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SARS-CoV-2 变异株可能影响唾液 RT-PCR 检测的敏感性。

SARS-CoV-2 Variants May Affect Saliva RT-PCR Assay Sensitivity.

机构信息

Keck School of Medicine, University of Southern California, Los Angeles, California, United States.

Division of Infectious Diseases, Children's Hospital Los Angeles, Los Angeles, California, United States.

出版信息

J Appl Lab Med. 2024 Nov 4;9(6):927-937. doi: 10.1093/jalm/jfae095.

Abstract

BACKGROUND

Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants demonstrate predilection for different regions of the respiratory tract. While saliva-based reverse transcription-polymerase chain reaction (RT-PCR) testing is a convenient, cost-effective alternative to nasopharyngeal swabs (NPS), few studies to date have investigated whether saliva sensitivity differs across variants of concern.

METHODS

SARS-CoV-2 RT-PCR was performed on paired NPS and saliva specimens collected from individuals with acute coronavirus disease 2019 (COVID-19) symptoms or exposure to a COVID-19 household contact. Viral genome sequencing of NPS specimens and Los Angeles County surveillance data were used to determine the variant of infection. Saliva sensitivity was calculated using NPS-positive RT-PCR as the reference standard. Factors contributing to the likelihood of saliva SARS-CoV-2 RT-PCR positivity were evaluated with univariate and multivariable analyses.

RESULTS

Between June 2020 and December 2022, 548 saliva samples paired with SARS-CoV-2 positive NPS samples were tested by RT-PCR. Overall, saliva sensitivity for SARS-CoV-2 detection was 61.7% (95% CI, 57.6%-65.7%). Sensitivity was highest with Delta infection (79.6%) compared to pre-Delta (58.5%) and Omicron (61.5%) (P = 0.003 and 0.01, respectively). Saliva sensitivity was higher in symptomatic individuals across all variants compared to asymptomatic cases [pre-Delta 80.6% vs 48.3% (P < 0.001), Delta 100% vs 72.5% (P = 0.03), Omicron 78.7% vs 51.2% (P < 0.001)]. Infection with Delta, symptoms, and high NPS viral load were independently associated with 2.99-, 3.45-, and 4.0-fold higher odds of SARS-CoV-2 detection by saliva-based RT-PCR (P = 0.004, <0.001, and <0.001), respectively.

CONCLUSIONS

As new variants emerge, evaluating saliva-based testing approaches may be crucial to ensure effective virus detection.

摘要

背景

严重急性呼吸综合征冠状病毒 2 型(SARS-CoV-2)变异株对呼吸道的不同部位具有倾向性。虽然基于唾液的逆转录-聚合酶链反应(RT-PCR)检测是一种方便、具有成本效益的替代鼻咽拭子(NPS)的方法,但迄今为止,很少有研究调查唾液检测对不同关注变异株的敏感性是否存在差异。

方法

对有急性 2019 年冠状病毒病(COVID-19)症状或与 COVID-19 家庭接触者接触的个体采集的 NPS 和唾液标本进行 SARS-CoV-2 RT-PCR。使用 NPS 标本的病毒基因组测序和洛杉矶县监测数据来确定感染的变异株。使用 NPS 阳性 RT-PCR 作为参考标准来计算唾液 SARS-CoV-2 RT-PCR 的敏感性。使用单变量和多变量分析评估影响唾液 SARS-CoV-2 RT-PCR 阳性的可能性的因素。

结果

2020 年 6 月至 2022 年 12 月,对 548 份与 SARS-CoV-2 阳性 NPS 样本配对的唾液样本进行了 RT-PCR 检测。总体而言,唾液检测 SARS-CoV-2 的敏感性为 61.7%(95%CI,57.6%-65.7%)。与 Delta 株(79.6%)相比,Delta 株之前(58.5%)和 Omicron 株(61.5%)的敏感性更高(P = 0.003 和 0.01)。在所有变异株中,症状性个体的唾液敏感性均高于无症状个体[Delta 株之前为 80.6%比 48.3%(P < 0.001),Delta 株为 100%比 72.5%(P = 0.03),Omicron 株为 78.7%比 51.2%(P < 0.001)]。Delta 感染、症状和高 NPS 病毒载量与唾液 RT-PCR 检测 SARS-CoV-2 的可能性分别高出 2.99 倍、3.45 倍和 4.0 倍(P = 0.004、<0.001 和 <0.001)。

结论

随着新变异株的出现,评估基于唾液的检测方法可能对于确保有效的病毒检测至关重要。

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