Characteristics of Yersinia pseudotuberculosis isolated from animals in Brazil

J Appl Microbiol. 1998 Oct;85(4):703-7. doi: 10.1111/j.1365-2672.1998.00579.x.

Abstract

Strains (105) of Yersinia pseudotuberculosis isolated in Brazil between 1982 and 1990 were bio-serotyped. They were also studied for plasmid profile, autoagglutination and calcium dependence at 37 degrees C, Congo red uptake, pyrazinamidase activity, esculin hydrolysis, salicin fermentation and drug sensitivity: 95.24% were biotype 2, serogroup O:3; 2.86% were biotype 1, serogroup O:1; and 1.90% were biotype 2, non-agglutinable. Plasmids were found in 77.14% of the strains (one in each strain). There was total correlation between the presence of the virulence plasmid and autoagglutination, calcium dependence at 37 degrees C and Congo red uptake. The esculin, salicin and pyrazinamidase tests were not efficient in differentiating pathogenic from non-pathogenic Y. pseudotuberculosis isolates. All strains were highly sensitive to the drugs used. These results indicate that Y. pseudotuberculosis is a potential pathogen for humans in Brazil, especially because the bio-serogroups detected among animals are those most frequently associated with human diseases.

MeSH terms

  • Amidohydrolases / metabolism
  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Bacterial Typing Techniques
  • Benzyl Alcohols / metabolism
  • Calcium / metabolism
  • Congo Red / metabolism
  • Esculin / metabolism
  • Feces / microbiology
  • Glucosides
  • Humans
  • Microbial Sensitivity Tests
  • Plasmids / analysis
  • Serotyping
  • Virulence
  • Yersinia pseudotuberculosis / classification*
  • Yersinia pseudotuberculosis / isolation & purification
  • Yersinia pseudotuberculosis / pathogenicity
  • Yersinia pseudotuberculosis / physiology*
  • Yersinia pseudotuberculosis Infections / microbiology
  • Yersinia pseudotuberculosis Infections / veterinary*

Substances

  • Anti-Bacterial Agents
  • Benzyl Alcohols
  • Glucosides
  • Esculin
  • Congo Red
  • salicin
  • Amidohydrolases
  • pyrazinamide deamidase
  • Calcium