Evidence map›Paper›PMID 22985268›Full record

ArticleBMC microbiology2012

Clinical isolates of Yersinia enterocolitica biotype 1A represent two phylogenetic lineages with differing pathogenicity-related properties.

Leila M Sihvonen, Kaisa Jalkanen, Elisa Huovinen, Susanna Toivonen, Jukka Corander, Markku Kuusi, Mikael Skurnik, Anja Siitonen, Kaisa Haukka

Abstract read
In one paragraph

Article in BMC microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

  1. HighMicrobiology spectrum · 2026
    Article
  2. International journal of systematic and evolutionary microbiology · 2026
    Article
  3. The Gene Ail for the Attachment-Invasion Locus Protein ofInternational journal of molecular sciences · 2025
    Article
  4. Article
  5. EnteropathogenicPathogens (Basel, Switzerland) · 2024
    Article
  6. Yersiniosis in New Zealand.Pathogens (Basel, Switzerland) · 2021
    Review
  7. Article
  8. Viruses · 2019
    Review
  9. Article
  10. Article
  11. Article
  12. Campylobacteriosis, Salmonellosis, Yersiniosis, and Listeriosis as Zoonotic Foodborne Diseases: A Review.International journal of environmental research and public health · 2018
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

Leila M SihvonenBacteriology Unit, National Institute for Health and Welfare, Helsinki, Finland.
Kaisa Jalkanen
Elisa Huovinen
Susanna Toivonen
Jukka Corander
Markku Kuusi
Mikael Skurnik
Anja Siitonen
Kaisa Haukka

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundY. enterocolitica biotype (BT) 1A strains are often isolated from human clinical samples but their contribution to disease has remained a controversial topic. Variation and the population structure among the clinical Y. enterocolitica BT 1A isolates have been poorly characterized. We used multi-locus sequence typing (MLST), 16S rRNA gene sequencing, PCR for ystA and ystB, lipopolysaccharide analysis, phage typing, human serum complement killing assay and analysis of the symptoms of the patients to characterize 298 clinical Y. enterocolitica BT 1A isolates in order to evaluate their relatedness and pathogenic potential.

resultsA subset of 71 BT 1A strains, selected based on their varying LPS patterns, were subjected to detailed genetic analyses. The MLST on seven house-keeping genes (adk, argA, aroA, glnA, gyrB, thrA, trpE) conducted on 43 of the strains discriminated them into 39 MLST-types. By Bayesian analysis of the population structure (BAPS) the strains clustered conclusively into two distinct lineages, i.e. Genetic groups 1 and 2. The strains of Genetic group 1 were more closely related (97% similarity) to the pathogenic bio/serotype 4/O:3 strains than Genetic group 2 strains (95% similarity). Further comparison of the 16S rRNA genes of the BT 1A strains indicated that altogether 17 of the 71 strains belong to Genetic group 2. On the 16S rRNA analysis, these 17 strains were only 98% similar to the previously identified subspecies of Y. enterocolitica. The strains of Genetic group 2 were uniform in their pathogenecity-related properties: they lacked the ystB gene, belonged to the same LPS subtype or were of rough type, were all resistant to the five tested yersiniophages, were largely resistant to serum complement and did not ferment fucose. The 54 strains in Genetic group 1 showed much more variation in these properties. The most commonly detected LPS types were similar to the LPS types of reference strains with serotypes O:6,30 and O:6,31 (37%), O:7,8 (19%) and O:5 (15%).

conclusionsThe results of the present study strengthen the assertion that strains classified as Y. enterocolitica BT 1A represent more than one subspecies. Especially the BT 1A strains in our Genetic group 2 commonly showed resistance to human serum complement killing, which may indicate pathogenic potential for these strains. However, their virulence mechanisms remain unknown.

Indexed as

Genetic VariationBacterial Typing TechniquesBacteriophage TypingBlood Bactericidal ActivityCluster AnalysisComplement System ProteinsDNA, BacterialDNA, RibosomalHumansMicrobial ViabilityMolecular Sequence DataMultilocus Sequence TypingPhylogenyPolymerase Chain ReactionRNA, Ribosomal, 16SVirulenceComplement System ProteinsDNA, BacterialDNA, RibosomalRNA, Ribosomal, 16S

Identifiers

PMID22985268
PMCPMC3512526

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.