| Literature DB >> 28400007 |
Maria Francesca Peruzy1, Nicoletta Murru1, Anna Giannina Perugini2, Federico Capuano2, Elisabetta Delibato3, Raffaelina Mercogliano1, Hannu Korkeala4, Yolande Therese Rose Proroga5.
Abstract
Yersinia enterocolitica comprises six biotypes 1A, 1B, 2, 3, 4, and 5. The virulence of the strains belonging to biotypes 1B and 2-5 depends on the presence of both chromosomal and plasmid-borne genes. Strains belonging to biotype 1A do not carry the virulence plasmid pYV. However, they carry other virulence genes, such as ystB and hreP. The aim of this study was to investigate the distribution of yadA, virF, inv, ystA, ystB, myfA, hreP and ymoA virulence genes in Y. enterocolitica strains in order to select the target genes that could be used for the development of a probe-specific real-time PCR to determine the presence of Y. enterocolitica in food samples. A total of 161 Y. enterocolitica strains isolated in eight countries and grouped into biotypes 1A, 2 (serotypes O3, O5 and O9), 3 (serotypes O3 and O9) and 4 (serotype O3) were examined for virulence genes. The most common virulence-associated gene in pathogenic Y. enterocolitica proved to be ystA, which can therefore be considered the best target gene to be amplified in order to evaluate the presence of pathogenic biotypes. By contrast, to identify Y. enterocolitica 1A strains, ystB, which codes for the enterotoxin YstB, can be proposed. This has been found in all non-pathogenic biotypes studied, but never in pathogenic biotypes.Entities:
Keywords: Sybr green RT-PCR; Y. enterocolitica; ystA gene; ystB gene
Mesh:
Substances:
Year: 2017 PMID: 28400007 DOI: 10.1016/j.fm.2017.03.004
Source DB: PubMed Journal: Food Microbiol ISSN: 0740-0020 Impact factor: 5.516