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作 者:董宏杰 张俊梅[1,2] 王帅 王宏伟[1] 张坤迪[1] 胡玮 谢晓鸿[2] 谢时灵 谷立川 DONG Hongjie;ZHANG Junmei;WANG Shuai;WANG Hongwei;ZHANG Kundi;HU Wei;XIE Xiaohong;XIE Shiling;GU Lichuan(State Key Laboratory of Microbial Technology,Shandong University,Qingdao 266000,Shandong,China;Shandong Shtars Medical Technology Co.,Ltd.,Jinan 250000,Shandong,China;Shandong Shtars Biological Industry Co.,Ltd.,Jinan 250000,Shandong,China)
机构地区:[1]山东大学微生物技术国家重点实验室,山东青岛266000 [2]山东仕达思医疗科技有限公司,山东济南250000 [3]山东仕达思生物产业有限公司,山东济南250000
出 处:《山东大学学报(医学版)》2021年第4期1-5,16,共6页Journal of Shandong University:Health Sciences
基 金:山东省重点研发计划(2020CXGC011305)。
摘 要:目的探究在新型冠状病毒样本混合检测中,稀释混样检测和混采检测的合理样本数量,为大人群样本的核酸筛查提供更为快捷有效的检测方案。方法设计一种利用注射器纯化柱进行大体积样本保存液核酸提取方法,在稀释混样检测和混采检测中,对比使用该方法将全部样本保存液提取核酸和只取200μL样本保存液提取核酸时检测结果的差异。结果稀释混样检测中,对于单独一份阳性样本,取全部保存液样本提取核酸时ORF1ab基因和N基因的Ct值比取200μL保存液样本提取核酸时分别小3.583、2.904;当1份阳性样本与9份、19份阴性样本混合后,将全部样本保存液提取核酸,不同混合人份检测的Ct值差异无统计学意义(P>0.05);当混合样本多于20份时,Ct值明显变大。混采检测中,取所有保存液样本提取核酸检测所得Ct值明显小于只取200μL保存液样本提取核酸所得Ct值(目前通行方案)。结论在新型冠状病毒混合检测中,采用注射器纯化柱法将全部样本的混合保存液提取核酸,稀释混样检测时,可将混合人数上限由20人提高到50人;采用混采检测时,可以明显降低核酸检测的Ct值,从而提高检出率,减少混合检测过程中假阴性现象的发生。Objective To determine the reasonable sample sizes of diluted mixed sample test and n-in-1 test in the detection of SARS-CoV-2,so as to provide a more efficient scheme for nucleic acid screening of large samples.Methods A method was designed to extract nucleic acid from the preservation solution of large volume samples using a syringe purification column.In both diluted mixed sample test and n-in-1 test,this method was used in the extraction of nucleic acid from the total preservation solution and from 200μL solution.The test results were compared.Results In diluted mixed sample test,for a single positive sample,the Ct values of ORF1 ab gene and N gene were 3.583 and 2.904 lower from the total preservation solution than from the 200μL solution;when one positive sample was mixed with 9 negative samples and 19 negative samples,there was no statistical difference in Ct values between the two sample sizes(P>0.05);when the number of mixed samples was more than 20,the Ct values increased significantly.In the n-in-1 test,the Ct values of nucleic acid extracted from total preservation solution was significantly lower than that from 200μL solution(the current scheme).Conclusion In mixed sample detection,using a syringe purification column to extract nucleic acid from the total preservation solution can increase the maximum number of sample size from 20 to 50.With this strategy,the Ct values of nucleic acid test can be significantly reduced,so as to improve the detection rate and reduce the number of false-negative cases in n-in-1 test.
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