Can selection for resistance to OsHV-1 infection modify susceptibility to Vibrio aestuarianus infection in Crassostrea gigas? First insights from experimental challenges using primary and successive exposures

Since 2008, the emergent virus OsHV-1µvar has provoked massive mortality events in Crassostrea gigas spat and juveniles in France. Since 2012, mortality driven by the pathogenic bacteria Vibrio aestuarianus has stricken market-sized adults. A hypothesis to explain the sudden increase in mortality ob...

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Published in:Veterinary Research
Main Authors: Azéma, Patrick, Travers, Marie-Agnès, De Lorgeril, Julien, Tourbiez, Delphine, Dégremont, Lionel
Format: Text
Language:English
Published: BioMed Central 2015
Subjects:
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673786/
http://www.ncbi.nlm.nih.gov/pubmed/26646058
https://doi.org/10.1186/s13567-015-0282-0
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spelling ftpubmed:oai:pubmedcentral.nih.gov:4673786 2023-05-15T15:58:22+02:00 Can selection for resistance to OsHV-1 infection modify susceptibility to Vibrio aestuarianus infection in Crassostrea gigas? First insights from experimental challenges using primary and successive exposures Azéma, Patrick Travers, Marie-Agnès De Lorgeril, Julien Tourbiez, Delphine Dégremont, Lionel 2015-12-09 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673786/ http://www.ncbi.nlm.nih.gov/pubmed/26646058 https://doi.org/10.1186/s13567-015-0282-0 en eng BioMed Central http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673786/ http://www.ncbi.nlm.nih.gov/pubmed/26646058 http://dx.doi.org/10.1186/s13567-015-0282-0 © Azéma et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. CC0 PDM CC-BY Research Article Text 2015 ftpubmed https://doi.org/10.1186/s13567-015-0282-0 2015-12-13T01:28:07Z Since 2008, the emergent virus OsHV-1µvar has provoked massive mortality events in Crassostrea gigas spat and juveniles in France. Since 2012, mortality driven by the pathogenic bacteria Vibrio aestuarianus has stricken market-sized adults. A hypothesis to explain the sudden increase in mortality observed in France since 2012 is that selective pressure due to recurrent viral infections could have led to a higher susceptibility of adults to Vibrio infection. In our study, two OsHV-1-resistant lines (AS and BS) and their respective controls (AC and BC) were experimentally challenged in the laboratory to determine their level of susceptibility to V. aestuarianus infection. At the juvenile stage, the selected lines exhibited lower mortality (14 and 33%) than the control lines (71 and 80%), suggesting dual-resistance to OsHV-1 and V. aestuarianus in C. gigas. Interestingly, this pattern was not observed at the adult stage, where higher mortality was detected for AS (68%) and BC (62%) than AC (39%) and BS (49%). These results were confirmed by the analysis of the expression of 31 immune-related genes in unchallenged oysters. Differential gene expression discriminated oysters according to their susceptibility to infection at both the juvenile and adult stages, suggesting that resistance to V. aestuarianus infection resulted in complex interactions between the genotype, stage of development and immunity status. Finally, survivors of the V. aestuarianus challenge at the juvenile stage still exhibited significant mortality at the adult stage during a second and third V. aestuarianus challenge, indicating that these survivors were not genetically resistant. Text Crassostrea gigas PubMed Central (PMC) Veterinary Research 46 1
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Research Article
spellingShingle Research Article
Azéma, Patrick
Travers, Marie-Agnès
De Lorgeril, Julien
Tourbiez, Delphine
Dégremont, Lionel
Can selection for resistance to OsHV-1 infection modify susceptibility to Vibrio aestuarianus infection in Crassostrea gigas? First insights from experimental challenges using primary and successive exposures
topic_facet Research Article
description Since 2008, the emergent virus OsHV-1µvar has provoked massive mortality events in Crassostrea gigas spat and juveniles in France. Since 2012, mortality driven by the pathogenic bacteria Vibrio aestuarianus has stricken market-sized adults. A hypothesis to explain the sudden increase in mortality observed in France since 2012 is that selective pressure due to recurrent viral infections could have led to a higher susceptibility of adults to Vibrio infection. In our study, two OsHV-1-resistant lines (AS and BS) and their respective controls (AC and BC) were experimentally challenged in the laboratory to determine their level of susceptibility to V. aestuarianus infection. At the juvenile stage, the selected lines exhibited lower mortality (14 and 33%) than the control lines (71 and 80%), suggesting dual-resistance to OsHV-1 and V. aestuarianus in C. gigas. Interestingly, this pattern was not observed at the adult stage, where higher mortality was detected for AS (68%) and BC (62%) than AC (39%) and BS (49%). These results were confirmed by the analysis of the expression of 31 immune-related genes in unchallenged oysters. Differential gene expression discriminated oysters according to their susceptibility to infection at both the juvenile and adult stages, suggesting that resistance to V. aestuarianus infection resulted in complex interactions between the genotype, stage of development and immunity status. Finally, survivors of the V. aestuarianus challenge at the juvenile stage still exhibited significant mortality at the adult stage during a second and third V. aestuarianus challenge, indicating that these survivors were not genetically resistant.
format Text
author Azéma, Patrick
Travers, Marie-Agnès
De Lorgeril, Julien
Tourbiez, Delphine
Dégremont, Lionel
author_facet Azéma, Patrick
Travers, Marie-Agnès
De Lorgeril, Julien
Tourbiez, Delphine
Dégremont, Lionel
author_sort Azéma, Patrick
title Can selection for resistance to OsHV-1 infection modify susceptibility to Vibrio aestuarianus infection in Crassostrea gigas? First insights from experimental challenges using primary and successive exposures
title_short Can selection for resistance to OsHV-1 infection modify susceptibility to Vibrio aestuarianus infection in Crassostrea gigas? First insights from experimental challenges using primary and successive exposures
title_full Can selection for resistance to OsHV-1 infection modify susceptibility to Vibrio aestuarianus infection in Crassostrea gigas? First insights from experimental challenges using primary and successive exposures
title_fullStr Can selection for resistance to OsHV-1 infection modify susceptibility to Vibrio aestuarianus infection in Crassostrea gigas? First insights from experimental challenges using primary and successive exposures
title_full_unstemmed Can selection for resistance to OsHV-1 infection modify susceptibility to Vibrio aestuarianus infection in Crassostrea gigas? First insights from experimental challenges using primary and successive exposures
title_sort can selection for resistance to oshv-1 infection modify susceptibility to vibrio aestuarianus infection in crassostrea gigas? first insights from experimental challenges using primary and successive exposures
publisher BioMed Central
publishDate 2015
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673786/
http://www.ncbi.nlm.nih.gov/pubmed/26646058
https://doi.org/10.1186/s13567-015-0282-0
genre Crassostrea gigas
genre_facet Crassostrea gigas
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673786/
http://www.ncbi.nlm.nih.gov/pubmed/26646058
http://dx.doi.org/10.1186/s13567-015-0282-0
op_rights © Azéma et al. 2015
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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