环介导等温扩增(LAMP)技术在卡波病毒诊断中的评价与优化及其与PCR方法的比较

Q3 Veterinary
Archives of Razi Institute Pub Date : 2024-12-31 eCollection Date: 2024-12-01 DOI:10.32592/ARI.2024.79.6.1183
M Edrisi, H R Varshovi, S Safi, M H Shahhoseiny
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引用次数: 0

摘要

绵羊痘(SP)、山羊痘(GP)和疙瘩性皮肤病(LSD)是由capv病毒(capv)的亚种引起的。它们是绵羊、山羊和牛的重要病原体。致病菌是在南非首次分离出的CaPV病毒。导致羊痘(SP)、山羊痘(GP)和肿块性皮肤病(LSD)的病毒在形态上难以区分,并且已经适应了不同的宿主物种(4)。从血清学上讲,区分这些病毒具有挑战性,并且它们之间存在交叉免疫(2)。本研究对一种新型环介导等温扩增(LAMP)技术进行了评价和优化,并与聚合酶链反应(PCR)方法进行了比较。从CaPV的p32保护基因中选择LAMP引物。采用Safe-Red荧光染料监测阳性病例在320 nm波长处由红色变为明黄色,并通过电泳记录最终结果。提出的capripox病毒LAMP检测显示出高特异性,并且不会与其他具有类似临床症状的痘病毒科病毒发生交叉反应。将优化后的LAMP法与PCR法进行比较。LAMP和PCR的诊断敏感性完全相同(100%)。使用30份疑似肿块性皮肤病的牛皮肤样本,以及16份额外样本,包括9份阳性参考,5份阴性参考和2份阴性对照,评估LAMP试验的特异性。采用阴性参考样本评价LSDV的诊断敏感性。拟议的LAMP检测方法实施简单,成本效益高,灵敏度高,特别适合在资源有限的欠发达地区、实验室和设施中检测capripox病毒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation and Optimization of Loop-Mediated Isothermal Amplification (LAMP) Technique for Capripoxvirus Diagnosis and Its Comparison with PCR Method.

Sheep pox (SP), goat pox (GP), and lumpy skin disease (LSD) are caused by subspecies of the capripox virus (CaPVs). They are significant pathogens of sheep, goats, and cattle. The causative agent is the capripox virus (CaPV), which was first isolated in South Africa. The viruses responsible for sheep pox (SP), goat pox (GP), and lumpy skin disease (LSD) are morphologically indistinguishable and have been adapted to different host species (4). Serologically, distinguishing between these viruses is challenging, and cross-immunity exists among them (2). The present study reports the evaluation and optimization of a novel loop-mediated isothermal amplification (LAMP) technique for the rapid detection of capripox viruses (CaPVs) and compares it with the polymerase chain reaction (PCR) method. LAMP primers were selected from the P32-protected gene of CaPV. The Safe-Red fluorescent dye was used to monitor the color change from red to bright yellow at a wavelength of 320 nm in positive cases, and the final results were documented through electrophoresis. The proposed LAMP test for the capripox virus demonstrated high specificity and did not cross react with other viruses in the Poxviridae family that present similar clinical symptoms. The optimized LAMP test was then compared with the PCR. The diagnostic sensitivity of LAMP and PCR was found to be identical (100%). The specificity of the LAMP test was evaluated using 30 samples of cow skin that were suspected of lumpy skin disease, along with16 additional samples, including nine positive references, fivenegative references, and two negative controls. A negative reference sample was used to assess the diagnostic sensitivity of LSDV. The proposed LAMP test is simple to implement, cost-effective, and highly sensitive, making it particularly well-suited for the detection of the capripox virus in less developed regions, laboratories, and facilities with limited resources.

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来源期刊
Archives of Razi Institute
Archives of Razi Institute Veterinary-Veterinary (all)
CiteScore
1.50
自引率
0.00%
发文量
108
审稿时长
12 weeks
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