环境卫生监测对鼠肺囊虫感染的检测与修复。

Lauren M Habenicht, Shari Hamilton, Marcia L Hart, Michael K Fink, Derek L Fong, Jori K Leszczynski, Christopher A Manuel
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引用次数: 0

摘要

与床褥脏哨(SBS)血清学相比,PCR检测在环境卫生监测中的灵敏度提高,可以识别被认为排除在研究动物设施之外的啮齿动物病原体。鼠类病原体监测排气粉尘检测结果显示,有3个菌落存在鼠肺囊虫,这是以往SBS血清学检测中未发现的。本病例系列描述了用于识别、消除或分离感染鼠腹假体的动物的后续检测过程。在单独通风的笼子(IVC)架子上对架子、排和笼子水平的排气粉尘进行PCR检测,以确定所有感染的笼子。根据我们的经验,IVCs和标准的笼子处理方法足以在免疫系统改变的小鼠中控制这种有机体,这可能是慢性鼠单胞杆菌感染的温床。具有活跃的小鼠进口计划的机构仍然面临从仍然依赖SBS血清学来鉴定该病原体的机构接收鼠腹假体阳性动物的持续风险。鼠笼产生的粉尘的PCR检测可用于定位在IVC架上饲养的鼠腹假单胞菌感染的小鼠。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection and Remediation of Pneumocystis murina Infections by Environmental Health Monitoring.

The increased sensitivity of PCR testing for environmental health monitoring compared with soiled bedding sentinel (SBS) serology can identify rodent pathogens thought to be excluded from a research animal facility. Exhaust dust testing for rodent pathogen surveillance revealed the presence of Pneumocystis murina in 3 colonies that was undetected in previous years of SBS serologic testing. This case series describes the process of follow-up testing used to identify and eliminate or isolate animals infected with P. murina. PCR testing of exhaust dust at the rack, row, and cage level on individually ventilated cage (IVC) racks was leveraged to identify all infected cages. Based on our experience, IVCs and standard cage handling practices are sufficient to contain this organism in mice with altered immune systems, which can harbor chronic P. murina infections. Institutions with an active mouse import program are at ongoing risk of accepting P. murina-positive animals from institutions still relying on SBS serology to identify this pathogen. PCR testing of rodent cage-generated dust can be used to pinpoint P. murina-infected mice housed on IVC racks.

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