Challenges in the diagnosis of SARS-CoV-2 (COVID-19) infection

M. Pal, M. Bulcha, Wakuma Mitiku Bune
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Abstract

The etiological diagnosis of COVID-19 is only feasible by detecting nucleic acid content (i.e., RNA) of SARS-CoV-2 in the biological samples, which is an almost logical result of this clear connotation.5,6 Despite the fact that the SARS-CoV-2 nucleic acid real-time polymerase chain reaction (PCR) test has become the gold standard for diagnosing SARS-CoV-2 infection thoroughout the world. However, these real-time PCR test kits have a number of drawbacks. Aside from the sample collection and transportation limitations, as well as kit results, the overall positive rate of RT-PCR for throat swab samples was estimated to be between 30% and 60% at first presentation. There are two types of SARS–CoV-2 experiments: those that detect the virus itself and those that detect the host’s reaction to the virus. While the virus can be cultured, this is a dangerous procedure that is not done in clinical laboratories on a regular basis.5-7
SARS-CoV-2 (COVID-19)感染诊断中的挑战
只有通过检测生物样本中SARS-CoV-2的核酸含量(即RNA)才能进行COVID-19的病原学诊断,这几乎是这一明确内涵的逻辑结果。5,6尽管SARS-CoV-2核酸实时聚合酶链反应(PCR)检测已成为全球诊断SARS-CoV-2感染的金标准。然而,这些实时PCR检测试剂盒有一些缺点。除了样本收集和运输的限制,以及试剂盒结果,喉拭子样本的RT-PCR总体阳性率在首次呈现时估计在30%至60%之间。有两种类型的SARS-CoV-2实验:检测病毒本身的实验和检测宿主对病毒反应的实验。虽然病毒可以培养,但这是一个危险的过程,在临床实验室中不经常进行
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