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Cited by 57Yersinia bacterium, plague, ectoparasites researchEscherichia coli research studiesMicrobial infections and disease research

Yersinia adhesins: An arsenal for infection

Chauhan, Nandini, Wrobel, Agnieszka, Skurnik, Mikael, Leo, Jack C.·2016·PROTEOMICS - CLINICAL APPLICATIONS
DOI 10.1002/prca.201600012
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Abstract

The Yersiniae are a group of Gram-negative coccobacilli inhabiting a wide range of habitats. The genus harbors three recognized human pathogens: Y. enterocolitica and Y. pseudotuberculosis, which both cause gastrointestinal disease, and Y. pestis, the causative agent of plague. These three organisms have served as models for a number of aspects of infection biology, including adhesion, immune evasion, evolution of pathogenic traits, and retracing the course of ancient pandemics. The virulence of the pathogenic Yersiniae is heavily dependent on a number of adhesin molecules. Some of these, such as the Yersinia adhesin A and invasin of the enteropathogenic species, and the pH 6 antigen of Y. pestis, have been extensively studied. However, genomic sequencing has uncovered a host of other adhesins present in these organisms, the functions of which are only starting to be investigated. Here, we review the current state of knowledge on the adhesin molecules present in the Yersiniae, and their functions and putative roles in the infection process.

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  • YadA is a central virulence factor of Y. enterocolitica and mediates binding to host cells and extracellular matrix components, evasion of phagocytosis, and serum resistance.

    “YadA is a central virulence factor of Y. enterocolitica and, in addition to autoaggregation, mediates binding to host cells and extracellular matrix components, evasion of phagocytosis, and serum resistance [139].”

    From Bacterial autoaggregation (2018) · cites this paper as [139]

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Authors
Chauhan, N., Wrobel, A., Skurnik, M., & Leo, J. C.
Affiliations
  • University of Oslo (NO)
  • Evolution and Genetics Department of Biosciences University of Oslo Oslo Norway
  • University of Helsinki (FI)
Corresponding author
Leo, Jack C.
ORCID
Venue
PROTEOMICS - CLINICAL APPLICATIONS
Publisher
Wiley
Published
2016-05-17
Volume
10
Issue
9-10
Pages
949-963
ISSN
  • 1862-8346 (ISSN-L)
  • 1862-8354
DOI
10.1002/prca.201600012
OpenAlex
W2341359807
Cited by
57
References
171
Citations by year
2026: 3 · 2025: 4 · 2024: 4 · 2023: 4 · 2022: 7 · 2021: 4 · 2020: 11 · 2019: 5 · 2018: 11 · 2017: 4
FWCI
0.89
Type
journal article
Language
en
Open access
closed
Licence
onlinelibrary.wiley.com/termsAndConditions#vor (vor)
Locations
  • PROTEOMICS - CLINICAL APPLICATIONS (publishedVersion)
  • PubMed (publishedVersion)
  • Nottingham Trent University's Institutional Repository (Nottingham Trent Repository) (acceptedVersion)
Funders
VISTA, a basic research program funded by Statoil, conducted in close collaboration with The Norwegian Academy of Science and Letters
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Yersinia bacterium, plague, ectoparasites research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Escherichia coli research studies
  • Life Sciences › Immunology and Microbiology › Microbiology › Microbial infections and disease research
Keywords
Yersinia, adhesins, Yersinia enterocolitica, Yersinia pseudotuberculosis, Yersinia pestis, bacterial adhesion, virulence factors, immune evasion, invasin, infection biology
MeSH terms
Protein Conformation, beta-Strand, Animals, Humans, Fimbriae, Bacterial, Yersinia, Yersinia Infections, Adhesins, Bacterial

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