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在巴西野外条件下通过实时逆转录聚合酶链反应诊断口蹄疫

Diagnosis of foot-and mouth disease by real time reverse transcription polymerase chain reaction under field conditions in Brazil.

作者信息

Paixão Tatiane A, Neta Alcina V Carvalho, Paiva Naimes O, Reis Jorge R, Barbosa Meirivan S, Serra Claudia V, Silva René R, Beckham Tammy R, Martin Barbara M, Clarke Neville P, Adams L Garry, Santos Renato L

机构信息

Departamento de Clínica e Cirurgia Veterinária, Escola de Veterinária da Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.

出版信息

BMC Vet Res. 2008 Dec 31;4:53. doi: 10.1186/1746-6148-4-53.

Abstract

BACKGROUND

Foot-and-mouth disease (FMD) is an economically important and highly contagious viral disease that affects cloven-hoofed domestic and wild animals. Virus isolation and enzyme-linked immunosorbent assay (ELISA) are the gold standard tests for diagnosis of FMD. As these methods are time consuming, assays based on viral nucleic acid amplification have been developed.

RESULTS

A previously described real-time reverse transcriptase polymerase chain reaction (RT-PCR) assay with high sensitivity and specificity under laboratorial and experimental conditions was used in the current study. To verify the applicability of this assay under field conditions in Brazil, 460 oral swabs from cattle were collected in areas free of FMD (n = 200) and from areas with outbreaks of FMD (n = 260). Three samples from areas with outbreaks of FMD were positive by real-time RT-PCR, and 2 of those samples were positive by virus isolation and ELISA. Four other samples were considered inconclusive by real-time RT-PCR (threshold cycle [Ct] > 40); whereas all 200 samples from an area free of FMD were real-time RT-PCR negative.

CONCLUSION

real-time RT-PCR is a powerful technique for reliable detection of FMDV in a fraction of the time required for virus isolation and ELISA. However, it is noteworthy that lack of infrastructure in certain areas with high risk of FMD may be a limiting factor for using real-time RT-PCR as a routine diagnostic tool.

摘要

背景

口蹄疫(FMD)是一种具有重要经济影响且传染性极强的病毒性疾病,可感染偶蹄类家畜和野生动物。病毒分离和酶联免疫吸附测定(ELISA)是诊断口蹄疫的金标准检测方法。由于这些方法耗时较长,基于病毒核酸扩增的检测方法已被开发出来。

结果

本研究使用了一种先前描述的在实验室和实验条件下具有高灵敏度和特异性的实时逆转录聚合酶链反应(RT-PCR)检测方法。为验证该检测方法在巴西田间条件下的适用性,从无口蹄疫地区(n = 200)和有口蹄疫疫情地区(n = 260)收集了460份牛的口腔拭子。来自有口蹄疫疫情地区的3份样本通过实时RT-PCR呈阳性,其中2份样本通过病毒分离和ELISA呈阳性。另外4份样本通过实时RT-PCR被认为结果不确定(阈值循环数[Ct] > 40);而来自无口蹄疫地区的所有200份样本实时RT-PCR均为阴性。

结论

实时RT-PCR是一种强大的技术,能够在病毒分离和ELISA所需时间的一小部分内可靠地检测口蹄疫病毒。然而,值得注意的是,在某些口蹄疫高风险地区缺乏基础设施可能是将实时RT-PCR用作常规诊断工具的一个限制因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aca9/2631516/4a60e5866a5c/1746-6148-4-53-1.jpg

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