Author:
Schaake Julia,Drees Anna,Grüning Petra,Uliczka Frank,Pisano Fabio,Thiermann Tanja,von Altrock Alexandra,Seehusen Frauke,Valentin-Weigand Peter,Dersch Petra
Abstract
ABSTRACTIn this study, an oral minipig infection model was established to investigate the pathogenicity ofYersinia enterocoliticabioserotype 4/O:3. O:3 strains are highly prevalent in pigs, which are usually symptomless carriers, and they represent the most common cause of human yersiniosis. To assess the pathogenic potential of the O:3 serotype, we compared the colonization properties ofY. enterocoliticaO:3 with O:8, a highly mouse-virulentY. enterocoliticaserotype, in minipigs and mice. We found that O:3 is a significantly better colonizer of swine than is O:8. Coinfection studies with O:3 mutant strains demonstrated that small variations within the O:3 genome leading to higher amounts of the primary adhesion factor invasin (InvA) improved colonization and/or survival of this serotype in swine but had only a minor effect on the colonization of mice. We further demonstrated that a deletion of theinvAgene abolished long-term colonization in the pigs. Our results indicate a primary role for invasin in naturally occurringY. enterocoliticaO:3 infections in pigs and reveal a higher adaptation of O:3 than O:8 strains to their natural pig reservoir host.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
16 articles.
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