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A method for microbial decontamination of Acanthamoeba cultures using the peritoneal cavity of mice简

机译:一种利用小鼠腹腔对棘阿米巴培养物进行微生物去污的方法

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Objective: To evaluate whether the inoculation of contaminated cultures in the peritoneal cavity of mice could implement decontamination of Acanthamoeba cultures.Methods: Suspensions of Acanthamoeba, Acanthamoeba polyphaga ATCC 30461, or Acanthamoeba spp. isolated from soil(Un B13 strain) were inoculated in the peritoneal cavity of Swiss mice(n = 24). After 1, 6, 12, or 24 h of exposure the peritoneal cavity was washed and assessed for the presence of bacteria, fungi, and Acanthamoeba.Results: After 1 h of intraperitoneal inoculation at least 97% of the bacteria and 96% of the fungi(P < 0.05) and 99% of the bacteria(P < 0.05) were successfully eliminated from the ATCC 30461 strain and from the soil isolate Un B13 strain, respectively. This method also allowed the recovery of most trophozoites and cysts from both Acanthamoeba cultures at the end of 24 h.Conclusions: Our data demonstrated that this technique has great potential for decontamination of Acanthamoeba cultures in a short period of time.
机译:目的:评价小鼠腹膜腔内的受污染培养物的接种是否可以实施Acanthamoeba培养物的净化。方法:Acanthamoeba,Acanthamoeba Polyphaga ATCC 30461或Acanthamoeba SPP的悬浮液。接种来自土壤(UN B13菌株)的瑞士小鼠的腹膜腔(n = 24)。在接触1,6,12或24小时后,洗涤腹膜腔并评估细菌,真菌和acanthamoeba.results:1小时后,腹膜内接种至少97%的细菌和96%的细菌真菌(P <0.05)和99%的细菌(P <0.05)分别从ATCC 30461菌株和土壤分离株UN B13菌株成功消除。该方法还允许在24小时结束时从Acanthamoeba培养物中恢复大多数滋养体和囊肿:我们的数据表明,这种技术在短时间内具有巨大净化Acanthamoba培养的潜力。

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