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First Report on Detection and Complete Genomic Analysis of a Novel CRESS DNA Virus from Sea Turtles

To date, only a handful of viruses have been identified in sea turtles. Although eukaryotic circular Rep (replication initiation protein)-encoding single-stranded DNA (CRESS DNA) viruses have been reported from a wide variety of terrestrial species, and some of these viruses have been associated wit...

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Autores principales: Gainor, Kerry, Stewart, Kimberly M., Picknell, Angela, Russ, Morgan, Makela, Noah, Watson, Kierra, Mancuso, Diana M., Malik, Yashpal Singh, Ghosh, Souvik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142553/
https://www.ncbi.nlm.nih.gov/pubmed/37111487
http://dx.doi.org/10.3390/pathogens12040601
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author Gainor, Kerry
Stewart, Kimberly M.
Picknell, Angela
Russ, Morgan
Makela, Noah
Watson, Kierra
Mancuso, Diana M.
Malik, Yashpal Singh
Ghosh, Souvik
author_facet Gainor, Kerry
Stewart, Kimberly M.
Picknell, Angela
Russ, Morgan
Makela, Noah
Watson, Kierra
Mancuso, Diana M.
Malik, Yashpal Singh
Ghosh, Souvik
author_sort Gainor, Kerry
collection PubMed
description To date, only a handful of viruses have been identified in sea turtles. Although eukaryotic circular Rep (replication initiation protein)-encoding single-stranded DNA (CRESS DNA) viruses have been reported from a wide variety of terrestrial species, and some of these viruses have been associated with clinical conditions in certain animals, limited information is available on CRESS DNA viruses from marine life. The present study aimed to investigate the presence of CRESS DNA viruses in sea turtles. In the present study, two (samples T3 and T33) of the 34 cloacal samples from 31 sea turtles (found in ocean waters around the Caribbean Islands of St. Kitts and Nevis) tested positive for CRESS DNA viruses by a pan-rep nested PCR assay. The partial Rep sequence of T3 shared 75.78% of a deduced amino acid (aa) identity with that of a CRESS DNA virus (classified under family Circoviridae) from a mollusk. On the other hand, the complete genome (2428 bp) of T33 was determined by an inverse nested PCR assay. The genomic organization of T33 mirrored those of type II CRESS DNA viral genomes of cycloviruses, characterized by the putative “origin of replication” in the 5’-intergenic region, and the putative Capsid (Cap)- and Rep-encoding open reading frame on the virion-sense- and antisense-strand, respectively. The putative Rep (322 aa) of T33 retained the conserved “HUH endonuclease” and the “super 3 family helicase” domains and shared pairwise aa identities of ~57% with unclassified CRESS DNA viruses from benthic sediment and mollusks. Phylogenetically, the T33 Rep formed a distinct branch within an isolated cluster of unclassified CRESS DNA viruses. The putative Cap (370 aa) of T33 shared maximum pairwise aa identity of 30.51% with an unclassified CRESS DNA virus from a capybara. Except for a blood sample from T33 that tested negative for CRESS DNA viruses, other tissue samples were not available from the sea turtles. Therefore, we could not establish whether the T3 and T33 viral strains infected the sea turtles or were of dietary origin. To our knowledge, this is the first report on the detection of CRESS DNA viruses from sea turtles, adding yet another animal species to the rapidly expanding host range of these viruses. Complete genome analysis of T33 identified a novel, unclassified CRESS DNA virus, providing insights into the high genetic diversity between viruses within the phylum Cressdnaviricota. Considering that sea turtles are an at-risk species, extensive studies on virus discovery, surveillance, and pathogenesis in these marine animals are of the utmost importance.
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spelling pubmed-101425532023-04-29 First Report on Detection and Complete Genomic Analysis of a Novel CRESS DNA Virus from Sea Turtles Gainor, Kerry Stewart, Kimberly M. Picknell, Angela Russ, Morgan Makela, Noah Watson, Kierra Mancuso, Diana M. Malik, Yashpal Singh Ghosh, Souvik Pathogens Communication To date, only a handful of viruses have been identified in sea turtles. Although eukaryotic circular Rep (replication initiation protein)-encoding single-stranded DNA (CRESS DNA) viruses have been reported from a wide variety of terrestrial species, and some of these viruses have been associated with clinical conditions in certain animals, limited information is available on CRESS DNA viruses from marine life. The present study aimed to investigate the presence of CRESS DNA viruses in sea turtles. In the present study, two (samples T3 and T33) of the 34 cloacal samples from 31 sea turtles (found in ocean waters around the Caribbean Islands of St. Kitts and Nevis) tested positive for CRESS DNA viruses by a pan-rep nested PCR assay. The partial Rep sequence of T3 shared 75.78% of a deduced amino acid (aa) identity with that of a CRESS DNA virus (classified under family Circoviridae) from a mollusk. On the other hand, the complete genome (2428 bp) of T33 was determined by an inverse nested PCR assay. The genomic organization of T33 mirrored those of type II CRESS DNA viral genomes of cycloviruses, characterized by the putative “origin of replication” in the 5’-intergenic region, and the putative Capsid (Cap)- and Rep-encoding open reading frame on the virion-sense- and antisense-strand, respectively. The putative Rep (322 aa) of T33 retained the conserved “HUH endonuclease” and the “super 3 family helicase” domains and shared pairwise aa identities of ~57% with unclassified CRESS DNA viruses from benthic sediment and mollusks. Phylogenetically, the T33 Rep formed a distinct branch within an isolated cluster of unclassified CRESS DNA viruses. The putative Cap (370 aa) of T33 shared maximum pairwise aa identity of 30.51% with an unclassified CRESS DNA virus from a capybara. Except for a blood sample from T33 that tested negative for CRESS DNA viruses, other tissue samples were not available from the sea turtles. Therefore, we could not establish whether the T3 and T33 viral strains infected the sea turtles or were of dietary origin. To our knowledge, this is the first report on the detection of CRESS DNA viruses from sea turtles, adding yet another animal species to the rapidly expanding host range of these viruses. Complete genome analysis of T33 identified a novel, unclassified CRESS DNA virus, providing insights into the high genetic diversity between viruses within the phylum Cressdnaviricota. Considering that sea turtles are an at-risk species, extensive studies on virus discovery, surveillance, and pathogenesis in these marine animals are of the utmost importance. MDPI 2023-04-15 /pmc/articles/PMC10142553/ /pubmed/37111487 http://dx.doi.org/10.3390/pathogens12040601 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Gainor, Kerry
Stewart, Kimberly M.
Picknell, Angela
Russ, Morgan
Makela, Noah
Watson, Kierra
Mancuso, Diana M.
Malik, Yashpal Singh
Ghosh, Souvik
First Report on Detection and Complete Genomic Analysis of a Novel CRESS DNA Virus from Sea Turtles
title First Report on Detection and Complete Genomic Analysis of a Novel CRESS DNA Virus from Sea Turtles
title_full First Report on Detection and Complete Genomic Analysis of a Novel CRESS DNA Virus from Sea Turtles
title_fullStr First Report on Detection and Complete Genomic Analysis of a Novel CRESS DNA Virus from Sea Turtles
title_full_unstemmed First Report on Detection and Complete Genomic Analysis of a Novel CRESS DNA Virus from Sea Turtles
title_short First Report on Detection and Complete Genomic Analysis of a Novel CRESS DNA Virus from Sea Turtles
title_sort first report on detection and complete genomic analysis of a novel cress dna virus from sea turtles
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142553/
https://www.ncbi.nlm.nih.gov/pubmed/37111487
http://dx.doi.org/10.3390/pathogens12040601
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