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Sequence analysis of a normalized cDNA library of Mytilus edulis hemocytes exposed to Vibrio splendidus LGP32 strain☆

Identifieur interne : 000193 ( Pmc/Curation ); précédent : 000192; suivant : 000194

Sequence analysis of a normalized cDNA library of Mytilus edulis hemocytes exposed to Vibrio splendidus LGP32 strain☆

Auteurs : Marion Tanguy [France, Canada] ; Patty Mckenna [Canada] ; Sophie Gauthier-Clerc [Canada] ; Jocelyne Pellerin [Canada] ; Jean-Michel Danger [France] ; Ahmed Siah [Canada]

Source :

RBID : PMC:3908323

Abstract

In the past decades, reports on bivalves' pathogens and associated mortalities have steadily increased. To face pathogenic micro-organisms, bivalves rely on innate defenses established in hemocytes which are essentially based on phagocytosis and cytotoxic reactions. As a step towards a better understanding of the molecular mechanisms involved in the mussel Mytilus edulis innate immune system, we constructed and sequenced a normalized cDNA library specific to M. edulis hemocytes unchallenged (control) and challenged with Vibrio splendidus LGP32 strain for 2, 4 and 6 h. A total of 1,024,708 nucleotide reads have been generated using 454 pyrosequencing. These reads have been assembled and annotated into 19,622 sequences which we believe cover most of the M. edulis hemocytes transcriptome. These sequences were successfully assigned to biological process, cellular component, and molecular function Gene Ontology (GO) categories. Several transcripts related to immunity and stress such as some fibrinogen related proteins and Toll-like receptors, the complement C1qDC, some antioxidant enzymes and antimicrobial peptides have already been identified. In addition, Toll-like receptors signaling pathways and the lysosome and apoptosis mechanisms were compared to KEGG reference pathways. As an attempt for large scale RNA sequencing, this study focuses on identifying and annotating transcripts from M. edulis hemocytes regulated during an in vitro experimental challenge with V. splendidus. The bioinformatic analysis provided a reference transcriptome, which could be used in studies aiming to quantify the level of transcripts using high-throughput analysis such as RNA-Seq.


Url:
DOI: 10.1016/j.rinim.2013.04.001
PubMed: 24600557
PubMed Central: 3908323

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PMC:3908323

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LGP32 strain
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LGP32 strain
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<name sortKey="Siah, Ahmed" sort="Siah, Ahmed" uniqKey="Siah A" first="Ahmed" last="Siah">Ahmed Siah</name>
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<wicri:regionArea>Department of Pathology & Microbiology, Atlantic Veterinary College (AVC), University of Prince Edward Island, 550 University Avenue, Charlottetown, PE</wicri:regionArea>
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<p>In the past decades, reports on bivalves' pathogens and associated mortalities have steadily increased. To face pathogenic micro-organisms, bivalves rely on innate defenses established in hemocytes which are essentially based on phagocytosis and cytotoxic reactions. As a step towards a better understanding of the molecular mechanisms involved in the mussel
<italic>Mytilus edulis</italic>
innate immune system, we constructed and sequenced a normalized cDNA library specific to
<italic>M. edulis</italic>
hemocytes unchallenged (control) and challenged with
<italic>Vibrio splendidus</italic>
LGP32 strain for 2, 4 and 6 h. A total of 1,024,708 nucleotide reads have been generated using 454 pyrosequencing. These reads have been assembled and annotated into 19,622 sequences which we believe cover most of the
<italic>M. edulis</italic>
hemocytes transcriptome. These sequences were successfully assigned to biological process, cellular component, and molecular function Gene Ontology (GO) categories. Several transcripts related to immunity and stress such as some fibrinogen related proteins and Toll-like receptors, the complement C1qDC, some antioxidant enzymes and antimicrobial peptides have already been identified. In addition, Toll-like receptors signaling pathways and the lysosome and apoptosis mechanisms were compared to KEGG reference pathways. As an attempt for large scale RNA sequencing, this study focuses on identifying and annotating transcripts from
<italic>M. edulis</italic>
hemocytes regulated during an
<italic>in vitro</italic>
experimental challenge with
<italic>V. splendidus</italic>
. The bioinformatic analysis provided a reference transcriptome, which could be used in studies aiming to quantify the level of transcripts using high-throughput analysis such as RNA-Seq.</p>
</div>
</front>
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<pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front>
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<journal-id journal-id-type="nlm-ta">Results Immunol</journal-id>
<journal-id journal-id-type="iso-abbrev">Results Immunol</journal-id>
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<journal-title>Results in Immunology</journal-title>
</journal-title-group>
<issn pub-type="epub">2211-2839</issn>
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</publisher>
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<article-id pub-id-type="doi">10.1016/j.rinim.2013.04.001</article-id>
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<subject>Article</subject>
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</article-categories>
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<article-title>Sequence analysis of a normalized cDNA library of
<italic>Mytilus edulis</italic>
hemocytes exposed to
<italic>Vibrio splendidus</italic>
LGP32 strain
<sup>
<xref ref-type="fn" rid="d32e808"></xref>
</sup>
</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Tanguy</surname>
<given-names>Marion</given-names>
</name>
<xref rid="aff0001" ref-type="aff">a</xref>
<xref rid="aff0002" ref-type="aff">b</xref>
<xref rid="aff0003" ref-type="aff">c</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>McKenna</surname>
<given-names>Patty</given-names>
</name>
<xref rid="aff0003" ref-type="aff">c</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Gauthier-Clerc</surname>
<given-names>Sophie</given-names>
</name>
<xref rid="aff0002" ref-type="aff">b</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Pellerin</surname>
<given-names>Jocelyne</given-names>
</name>
<xref rid="aff0002" ref-type="aff">b</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Danger</surname>
<given-names>Jean-Michel</given-names>
</name>
<email>jean-michel.danger@univ-lehavre.fr</email>
<xref rid="aff0001" ref-type="aff">a</xref>
<xref rid="cor0001" ref-type="corresp">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Siah</surname>
<given-names>Ahmed</given-names>
</name>
<email>ahmed.siah@cahs-bc.ca</email>
<xref rid="aff0003" ref-type="aff">c</xref>
<xref rid="aff0004" ref-type="aff">d</xref>
<xref rid="cor0002" ref-type="corresp">**</xref>
</contrib>
</contrib-group>
<aff id="aff0001">
<label>a</label>
Laboratory of Ecotoxicology, University of Le Havre, 25 rue Philippe Lebon, BP540, 76058 Le Havre, France</aff>
<aff id="aff0002">
<label>b</label>
Institute of Marine Science, University of Quebec at Rimouski, 310 allée des Ursulines, Rimouski, Québec, Canada G5L 3A1</aff>
<aff id="aff0003">
<label>c</label>
Department of Pathology & Microbiology, Atlantic Veterinary College (AVC), University of Prince Edward Island, 550 University Avenue, Charlottetown, PE, Canada C1A 4P3</aff>
<aff id="aff0004">
<label>d</label>
British Columbia Centre for Aquatic Health Sciences (BC CAHS), 871A Island Highway, Campbell River, BC, Canada V9W 2C2</aff>
<author-notes>
<corresp id="cor0001">
<label>*</label>
Corresponding author. Jean-Michel Danger, PhD, Laboratory of Ecotoxicology, University of Le Havre, 25 rue Philippe Lebon, BP540, 76058 Le Havre, France, Tel.: +33 2 32 74 43 02; fax: +33 2 32 74 43 14.
<email>jean-michel.danger@univ-lehavre.fr</email>
</corresp>
<corresp id="cor0002">
<label>**</label>
Corresponding author at: British Columbia Centre for Aquatic Health Sciences (BC CAHS), 871A Island Highway, V9W 2C2, Campbell River, BC, Canada. Tel.: +1 250 286 6102; fax: +1 250 286 6103.
<email>ahmed.siah@cahs-bc.ca</email>
</corresp>
</author-notes>
<pub-date pub-type="pmc-release">
<day>30</day>
<month>4</month>
<year>2013</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="epub">
<day>30</day>
<month>4</month>
<year>2013</year>
</pub-date>
<pub-date pub-type="collection">
<year>2013</year>
</pub-date>
<volume>3</volume>
<fpage>40</fpage>
<lpage>50</lpage>
<history>
<date date-type="received">
<day>27</day>
<month>12</month>
<year>2012</year>
</date>
<date date-type="rev-recd">
<day>12</day>
<month>4</month>
<year>2013</year>
</date>
<date date-type="accepted">
<day>16</day>
<month>4</month>
<year>2013</year>
</date>
</history>
<permissions>
<copyright-statement>© 2013 The Authors</copyright-statement>
<copyright-year>2013</copyright-year>
</permissions>
<abstract>
<p>In the past decades, reports on bivalves' pathogens and associated mortalities have steadily increased. To face pathogenic micro-organisms, bivalves rely on innate defenses established in hemocytes which are essentially based on phagocytosis and cytotoxic reactions. As a step towards a better understanding of the molecular mechanisms involved in the mussel
<italic>Mytilus edulis</italic>
innate immune system, we constructed and sequenced a normalized cDNA library specific to
<italic>M. edulis</italic>
hemocytes unchallenged (control) and challenged with
<italic>Vibrio splendidus</italic>
LGP32 strain for 2, 4 and 6 h. A total of 1,024,708 nucleotide reads have been generated using 454 pyrosequencing. These reads have been assembled and annotated into 19,622 sequences which we believe cover most of the
<italic>M. edulis</italic>
hemocytes transcriptome. These sequences were successfully assigned to biological process, cellular component, and molecular function Gene Ontology (GO) categories. Several transcripts related to immunity and stress such as some fibrinogen related proteins and Toll-like receptors, the complement C1qDC, some antioxidant enzymes and antimicrobial peptides have already been identified. In addition, Toll-like receptors signaling pathways and the lysosome and apoptosis mechanisms were compared to KEGG reference pathways. As an attempt for large scale RNA sequencing, this study focuses on identifying and annotating transcripts from
<italic>M. edulis</italic>
hemocytes regulated during an
<italic>in vitro</italic>
experimental challenge with
<italic>V. splendidus</italic>
. The bioinformatic analysis provided a reference transcriptome, which could be used in studies aiming to quantify the level of transcripts using high-throughput analysis such as RNA-Seq.</p>
</abstract>
<kwd-group>
<title>Keywords</title>
<kwd>Transcriptome</kwd>
<kwd>Hemocyte</kwd>
<kwd>
<italic>Mytilus edulis</italic>
</kwd>
<kwd>454 Pyrosequencing</kwd>
<kwd>
<italic>Vibrio splendidus</italic>
</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>

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