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唾液用于 SARS-CoV-2 的诊断:来自印度的首次报告。

Saliva for diagnosis of SARS-CoV-2: First report from India.

机构信息

Department of Microbiology, ICMR-Regional Medical Research Centre (Dept. of Health Research, Ministry of Health & Family Welfare, Govt. of India), Bhubaneswar, India.

Department of Microbiology, IMS & SUM Hospital, Bhubaneswar, India.

出版信息

J Med Virol. 2021 Apr;93(4):2529-2533. doi: 10.1002/jmv.26719. Epub 2020 Dec 23.

Abstract

There are very few studies in search of an alternate and convenient diagnostic tool which can substitute nasopharyngeal swab (NPS) specimen for detection of SARS-CoV-2. In the study we analyzed, the comparison and agreement between the feasibility of using the saliva in comparison to NPS for diagnosis of SARS-CoV-2. A total number of 74 patients were enrolled for this study. We analyzed and compared the NPS and saliva specimen collected within 48 h after the symptom onset. We carried out real-time quantitative polymerase chain reaction, gene sequencing for the detection and determination SARS-CoV-2 specific genes. Phylogenetic tree was constructed to establish the isolation of viral RNA from saliva. We used the Bland-Altman model to identify the agreement between two specimens. This study showed a lower cycle threshold (C ) mean value for the detection of SARS-CoV-2 ORF1 gene (mean, 27.07; 95% confidence interval [CI], 25.62 to 28.52) in saliva methods than that of NPS (mean 28.24; 95% CI, 26.62 to 29.85) specimen although the difference is statistically nonsignificant (p > .05). Bland-Altman analysis produced relatively smaller bias and high agreement between these two clinical specimens. Phylogenetic analysis with the RdRp and S gene confirmed the presence of SARS-CoV-2 in the saliva samples. Saliva represented a promising tool in COVID-19 diagnosis and the collection method would reduce the exposure risk of frontline health workers which is one of the major concerns in primary healthcare settings.

摘要

目前很少有研究在寻找一种替代的、便捷的诊断工具,可以替代鼻咽拭子(NPS)标本来检测 SARS-CoV-2。在我们分析的研究中,比较并评估了使用唾液替代 NPS 进行 SARS-CoV-2 诊断的可行性。共有 74 名患者入组了这项研究。我们分析和比较了在症状出现后 48 小时内采集的 NPS 和唾液标本。我们进行了实时定量聚合酶链反应,基因测序以检测和确定 SARS-CoV-2 特异性基因。构建了系统发生树以确定从唾液中分离病毒 RNA。我们使用 Bland-Altman 模型来识别两种标本之间的一致性。这项研究表明,唾液方法检测 SARS-CoV-2 ORF1 基因的循环阈值(C)平均值较低(平均值 27.07;95%置信区间 [CI],25.62 至 28.52),而 NPS 标本(平均值 28.24;95% CI,26.62 至 29.85)的检测值虽然统计学上无显著差异(p>.05)。Bland-Altman 分析产生了这两种临床标本之间相对较小的偏差和高度一致性。用 RdRp 和 S 基因进行的系统发生分析证实了 SARS-CoV-2 存在于唾液样本中。唾液是 COVID-19 诊断的有前途的工具,其采集方法将降低一线卫生工作者的暴露风险,这是初级保健环境中的主要关注点之一。

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