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DOI 10.1016/j.meegid.2013.02.009

Медицинская библиотека · Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2013

Genetic diversity and molecular evolution of the rabies virus matrix protein gene in China.

Wu Hui, Wang Lihua, Tao Xiaoyan, Li Hao, Rayner Simon, Liang Guodong, Tang Qing

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

To investigate the diversity of rabies virus (RABV) matrix protein (M) gene in the current Chinese rabies epidemic, we fully examined M gene of 63 street RABVs (Virus isolated from naturally infected animals), and performed phylogenetic and mutational analysis. Our results indicate that the Chinese RABV M gene is well conserved with 90.6% to 100% amino acid similarity. Analysis of the mutations indicates that the sequences can be divided into four groups with each group defined by distinct substitutions. The PPxY motif and residue E58, which are essential for efficient virus production and pathogenicity, were completely conserved. The estimated mean rate of nucleotide substitution was 4.6×10(-4) substitutions per site per year, and the estimated average time of the most recent common ancestor (TMRCA) was 265 years ago based on the M gene of Chinese street RABVs, which are similar to previously reported values for the glycoprotein (G) and nucleoprotein (N) gene. This indicates that the genomic RNA of RABVs circulating worldwide is stable; G, N and M genes are evolving at a similar rate. This study showed that although the Chinese RABV strains could be divided into distinct clades based on the phylogenetic analysis, their functional domains of M proteins were highly conserved.

Для цитирования: Wu Hui, Wang Lihua, Tao Xiaoyan, Li Hao, Rayner Simon, Liang Guodong, Tang Qing. Genetic diversity and molecular evolution of the rabies virus matrix protein gene in China.. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases. 2013. DOI: 10.1016/j.meegid.2013.02.009.

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