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Reverse Genetics Mediated Recovery of Infectious Murine Norovirus
Published on: June 24, 2012
[Isolation, identification and genetic analysis of a murine norovirus strain]
Abstract:
Murine norovirus (MNV) was first discovered in mice in 2003. MNV is a member of the genus Norovirus in the family Caliciviridae. It is one of the most important and prevalent pathogens of laboratory mice, and almost all mouse strains are susceptible to MNV infection. In this study, a MNV strain was isolated from the cecal contents of infected mice and identified by the cytopathic effect (CPE) assay, virus plaque assay, 50% tissue culture infectious dose (TCID50) assay, electron microscopy, indirect immunofluorescence assay (IFA) and nucleotide sequencing. On infection, the RAW264.7 cell line showed obvious cytopathic effects within 24 to 48 hours post-inoculation, as infected cells became rounded, bright and shrunken, with ultimate disintegration of the cell sheet. After the isolation of the MNV virus, the virus was plaque-purified in RAW264.7 cells. The TCID50 of the virus was 10(5.25/0.1 mL. Electron microscopic observations of the purified virus showed the presence of spherical and non-enveloped viral particles that were 30 to 35 nm in diameter. According to the identification results, the isolate was named as MNV Guangzhou/K162/09/CHN. Thereafter, five overlapping gene fragments that covered the entire open reading frame (ORF) were amplified by RT-PCR, and the 3'-untranslated region (UTR) and 5'-UTR were amplified using the 3'-rapid amplification of cDNA ends (RACE) and the 5'-RACE method, respectively. Each of the gene fragments were cloned and sequenced, and whole genome sequences of the strain were obtained by assembling the cDNA fragment sequences. The results showed that the length of the complete genome was 7 380 nucleotides (GenBank accession number: HQ317203). The comparison of nucleotide and deduced amino acid sequences of the isolate was performed against other MNV strains in the GenBank database. A phylogenetic tree based on VP1 nucleotide sequences was constructed using MEGA5.0 software. The homology of nucleotides between the MNV Guangzhou/K162/09/CHN strain and other MNV isolates ranged from 87.4% to 89.7%. Phylogenetic analysis showed that there was a close genetic relationship between the Guangzhou/K162/09/CHN strain and MNV strains isolated from Japan (S7-P2 and S7-PP3 isolates), Korea (K4 isolate), and Germany (Berlin/04/06/DE and Berlin/05/06/DE isolates). This is the first report of the isolation and identification of MNV in China, and the first report of the genetic analysis of its complete genome.
Insights
This study reports the first isolation and complete genome sequencing of Murine norovirus (MNV) in China. The findings provide crucial insights into MNV epidemiology and genetic diversity in laboratory mice.
Area of Science:
- Virology
- Molecular Biology
Context:
- Murine norovirus (MNV) is a significant pathogen in laboratory mice, affecting research reproducibility.
- Understanding MNV prevalence and genetic characteristics is vital for animal health and research integrity.
Purpose:
- To isolate and identify a novel strain of Murine norovirus (MNV) from infected mice in China.
- To determine the complete genome sequence of the identified MNV strain and analyze its genetic relationship with other known MNV strains.
Summary:
- A MNV strain, designated MNV Guangzhou/K162/09/CHN, was successfully isolated from mouse cecal contents using various assays including CPE, plaque assay, and TCID50.
- The complete genome sequence (7,380 nucleotides) was determined, revealing an 87.4%–89.7% nucleotide homology with other MNV strains.
- Phylogenetic analysis indicated a close genetic relationship between the Chinese isolate and strains from Japan, Korea, and Germany.
Impact:
- This research marks the first report of MNV isolation and complete genome characterization in China.
- The findings contribute to a better understanding of MNV genetic diversity and geographical distribution.
- Establishes a foundation for future studies on MNV pathogenesis and control in research settings.

