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Virus research2015; 210; 271-278; doi: 10.1016/j.virusres.2015.08.021

Identification of G and P genotype-specific motifs in the predicted VP7 and VP4 amino acid sequences.

Abstract: Equine rotavirus (ERV) strain L338 (G13P[18]) has a unique G and P genotype. However, the evolutionary relationship of L338 with other ERVs is still unknown. Here whole genome analysis of the L338 ERV strain was independently performed. Its genotype constellations were determined as G13-P[18]-I6-R9-C9-M6-A6-N9-T12-E14-H11, confirming previous genotype assignments. The L338 strain only shared the P[18] and I6 genotypes with other ERVs. The nucleotide sequences of the other 9 RNA segments were different from those of cogent genes of all other group A rotavirus (RVA) strains including ERVs and formed unique phylogenetic lineages. The L338 evolutionary footprints were tentatively identified in both VP7 and VP4 amino acid sequences: two regions were found in VP7 and twelve in VP4. The conserved regions shared between L338 and other group A rotavirus strains (RVAs) indicated that L338 was more closely related genomically to animal and human RVAs other than ERVs, suggesting that L338 may not be an endogenous equine RV but have emerged as an interspecies reassortant with other RVA strains. Furthermore, genotype-specific motifs of all 27 G and 37 P types were identified in regions 7-1a (aa 91-100) of VP7 and regions 8-1 (aa146-151) and 8-3 (aa113-118 and 125-135) of VP4 (VP8*).
Publication Date: 2015-08-28 PubMed ID: 26321159DOI: 10.1016/j.virusres.2015.08.021Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research studied the genotypic qualities of L338, a unique equine rotavirus strain, and the evolutionary relationship it shares with other equine rotavirus strains. Upon analysis, the researchers suggest that this particular strain may be the result of an interspecies reassortant with other group A rotavirus strains.

Overview of the L338 Strain

  • The L338 strain of equine rotavirus (ERV) was found to be a unique G13P[18] genotype – this meant it was different from other ERVs in terms of its genetic components.
  • Its genotype constellations were confirmed as G13-P[18]-I6-R9-C9-M6-A6-N9-T12-E14-H11. These ‘constellations’ represent the different components of the strain’s genetic makeup.
  • Of these genotype constellations, the L338 strain was only found to share its P[18] and I6 genotypes with other ERVs – its remaining 9 RNA segments were unique.

Evolutionary Relationship with Other ERVs

  • The researchers found that the unique RNA segments of the L338 strain form unique phylogenetic lineages – these are evolutionary links that show the development of the strain over time.
  • These lineages were found to be distinct from the cogent genes of all other group A rotavirus (RVA) strains – including other ERVs.
  • However, the L338 strain did share conserved regions with other RVA strains, indicating a closer genomic relationship with these strains as opposed to other ERVs.
  • This led to the suggestion that the L338 strain is not an endogenous equine RV, but rather, it may have evolved as an interspecies reassortant with other RVA strains. The term ‘reassortant’ means that the strain may have emerged due to the mixing or recombination of genes from different species.

Identification of Genotype-specific Motifs

  • The researchers also identified genotype-specific motifs in the VP7 and VP4 amino acid sequences of the L338 strain. Motifs are recurring elements that serve a specific function.
  • They were able to find two regions in the VP7 sequence and twelve in the VP4 sequence, which were representative of the evolutionary footprints of L338.
  • These ‘footprints’ provide insights about the evolutionary history and genetic variation of the strain.
  • All 27 G and 37 P type genotypes were identified in specific regions of VP7 and VP4, further indicating the unique genetic makeup of this strain.

Cite This Article

APA
Ma Y. (2015). Identification of G and P genotype-specific motifs in the predicted VP7 and VP4 amino acid sequences. Virus Res, 210, 271-278. https://doi.org/10.1016/j.virusres.2015.08.021

Publication

ISSN: 1872-7492
NlmUniqueID: 8410979
Country: Netherlands
Language: English
Volume: 210
Pages: 271-278
PII: S0168-1702(15)30053-8

Researcher Affiliations

Ma, Yongping
  • Department of Biochemistry and Molecular Biology, Molecular Medicine and Cancer Research Center, Chongqing Medical University, Yu Zhong District, Yi Xue Yuan Road #1, Chongqing 400016, China. Electronic address: yongpingm@yahoo.com.

MeSH Terms

  • Amino Acid Motifs
  • Amino Acid Sequence
  • Animals
  • Antigens, Viral
  • Capsid Proteins / chemistry
  • Capsid Proteins / genetics
  • Genome, Viral
  • Genotype
  • Horses
  • Molecular Sequence Data
  • RNA, Viral / genetics
  • Rotavirus / chemistry
  • Rotavirus / genetics
  • Sequence Analysis, DNA

Citations

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