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Infection and Immunity, November 2006, p. 6287-6292, Vol. 74, No. 11
0019-9567/06/$08.00+0 doi:10.1128/IAI.00363-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Timothy J. Johnson,1
James R. Johnson,2
Connie Clabots,2
Catherine M. Logue,3 and
Lisa K. Nolan1*
Department of Veterinary Microbiology and Preventive Medicine, College of Veterinary Medicine, Iowa State University, Ames, Iowa 50011,1 Mucosal and Vaccine Research Center, VA Medical Center, and Department of Medicine, University of Minnesota, Minneapolis, Minnesota,2 Department of Veterinary and Microbiological Sciences, North Dakota State University, Fargo, North Dakota 581053
Received 6 March 2006/ Returned for modification 22 May 2006/ Accepted 17 August 2006
We have found an avian pathogenic Escherichia coli (APEC) plasmid, pAPEC-O2-ColV, which contains many of the genes associated with APEC virulence and also shows similarity in content to a plasmid and pathogenicity island of human uropathogenic E. coli (UPEC). To test the possible role of this plasmid in virulence, it was transferred by conjugation along with a large R plasmid, pAPEC-O2-R, into a commensal avian E. coli strain. The transconjugant was compared to recipient strain NC, UPEC strain HE300, and donor strain APEC O2 using various assays, including lethality for chicken embryos, growth in human urine, and ability to cause urinary tract infection in mice. The transconjugant killed significantly more chicken embryos than did the recipient. In human urine, APEC O2 grew at a rate equivalent to that of UPEC strain HE300, and the transconjugant showed significantly increased growth compared to the recipient. The transconjugant also significantly outcompeted the recipient in colonization of the murine kidney. These findings suggest that APEC plasmids, such as pAPEC-O2-ColV, contribute to the pathogenesis of avian colibacillosis. Moreover, since avian E. coli and their plasmids may be transmitted to humans, evaluation of APEC plasmids as possible reservoirs of urovirulence genes for human UPEC may be warranted.
Published ahead of print on 5 September 2006.
Present address: Department of Veterinary Molecular Biology, Montana State University, Bozeman, MT 59718.
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