Colibactin, a genotoxin, encoded by the pathogenicity island of belonging to the B2 phylogroup has been reported as a determinant of bacterial pathogenicity. The present study was carried out to detect the pathogenicity island in extraintestinal pathogenic (ExPEC) isolated from a tertiary hospital in Pune, India. Of 462 isolates analyzed, the genomic island was detected in 35 (7.6%) isolates, which predominantly belonged to pathogenic phylogroup B2 (97%), and harbored virulence genes such as , and . Biofilm formation assay revealed 21 of the 35 carrying isolates to be strong (SBF > 1.0), 10 isolates to be moderate (SBF = 0.5-1.0), and 4 as weak (SBF < 0.5) biofilm formers. All of the carrying isolates proved resistant against bactericidal activity of human serum. Assays carried out to detect antimicrobial susceptibility revealed 11% of these isolates to be multidrug resistant, 37% producing ESBL and 25% were positive for . The observed prevalence of multidrug resistance and colibactin producing characteristics among pathogenic belonging to phylogenetic group B2 advocate urgent need for broader surveillance in order to understand and prevent transmission of these ExPEC in community and hospital settings.
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http://dx.doi.org/10.3389/fmicb.2018.02631 | DOI Listing |
Mol Phylogenet Evol
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Biology, Universita degli Studi di Roma Tor Vergata, Italy.
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Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, Texas, USA.
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Centre for Environmental Health, Hasselt University, Hasselt, Belgium.
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Department of Genetics, The Edison Family Center for Genome Sciences & Systems Biology, Washington University School of Medicine, St. Louis, MO 63110, USA.
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Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.
Alcohol consumption is an important risk factor for multiple diseases. It is typically assessed via self-report, which is open to measurement error through recall bias. Instead, molecular data such as blood-based DNA methylation (DNAm) could be used to derive a more objective measure of alcohol consumption by incorporating information from cytosine-phosphate-guanine (CpG) sites known to be linked to the trait.
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