Prevalence and pathologic characterization of mouse kidney parvovirus in sentinel CD1 mice Journal Article


Authors: Ge, Z.; Feng, Y.; Parry, N. M.; Annamalai, D.; Carrasco, S. E.; Guo, M.; Muthupalani, S.; Erdman, S. E.; Fox, J. G.
Article Title: Prevalence and pathologic characterization of mouse kidney parvovirus in sentinel CD1 mice
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. © 2024 American Association for Laboratory Animal Science. All rights reserved.
Keywords: controlled study; genetics; nonhuman; polymerase chain reaction; mouse; animal; animals; mice; animal tissue; kidney disease; prevalence; animal experiment; animal model; in vivo study; pathology; virology; liver; disease severity; kidney; virus rna; veterinary medicine; real time polymerase chain reaction; pathogenicity; epidemiology; feces; virus detection; virus transmission; liver injury; kidney diseases; cell nucleus inclusion body; parvovirus; rodent diseases; kidney tubule cell; female; article; parvoviridae; interstitial nephritis; cd-1 mouse; inclusion body nephropathy; parvoviridae infections; ibn; mkpv; mouse kidney parvovirus; mucpv; murine chapparvovirus; parvovirus infection; rodent disease; b6.il2rrag2w; c57bl/6 il2rg<sup>-/-</sup>rag2<sup>-/-</sup>ckit<sup>w-sh</sup> mice; clin; chronic lymphoplasmacytic interstitial nephritis; sentinel species
Journal Title: Comparative Medicine
Volume: 74
Issue: 5
ISSN: 1532-0820
Publisher: American Association for Laboratory Animal Science  
Date Published: 2024-10-01
Start Page: 344
End Page: 351
Language: English
DOI: 10.30802/aalas-cm-24-000015
PUBMED: 39503174
PROVIDER: scopus
PMCID: PMC11524405
DOI/URL:
Notes: Article -- Source: Scopus
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