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利用常用于监测食品中微生物群落结构的通用引物检测与明串珠菌科相关的扩增偏差。

Detection of an amplification bias associated to Leuconostocaceae family with a universal primer routinely used for monitoring microbial community structures within food products.

作者信息

Poirier Simon, Rué Olivier, Coeuret Gwendoline, Champomier-Vergès Marie-Christine, Loux Valentin, Chaillou Stéphane

机构信息

MICALIS, INRA AgroParisTech, Université Paris-Saclay, Domaine de Vilvert, 78350, Jouy-en-Josas, France.

MaIAGE, INRA, Université Paris-Saclay, Domaine de Vilvert, 78350, Jouy-en-Josas, France.

出版信息

BMC Res Notes. 2018 Nov 8;11(1):802. doi: 10.1186/s13104-018-3908-2.

Abstract

OBJECTIVES

Sequencing of 16S rDNA V3-V4 region is widely applied for food community profiling. However, two different universal forward primers (named here MUYZER-primer1 and KLINDWORTH-primer2) targeting an identical conservative sequence upstream of the V3 region of 16S rRNA gene, and only distinguished by a single mismatch are both used. This study was carried out to compare whether the accuracy of food microbiota analysis would depend on the choice of one of these two primers.

RESULTS

Alignment of both primers with common food-borne bacteria 16S sequences revealed that the mismatch between both primers might specifically affect the amplification of Leuconostoc, Oenococcus and Fructobacillus species but not Weissella species. Food products containing either Leuconostoc and/or Weissella were selected for a detection test. As expected from our in silico analysis, our study showed that this mismatch induced a strong biased amplification specifically associated to the OTUs belonging to the genus Leuconostoc but not to the genus Weissella. In presence of Muyzer-primer1, none of the sequences expected for Leuconostoc genus was detected whereas those sequences were correctly amplified with Klindworth-primer2. Since Leuconostoc is an important genus in food, agro-environments and in digestive tract of animals, we recommend that Muyzer-primer1 should thus be abandoned for the bacterial characterization of their associated microbiota.

摘要

目的

16S rDNA V3 - V4区域测序广泛应用于食品群落分析。然而,两种不同的通用正向引物(此处命名为MUYZER - primer1和KLINDWORTH - primer2)靶向16S rRNA基因V3区域上游的相同保守序列,且仅相差一个错配碱基,二者都被使用。本研究旨在比较食品微生物群分析的准确性是否取决于这两种引物之一的选择。

结果

两种引物与常见食源细菌16S序列的比对显示,两种引物之间的错配可能会特异性影响明串珠菌属、酒球菌属和果糖杆菌属物种的扩增,但不影响魏斯氏菌属物种的扩增。选择含有明串珠菌属和/或魏斯氏菌属的食品进行检测试验。正如我们在计算机模拟分析中所预期的,我们的研究表明,这种错配导致了强烈的偏向性扩增,特别是与属于明串珠菌属的操作分类单元相关,而与魏斯氏菌属无关。在使用Muyzer - primer1时,未检测到任何预期的明串珠菌属序列,而使用Klindworth - primer2时这些序列被正确扩增。由于明串珠菌属在食品、农业环境和动物消化道中是一个重要的属,我们建议在对其相关微生物群进行细菌鉴定时应放弃使用Muyzer - primer1。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2a3/6225703/d085c3c42a6c/13104_2018_3908_Fig1_HTML.jpg

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