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. 2011 Sep 14;2011:727313. doi: 10.4061/2011/727313

Table 1.

Comparison of selected phenotypic expression of pYV-bearing Y. enterocolitica, Y. pseudotuberculosis, and Y. pestis (adapted from [7]).

Organisma Strain CMb CV bindingc Lcrd CR-uptakee AAf HPg Plasmidh
Y. enterocolitica GER + + + + + + +
Y. enterocolitica-RE GER + + + + + + +
Y. enterocolitica-C GER
Y. pseudotuberculosis PB1/+ + + + + + + +
Y. pseudotuberculosis-RE PB1/+ + + + + + + +
Y. pseudotuberculosis-C PB1/+
Y. pestis KIM5 + + + +
Y. pestis-RE KIM5
Y. pestis-C KIM5
pYV-less Y. pestis Kuma

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.