Journal of General Virology · 1994 · 91 citations · 9 references
Life SciencesMolecular BiologyMolecular GeneticsGenomicsMolecular VirologyVirologyAnimal VirusesViral GeneticsViral Genome OrganizationViral GenomicsViral Rna BiologyVirus Genome OrganizationGenetic Diversity Of VirusesGeographic Origin AssignmentGeographic Origin DataGeographic Origin ProfilingGeographic Origin VerificationViral Genetic VariationViral Genome SequencingVirus Evolutionary Relationships
An experimental scheme was developed for direct sequence analysis of Puumala virus-containing specimens from wild rodents (Clethrionomys glareolus). Total RNA isolated from rodent lung tissues was reverse-transcribed in the presence of a universal 11 nucleotide primer complementary to all three viral RNA segments followed by amplification in a PCR with gene-specific primers. A full-length PCR product of approximately 1800 bp from the S segment encoding the viral nucleoprotein and a product of approximately 900 bp from the M segment (encoding the C-terminal two-thirds of the G2 protein and including the 3' non-coding region) of Puumala virus (from C. glareolus trapped in Udmurtia) were prepared and sequenced. No pronounced differences to Vero cell-grown viruses were seen. The Udmurtia/894Cg/91 strain was more closely related to the Bashkiria/CG18-20/84 strain than to the Finnish prototype strain of Puumala virus, Sotkamo/V-2969/81. Thus there is a correlation with the geographic origin of the three strains. The results indicate the occurrence of genetic drift and different selection pressures leading to (i) clustering of mutations, (ii) a lower frequency of nucleotide substitutions in the coding than in the 3' noncoding regions and (iii) a higher frequency of amino acid substitutions in G2 than in the N protein.
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