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Das, L.

Publications and source records attributed to Das, L..

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Pufferfish (Tetraodon cutcutia) sampled from freshwater river serves an intermediate reservoir of sucrose nonfermenting variant of Vibrio cholerae PS-4.

This study describes the genomic characteristics of Vibrio cholerae strain PS-4, which fails to ferment sucrose on thiosulfate{square}citrate{square}bile salt{square}sucrose (TCBS) agar medium. This bacterium was isolated from skin mucus of a freshwater pufferfish. In order to understand the sucrose nonfermenting phenotype, the genome of the strain PS-4 was sequenced. The gene encoding the sucrose specific phosphotransferase system IIB (sucR) was absent, resulting for the defective sucrose fermenting phenotype. In contrast, genes encoding glucose-specific transport system IIB (ptsG) and fructose specific transport system IIB (fruA) were present and showing acid production while growing with respective sugars. The overall genome relatedness indices (OGRI) such as in silico DDH, average nucleotide identity (ANI) and average amino acid identity (AAI) were above the threshold value, i.e., 70% and 95-96%, respectively. Phylogenomic analysis based on genome wide core genes and the non-recombinant core-genes, strain PS-4 clustered with Vibrio cholerae ATCC 14035T. Further, genes encoding ctx, zot, ace, tcp and rfb were absent. It showed hemolytic activity and reacted strongly to the R antibody. This is the first report on the existence of Vibrio cholerae from the pufferfish adds to our knowledge of the new ecological niche of this bacterium. IMPORTANCEVibrio cholerae, the causative agent of cholera, is a natural inhabitant of aquatic environments. It ferments sucrose, producing characteristic yellow colonies on TCBS agar. Vibrio cholerae strain PS-4 described in this study was a sucrose nonfermenting variant associated with pufferfish skin and did not produce yellow colonies on TCBS agar. Genes encoding sucrose specific phosphotransferase system IIB (sucR) was absent. The observed phenotype in the characteristic metabolic pathway indicates niche specific adaptive evolution for this bacterium. Our study suggested that nonfermenting phenotype on TCBS agar may not be considered always for Vibrio cholerae species delineation.

microbiology↗

Phenotypic and molecular characterization of extended spectrum β-lactamase producing Escherichia coli and Klebsiella pneumoniae isolates from various samples of animal origin from Assam, India

Extended-spectrum beta-lactamase (ESBL) producing Enterobacteriaceae has become a major threat globally. Here we have characterized ESBL producing E. coli and K. pneumoniae from various sources, studied antibiogram and resistance gene profiles. Out of 385 samples, 31 (8.05%) were positive for ESBL producing E. coli. Such isolates could be recovered from 10.05, 8.33, 15.63, 6.67 and 4.35 per cent of cattle milk, curd, chicken, pork and cattle faeces samples, respectively. A total of 59 (15.32%) samples were positive for ESBL producing K. pneumoniae, which were isolated from 14.35, 6.25, 21.43 and 34.78 per cent cattle milk, chicken, beef and cattle faeces, respectively. All the 90 isolates were confirmed as ESBL producers by CDT and ESBL-E strip tests. Antibiogram revealed that 74.19% and 69.49% of the ESBL producing E. coli and K. pneumoniae isolates, respectively showed resistance to ceftizoxime, 25.81% and 23.73% to both co-trimoxazole and tetracycline, 19.35% and 25.42% to ciprofloxacin, 9.68% and 16.95% to chloramphenicol, 3.23% and 5.08% to pipercillin-tazobactam, and 3.23% and 3.39% to gentamicin. Resistance gene profiling showed blaCTX-M gene as most predominant (100%). The blaTEM gene was found in 54.84% and 55.93%, blaSHV gene in 90.32% and 77.97%, Sul 1 gene in 90.32% and 86.44% of ESBL producing E. coli and K. pneumoniae isolates, respectively. The Int1 gene was detected in 70.97% and 62.71% isolates, while qnrB gene was found in 3.23% and 10.17% of E. coli and K. pneumoniae isolates, respectively.

molecular biology↗