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基于TaqMan探针的定量实时PCR技术在养殖环境和鱼组织中快速检测和定量多子小瓜虫的方法建立及应用

Establishment and application of TaqMan probe-based quantitative real-time PCR for rapid detection and quantification of Ichthyophthirius multifiliis in farming environments and fish tissues.

作者信息

Guo Shu-Quan, Fu Yao-Wu, Hou Ting-Long, Huang Shi-Lu, Zhang Qi-Zhong

机构信息

Department of Ecology, Jinan University, Engineering Research Center of Tropical and Subtropical Aquatic Ecological Engineering, Ministry of Education, Key Laboratory of Eutrophication and Red Tide Prevention of Guangdong Higher Education Institutes, West 601 Huangpu Avenue, Tianhe District, Guangzhou 510632, PR China.

Department of Ecology, Jinan University, Engineering Research Center of Tropical and Subtropical Aquatic Ecological Engineering, Ministry of Education, Key Laboratory of Eutrophication and Red Tide Prevention of Guangdong Higher Education Institutes, West 601 Huangpu Avenue, Tianhe District, Guangzhou 510632, PR China.

出版信息

Vet Parasitol. 2025 Feb;334:110381. doi: 10.1016/j.vetpar.2024.110381. Epub 2024 Dec 26.

Abstract

Ichthyophthirius multifiliis, a pathogenic ciliate, is a crucial pathogen of freshwater fish and can result in severe economic loss in the aquaculture industry worldwide. It is necessary to develop a sensitive and accurate method for detecting I. multifiliis in farming environments and fish skin and gills to protect fishes from infection of the parasite due to a lack of both safe and effective treatment drugs. The present study established a new TaqMan probe-based quantitative PCR (qPCR) detection method targeting the coding region of the cathepsin L cysteine protease (ICP2) gene of I. multifiliis. The sensitivity, specificity, reproducibility and application for detection and diagnosis of the TaqMan probe-based qPCR method were evaluated. In addition, the linear model between the cycle threshold (Ct) and the logarithmic starting quantity (SQ) of the number of theronts per 1 L of sterile water was developed as Ct = -3.312lg(SQ)+ 34.47 with an R of 0.9636 and a minimum detection limit of 4 theronts per 1 L of water and could be employed to determine the theront number based on Ct value. The results of the detection of trial infection samples with the TaqMan probe-based qPCR method showed that the tissues of fish individuals infected with I. multifiliis and the tank water samples were positive detection signals. In contrast, the tissues and water samples from uninfected fish individuals and tanks containing healthy fish showed no signals. The detection results demonstrated the reliability of this detection method. Overall, the novel TaqMan probe-based qPCR method with high sensitivity and specificity as well as repeatability for detection of I. multifiliis was a valuable tool in detecting the parasite in farming water, pond sediments, and fish tissues and could provide early warning for prevention of the disease caused by I. multifiliis.

摘要

多子小瓜虫(Ichthyophthirius multifiliis)是一种致病性纤毛虫,是淡水鱼的重要病原体,可在全球水产养殖业中造成严重经济损失。由于缺乏安全有效的治疗药物,有必要开发一种灵敏准确的方法来检测养殖环境以及鱼的皮肤和鳃中的多子小瓜虫,以保护鱼类免受该寄生虫感染。本研究建立了一种基于TaqMan探针的新型定量PCR(qPCR)检测方法,该方法针对多子小瓜虫组织蛋白酶L半胱氨酸蛋白酶(ICP2)基因的编码区。对基于TaqMan探针的qPCR方法的灵敏度、特异性、重复性以及检测和诊断应用进行了评估。此外,还建立了每1升无菌水中稚虫数量的循环阈值(Ct)与对数起始量(SQ)之间的线性模型,即Ct = -3.312lg(SQ)+ 34.47,R为0.9636,最低检测限为每1升水4个稚虫,可用于根据Ct值确定稚虫数量。用基于TaqMan探针的qPCR方法检测试验感染样本的结果表明,感染多子小瓜虫的鱼个体组织和养殖池水样本检测到阳性信号。相比之下,未感染鱼个体的组织和含有健康鱼的养殖池的水样未显示信号。检测结果证明了该检测方法的可靠性。总体而言,基于TaqMan探针的新型qPCR方法具有高灵敏度、特异性以及重复性,是检测养殖水体、池塘沉积物和鱼组织中该寄生虫的宝贵工具,可为预防多子小瓜虫引起的疾病提供早期预警。

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