2022
DOI: 10.1016/j.psj.2021.101538
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Prevalence of qnrS-positive Escherichia coli from chicken in Thailand and possible co-selection of isolates with plasmids carrying qnrS and trimethoprim-resistance genes under farm use of trimethoprim

Abstract: One hundred and twenty chicken samples from feces (n = 80), the carcass surface at slaughter at 2 meat chicken farms (n = 20), and retail chicken meat from 5 markets (n = 20) collected during 2018 and 2019 were examined for the prevalence of plasmid-mediated quinolone resistance ( PMQR ) in Escherichia coli . We detected qnrS -positive E. coli in a total of 74 samples from feces (n = 59), the carcass surface (n = 7), an… Show more

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Cited by 5 publications
(3 citation statements)
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“…Regarding present isolates, quinolones are not used in the treatment of children infections, thereby ETEC have a limited exposure to quinolones, and the presence of mechanisms leading to low-levels of quinolone resistance with a low impact on bacterial fitness might be a good evolutive strategy. Furthermore, the use of other antimicrobial agents might favour the co-selection of genetic structures (Vien et al, 2012;Murase et al, 2022).…”
Section: Discussionmentioning
confidence: 99%
“…Regarding present isolates, quinolones are not used in the treatment of children infections, thereby ETEC have a limited exposure to quinolones, and the presence of mechanisms leading to low-levels of quinolone resistance with a low impact on bacterial fitness might be a good evolutive strategy. Furthermore, the use of other antimicrobial agents might favour the co-selection of genetic structures (Vien et al, 2012;Murase et al, 2022).…”
Section: Discussionmentioning
confidence: 99%
“…They suggested that fecal excretion is one of the reasons for the prevalence of MDR bacteria. The PMQR gene qnrS is prevalent in chicken feces ( 22 , 37 , 38 ). The qnrS gene was also found in the chicken feed ( 22 ).…”
Section: Discussionmentioning
confidence: 99%
“…The final volume of each reaction mixture was at 25 μL containing 12.5 μL of 2× GoTaq ® Green Master Mix (Promega, USA), 0.2 μM of each primer for each gene, and 2 μL of extracted DNA. No template DNA was included as a negative control and DNA of Escherichia coli containing PMQR genes was included as a positive control (Murase et al, 2022). PCR products were separated by electrophoresis with 1.5% agarose gel in 1×TBE buffer and were visualized under UV light using a gel documentation system (Bio-Rad, USA).…”
Section: Pcr Detection Of Plasmid-mediated Quinolone Resistance (Pmqr...mentioning
confidence: 99%