首页> 外文期刊>Canadian Journal of Veterinary Research >Comparison of the selection of antimicrobial resistance in fecal Escherichia coli during enrofloxacin administration with a local drug delivery system or with intramuscular injections in a swine model
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Comparison of the selection of antimicrobial resistance in fecal Escherichia coli during enrofloxacin administration with a local drug delivery system or with intramuscular injections in a swine model

机译:恩洛沙星局部给药系统或猪模型肌肉注射恩诺沙星给药过程中对大肠埃希菌耐药性选择的比较

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This study evaluated, for the first time, the selection of antibiotic resistance in fecal Escherichia coli, a potential reservoir of genes of resistance, during the prolonged exposure to fluoroquinolones after the implantation of a local drug delivery system (LDDS) in a swine model. Fourteen pigs were randomly assigned to group IM (5 mg/kg/day of intramuscular enrofloxacin — EFX) or LD (surgical implantation of EFX-polymethyl-methacrylate perifemoral implants). Blood samples were collected daily for determination of plasma EFX and ciprofloxacin (CFX) concentrations. Fecal samples were collected daily to determine the E. coli counts and the susceptibility patterns of its isolates as evaluated by antibiotic disk diffusion tests. In both groups, EFX administration significantly reduced the bacterial counts after 2 days. During recolonization, the bacterial counts remained lower than baseline in group IM but not significantly, and almost reached pre-treatment levels in group LD. Susceptibility to EFX, CFX, and nalidixic acid of recolonizing E. coli in LD pigs slightly decreased but remained within the limit of “susceptible” isolates. In contrast, quinolone susceptibility of recolonizing E. coli in IM pigs dropped dramatically (P < 0.0001). In addition, intramuscular exposure to fluoroquinolones significantly decreased the susceptibility of E. coli to ampicillin and trimethoprim-sulfamethoxazole (P < 0.05). In conclusion, the use of a dosing regimen that minimized the intestinal output of fluoroquinolones also minimized the selection of resistance to several classes of antibiotics. This could represent another advantage of LDDS usage compared to long-lasting systemic administration of fluoroquinolones.
机译:这项研究首次评估了在猪模型中植入局部药物递送系统(LDDS)后长时间暴露于氟喹诺酮类药物时,粪便大肠杆菌中的抗生素耐药性的选择,大肠杆菌是潜在的耐药基因库。 14只猪被随机分为IM组(5 mg / kg /天,肌内恩诺沙星-EFX)或LD组(EFX-聚甲基丙烯酸甲酯围手术期植入物的外科植入)。每天采集血样,以测定血浆EFX和环丙沙星(CFX)浓度。每天收集粪便样品,以确定其细菌计数,并通过抗生素圆盘扩散试验评估其分离物的敏感性。在两组中,EFX给药均在2天后显着减少了细菌计数。在重新定殖期间,IM组的细菌计数仍低于基线,但不显着,LD组几乎达到治疗前水平。 LD猪对EFX,CFX和重新定殖的大肠杆菌的萘啶酸的敏感性稍有下降,但仍在“易感”分离株的范围内。相比之下,IM猪中重新定殖的大肠杆菌的喹诺酮敏感性大大降低(P <0.0001)。此外,肌内暴露于氟喹诺酮类药物可显着降低大肠杆菌对氨苄西林和甲氧苄啶-磺胺甲基异恶唑的敏感性(P <0.05)。总之,使用最小化氟喹诺酮类药物肠道剂量的给药方案,还可以最小化对几种抗生素的抗药性选择。与氟喹诺酮类药物的长期全身给药相比,这可能代表使用LDDS的另一个优势。

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