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Characterization of four Escherichia albertii isolates collected from animals living in Antarctica and Patagonia
L. Grillová, I. Sedláček, G. Páchníková, E. Staňková, P. Švec, P. Holochová, L. Micenková, J. Bosák, I. Slaninová, D. Šmajs,
Language English Country Japan
Document type Journal Article
NLK
Free Medical Journals
from 1991
J-STAGE (Japan Science & Technology Information Aggregator, Electronic) - English
from 1991
J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - English
from 1991
PubMed Central
from 2013
Europe PubMed Central
from 2013
Open Access Digital Library
from 1991-01-01
Open Access Digital Library
from 2013-01-01
PubMed
29249728
DOI
10.1292/jvms.17-0492
Knihovny.cz E-resources
- MeSH
- Charadriiformes microbiology MeSH
- Escherichia genetics isolation & purification metabolism MeSH
- Feces microbiology MeSH
- Multilocus Sequence Typing veterinary MeSH
- Polymerase Chain Reaction veterinary MeSH
- Electrophoresis, Gel, Pulsed-Field veterinary MeSH
- Ribotyping veterinary MeSH
- RNA, Ribosomal, 16S genetics MeSH
- Spheniscidae microbiology MeSH
- Seals, Earless microbiology MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Antarctic Regions MeSH
- Chile MeSH
Escherichia albertii is a recently discovered species with a limited number of well characterized strains. The aim of this study was to characterize four of the E. albertii strains, which were among 41 identified Escherichia strains isolated from the feces of living animals on James Ross Island, Antarctica, and Isla Magdalena, Patagonia. Sequencing of 16S rDNA, automated ribotyping, and rep-PCR were used to identify the four E. albertii isolates. Phylogenetic analyses based on multi-locus sequence typing showed these isolates to be genetically most similar to the members of E. albertii phylogroup G3. These isolates encoded several virulence factors including those, which are characteristic of E. albertii (cytolethal distending toxin and intimin) as well as bacteriocin determinants that typically have a very low prevalence in E. coli strains (D, E7). Moreover, E. albertii protein extracts caused cell cycle arrest in human cell line A375, probably because of cytolethal distending toxin activity.
References provided by Crossref.org
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