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Partial N Gene Sequencing for SARS-CoV-2 Verification and Pathway Tracing

机译:SARS-COV-2验证和途径跟踪的部分N基因测序

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摘要

When SARS-CoV-2 prevalence is low, many RT-qPCR-positive test results are false positives. Sequencing of a 398-bp cDNA PCR amplicon derived from a highly conserved segment with single nucleotide polymorphisms of the nucleocapsid (N) gene in presumptive positive samples can verify true positives and differentiate at least 27 phylogenetically distinct strains of SARS-CoV-2 for helping track virus strain movement between individuals and across geographical areas. We report using this partial N gene sequencing method to confirm a case of mild COVID-19 disease. The patient was first seen on March 15, 2020, in the emergency department of the university hospital in Dublin, Ireland. RT-qPCR test on a nasopharyngeal swab sample was positive for SARS-CoV-2. Partial sequencing of the N gene in the residue of the tested RNA extract showed a characteristic set of 3-consecutive GGG-to-AAC mutations at positions 28881, 28882, 28883, which is known to first appear in samples collected in Continental Europe in February 2020. Using this sequencing-based method to re-test 9 reference nasopharyngeal swab samples supplied by the Connecticut State Department of Public Health Microbiology Laboratory revealed that 2 of the 9 positive samples had a single nucleotide mutation in the 398-base segment of the SARS-CoV-2 N gene. One of the 2 mutant samples showed a mutation at position 28821, which was first reported in a sample recently collected in the neighboring New York state. The other sample showed a novel frameshift nucleotide “A” insertion between position 29051 and position 29057, which co-existed with its wildtype parental virus in one sample. Routine sequencing of RT-qPCR-positive samples can minimize or eliminate false-positive SARS-CoV-2 test results that may cause unnecessary anxiety among the population and prevent false-positive tests from shutting down schools and workplaces unnecessarily as businesses try to resume normal operations in the community.
机译:当SARS-COV-2流行率低时,许多RT-QPCR阳性测试结果是误报。源自高度保守段的398-BP cDNA PCR扩增子的测序,所述预防阳性样品中的核衣壳(n)基因的单核苷酸多态性衍生,可以验证真实的阳性,并分化至少27个系统源性不同的SARS-COV-2菌株进行帮助在个人和地理区域之间跟踪病毒应变运动。我们通过这种部分N基因测序方法报告以确认轻度Covid-19疾病的情况。患者首次于2020年3月15日在爱尔兰都柏林大学医院的急诊部门看到。鼻咽拭子样品上的RT-QPCR测试对于SARS-COV-2是阳性的。在测试的RNA提取物残余物中的N基因的部分测序显示出在2月28881,2882,28883的位置的3-连续的GGG-AAC突变中的特征组3-连续的3-2882,28833,其已知首先出现在2月份欧洲大陆收集的样品中2020.使用基于测序的方法来重新测试9型参考鼻咽拭子样本,康涅狄格州公共卫生微生物学实验室提供的,9个阳性样品中的2个阳性样品中的2个核苷酸突变在SARS的398碱基部分中具有单一的核苷酸突变-cov-2 n基因。其中2个突变样本中的一种在28821的位置显示出突变,该突变在最近在邻近的纽约状态收集的样品中首次报道。其他样品在位置29051和位置29057之间插入的新型框架核苷酸“a”插入,其在一个样品中与其野生型父母病毒共存。常规测序RT-QPCR阳性样品可以最小化或消除假阳性SARS-COV-2测试结果,可能导致人口中不必要的焦虑,并防止由于业务试图恢复正常而不必要地关闭学校和工作场所的假阳性测试社区的运营。

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