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Analysis of Yersinia enterocolitica Effector Translocation into Host Cells Using Beta-lactamase Effector Fusions
Published on: October 13, 2015
[Enteropathogenic yersinias: pathogenicity factors and new diagnostic methods]
1Institut für Hygiene und Mikrobiologie der Universität Würzburg.
Abstract:
A limited number of serotypes of Yersinia enterocolitica and Y. pseudotuberculosis is enteropathogenic for humans. During the last decade molecular biology contributed significantly to the understanding of the pathogenicity of these enteric agents. All human pathogenic Yersiniae harbour a 70-kilobase plasmid which is essential for virulence expression. Presently, thirteen plasmid-encoded polypeptides have been identified. Two of them have been identified as true outer membrane proteins and at least ten are secreted into the culture medium. Plasmid-mediated pathogenic functions are survival in serum, resistance to phagocytosis, cell adhesion, and cytotoxicity. As chromosomal determinants two invasions, one heat-stable enterotoxin and one iron-utilization system have been identified. The contribution of the iron-uptake system to mouse lethality has been clearly demonstrated. The plasmid-encoded proteins have been turned out to be more suitable antigens for serologic diagnosis of yersiniosis (immunoblotting and indirect immunofluorescence) than whole bacterial antigens.
Insights
Molecular biology advances understanding of human pathogenic Yersinia species. Plasmid-encoded proteins are key virulence factors and better diagnostic antigens for yersiniosis than whole bacterial antigens.
Area of Science:
- Microbiology
- Molecular Biology
- Immunology
Background:
- Certain Yersinia enterocolitica and Y. pseudotuberculosis serotypes cause human enteropathogenic infections.
- Molecular biology has significantly advanced the understanding of Yersinia pathogenicity in the last decade.
Purpose of the Study:
- To elucidate the role of plasmid-encoded factors in Yersinia pathogenicity.
- To identify suitable antigens for serologic diagnosis of yersiniosis.
Main Methods:
- Identification of plasmid-encoded polypeptides.
- Characterization of plasmid-mediated pathogenic functions.
- Analysis of chromosomal determinants including invasion factors, enterotoxin, and iron-utilization systems.
- Serologic diagnosis using immunoblotting and indirect immunofluorescence.
Main Results:
- Human pathogenic Yersiniae possess a 70-kilobase virulence plasmid.
- Thirteen plasmid-encoded polypeptides identified; two are outer membrane proteins, ten are secreted.
- Plasmid functions include serum survival, phagocytosis resistance, cell adhesion, and cytotoxicity.
- Chromosomal factors include invasion determinants, heat-stable enterotoxin, and an iron-utilization system.
- Iron-uptake system contributes to mouse lethality.
- Plasmid-encoded proteins are superior antigens for diagnosing yersiniosis compared to whole bacterial antigens.
Conclusions:
- The 70-kilobase plasmid is essential for virulence in pathogenic Yersinia species.
- Plasmid-encoded proteins are crucial for Yersinia pathogenesis and serve as effective diagnostic targets.
- Molecular insights into Yersinia pathogenicity enhance diagnostic strategies for yersiniosis.
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