Davis Cheryl, DeOliveira Shushawna, Jumbo Adiebonye
Laboratory Manager, Tuskegee Health Disparities Diagnostic Center, Tuskegee University, Carver Research Building, Room 30, Tuskegee, Alabama 36088, 334-421-7024, Email:
Associate Dean, School of Health Professions, State University of New York Downstate Health Sciences University, 450 Clarkson Avenue, MSC 94, Brooklyn, NY 11203, (718) 270-7738, Fax: (718) 270-7702, Email:
J Healthc Sci Humanit. 2024 Fall;14(1):62-72.
COVID-19 variants continue to infect thousands of people even though the end of the pandemic was announced on May 11, 2023. Nextstrain CoVariants (CoVariants) genomic databases provide detailed information about more than 31 variants of COVID-19 viruses that have been identified through genomic sequencing, showing the mutations they carry. Mutated viruses may yield a negative result for a gene target using a PCR test that has a positive COVID-19 test result. This negative gene target result is known as gene target dropout/failure, not a negative COVID-19 test result. The Centers for Disease Control and Prevention (CDC), World Health Organization (WHO), and CoVariants utilize gene target dropout/failure as a Variant of Concern (VOC) screening method until the genomic sequencing is performed. The Thermofisher TaqPath COVID-19 Combo kit (TaqPath), a real-time RT-PCR test, detects COVID-19 nucleic acids in respiratory specimens. TaqPath PCR COVID-19 target profile data was retrieved from the Tuskegee Health Disparities Diagnostic Center COVID-19 clinical laboratory. The results revealed an association between the TaqPath results date tested and CoVariants tracking announced and end dates for S gene target dropout/failure (SGTF). This study highlights the usefulness of TaqPath COVID-19 Combo Kit gene target profiles in monitoring and mitigating the spread of emerging COVID-19 variants, without genomic sequencing.
尽管2023年5月11日宣布大流行结束,但新冠病毒变异株仍在持续感染数千人。Nextstrain CoVariants(CoVariants)基因组数据库提供了有关通过基因组测序鉴定出的31种以上新冠病毒变异株的详细信息,展示了它们携带的突变。使用对新冠病毒检测呈阳性的聚合酶链反应(PCR)检测时,突变病毒可能会导致基因靶点出现阴性结果。这种基因靶点阴性结果被称为基因靶点缺失/失败,而非新冠病毒检测阴性结果。在进行基因组测序之前,美国疾病控制与预防中心(CDC)、世界卫生组织(WHO)以及CoVariants将基因靶点缺失/失败用作关注变异株(VOC)的筛查方法。赛默飞TaqPath新冠病毒组合检测试剂盒(TaqPath)是一种实时逆转录PCR检测方法,可检测呼吸道标本中的新冠病毒核酸。TaqPath新冠病毒PCR靶点谱数据取自塔斯基吉健康差异诊断中心新冠病毒临床实验室。结果显示,TaqPath检测结果日期与CoVariants追踪公布的日期以及S基因靶点缺失/失败(SGTF)的结束日期之间存在关联。本研究强调了TaqPath新冠病毒组合检测试剂盒基因靶点谱在监测和缓解新出现的新冠病毒变异株传播方面的有用性,而无需进行基因组测序。