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Serotype-related HEp-2 Cell Interaction of Yersinia Enterocolitica

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Journal Infect Immun
Date 1986 Apr 1
PMID 2870030
Citations 8
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Abstract

The ability of human clinical isolates of Yersinia enterocolitica to interact with HEp-2 cells was found to vary considerably between the serotypes O:3, O:8, and O:9. Although all three serotypes adhered initially to the cell surface, regardless of incubation temperature of the bacterial inoculum or presence of the 40- to 48-megadalton virulence plasmid, the ability to localize intracellularly was not uniformly expressed. By using a combined light optical method based on differential interference contrast and UV incident light microscopy, we found that in serotype O:3, resistance to internalization was dependent upon prior growth at 37 degrees C and carriage of the virulence plasmid; in serotype O:9, this property was plasmid dependent but not temperature dependent; in serotype O:8, it was constitutive. The ability of serotype O:3 to resist internalization was correlated with the expression of plasmid-associated fibrillae on the bacterial surface. No relationship between fibrillation and HEp-2 cell interaction was apparent for serotype O:8 or O:9. Serotypes O:8 and O:9, unlike the O:3 strains studied, associated with HEp-2 cells in greater number after cultivation at 22 degrees C than after cultivation at 37 degrees C. We failed to establish a correlation between the expression of surface fibrillae and the ability to evoke guinea pig conjunctivitis.

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References
1.
Aulisio C, Hill W, Stanfield J, Sellers Jr R . Evaluation of virulence factor testing and characteristics of pathogenicity in Yersinia enterocolitica. Infect Immun. 1983; 40(1):330-5. PMC: 264852. DOI: 10.1128/iai.40.1.330-335.1983. View

2.
Portnoy D, Wolf-Watz H, Bolin I, Beeder A, Falkow S . Characterization of common virulence plasmids in Yersinia species and their role in the expression of outer membrane proteins. Infect Immun. 1984; 43(1):108-14. PMC: 263395. DOI: 10.1128/iai.43.1.108-114.1984. View

3.
Bolin I, Norlander L, Wolf-Watz H . Temperature-inducible outer membrane protein of Yersinia pseudotuberculosis and Yersinia enterocolitica is associated with the virulence plasmid. Infect Immun. 1982; 37(2):506-12. PMC: 347563. DOI: 10.1128/iai.37.2.506-512.1982. View

4.
Kapperud G . Yersinia enterocolitica and Yersinia like microbes isolated from mammals and water in Norway and Denmark. Acta Pathol Microbiol Scand B. 1977; 85(2):129-35. DOI: 10.1111/j.1699-0463.1977.tb01686.x. View

5.
Skurnik M, Bolin I, Heikkinen H, PIHA S, Wolf-Watz H . Virulence plasmid-associated autoagglutination in Yersinia spp. J Bacteriol. 1984; 158(3):1033-6. PMC: 215546. DOI: 10.1128/jb.158.3.1033-1036.1984. View