首页> 外文会议>Annual Meeting of the European Aquaculture Society >THERMAL CHALLENGE AS A SANITARY QUALIFICATION TEST OF OYSTER SPATS Crassostrea gigas AND OF THEIR ECOSYSTEMS WITH REGARD TO THE HERPESVIRUS OSHV-1 MVAR
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THERMAL CHALLENGE AS A SANITARY QUALIFICATION TEST OF OYSTER SPATS Crassostrea gigas AND OF THEIR ECOSYSTEMS WITH REGARD TO THE HERPESVIRUS OSHV-1 MVAR

机译:热挑战作为牡蛎斯科斯科斯特拉斯·克斯索斯特雷斯和其生态系统的卫生挑战,关于疱疹病毒OSHV-1 MVAR

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Since 2008, mass mortalities of juvenile oysters Crassostrea gigas associated with ostreid herpevirus OsHV-1 uVar (Segarra et al. 2010) have occurred along all coasts of France when sea water temperature is higher than 16°C (Pernet etal. 2012). Laboratory experiments have established a direct link between the oyster mortalities and the infection by OsHV-1 uVar (Schikorski et al. 2011). OsFfV-1 DNA can be quantified and detected by quantitative polymerase chain reaction (qPCR) above a threshold of 102 copies mg'1 of wet tissues (Pepin et al. 2008). But this threshold does not allow to identify any asymptomatic individuals. In this context, we proposed a two-step methodological approach to qualify the sanitary status of C. gigas spats and of their ecosystems. The first step consisted in testing under laboratory conditions a thermal challenge based on a sharp increase in water temperature (>16°C) to test the sanitary status of C. gigas spats with regard to OsHV-1 uVar. In the second step, spats thatwere produced under a standardized laboratory protocol and that were qualified as naive after the thermal challenge with regard to OsHV-1 uVar (i.e. naive standardised spats, NSS) were deployed in the field (Brest Harbour) for a OsHV-1 uVar imprint. Then they were brought back to the laboratory for a 21°C thermal challenge to reveal the disease. The objective of this study was to determine the periods and the duration of OsHV-1 uVar infectivity in the ecosystem. The aim of this sanitary qualificationmethod was to provide an objective and accurate test to determine the status of oysters which can be used as a management tool of OsHV-1 uVar sanitary risk.
机译:自2008年以来,当海水温度高于16°C(2012年)时,沿着鸵鸟Herpevirus oshv-1 UVAR(Segarra等,2010)的少年牡蛎鲫鱼(Segarra等,2010)。实验室实验已经建立了牡蛎死亡率与OSHV-1 UVAR感染之间的直接联系(Schikorski等人。2011)。通过定量聚合酶链反应(QPCR)可以量化和检测OSFFV-1 DNA,湿组织的102份Mg'1的阈值(Pepin等,2008)。但此阈值不允许识别任何无症状的个体。在这方面,我们提出了一种两步的方法论方法,以资格获得C. Gigas Spats和其生态系统的卫生地位。在实验室条件下进行测试的第一步是基于水温(> 16℃)的急剧增加,以测试C. Gigas Spats关于OSHV-1 UVAR的卫生状态的热攻击。在第二步中,在标准化实验室协议下产生的斯帕茨在欧洲欧洲贸易厅(即天真标准化的斯科斯,NSS)的热挑战之后,在热挑战之后,在卫生(布雷斯特港)的热挑战之后-1 UVAR印记。然后他们被带回实验室进行了21°C的热挑战以揭示疾病。本研究的目的是确定生态系统中OSHV-1 UVAR感染性的时期和持续时间。这种卫生资格化方法的目的是提供一个客观准确的测试,以确定牡蛎的状况,可用作欧沙-1 UVAR卫生风险的管理工具。

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