Review Article
Virulence Plasmid (pYV)-Associated Expression of Phenotypic Virulent Determinants in Pathogenic Yersinia Species: A Convenient Method for Monitoring the Presence of pYV under Culture Conditions and Its Application for Isolation/Detection of Yersinia pestis in Food
Table 1
Comparison of selected phenotypic expression of pYV-bearing Y. enterocolitica, Y. pseudotuberculosis, and Y. pestis (adapted from [7]).
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
aCells recovered from red pinpoint colonies and subcultured in BHI broth at 28°C are designated as RE. The pYV-negative strains of Y. enterocolitica, Y. pseudotuberculosis, and Y. pestis are designated as C (cured). bCM: colony morphology. On calcium-adequate BHA (1500 μM Ca2+), and TSA (1400 μM Ca2+) the P+ cells appeared as small colonies (1.13 mm in diameter) as compared to larger P− colonies (2.4 mm in diameter). cCV binding: crystal violet binding. The P+ cells appeared as small dark-violet colonies, and the P− cells showed large white colonies on calcium-adequate BHA (1500 μM Ca2+) and TSA (1400 μM Ca2+), low-calcium CR-BHO (238 μM Ca2+), CR-TSO (311 μM Ca2+), and calcium-deficient CR-MOX. dLcr: low calcium response/calcium-dependent growth. P+ cells appeared as pinpoint colonies (0.36 in diameter), and P− cells appeared large colonies (1.37 in diameter) on low-calcium CR-BHO (238 μM Ca2+), CR-TSO (311 μM Ca2+), and calcium-deficient CR-MOX. eCR-Uptake: Congo red-uptake. The P+ cells appeared as red pinpoint colonies (0.36 in diameter), and the P− cells appeared large white or light orange colonies (1.13 mm in diameter) on calcium-deficient CR-MOX. fAA: autoagglutination. The P+ cells agglutinated. The P− cells remained dispersed. gHP: hydrophobicity by latex particles. The P+ cells formed clumps showing hydrophobicity. The P− cells remained dispersed. hPlasmid: presence of 70-kb pYV by PCR assay. |