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采用SYBR Green I化学法通过实时荧光定量PCR对新喀里多尼亚虾类93综合征的病原体——凡纳滨对虾弧菌进行定量分析。

Quantification of Vibrio penaeicida, the etiological agent of Syndrome 93 in New Caledonian shrimp, by real-time PCR using SYBR Green I chemistry.

作者信息

Goarant Cyrille, Merien Fabrice

机构信息

IFREMER, Département Aquaculture en Nouvelle-Calédonie, BP 2059, 98846 Nouméa Cedex, Nouvelle-Calédonie.

出版信息

J Microbiol Methods. 2006 Oct;67(1):27-35. doi: 10.1016/j.mimet.2006.02.013. Epub 2006 Apr 17.

DOI:10.1016/j.mimet.2006.02.013
PMID:16616385
Abstract

Shrimp farming is a small but growing industry in New Caledonia. Since 1993, "Syndrome 93" has been affecting New Caledonian shrimp farming industry every cold season, causing severe epizootic mortalities in grow-out ponds and significant losses. Highly pathogenic strains of Vibrio penaeicida are considered the etiological agent of the disease in Litopenaeus stylirostris. On one hand, studies demonstrated that healthy shrimp may carry V. penaeicida for weeks with a high overall prevalence, regardless of any seasonal pattern or temperature conditions. On the other hand, larvae are free of V. penaeicida and are also resistant to experimental infection. V. penaeicida is frequently detected in incoming water pumped from the bays, which was shown, by a molecular typing study, to be the infectious source. This particular epidemiological pattern highlights the major role of the factors that trigger and aggravate the disease in grow-out ponds, where shrimp populations carry the pathogen all year round. In order to gain a better understanding of "Syndrome 93" epidemiology, quantification of V. penaeicida both in shrimp and the shrimp farm ecosystem is necessary. This article describes the steps in the successful development of a real-time PCR quantification assay of V. penaeicida in shrimp haemolymph, seawater (from ponds or bays) and sediment pore water, including the choice of an accurate extraction technique. The entire detection method; including sample processing, DNA extraction and real-time PCR amplification, can be completed within 4 h.

摘要

对虾养殖在新喀里多尼亚是一个规模较小但不断发展的产业。自1993年以来,“93综合征”每年寒冷季节都会影响新喀里多尼亚的对虾养殖业,导致养成池中出现严重的流行病死亡情况,并造成重大损失。致病性很强的 penaeicida 弧菌菌株被认为是斯氏滨对虾疾病的病原体。一方面,研究表明健康的对虾可能携带 penaeicida 弧菌数周,总体患病率很高,且不受任何季节模式或温度条件的影响。另一方面,幼体没有携带 penaeicida 弧菌,并且对实验感染具有抗性。在从海湾抽取的进水口中经常检测到 penaeicida 弧菌,分子分型研究表明这是感染源。这种特殊的流行病学模式突出了在养成池中引发和加重疾病的因素的主要作用,在养成池中对虾种群全年都携带病原体。为了更好地了解“93综合征”的流行病学,有必要对对虾和对虾养殖生态系统中的 penaeicida 弧菌进行定量分析。本文描述了成功开发对虾血淋巴、海水(来自池塘或海湾)和沉积物孔隙水中 penaeicida 弧菌实时荧光定量PCR检测方法的步骤,包括选择准确的提取技术。整个检测方法,包括样品处理、DNA提取和实时荧光定量PCR扩增,可在4小时内完成。

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