4.6 Article

Antimicrobial Resistance of Non-O157 Shiga Toxin-Producing Escherichia coli Isolated from Humans and Domestic Animals

Journal

ANTIBIOTICS-BASEL
Volume 10, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/antibiotics10010074

Keywords

Shiga toxin-producing Escherichia coli; STEC infection; antimicrobial drugs; multidrug resistance; whole genome sequencing

Funding

  1. National Natural Science Foundation of China [81772152, 81701977]
  2. National Science and Technology Major Project [2018ZX10201001-006, 2018ZX10301407-002]

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This study investigated the antimicrobial resistance of non-O157 Shiga toxin-producing Escherichia coli (STEC) strains in China, revealing diverse resistance patterns and the presence of various resistance genes among strains from different sources. Whole genome analysis showed genetic diversity among STEC strains from different sources, with some strains tending to cluster closely within the phylogenetic tree. These findings provide valuable information for monitoring and guiding the use of antimicrobial drugs in the management of multidrug resistant STEC strains among animals and humans.
Non-O157 Shiga toxin-producing Escherichia coli (STEC) is an important pathogen that can cause zoonotic diseases. To investigate the antimicrobial resistance of STEC in China, non-O157 STEC isolates, recovered from domestic animals and humans from 12 provinces, were analyzed using antimicrobial susceptibility testing and whole genome characterization. Out of the 298 isolates tested, 115 strains showed resistance to at least one antimicrobial and 85 strains showed multidrug resistance. The highest resistance rate was to tetracycline (32.6%), followed by nalidixic acid (25.2%) and chloramphenicol and azithromycin (both 18.8%). However, imipenem and meropenem were effective against all isolates. Antimicrobial resistance patterns varied among strains from different sources. Strains from pig, sheep, humans, and cattle showed resistance rates of 100.0%, 46.9%, 30.3%, and 6.3% to one or more antimicrobials, respectively. Forty-three genes related to 11 antimicrobial classes were identified among these strains. The colistin-resistance gene mcr was only carried by strains from pigs. A new fosfomycin-resistant gene, fosA7, was detected in strains from humans, cattle, and sheep. Whole genome phylogenetic analysis showed that strains from the four sources were genetically diverse and scattered throughout the phylogenetic tree; however, some strains from the same source had a tendency to cluster closely. These results provide a reference to monitor the emergence and spread of multidrug resistant STEC strains among animals and humans. Furthermore, with a better understanding of antimicrobial genotypes and phenotypes among the diverse STEC strains obtained, this study could guide the administration of antimicrobial drugs in STEC infections when necessary.

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