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Published on: November 1, 2011
Characterization of the sigmaC-encoding gene from musocvy duck reovirus
Yun Zhang1, Ming Liu, Qilin Hu
1National Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute of Chinese Academy of Agricultural Sciences, China. yunzhang03@yahoo.com
Abstract:
The sigmaC-encoding gene of two muscovy duck reovirus (DRV) S14 and C4 strains were cloned and completely sequenced. The open reading frame (ORF) comprised 810 bp and encoded 269 amino acids with a predicated molecular mass of 29.5 kDa. Expressed sigmaC fusion protein in Escherichia coli BL21 strain could be detected by Western blotting under duck anti-reovirus polyclonal serum. There are two large gap insertions at the N-terminal part of the DRV sigmaC when necessary to optimize the alignment of the amino acid sequences of the DRV sigmaC had a heptapeptide repeat and leucine zipper patterns structurally related to ARV sigmaC. All DRVs grouped into one specified genogroup within Orthoreoviruses genus subgroup II. The degree of differences between the S14/C4 and ARV was only 23-24%, and 21-22%, respectively, at both the nucleotide and deduced amino acid levels, suggested that DRVs are quite different from ARVs and should give a precise classification for DRVs in Orthoreovirus genus.
Insights
This study sequenced the sigmaC gene from Muscovy duck reoviruses (DRV), revealing unique genetic features. These findings support a distinct classification for DRVs within the Orthoreovirus genus.
Area of Science:
- Virology
- Molecular Biology
- Genomics
Background:
- Muscovy duck reoviruses (DRV) are avian pathogens.
- The sigmaC protein is a key outer-capsid protein of Orthoreoviruses, involved in cell attachment and penetration.
- Understanding DRV genetic makeup is crucial for disease control and classification.
Purpose of the Study:
- To clone, sequence, and analyze the sigmaC gene from Muscovy duck reovirus (DRV) strains S14 and C4.
- To compare the genetic and structural characteristics of DRV sigmaC with other avian reoviruses (ARV).
- To determine the phylogenetic position of DRVs within the Orthoreovirus genus.
Main Methods:
- Cloning and complete sequencing of the sigmaC-encoding gene from DRV S14 and C4 strains.
- Analysis of the open reading frame (ORF) and deduced amino acid sequence.
- Expression of DRV sigmaC fusion protein in Escherichia coli and detection via Western blotting.
- Sequence alignment and phylogenetic analysis with other reoviruses.
Main Results:
- The DRV sigmaC gene's ORF is 810 bp, encoding 269 amino acids (29.5 kDa).
- DRV sigmaC exhibits structural similarities to ARV sigmaC, including heptapeptide repeats and leucine zipper patterns.
- Phylogenetic analysis places all DRVs in a distinct genogroup within Orthoreoviruses genus subgroup II.
- DRV S14/C4 showed significant nucleotide (23-24%) and amino acid (21-22%) differences compared to ARV.
Conclusions:
- DRVs possess unique genetic and structural features distinguishing them from ARVs.
- The genetic divergence supports a precise classification of DRVs as a separate group within the Orthoreovirus genus.
- Further research into DRV pathogenesis and host interactions is warranted.
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