Droplet Digital PCR Enhances Sensitivity of Canine Distemper Virus Detection.

IF 3.8 3区 医学 Q2 VIROLOGY
Viruses-Basel Pub Date : 2024-10-31 DOI:10.3390/v16111720
Victoria Iribarnegaray, Guillermo Godiño, Camila Larrañaga, Kanji Yamasaki, José Manuel Verdes, Rodrigo Puentes
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Abstract

Canine distemper virus (CDV) poses a substantial threat to diverse carnivorans, leading to systemic and often fatal diseases. Accurate and prompt diagnosis is paramount for effective management and curbing further transmission. This study evaluates the diagnostic performance of droplet digital PCR (ddPCR) in comparison to conventional reverse-transcription (RT-PCR) and quantitative reverse-transcription real-time PCR (RT-qPCR). Seventy-six clinical samples were collected from dogs with CDV symptoms diagnosed by specialized veterinarians, and sixteen samples from apparently healthy individuals. Conventional PCR, quantitative real-time PCR, and ddPCR were deployed, and their diagnostic capabilities were meticulously assessed. DdPCR exhibited heightened analytical sensitivity, reaching a detection limit of 3 copies/μL, whereas RT-qPCR had a detection limit of 86 copies/μL. The comparative analysis between clinical diagnosis and molecular techniques, including RT-PCR and RT-qPCR, demonstrated low concordance, with Kappa coefficients of 0.268 and 0.324, respectively. In contrast, ddPCR showed a moderate concordance, with a Kappa coefficient of 0.477. The sensitivity was 42.4% for RT-PCR, 57.9% for RT-qPCR, and 72.4% for ddPCR, with 100% specificity for all methods. This study underscores ddPCR's superior sensitivity and agreement with clinical CDV diagnosis, even at low viral concentrations, suggesting it as a promising alternative for CDV diagnosis.

液滴数字 PCR 提高了犬瘟热病毒检测的灵敏度。
犬瘟热病毒(CDV)对各种食肉动物构成严重威胁,可导致全身性疾病,而且往往是致命性疾病。准确及时的诊断对于有效管理和遏制进一步传播至关重要。本研究评估了液滴数字 PCR(ddPCR)与传统反转录(RT-PCR)和定量反转录实时 PCR(RT-qPCR)相比的诊断性能。从经专业兽医诊断出现 CDV 症状的狗身上采集了 76 份临床样本,从表面健康的人身上采集了 16 份样本。对常规 PCR、定量实时 PCR 和 ddPCR 进行了部署,并对它们的诊断能力进行了细致的评估。DdPCR 的分析灵敏度更高,检测限为 3 个拷贝/μL,而 RT-qPCR 的检测限为 86 个拷贝/μL。临床诊断与分子技术(包括 RT-PCR 和 RT-qPCR)之间的比较分析表明,两者的一致性较低,Kappa 系数分别为 0.268 和 0.324。相比之下,ddPCR 显示出中等程度的一致性,Kappa 系数为 0.477。RT-PCR 的灵敏度为 42.4%,RT-qPCR 为 57.9%,ddPCR 为 72.4%,所有方法的特异性均为 100%。这项研究强调了 ddPCR 的灵敏度和与临床 CDV 诊断的一致性,即使在病毒浓度较低的情况下也是如此,这表明它是 CDV 诊断的一种很有前途的替代方法。
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来源期刊
Viruses-Basel
Viruses-Basel VIROLOGY-
CiteScore
7.30
自引率
12.80%
发文量
2445
审稿时长
1 months
期刊介绍: Viruses (ISSN 1999-4915) is an open access journal which provides an advanced forum for studies of viruses. It publishes reviews, regular research papers, communications, conference reports and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. We also encourage the publication of timely reviews and commentaries on topics of interest to the virology community and feature highlights from the virology literature in the ''News and Views'' section. Electronic files or software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material.
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