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更新一种用于贝类中 GII 诺如病毒特异性检测的新型半巢式 PCR 引物对。

Updating a New Semi-nested PCR Primer Pair for the Specific Detection of GII Norovirus in Oysters.

机构信息

College of Food Science and Technology, Shanghai Ocean University, Shanghai, China.

Laboratory of Quality and Safety Risk Assessment for Aquatic Products on Storage and Preservation (Shanghai), Ministry of Agriculture and Rural Affairs, Shanghai, China.

出版信息

Food Environ Virol. 2022 Jun;14(2):149-156. doi: 10.1007/s12560-022-09511-6. Epub 2022 Jan 31.

Abstract

Oysters are major transmission vectors of noroviruses (NoVs) in the environment. Outbreaks of NoVs are often associated with the consumption of NoV-contaminated oysters. Laboratory confirmation of suspected oyster samples is a critical step in the surveillance and control of NoVs. Because of non-specific amplification, false-positive results are frequently obtained by semi-nested RT-PCR with the presently widely used primer set (G2SKF/G2SKR). Here, a novel universal PCR primer set N (NG2OF/NG2OR) specific for genogroup II (GII) NoVs was designed based on all GII NoV sequences available in public databases. Specific products were obtained with the primer set N when the NoV-positive oysters, spiked with each of five representative genotypes of GII NoVs (GII.17, GII.13, GII.4, GII.3, and GII.12), were subjected to analyzing. No products were detected with the primer set N for the NoV-negative oysters, while the primer set C gave various non-specific bands. Twenty-three out of 156 fresh oyster samples were NoV-positive with both the primer set N and the classic primer set, while eight were NoV-positive solely with the primer set N. Compared with the classic primer set, the newly designed primer set N had a higher detection rate and improved specificity for GII NoVs in oyster samples. These results show that the novel PCR primer pair is specific and applicable for the detection of GII NoVs in oysters.

摘要

牡蛎是环境中诺如病毒(NoV)的主要传播载体。NoV 的爆发通常与食用受 NoV 污染的牡蛎有关。疑似牡蛎样本的实验室确认是 NoV 监测和控制的关键步骤。由于非特异性扩增,目前广泛使用的引物组(G2SKF/G2SKR)的半巢式 RT-PCR 经常会得到假阳性结果。在这里,根据公共数据库中所有 GII NoV 序列,设计了一种新型通用 PCR 引物组 N(NG2OF/NG2OR),用于特异性扩增 GII NoV。当用引物组 N 分析用五种代表性 GII NoV 基因型(GII.17、GII.13、GII.4、GII.3 和 GII.12)之一对 NoV 阳性牡蛎进行加标时,可获得特异性产物。用引物组 N 未检测到 NoV 阴性牡蛎的产物,而引物组 C 则产生各种非特异性条带。用引物组 N 和经典引物组均检测到 156 个新鲜牡蛎样本中的 23 个为 NoV 阳性,而仅用引物组 N 检测到 8 个为 NoV 阳性。与经典引物组相比,新设计的引物组 N 对牡蛎样本中的 GII NoV 具有更高的检测率和特异性。这些结果表明,新型 PCR 引物对特异性适用于牡蛎中 GII NoV 的检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae37/8802746/222e639ce005/12560_2022_9511_Fig1_HTML.jpg

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