用于检测和绝对定量奥罗普切病毒的 ddPCR

Viruses Pub Date : 2024-09-07 DOI:10.3390/v16091426
Elena Pomari, Andrea Matucci, Silvia Accordini, Rebeca Passarelli Mantovani, Natasha Gianesini, Antonio Mori, Concetta Castilletti
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摘要

背景:Oropouche病毒(OROV)是一种分段RNA病毒,属于Peribunyaviridae科Orthobunyavirus属。本文采用内部液滴数字 PCR(ddPCR)测定法检测和定量 OROV。方法使用人类看家基因 RPP30 对 ddPCR 反应进行双链检测。在全血、血清和尿液中进行了检测限(LoD)分析。共对 28 份临床样本(全血 9 份、血清 11 份、尿液 8 份)进行了检测,其中 16 份样本在常规分子诊断(终点和实时 PCR)中检测结果呈阳性。结果使用 OROV 的 10 倍序列稀释液进行的 ddPCR 的 LoD 在所有生物基质中均检测到 1 cp/µL。与常规分子诊断相比,ddPCR 检测对全血和血清的灵敏度为 100%,对尿液的灵敏度为 75%,这表明 ddPCR 的阳性率更高。结论我们建立了一种基于 ddPCR 的高灵敏度和高特异性的 OROV RNA 定量检测方法。这种检测方法能够定量监测 OROV 的病毒载量,除实验室诊断外,还有助于揭示发病机制,填补这一被忽视疾病的知识空白,并有助于病媒控制计划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ddPCR for the Detection and Absolute Quantification of Oropouche Virus
Background: Oropouche virus (OROV) is a segmented RNA virus belonging to the genus Orthobunyavirus in the family Peribunyaviridae. Herein, an in-house droplet digital PCR (ddPCR) assay was used for the detection and quantification of OROV. Methods: The ddPCR reaction was assessed as duplex assay using the human housekeeping gene RPP30. Limit of detection (LoD) analysis was performed in whole blood, serum, and urine. The assay was executed on a total of 28 clinical samples (whole blood n = 9, serum n = 11, and urine n = 8), of which 16 specimens were tested positive at the routine molecular diagnostics (endpoint and real-time PCRs). Results: The LoD of the ddPCR performed using 10-fold serial dilution of OROV detected up to 1 cp/µL in all the biological matrices. Compared to the routine molecular diagnostics, the ddPCR assay showed 100% sensitivity for whole blood and serum and 75% for urine, highlighting higher positive rate of ddPCR. Conclusion: We have established a quantitative RNA detection method of OROV with high sensitivity and specificity based on ddPCR. This test is capable of quantitatively monitoring the viral load of OROV and can contribute, in addition to laboratory diagnosis, to shed light on the pathogenesis, filling in the knowledge gaps of this neglected disease and to the vector control programs.
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