Detection of virulence factors of Escherichia coli focused on prevalence of EAST1 toxin in stool of diarrheic and non-diarrheic piglets and presence of adhesion involving virulence factors in astA positive strains
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
21864997
DOI
10.1016/j.vetmic.2011.07.029
PII: S0378-1135(11)00425-1
Knihovny.cz E-zdroje
- MeSH
- bakteriální adheze fyziologie MeSH
- bakteriální adheziny genetika metabolismus MeSH
- bakteriální fimbrie genetika metabolismus MeSH
- enterotoxigenní Escherichia coli izolace a purifikace MeSH
- enterotoxiny izolace a purifikace metabolismus MeSH
- Escherichia coli genetika izolace a purifikace metabolismus patogenita MeSH
- faktory virulence metabolismus MeSH
- feces mikrobiologie MeSH
- infekce vyvolané Escherichia coli patologie veterinární MeSH
- nemoci prasat epidemiologie mikrobiologie MeSH
- polymerázová řetězová reakce veterinární MeSH
- prasata MeSH
- prevalence MeSH
- proteiny z Escherichia coli genetika metabolismus MeSH
- průjem mikrobiologie patologie veterinární MeSH
- shiga toxin metabolismus MeSH
- virulence MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Česká republika MeSH
- Názvy látek
- bakteriální adheziny MeSH
- enterotoxiny MeSH
- faktory virulence MeSH
- proteiny z Escherichia coli MeSH
- shiga toxin MeSH
Between 2005 and 2009, a total of 800 Escherichia coli strains isolated from piglets with diarrhea were tested for the presence of enteroaggregative heat-stable enterotoxin EAST1, heat-labile (LT) and heat-stable enterotoxins (STa) and shigatoxin (Stx2e) by PCR with the purpose of investigating the present distribution of virulence factors on swine farms in the Czech Republic. The isolates were analyzed for their O-serogroup, fimbrial (K88, K99, 987P, F41, F18) and nonfimbrial adhesins (adhesin involved in diffuse adherence AIDA and porcine attaching and effacing-associated factor PAA). The detection rates of ETEC and STEC isolates were 36.5% and 7.75%, respectively, which implies that ETEC play the major role in E. coli infections in Czech herds. Generally, the most common serotype was O149:K88 which possessed genetic determinants for LT and EAST1. None of the tested E. coli isolates was positive for genes K99, 987P and F41. It was shown that out of 800 E. coli strains isolated from pigs, 277 were EAST1 positive and 74% from the latter were identified as ETEC. Of the fimbrial adhesins, K88 and F18 were commonly detected. Over 80% of K88/EAST1 positive strains possessed the gene for paa. We detected no EAE isolate positive for fimbrial adhesins or PAA and AIDA. The AIDA was more often associated with F18 than with K88. The gene astA was also identified among E. coli isolates of non-diarrheic piglets. We tested rectal swab samples collected from apparently healthy piglets on three farms. On all farms, E. coli astA positive strains (26.66%, 90.00% and 46.66% astA positive animals) were isolated. Our results showed a significantly higher prevalence of astA positive E. coli isolates among apparently healthy piglets in comparison with diarrheic piglets. The question remains as to what is the role of the astA gene in the pathogenesis of porcine colibacillosis and as a virulence factor.
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