Epidemiological and phylogenetic analysis of institutional mouse parvoviruses

Mouse parvoviruses (MPVs) are small, single-stranded, 5kb DNA viruses that are subclinical and endemic in many laboratory mouse colonies. MPVs cause more distinctive deleterious effects in immune-compromised or genetically-engineered mice than immuno-competent mice. At the University of Louisville (...

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Veröffentlicht in:Experimental and molecular pathology 2013-08, Vol.95 (1), p.32-37
Hauptverfasser: Joh, Joongho, Proctor, Mary L., Ditslear, Janice L., King, William W., Sundberg, John P., Jenson, A. Bennett, Ghim, Shin-Je
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Sprache:eng
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Zusammenfassung:Mouse parvoviruses (MPVs) are small, single-stranded, 5kb DNA viruses that are subclinical and endemic in many laboratory mouse colonies. MPVs cause more distinctive deleterious effects in immune-compromised or genetically-engineered mice than immuno-competent mice. At the University of Louisville (U of L), there was an unexpected increase of MPV sero-positivity for MPV infections in mouse colonies between January 2006 and February 2007, resulting in strategic husbandry changes aimed at controlling MPV spread throughout the animal facility. To investigate these MPVs, VP2 genes of seven MPVs were cloned and sequenced from eight documented incidences by PCR technology. The mutations in these VP2 genes were compared to those found at the Genbank database (NCBI; http://www.ncbi.nlm.nih.gov) and an intra-institutional phylogenetic tree for MPV infections at U of L was constructed. We discovered that the seven MPV isolates were different from those in Genbank and were not identical to each other. These MPVs were designated MPV-UL1 to 7; none of them were minute virus of mice (MVMs). Four isolates could be classified as MPV1, one was classified as MPV2, and two were defined as novel types with less than 96% and 94% homology with existing MPV types. Considering that all seven isolates had mutations in their VP2 genes and no mutations were observed in VP2 genes of MPV during a four-month time period of incubation, we concluded that all seven MPVs isolated at U of L between 2006 and 2007 probably originated from different sources. Serological survey for MPV infections verified that each MPV outbreak was controlled without further contamination within the institution. •VP2 genes of 7 primary MPVs were cloned from 8 occurrences at U of Louisville.•The seven MPV isolates were different from those in Genbank and from each other.•An intra-institutional MPV phylogenetic tree was constructed based on VP2 sequences.•All seven primary MPV isolates most likely originated from different sources.
ISSN:0014-4800
1096-0945
DOI:10.1016/j.yexmp.2013.03.009