O'Connell Kathryn A, Tigyi Gabor J, Livingston Robert S, Johnson Daniel L, Hamilton David J
Departments of Comparative Medicine, University of Tennessee Health Science Center, Memphis, Tennessee;, Email:
Departments of Physiology, University of Tennessee Health Science Center, Memphis, Tennessee.
J Am Assoc Lab Anim Sci. 2021 Mar 1;60(2):160-167. doi: 10.30802/AALAS-JAALAS-20-000086. Epub 2021 Feb 24.
Recent studies have evaluated alternatives to the use of live animals in colony health monitoring. Currently, an alternative method that is suitable for all rack types and that has been verified to detect the infectious agents most commonly excluded from mouse colonies is unavailable. We compared the use of filter paper placed on the inside floor of mouse cages to the traditional use of sentinel mice in the detection of several prevalent murine pathogens including mouse hepatitis virus (MHV), murine norovirus (MNV), minute virus of mice (MVM), mouse parvovirus (MPV), Theiler murine encephalomyelitis virus (TMEV), spp., and Experimental groups comprised 7 cages containing either 2 pieces of filter paper on the cage floor or 2 ICR sentinel mice. Soiled bedding from pet-store mice was transferred to the experimental cages weekly for 8 wk. At 1 and 2 mo after bedding transfer, the filter papers were evaluated by PCR and sentinel mice were tested by serology and fecal PCR. Filter papers detected all pathogens as effectively (MHV, MNV, MPV, MVM, TMEV and ) or more effectively ( spp.) than sentinel mice at both time points. Filter papers more readily detected pathogens with a high copy number per RT-PCR analysis than a low copy number. spp. were not detected by sentinel mice at either time point. These results indicate that the use of filter paper placed on the interior floor of empty mouse cages and exposed to soiled bedding is efficient in detecting bacteria, endoparasites, and most of the common mouse viruses included in an animal health monitoring program.
最近的研究评估了在群体健康监测中替代使用活体动物的方法。目前,一种适用于所有笼架类型且已被验证能检测出小鼠群体中最常见被排除的传染原的替代方法尚不存在。我们将放置在小鼠笼内底部的滤纸的使用与传统的哨兵小鼠的使用进行了比较,以检测几种常见的鼠类病原体,包括小鼠肝炎病毒(MHV)、鼠诺如病毒(MNV)、小鼠微小病毒(MVM)、小鼠细小病毒(MPV)、泰勒氏鼠脑脊髓炎病毒(TMEV)、 属 以及 。实验组包括7个笼子,每个笼子的笼底放置2张滤纸或2只ICR哨兵小鼠。每周将宠物店小鼠的脏垫料转移到实验笼中,持续8周。在垫料转移后的1个月和2个月,通过PCR评估滤纸,通过血清学和粪便PCR检测哨兵小鼠。在两个时间点,滤纸检测到所有病原体的效果(MHV、MNV、MPV、MVM、TMEV和 )与哨兵小鼠相当,或( 属 )比哨兵小鼠更有效。与低拷贝数的病原体相比,滤纸在每次RT-PCR分析中更容易检测到高拷贝数的病原体。在两个时间点,哨兵小鼠均未检测到 属 。这些结果表明,将滤纸放置在空小鼠笼的内部底部并使其接触脏垫料,在检测动物健康监测项目中包括的细菌、内寄生虫和大多数常见小鼠病毒方面是有效的。