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用于检测小鼠细小病毒和小鼠肝炎病毒的脏垫料转移的可靠性

Reliability of soiled bedding transfer for detection of mouse parvovirus and mouse hepatitis virus.

作者信息

Smith Peter C, Nucifora Michelle, Reuter Jon D, Compton Susan R

机构信息

Section of Comparative Medicine, Yale University School of Medicine, New Haven, CT, USA.

出版信息

Comp Med. 2007 Feb;57(1):90-6.

Abstract

Serologic monitoring of sentinel mice exposed to soiled bedding is a common method of detecting viral infections in mice. Because bedding transfer protocols vary, the sensitivity of this method has not been documented sufficiently. We examined the reliability of bedding transfer during various stages of infection with mouse parvovirus (MPV) and mouse hepatitis virus (MHV). Most mice exposed to bedding contaminated with MPV 0, 3, or 7 d previously seroconverted, whereas only mice exposed to bedding contaminated with MHV 4 h previously seroconverted, thus confirming the differing stabilities of these viruses. Index mice were inoculated with 30 times the infectious dose 50 (ID50) of MPV or 300 ID50 of MHV. At 3 d, 1 wk, and 2 wk postinoculation (PI), we transferred 25, 50, or 100 ml of bedding to cages of sentinel mice. Viral infection and shedding by index mice was confirmed by serology and fecal polymerase chain reaction assay. Transfer of soiled bedding between mice in static cages induced seroconversion of sentinel mice most reliably during peak viral shedding (1 wk PI for MPV and 3 d PI for MHV). Soiled bedding transfer between mice in individually ventilated cages induced a higher prevalence of sentinel seroconversion to MPV and MHV than that after transfer between mice in static cages. Our findings indicate that although soiled bedding transfer is an effective method for detecting MHV and MPV under optimal conditions, the method is less than 100% reliable under many conditions in contemporary mouse facilities.

摘要

对接触脏垫料的哨兵小鼠进行血清学监测是检测小鼠病毒感染的常用方法。由于垫料转移方案各不相同,该方法的敏感性尚未得到充分记录。我们研究了在感染小鼠细小病毒(MPV)和小鼠肝炎病毒(MHV)的不同阶段进行垫料转移的可靠性。大多数接触0、3或7天前被MPV污染的垫料的小鼠发生了血清转化,而只有接触4小时前被MHV污染的垫料的小鼠发生了血清转化,从而证实了这些病毒的稳定性不同。将指数小鼠接种30倍感染剂量50(ID50)的MPV或300 ID50的MHV。在接种后(PI)3天、1周和2周,我们将25、50或100毫升垫料转移到哨兵小鼠的笼子中。通过血清学和粪便聚合酶链反应分析证实指数小鼠的病毒感染和排毒情况。在静态笼子中,小鼠之间脏垫料的转移在病毒排毒高峰期(MPV为接种后1周,MHV为接种后3天)最可靠地诱导了哨兵小鼠的血清转化。与静态笼子中小鼠之间转移后相比,独立通风笼子中小鼠之间脏垫料的转移诱导哨兵小鼠对MPV和MHV血清转化的发生率更高。我们的研究结果表明,尽管脏垫料转移在最佳条件下是检测MHV和MPV的有效方法,但在当代小鼠设施的许多条件下,该方法的可靠性不到100%。

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