Prevalence and Pathologic Characterization of Mouse Kidney Parvovirus in Sentinel CD1 Mice.

Comparative medicine Pub Date : 2024-10-31 Print Date: 2024-10-01 DOI:10.30802/AALAS-CM-24-000015
Zhongming Ge, Yan Feng, Nicola M Parry, Damodaran Annamalai, Sebastian E Carrasco, Melody Guo, Sureshkumar Muthupalani, Susan E Erdman, James G Fox
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Abstract

Mouse kidney parvovirus (MKPV) infection can cause significant morbidity and mortality by inducing moderate to severe inclusion body nephropathy and kidney fibrosis in aged immunodeficient mice. However, MKPV infection in immunocompetent mice is associated with histopathologic findings ranging from absent to minimal or moderate lymphoplasmacytic interstitial nephritis without inclusion body in most cases. We surveyed the prevalence of MKPV via PCR from August 2019 through January 2021, using feces, kidneys, and livers collected and pooled from 2 sentinel mice [Crl:CD1(ICR)] (CD1) per surveillance cage (a total of 212 cages). CD1 mice used as dirty-bedding sentinels were housed for 6 mo in a separate cage on the same rack as colony mice used in research at the Massachusetts Institute of Technology and at the Whitehead Institute for Biomedical Research. MKPV quantitative PCR positivity was 16.04%, 14.62%, and 10.02% for feces, kidney, and liver, respectively. The aggregate prevalence of MKPV was 22.64% (48 of 212 samples). Thirty-three of 103 rooms (32.04%) were MKPV positive. MKPV-positive kidneys had more severe chronic lymphoplasmacytic interstitial nephritis (CLIN) than MKPV-negative kidneys; however, there was no significant difference in hepatic lesions between MKPV-positive and -negative livers. Although no overt intranuclear inclusion body nephropathy was noted in MKPV-positive CD1 kidneys, MKPV RNA was sporadically detected within tubular epithelial cells in MKPV-positive kidneys but not in MKPV-positive livers. Our study indicates that MKPV can be easily transmitted through soiled bedding. It highlights that CD1 mice can be used as sentinels to detect MKPV, emphasizing the importance of monitoring MKPV distribution using quantitative PCR in sentinel mice if MKPV needs to be excluded from a colony. Importantly, as MKPV infection is associated with mild to moderate CLIN, MKPV can potentially confound the interpretation of in vivo biomedical data.

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小鼠肾脏 Parvovirus 在哨兵 CD1 小鼠中的流行情况和病理特征。
小鼠肾脏细小病毒(MKPV)感染会诱发老年免疫缺陷小鼠中度至重度包涵体肾病和肾脏纤维化,从而导致严重的发病率和死亡率。然而,免疫功能正常的小鼠感染 MKPV 后,组织病理学检查结果从无包涵体到轻度或中度淋巴浆细胞性间质性肾炎不等。从 2019 年 8 月到 2021 年 1 月,我们通过 PCR 调查了 MKPV 的流行情况,使用的方法是从每个监测笼(共 212 个笼)中收集并汇集 2 只哨点小鼠[Crl:CD1(ICR)](CD1)的粪便、肾脏和肝脏。作为脏垫哨兵的 CD1 小鼠与麻省理工学院和怀特海生物医学研究所用于研究的群体小鼠在同一个架子上的单独笼子中饲养 6 个月。粪便、肾脏和肝脏中的 MKPV 定量 PCR 阳性率分别为 16.04%、14.62% 和 10.02%。MKPV 的总感染率为 22.64%(212 个样本中的 48 个)。103 个房间中有 33 个(32.04%)呈 MKPV 阳性。与 MKPV 阴性肾脏相比,MKPV 阳性肾脏的慢性淋巴细胞性间质性肾炎(CLIN)更为严重;然而,MKPV 阳性肝脏和阴性肝脏的肝脏病变并无明显差异。虽然在 MKPV 阳性的 CD1 肾脏中没有发现明显的核内包涵体肾病,但在 MKPV 阳性的肾脏中的肾小管上皮细胞内零星检测到 MKPV RNA,而在 MKPV 阳性的肝脏中则没有检测到。我们的研究表明,MKPV 很容易通过弄脏的床上用品传播。它强调了 CD1 小鼠可用作检测 MKPV 的哨兵小鼠,并强调了如果需要将 MKPV 从一个鼠群中排除,使用定量 PCR 在哨兵小鼠中监测 MKPV 分布的重要性。重要的是,由于 MKPV 感染与轻度至中度 CLIN 有关,因此 MKPV 可能会混淆体内生物医学数据的解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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