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Abstract

Pet turtles are a well-recognized source of human salmonellosis, posing a threat to human health, particularly children who commonly keep pet turtles. To date, the genomic characteristics of among pet turtles and children has not been well described. We investigated the prevalence, antimicrobial resistance (AMR) and genomic characteristics of from pet turtles in Beijing, China. In total, 9.6 % (46/480) of pet turtles were positive for with . Thompson being the dominant serovar (19/46) in 2019. Moreover, 80.4 % of were multi-drug resistant (MDR) and 60.7 % were resistant to ampicillin, streptomycin, sulfonamides and tetracycline (ASSuT). We further compared the genomes of . Thompson isolates from pet turtles (=19) with those from children with diarrhoea (=28) in the same region and year, most of which were sequence type (ST)26, with one novel ST7937 identified from a child-associated isolate. . Thompson isolates from children with diarrhoea exhibited less resistance than isolates from pet turtles. Most MDR isolates possessed multiple AMR genes, including the AmpC β-lactamase-encoding genes and which co-occurred with the IncA/C and IncHI plasmid replicon types. To the best of our knowledge, this is the first time that the gene has been detected from . Several pet turtle-associated . Thompson isolates comprised phylogenetically close clusters with those from children with diarrhoea (<20 SNP differences). Bayesian analysis demonstrated that the Chinese ST26 . Thompson strains had a recent evolutionary history and evolved into two major clades, with one clade acquiring various resistant plasmids. Our findings revealed the emergence of MDR among pet turtles in China and provided evidence for the interspecies transmission of . Thompson.

Funding
This study was supported by the:
  • the National Key R&D Program of China (Award 2020YFF0305002)
    • Principal Award Recipient: XiaoJing
  • This is an open-access article distributed under the terms of the Creative Commons Attribution License.
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/content/journal/mgen/10.1099/mgen.0.001164
2024-01-03
2025-11-09

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