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.
J Appl Lab Med. 2024 Nov 4;9(6):927-937. doi: 10.1093/jalm/jfae095.
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.
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.
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.
As new variants emerge, evaluating saliva-based testing approaches may be crucial to ensure effective virus detection.
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。
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。
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)。
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。