首页> 外文期刊>American Journal of Veterinary Research >Effects of subtherapeutic concentrations of antimicrobials on gene acquisition events in Yersinia, Proteus, Shigella, and Salmonella recipient organisms in isolated ligated intestinal loops of swine.
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Effects of subtherapeutic concentrations of antimicrobials on gene acquisition events in Yersinia, Proteus, Shigella, and Salmonella recipient organisms in isolated ligated intestinal loops of swine.

机译:亚治疗浓度的抗菌剂对猪结扎肠环中耶尔森菌,变形杆菌,志贺氏菌和沙门氏菌受体生物中基因获取事件的影响。

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摘要

Objective: To assess antimicrobial resistance and transfer of virulence genes facilitated by subtherapeutic concentrations of antimicrobials in swine intestines. Animals: 20 anesthetized pigs experimentally inoculated with donor and recipient bacteria. Procedures: 4 recipient pathogenic bacteria (Salmonella enterica serotype Typhimurium, Yersinia enterocolitica, Shigella flexneri, or Proteus mirabilis) were incubated with donor bacteria in the presence of subinhibitory concentrations of 1 of 16 antimicrobials in isolated ligated intestinal loops in swine. Donor Escherichia coli contained transferrable antimicrobial resistance or virulence genes. After coincubations, intestinal contents were removed and assessed for pathogens that acquired new antimicrobial resistance or virulence genes following exposure to the subtherapeutic concentrations of antimicrobials. Results: 3 antimicrobials (apramycin, lincomycin, and neomycin) enhanced transfer of an antimicrobial resistance plasmid from commensal E coli organisms to Yersinia and Proteus organisms, whereas 7 antimicrobials (florfenicol, hygromycin, penicillin G, roxarsone, sulfamethazine, tetracycline, and tylosin) exacerbated transfer of an integron (Salmonella genomic island 1) from Salmonella organisms to Yersinia organisms. Sulfamethazine induced the transfer of Salmonella pathogenicity island 1 from pathogenic to nonpathogenic Salmonella organisms. Six antimicrobials (bacitracin, carbadox, erythromycin, sulfathiazole, tiamulin, and virginiamycin) did not mediate any transfer events. Sulfamethazine was the only antimicrobial implicated in 2 types of transfer events. Conclusions and Clinical Relevance: 10 of 16 antimicrobials at subinhibitory or subtherapeutic concentrations augmented specific antimicrobial resistance or transfer of virulence genes into pathogenic bacteria in isolated intestinal loops in swine. Use of subtherapeutic antimicrobials in animal feed may be associated with unwanted collateral effects.
机译:目的:评估亚治疗浓度的猪肠道中的抗菌素耐药性和致病基因的转移。动物:20只麻醉猪经实验接种供体和受体细菌。程序:将4种受体病原菌(肠炎沙门氏菌血清型鼠伤寒,小肠结肠炎耶尔森氏菌,弗氏志贺氏菌或奇异变形杆菌)与供体细菌一起孵育,在猪中分离的结扎肠loop中,抑制浓度为16种抗菌素中的一种。供体大肠杆菌包含可转移的抗药性或毒力基因。共温育后,去除肠道内容物并评估在暴露于亚治疗浓度的抗菌剂后获得新的抗菌素耐药性或致病性基因的病原体。结果:3种抗微生物药物(apramycin,lincomycin和neomycin)增强了从普通大肠杆菌向耶尔森氏菌和变形杆菌生物体转移抗性质粒的能力,而7种抗微生物药物(氟苯尼考,潮霉素,青霉素G,罗沙酮,磺胺二甲嘧啶,四环素和四环素)整合子(沙门氏菌基因组岛1)从沙门氏菌生物体向耶尔森氏菌生物体的转移加剧。磺胺二甲嘧啶诱导沙门氏菌致病岛1从致病性沙门氏菌转移到非致病性沙门氏菌。六种抗微生物剂(杆菌肽,卡巴多昔,红霉素,磺胺噻唑,替米林和维吉尼亚霉素)未介导任何转移事件。磺胺二甲嘧啶是唯一涉及两种转移事件的抗菌剂。结论和临床意义:亚抑制或亚治疗浓度的16种抗菌药物中有10种增加了特定的抗药性,或者将毒力基因转移到了猪离体肠环中的致病菌中。在动物饲料中使用亚治疗性抗微生物药物可能会带来不良的附带影响。

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