The prevalence of .in pets is a potential concern for human health. However, little is known about the pet-related spp. in China. A total of 325 fecal samples were collected from dogs, cats, and pet foxes. spp. were isolated by culture, and MALDI-TOF MS was used to identify 110 spp. isolates in total. (30.2%, 98/325), (2.5%, 8/325), and (1.2%, 4/325) were the three found species. In dogs and cats, the prevalence of spp. was 35.0% and 30.1%, respectively. A panel of 11 antimicrobials was used to evaluate the antimicrobial susceptibility by the agar dilution method. Among isolates, ciprofloxacin had the highest rate of resistance (94.9%), followed by nalidixic acid (77.6%) and streptomycin (60.2%). Multidrug resistance (MDR) was found in 55.1% (54/98) of the isolates. Moreover, 100 isolates, including 88 , 8 , and 4 , had their whole genomes sequenced. By blasting the sequence against the VFDB database, virulence factors were identified. In total, 100% of isolates carried the , and genes. The gene was present in only 13.6% (12/88) of the isolates, while the gene was absent. By analyzing the sequence against the CARD database, we found that 89.8% (79/88) of isolates had antibiotic target alteration in the gene conferring resistance to fluoroquinolone, 36.4% (32/88) had the aminoglycoside resistance gene, and 19.3% (17/88) had the tetracycline resistance gene. The phylogenetic analysis using the K-mer tree method obtained two major clades among the isolates. All eight isolates in subclade 1 possessed the gene mutation, the aminoglycoside and tetracycline resistance genes, and were phenotypically resistant to six classes of antimicrobials. It has been established that pets are a significant source of spp. strains and a reservoir for them. This study is the first to have documented the presence of spp. in pets in Shenzhen, China. In this study, of subclade 1 required additional attention due to its broad MDR phenotype and relatively high gene prevalence.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267384 | PMC |
http://dx.doi.org/10.3389/fmicb.2023.1152719 | DOI Listing |
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