Morais Orlando Miguel, Azevedo Alves Manuel Rui, Fernandes Paulo Alexandre da Costa
Escola Superior de Tecnologia e Gestão, Instituto Politécnico de Viana do Castelo, Rua Escola Industrial e Comercial de Nun'Álvares, Viana do Castelo 4900-347, Portugal.
CISAS, Escola Superior de Tecnologia e Gestão, Instituto Politécnico de Viana do Castelo, Rua Escola Industrial e Comercial de Nun'Álvares, Viana do Castelo 4900-347, Portugal.
Adv Virol. 2022 Jun 1;2022:7442907. doi: 10.1155/2022/7442907. eCollection 2022.
The use of saliva directly as a specimen to detect viral RNA by RT-PCR has been tested for a long time as its advantages are relevant in terms of convenience and costs. However, as other body fluids, its proven inhibition effect on the amplification reaction can be troublesome and compromise its use in the detection of viral particles. The aim of the present work is to demonstrate that saliva pretreatment may influence the RT-PCR amplification of three gene targets of SARS-CoV-2 significantly. A pool of RNA from confirmed COVID-19 patients was used to test the influence of heat pretreatment of saliva samples at 95°C for 5, 10, 15 and 20 min on the amplification performance of ORF1ab, E, and N SARS-CoV-2 genes. Prolonged heating at 95°C significantly improves the Ct value shift, usually observed in the presence of saliva, increasing the limit of detection of viral genes ORF1ab, and . When tested using a cohort of COVID-19 patients' saliva, the increased time of heat pretreatment resulted in a significant increase in the detection sensitivity.
由于唾液在便利性和成本方面具有优势,长期以来人们一直在测试直接将其作为样本通过逆转录聚合酶链反应(RT-PCR)检测病毒RNA。然而,与其他体液一样,唾液对扩增反应已证实的抑制作用可能会带来麻烦,并影响其在病毒颗粒检测中的应用。本研究的目的是证明唾液预处理可能会显著影响严重急性呼吸综合征冠状病毒2(SARS-CoV-2)三个基因靶点的RT-PCR扩增。使用来自确诊的冠状病毒病(COVID-19)患者的RNA池,测试唾液样本在95°C下分别加热5、10、15和20分钟对SARS-CoV-2的开放阅读框1ab(ORF1ab)、包膜蛋白(E)和核衣壳蛋白(N)基因扩增性能的影响。在95°C下长时间加热显著改善了通常在有唾液存在时观察到的循环阈值(Ct)值变化,提高了病毒基因ORF1ab等的检测限。当使用一组COVID-19患者的唾液进行测试时,加热预处理时间的延长导致检测灵敏度显著提高。