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首页> 外文期刊>Diseases of Aquatic Organisms >DGGE-based detection method for Quahog Parasite Unknown (QPX)
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DGGE-based detection method for Quahog Parasite Unknown (QPX)

机译:基于DGGE的Quahog寄生虫未知(QPX)检测方法

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摘要

ABSTRACT: Quahog Parasite Unknown (QPX) is a significant cause of hard clam Mercenaria mercenaria mortality along the northeast coast of the United States. It infects both wild and cultured clams, often annually in plots that are heavily farmed. Subclinically infected clams can be identified by histological examination of the mantle tissue, but there is currently no method available to monitor the presence of QPX in the environment. Here, we report on a polymerase chain reaction (PCR)-based method that will facilitate the detection of QPX in natural samples and seed clams. With our method, between 10 and 100 QPX cells can be detected in 1 l of water, 1 g of sediment and 100 mg of clam tissue. Denaturing gradient gel electrophoresis (DGGE) is used to establish whether the PCR products are the same as those in the control QPX culture. We used the method to screen 100 seed clams of 15 mm, and found that 10 to 12% of the clams were positive for the presence of the QPX organism. This method represents a reliable and sensitive procedure for screening both environmental samples and potentially contaminated small clams.
机译:摘要:未知的Quahog寄生虫(QPX)是导致美国东北沿海硬蛤 Mesenaria mercenaria 死亡的重要原因。它通常会每年在大量耕种的土地上感染野生和养殖的蛤。亚临床感染的蛤can可以通过对地幔组织进行组织学检查来鉴定,但是目前尚无可用的方法来监测环境中QPX的存在。在这里,我们报告基于聚合酶链反应(PCR)的方法,该方法将有助于检测天然样品和蛤中的QPX。使用我们的方法,在1升水,1克沉积物和100毫克蛤lam组织中可以检测到10至100个QPX细胞。变性梯度凝胶电泳(DGGE)用于确定PCR产物是否与对照QPX培养物中的产物相同。我们使用该方法筛选了100个15毫米的蛤c,发现10%至12%的蛤for对QPX生物体呈阳性。该方法代表了一种既可靠又灵敏的程序,可以同时筛查环境样品和可能受污染的小蛤。

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