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首页> 外文期刊>Veterinary research >In vivo therapeutic efficacy and pharmacokinetics of colistin sulfate in an experimental model of enterotoxigenic Escherichia coli infection in weaned pigs
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In vivo therapeutic efficacy and pharmacokinetics of colistin sulfate in an experimental model of enterotoxigenic Escherichia coli infection in weaned pigs

机译:硫酸大肠菌素在断奶猪肠毒素性大肠杆菌感染实验模型中的体内治疗功效和药代动力学

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Enterotoxigenic Escherichia coli (ETEC: F4) associated with post-weaning diarrhea (PWD) in pigs has developed resistance against several antimicrobial families, leading to increased use of colistin sulfate (CS) for the treatment of this disease. The objective of this study was to determine the efficacy of oral CS treatment in experimental PWD due to ETEC: F4 challenge and determine the effect of this challenge on CS intestinal absorption. In this study, 96 pigs were divided into two trials based on CS dose (100 000 or 50 000?IU/kg). Fecal shedding of ETEC: F4, total E. coli , and CS-resistant E. coli , diarrhea scores, and weight changes were evaluated. Colistin sulfate plasma concentrations were determined by HPLC–MS/MS. Regardless of the dose, CS treatment resulted in a reduction of fecal ETEC: F4 and total E. coli shedding, and in diarrhea scores but only during the treatment period. However, CS treatment resulted in a slight increase in fecal shedding of CS resistant E. coli and did not prevent weight loss in challenged pigs. In addition, challenge with ETEC: F4 resulted in an increase of CS intestinal absorption. Our study is among the first to demonstrate that under controlled conditions, CS was effective in reducing fecal shedding of ETEC: F4 and total E. coli in experimental PWD. However, CS treatment was associated with a slight selection pressure on E. coli and did not prevent pig weight loss. Further studies are needed in field conditions, to better characterize CS therapeutic regimen efficacy and bacterial resistance dissemination.
机译:与猪断奶后腹泻(PWD)相关的肠毒素性大肠杆菌(ETEC:F4)对几种抗菌素家族产生了耐药性,导致硫酸粘菌素(CS)的使用增加。这项研究的目的是确定由于ETEC:F4攻击而在实验性​​PWD中口服CS治疗的疗效,并确定该挑战对CS肠道吸收的影响。在这项研究中,根据CS剂量(100,000或50,000?IU / kg)将96头猪分为两个试验。 ETEC的粪便脱落:F4,总大肠杆菌和CS抗性大肠杆菌,腹泻评分和体重变化进行了评估。硫酸共利斯汀血浆浓度通过HPLC-MS / MS测定。不论剂量如何,CS治疗均导致粪便ETEC:F4减少和大肠杆菌总脱落,以及腹泻评分降低,但仅限于治疗期间。但是,CS处理导致CS抗性大肠杆菌的粪便排出量略有增加,并且不能防止感染猪的体重减轻。此外,对ETEC:F4的攻击导致CS肠道吸收增加。我们的研究首次证明,在受控条件下,CS可有效减少实验性PWD中ETEC:F4和总大肠杆菌的粪便脱落。但是,CS处理与对大肠杆菌的轻微选择压力有关,并且不能防止猪体重减轻。在田间条件下需要进一步研究,以更好地表征CS治疗方案的功效和细菌耐药性的传播。

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