AI Article Synopsis

  • Escherichia coli is a significant cause of bacterial infections among tea tribe patients in Assam, India, with a study revealing high rates of multidrug resistance (MDR) and the presence of extended-spectrum β-lactamases (ESBLs).
  • Among 148 E. coli strains analyzed, there was a notable resistance to multiple antibiotics, including ampicillin and amoxicillin, and 26% of the isolates were identified as ESBL producers, contributing to the increasing resistance.
  • The study also utilized molecular modeling to understand the structure of ESBL proteins, emphasizing the role of previous exposure to low-quality antibiotics in rising drug resistance and aiding in future drug targeting strategies.

Article Abstract

Escherichia coli is a common major cause of bacterial infections in tea tribe patients of the northeast region of Assam, India. In this study, we documented multidrug resistance (MDR) and the prevalence of extended-spectrum β-lactamases (ESBLs) among 148 E. coli strains that were isolated from bacterial infections in tea tribe patients who had a history of self-medication. High prevalence of resistance to ampicillin (82%), amoxicillin (68%), cefixime (60%), norfloxacin (60%), nalidixic acid (60%), and co-trimoxazole (53%) was observed. Of 148 E. coli isolates, 38 (26%) were confirmed as ESBL producers. The ESBL genes were sequenced from highly resistant ESBL producing E. coli isolates. Molecular modeling was performed using MODELLER 9v10 software to determine the three-dimensional structure of a protein. This result indicates that the prevailing reason for the high prevalence of antibiotic resistance in this community is prior exposure to low-quality antibiotics, hence MDR in E. coli is increasing. ESBLs are enzymes that are produced by resistant bacteria that hydrolyze advanced generations of cephalosporin antibiotics and cause resistance, even in patients with community-acquired infections. So our results provide a framework for understanding the structure and possible binding sites of ESBL proteins for drug targeting, and the results were found to be reliable.

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Source
http://dx.doi.org/10.1089/mdr.2013.0088DOI Listing

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