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首页|期刊导航|农业生物技术学报|单增李斯特菌微滴式数字PCR检测方法的建立及在标准物质研制方面的应用

单增李斯特菌微滴式数字PCR检测方法的建立及在标准物质研制方面的应用

徐佳微 辛长卫 李铁山 赵格 曲志娜 赵建梅 高玉斌 张喜悦 王君玮

农业生物技术学报2024,Vol.32Issue(10):2413-2423,11.
农业生物技术学报2024,Vol.32Issue(10):2413-2423,11.DOI:10.3969/j.issn.1674-7968.2024.10.019

单增李斯特菌微滴式数字PCR检测方法的建立及在标准物质研制方面的应用

Establishment of Droplet Digital PCR Method for Detection of Listeria monocytogenes and Its Application in the Development of Reference Materials

徐佳微 1辛长卫 2李铁山 3赵格 4曲志娜 4赵建梅 4高玉斌 4张喜悦 4王君玮4

作者信息

  • 1. 中国动物卫生与流行病学中心致病微生物监测室,青岛 266032||青岛大学附属医院康复二科,青岛 266003
  • 2. 博爱县职业中等专业学校,博爱 454450
  • 3. 青岛大学附属医院康复二科,青岛 266003
  • 4. 中国动物卫生与流行病学中心致病微生物监测室,青岛 266032
  • 折叠

摘要

Abstract

Listeria monocytogenes is one of the most serious foodborne pathogens.The aim of this study is to establish a rapid,sensitive,and accurate droplet digital PCR(ddPCR)method for detecting L.monocytogenes,and apply the method to develop the reference materials.In the study,the ddPCR method was established with the invasion associated protein gene(iap)as the target gene,the reaction conditions were optimized,the specificity,sensitivity,and repeatability of the method were tested,and the established method was used to detect clinical samples and the standard material was developed by using the method.The results showed that the ddPCR method had the best amplification effect when the amount of 10 μmol/L primer was 1.5 μL,the amount of 10 μmol/L probe was 0.45 μL and the annealing temperature was 60℃.Finally,the ddPCR method for L.monocytogenes was established.The established ddPCR method had good specificity and did not cross-react with other non-specific strains.Repeatability test results showed that the coefficient of variation between groups was 1.57%~4.32%,which proved that the method had good repeatability.The method had high sensitivity,and the lower limit of detection was 6.65 copies/μL.The results of clinical samples showed that the ddPCR method and fluorescence quantitative PCR method were 100%consistent with the results of 47 clinical positive samples stored in the laboratory.This method was used to measure the uniformity and stability of the reference materials,and 9 laboratories determined the reference materials.The fixed value was 5.79×103 copies/μL,and the uncertainty was 0.47×103 copies/μL.The ddPCR method established in this study can be used for the detection of L.monocytogenes in the laboratory and the development of reference materials,etc.,and can be a technical means to monitor L.monocytogenes infection.

关键词

单核细胞增生李斯特菌/微滴式数字PCR(ddPCR)/iap基因/标准物质

Key words

Listeria monocytogenes/Droplet digital PCR(ddPCR)/iap gene/Reference material

分类

农业科技

引用本文复制引用

徐佳微,辛长卫,李铁山,赵格,曲志娜,赵建梅,高玉斌,张喜悦,王君玮..单增李斯特菌微滴式数字PCR检测方法的建立及在标准物质研制方面的应用[J].农业生物技术学报,2024,32(10):2413-2423,11.

基金项目

国家重点研发计划(2022YFC2303900 ()

2022YFD1301003) ()

中国动物卫生与流行病学中心创新基金(DW2021001-13) (DW2021001-13)

农业生物技术学报

OA北大核心CSTPCD

1674-7968

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