical microbiology ·Vol. 52 ·No. Pt 4 ·2003-04-00 ·Pages 289-294

Oyston PCF, Prior JL, Kiljunen S, Skurnik M, Hill J, Titball RW

Abstract

All strains of Yersinia pestis examined have been found to lack an O-antigen. In other members of the Enterobacteriaceae, the rough phenotype often results in attenuation. However, Y. pestis is the aetiological agent of bubonic plague. In evolving from the ancestral enteropathogenic Yersinia pseudotuberculosis, and with the development of an arthropod-vectored systemic pathogenesis, smooth LPS production is not necessary for Y. pestis virulence and the metabolic burden has been alleviated by inactivation of the O-antigen biosynthetic operon. To investigate this, Y. pestis strain KIM D27 was transformed with a plasmid carrying the operon encoding the O-antigen of Yersinia enterocolitica O : 3. Expression of the O-antigen could be detected in silver-stained gels. The receptor for bacteriophage phiYeO3-12 has been shown to be O-antigen, and infection by this bacteriophage results in lysis of Y. enterocolitica O : 3. Expression of the O-antigen in Y. pestis conferred sensitivity to lysis by phiYeO3-12. The O-antigen-expressing clone was shown to be as virulent in mice by the intravenous route of challenge as the rough wild-type. Assays showed no alteration in the ability of Y. pestis to resist lysis by cationic antimicrobial peptides, serum or polymyxin.

MeSH Terms
Animals Bacteriolysis/immunology Electrophoresis, Polyacrylamide Gel Female Mice Mice, Inbred BALB C O Antigens/biosynthesis,genetics Plague/microbiology Silver Staining Transformation, Bacterial Virulence Yersinia pestis/genetics,immunology,pathogenicity
Chemicals
O Antigens
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Oyston P C F
Microbiology, DSTL, CBS Porton Down, Salisbury, Wiltshire SP4 0JQ, UK 2Department of Medical Biochemistry and Molecular Biology, Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, 20520 Turku, Finland.
Prior J L
Microbiology, DSTL, CBS Porton Down, Salisbury, Wiltshire SP4 0JQ, UK 2Department of Medical Biochemistry and Molecular Biology, Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, 20520 Turku, Finland.
Kiljunen S
Microbiology, DSTL, CBS Porton Down, Salisbury, Wiltshire SP4 0JQ, UK 2Department of Medical Biochemistry and Molecular Biology, Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, 20520 Turku, Finland.
Skurnik M
Microbiology, DSTL, CBS Porton Down, Salisbury, Wiltshire SP4 0JQ, UK 2Department of Medical Biochemistry and Molecular Biology, Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, 20520 Turku, Finland.
Hill J
Microbiology, DSTL, CBS Porton Down, Salisbury, Wiltshire SP4 0JQ, UK 2Department of Medical Biochemistry and Molecular Biology, Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, 20520 Turku, Finland.
Titball R W
Microbiology, DSTL, CBS Porton Down, Salisbury, Wiltshire SP4 0JQ, UK 2Department of Medical Biochemistry and Molecular Biology, Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, 20520 Turku, Finland.
Article Info
Journal
Journal of medical microbiology
Abbr.
J Med Microbiol
ISSN
0022-2615
Published
2003-04-00
Pages
289-294
Language
English
Region
England
NLM ID
0224131
Subset
IM
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