|
|
||||||||
DIAGNOSTICS, TYPING AND IDENTIFICATION |
Division of Infection and Immunity, Institute of Biomedical and Life Sciences, Joseph Black Building, University of Glasgow, Glasgow G12 8QQ, UK
Correspondence Robert L. Davies r.l.davies{at}bio.gla.ac.uk
Received5 July 2002 Accepted15 September 2002
One hundred and fifty-eight porcine strains of Pasteurella multocida, recovered primarily from cases of pneumonic pasteurellosis or progressive atrophic rhinitis (PAR) in England and Wales, were characterized by determination of their capsular types, presence or absence of the toxA gene and molecular mass heterogeneity of the heat-modifiable (OmpA) and porin (OmpH) proteins. Eighteen groups (clones) of strains were identified on the basis of specific combinations of capsular type, toxA status and outer-membrane protein (OMP)-type. The data provided evidence that different subpopulations of P. multocida are responsible for pneumonia and PAR in pigs. The majority (88 %) of cases of pneumonia were associated exclusively with non-toxigenic capsular type A strains of OMP-types 1.1, 2.1, 3.1 and 5.1 and capsular type D isolates of OMP-type 6.1. These strains were recovered from widespread geographical locations within England and Wales over a 12-year period and represented mostly single sporadic cases. The association of a small number of P. multocida variants with the majority of cases of porcine pneumonia suggests that these strains are not opportunistic pathogens of low virulence but represent primary pathogens with a relatively high degree of virulence. In contrast, the majority (76 %) of cases of PAR were associated with toxA-containing capsular type D strains of OMP-type 4.1 and capsular type A and D strains of OMP-type 6.1. Toxigenic capsular type A strains associated with PAR and non-toxigenic capsular type A strains associated with pneumonia represent distinct subpopulations of P. multocida that can be differentiated by their OMP-types. The association of capsular types A and D with strains of the same OMP-types, and the absence and presence of the toxA gene in strains of the same OMP-types, suggest that horizontal transfer of capsular biosynthesis and toxA genes has occurred between strains representing certain subpopulations of P. multocida.
This article has been cited by other articles:
![]() |
X. Tang, Z. Zhao, J. Hu, B. Wu, X. Cai, Q. He, and H. Chen Isolation, Antimicrobial Resistance, and Virulence Genes of Pasteurella multocida Strains from Swine in China J. Clin. Microbiol., April 1, 2009; 47(4): 951 - 958. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Wheeler Outer membrane proteomics of Pasteurella multocida isolates to identify putative host-specificity determinants Bioscience Horizons, March 1, 2009; 2(1): 1 - 12. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Campoy, J. Aranda, G. Alvarez, J. Barbe, and M. Llagostera Isolation and Sequencing of a Temperate Transducing Phage for Pasteurella multocida. Appl. Envir. Microbiol., May 1, 2006; 72(5): 3154 - 3160. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Catry, K. Chiers, S. Schwarz, C. Kehrenberg, A. Decostere, and A. de Kruif Fatal Peritonitis Caused by Pasteurella multocida Capsular Type F in Calves J. Clin. Microbiol., March 1, 2005; 43(3): 1480 - 1483. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Christensen, M. Bisgaard, O. Angen, W. Frederiksen, and J. E. Olsen Characterization of Sucrose-Negative Pasteurella multocida Variants, Including Isolates from Large-Cat Bite Wounds J. Clin. Microbiol., January 1, 2005; 43(1): 259 - 270. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. L. Davies Genetic diversity among Pasteurella multocida strains of avian, bovine, ovine and porcine origin from England and Wales by comparative sequence analysis of the 16S rRNA gene Microbiology, December 1, 2004; 150(12): 4199 - 4210. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | J MED MICROBIOL | MICROBIOLOGY | J GEN VIROL | ALL SGM JOURNALS |