Turbot reovirus (SMReV) genome encoding a FAST protein with a non-AUG start site

Abstract Background A virus was isolated from diseased turbot Scophthalmus maximus in China. Biophysical and biochemical assays, electron microscopy, and genome electrophoresis revealed that the virus belonged to the genus Aquareovirus , and was named Scophthalmus maximus reovirus (SMReV). To the be...

Full description

Bibliographic Details
Published in:BMC Genomics
Main Authors: Ke, Fei, He, Li-Bo, Pei, Chao, Zhang, Qi-Ya
Format: Article in Journal/Newspaper
Language:English
Published: Springer Science and Business Media LLC 2011
Subjects:
Online Access:http://dx.doi.org/10.1186/1471-2164-12-323
https://link.springer.com/content/pdf/10.1186/1471-2164-12-323.pdf
https://link.springer.com/article/10.1186/1471-2164-12-323/fulltext.html
id crspringernat:10.1186/1471-2164-12-323
record_format openpolar
spelling crspringernat:10.1186/1471-2164-12-323 2023-05-15T18:15:47+02:00 Turbot reovirus (SMReV) genome encoding a FAST protein with a non-AUG start site Ke, Fei He, Li-Bo Pei, Chao Zhang, Qi-Ya 2011 http://dx.doi.org/10.1186/1471-2164-12-323 https://link.springer.com/content/pdf/10.1186/1471-2164-12-323.pdf https://link.springer.com/article/10.1186/1471-2164-12-323/fulltext.html en eng Springer Science and Business Media LLC https://creativecommons.org/licenses/by/4.0 https://creativecommons.org/licenses/by/4.0 CC-BY BMC Genomics volume 12, issue 1 ISSN 1471-2164 Genetics Biotechnology journal-article 2011 crspringernat https://doi.org/10.1186/1471-2164-12-323 2022-01-04T16:33:03Z Abstract Background A virus was isolated from diseased turbot Scophthalmus maximus in China. Biophysical and biochemical assays, electron microscopy, and genome electrophoresis revealed that the virus belonged to the genus Aquareovirus , and was named Scophthalmus maximus reovirus (SMReV). To the best of our knowledge, no complete sequence of an aquareovirus from marine fish has been determined. Therefore, the complete characterization and analysis of the genome of this novel aquareovirus will facilitate further understanding of the taxonomic distribution of aquareovirus species and the molecular mechanism of its pathogenesis. Results The full-length genome sequences of SMReV were determined. It comprises eleven dsRNA segments covering 24,042 base pairs and has the largest S4 genome segment in the sequenced aquareoviruses. Sequence analysis showed that all of the segments contained six conserved nucleotides at the 5' end and five conserved nucleotides at the 3' end (5'-GUUUUA ---- UCAUC-3'). The encoded amino acid sequences share the highest sequence identities with the respective proteins of aquareoviruses in species group Aquareovirus A. Phylogenetic analysis based on the major outer capsid protein VP7 and RNA-dependent RNA polymerase were performed. Members in Aquareovirus were clustered in two groups, one from fresh water fish and the other from marine fish. Furthermore, a fusion associated small transmembrane (FAST) protein NS22, which is translated from a non-AUG start site, was identified in the S7 segment. Conclusions This study has provided the complete genome sequence of a novel isolated aquareovirus from marine fish. Amino acids comparison and phylogenetic analysis suggested that SMReV was a new aquareovirus in the species group Aquareovirus A. Phylogenetic analysis among aquareoviruses revealed that VP7 could be used as a reference to divide the aquareovirus from hosts in fresh water or marine. In addition, a FAST protein with a non-AUG start site was identified, which partially contributed to the cytopathic effect caused by the virus infection. These results provide new insights into the virus-host and virus-environment interactions. Article in Journal/Newspaper Scophthalmus maximus Turbot Springer Nature (via Crossref) BMC Genomics 12 1
institution Open Polar
collection Springer Nature (via Crossref)
op_collection_id crspringernat
language English
topic Genetics
Biotechnology
spellingShingle Genetics
Biotechnology
Ke, Fei
He, Li-Bo
Pei, Chao
Zhang, Qi-Ya
Turbot reovirus (SMReV) genome encoding a FAST protein with a non-AUG start site
topic_facet Genetics
Biotechnology
description Abstract Background A virus was isolated from diseased turbot Scophthalmus maximus in China. Biophysical and biochemical assays, electron microscopy, and genome electrophoresis revealed that the virus belonged to the genus Aquareovirus , and was named Scophthalmus maximus reovirus (SMReV). To the best of our knowledge, no complete sequence of an aquareovirus from marine fish has been determined. Therefore, the complete characterization and analysis of the genome of this novel aquareovirus will facilitate further understanding of the taxonomic distribution of aquareovirus species and the molecular mechanism of its pathogenesis. Results The full-length genome sequences of SMReV were determined. It comprises eleven dsRNA segments covering 24,042 base pairs and has the largest S4 genome segment in the sequenced aquareoviruses. Sequence analysis showed that all of the segments contained six conserved nucleotides at the 5' end and five conserved nucleotides at the 3' end (5'-GUUUUA ---- UCAUC-3'). The encoded amino acid sequences share the highest sequence identities with the respective proteins of aquareoviruses in species group Aquareovirus A. Phylogenetic analysis based on the major outer capsid protein VP7 and RNA-dependent RNA polymerase were performed. Members in Aquareovirus were clustered in two groups, one from fresh water fish and the other from marine fish. Furthermore, a fusion associated small transmembrane (FAST) protein NS22, which is translated from a non-AUG start site, was identified in the S7 segment. Conclusions This study has provided the complete genome sequence of a novel isolated aquareovirus from marine fish. Amino acids comparison and phylogenetic analysis suggested that SMReV was a new aquareovirus in the species group Aquareovirus A. Phylogenetic analysis among aquareoviruses revealed that VP7 could be used as a reference to divide the aquareovirus from hosts in fresh water or marine. In addition, a FAST protein with a non-AUG start site was identified, which partially contributed to the cytopathic effect caused by the virus infection. These results provide new insights into the virus-host and virus-environment interactions.
format Article in Journal/Newspaper
author Ke, Fei
He, Li-Bo
Pei, Chao
Zhang, Qi-Ya
author_facet Ke, Fei
He, Li-Bo
Pei, Chao
Zhang, Qi-Ya
author_sort Ke, Fei
title Turbot reovirus (SMReV) genome encoding a FAST protein with a non-AUG start site
title_short Turbot reovirus (SMReV) genome encoding a FAST protein with a non-AUG start site
title_full Turbot reovirus (SMReV) genome encoding a FAST protein with a non-AUG start site
title_fullStr Turbot reovirus (SMReV) genome encoding a FAST protein with a non-AUG start site
title_full_unstemmed Turbot reovirus (SMReV) genome encoding a FAST protein with a non-AUG start site
title_sort turbot reovirus (smrev) genome encoding a fast protein with a non-aug start site
publisher Springer Science and Business Media LLC
publishDate 2011
url http://dx.doi.org/10.1186/1471-2164-12-323
https://link.springer.com/content/pdf/10.1186/1471-2164-12-323.pdf
https://link.springer.com/article/10.1186/1471-2164-12-323/fulltext.html
genre Scophthalmus maximus
Turbot
genre_facet Scophthalmus maximus
Turbot
op_source BMC Genomics
volume 12, issue 1
ISSN 1471-2164
op_rights https://creativecommons.org/licenses/by/4.0
https://creativecommons.org/licenses/by/4.0
op_rightsnorm CC-BY
op_doi https://doi.org/10.1186/1471-2164-12-323
container_title BMC Genomics
container_volume 12
container_issue 1
_version_ 1766188995376578560