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Published on: November 1, 2011
Characterization of M-class genome segments of muscovy duck reovirus S14
Yun Zhang1, Dongchun Guo, Hongwei Geng
1Avian Infectious Disease Division of National Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute of Chinese Academy of Agricultural Sciences, Harbin, PR China. yunzhang03@yahoo.com
Abstract:
This report documents the first sequence analysis of the entire M1, M2, and M3 genome segments of the muscovy duck reovirus (DRV) S14. The complete sequence of each of the three M gene segments was determined. The M1 genome segment was 2283 nucleotides in length and was predicted to encode muA protein of 732 residues. The Escherichia coli expressed M1 transcripts generated a 108kDa protein, as expected for muA. A cleavage product of muA, muA1, could be detected by Western blotting with duck anti-reovirus and mouse anti-muA polyclonal serum. muA was distributed diffusely in the cytoplasma and nucleus of transfected Vero cells, which provides evidence that muA might be functional related to the mammalian reovirus (MRV) mu2. The M2 gene was 2155 nucleotides in length and was predicted to encode muB major outer capsid protein of 676 amino acids. The M3 genome segment was 1996 nucleotides in length and was predicted to encode a muNS protein of 635 amino acids. It was unexpectedly found that 5'-termini of the M1 and M2 genes ended with 5'-ACUUUU and 5'-UCUUUU, respectively, instead of 5'-GCUUUU, which is present on most mRNAs of other avian reoviruses (ARV). The UCAUC 3'-terminal sequences of the S14 M1, M2, and M3 genome segments are shared by DRV, ARV, and MRV. Alignment of the DRV muA-, muB-, and muNS-encoding genes with ARV revealed 72.9-73.9%, 67.1-69.6%, and 69.4-70.8% nucleotide identity, respectively. The amino acid sequence homology between DRV and ARV ranged from 85.3 to 86.2% (muA), 75.0 to 76.5% (muB), and 78.4 to 79.8% (muNS). Phylogenetic analyses of the M1, M2, M3, and S-class [Kuntz-Simon, G., Le Gall-Recule, G., de Boisseson, C., Jestin, V., 2002. Muscovy duck reovirus sigmaC protein is a typically encoded by the smallest genome segment. J. Gen. Virol. 83, 1189-1200; Zhang, Y., Liu, M., Hu, Q.L., Ouyang, S.D., Tong, G.Z., 2006a. Characterization of the sigmaC-encoding gene from muscovy duck reovirus. Virus Genes 36, 169-174; Zhang, Y., Liu, M., Ouyan, S.D., Hu, Q.L., Guo, D.C., Han, Z., 2006b. Detection and identification of avian, duck, and goose reoviruses by RT-PCR: goose and duck reoviruses aggregated the same specified genogroup in Orthoreovirus Genus II. Arch. Virol. 151, 1525-1538] genome segments suggests that DRV and ARV share a recent common ancestor and that the two lineages have subsequently undergone host dependent evolution.
Insights
This study presents the first full genome sequence analysis of muscovy duck reovirus (DRV) M segments, revealing genetic similarities and differences with avian reoviruses (ARV). Findings suggest a recent common ancestor and host-driven evolution between DRV and ARV lineages.
Area of Science:
- Virology
- Genomics
- Molecular Biology
Background:
- Muscovy duck reovirus (DRV) is an avian pathogen.
- Understanding the genetic makeup of DRV is crucial for disease control and prevention.
Purpose of the Study:
- To perform the first complete sequence analysis of the M1, M2, and M3 genome segments of DRV S14.
- To compare the genetic sequences and phylogenetic relationships of DRV with other reoviruses, particularly avian reoviruses (ARV).
Main Methods:
- Complete sequencing of DRV S14 M1, M2, and M3 genome segments.
- In silico analysis of predicted protein sequences and functional domains.
- Western blotting to detect expressed proteins and cleavage products.
- Cell-based assays to determine protein localization.
- Sequence alignment and phylogenetic analysis with ARV and mammalian reovirus (MRV) sequences.
Main Results:
- The complete sequences of M1 (2283 nt), M2 (2155 nt), and M3 (1996 nt) segments were determined, encoding predicted muA, muB, and muNS proteins, respectively.
- Unexpected 5'-terminal sequences (5'-ACUUUU and 5'-UCUUUU) were found for M1 and M2, differing from typical ARV sequences.
- High nucleotide and amino acid sequence homology was observed between DRV and ARV M segments (72.9-73.9% nucleotide identity for M1, 85.3-86.2% amino acid identity for muA).
- Phylogenetic analysis indicated a recent common ancestor between DRV and ARV, with subsequent host-dependent evolution.
Conclusions:
- The genetic characterization of DRV M segments provides foundational data for understanding its biology.
- Sequence similarities and differences highlight the evolutionary relationship between DRV and ARV.
- The findings suggest that host specificity may have driven the divergence of these reovirus lineages.
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