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用于检测 COVID-19 患者样本中 SARS-CoV-2 的感染性测定。

Infectivity assay for detection of SARS-CoV-2 in samples from patients with COVID-19.

机构信息

Division of Microbiology, Virology Section, Osaka Institute of Public Health, Osaka, Japan.

Department of Viral Infections, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.

出版信息

J Med Virol. 2021 Oct;93(10):5917-5923. doi: 10.1002/jmv.27145. Epub 2021 Jun 29.

Abstract

Since the coronavirus disease 2019 (COVID-19) outbreak, laboratory diagnosis has mainly been conducted using reverse-transcription polymerase chain reaction (RT-PCR). Detecting the presence of an infectious virus in the collected sample is essential to analyze if a person can transmit infectious severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). However, there have been no quantitative investigations conducted for infectious SARS-CoV-2 in clinical samples. Therefore, in the present study, a rapid and simple focus-forming assay using the peroxidase-antiperoxidase technique was developed to quantify infectious SARS-CoV-2 titers in 119 samples (n = 52, nasopharyngeal swabs [NPS]; n = 67, saliva) from patients with COVID-19. Furthermore, the study findings were compared with the cycle threshold (Ct) values of real-time RT-PCR. The infectious virus titers in NPS samples and Ct values were inversely correlated, and no infectious virus could be detected when the Ct value exceeded 30. In contrast, a low correlation was observed between the infectious virus titers in saliva and Ct values (r = -0.261, p = 0.027). Furthermore, the infectious virus titers in the saliva were significantly lower than those in the NPS samples. Ten days after the onset of COVID-19 symptoms, the infectious virus was undetectable, and Ct values were more than 30 in NSP and saliva samples. The results indicate that patients whose symptoms subsided 10 days after onset, with Ct values more than 30 in NSP and saliva samples, were less likely to infect others.

摘要

自 2019 年冠状病毒病(COVID-19)爆发以来,实验室诊断主要采用逆转录聚合酶链反应(RT-PCR)进行。检测采集样本中是否存在传染性病毒对于分析患者是否能够传播传染性严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)至关重要。然而,目前尚未对临床样本中传染性 SARS-CoV-2 进行定量研究。因此,在本研究中,开发了一种使用过氧化物酶-抗过氧化物酶技术的快速简便的致病变异检测法,以定量分析 119 份 COVID-19 患者样本(n=52,鼻咽拭子[NPS];n=67,唾液)中的传染性 SARS-CoV-2 滴度。此外,还将研究结果与实时 RT-PCR 的循环阈值(Ct)值进行了比较。NPS 样本中的传染性病毒滴度与 Ct 值呈负相关,当 Ct 值超过 30 时,无法检测到传染性病毒。相比之下,唾液中的传染性病毒滴度与 Ct 值相关性较低(r=-0.261,p=0.027)。此外,唾液中的传染性病毒滴度明显低于 NPS 样本。COVID-19 症状出现 10 天后,可检测不到传染性病毒,且 NPS 和唾液样本的 Ct 值均超过 30。结果表明,症状缓解 10 天后 Ct 值超过 30 的 NSP 和唾液样本患者,其传染性较低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9039/8426682/aa07b3d5187e/JMV-93-5917-g003.jpg

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