Creation of Standard DNA for Detection and Quantification of White Spot Syndrome Virus in Shrimps by Real-time PCR (qPCR)

T. Cuong, Phan Tuấn Nghĩa, Nguyen Thi Hong Loan
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Abstract

White spot syndrome virus (WSSV) is a double stranded DNA virus that causes WSS diseases for many crustaceans including the Penaeidae family shrimp. In this study, standard DNA for detection and quantification of WSSV by real-time polymerase chain reaction (qPCR) method was created. A specific gene fragment of 126 bp from WSSV genome was successfully amplified by PCR and cloned into pGEM-T vector. qPCR calibration curves using the created recombinant pGEM vector harboring 126 bp gene fragment as the standard DNA at concentrations of 3x102 to 3x108 copies/mL showed to have good linear regression with an efficiency of 99.1%, correlation coefficient R2 of 0.998 and the slope of -3.344. The recombinant vector was also used as a positive standard for detection and quantification of WSSV in a number of WSSV-infected shrimp samples and the values ranging from 3.69x103 copies/mL to 1.25x108 copies/mL WSSV were found in the collected samples.
实时荧光定量PCR (qPCR)检测和定量对虾白斑综合征病毒标准DNA的建立
白斑综合征病毒(WSSV)是一种双链DNA病毒,可引起包括对虾科虾在内的许多甲壳类动物的白斑综合征疾病。本研究构建了实时荧光定量pcr (real-time polymerase chain reaction, qPCR)检测和定量WSSV的标准DNA。从WSSV基因组中成功扩增出126 bp的特异基因片段,并将其克隆到pGEM-T载体中。在3x102 ~ 3x108 copies/mL浓度下,以含126 bp基因片段的重组pGEM载体为标准DNA, qPCR校准曲线线性回归效果良好,效率为99.1%,相关系数R2为0.998,斜率为-3.344。将重组载体作为阳性标准物,在多份感染WSSV的对虾样本中进行WSSV的检测和定量,所收集的样本中WSSV的检测值在3.69 × 103 copies/mL ~ 1.25 × 108 copies/mL之间。
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