Hou Qiangchuan, Bai Xiaoye, Li Weicheng, Gao Xu, Zhang Faming, Sun Zhihong, Zhang Heping
Key Laboratory of Dairy Biotechnology and Engineering, Ministry of Education, Inner Mongolia Agricultural University, Hohhot, China.
Key Laboratory of Dairy Products Processing, Ministry of Agriculture, Inner Mongolia Agricultural University, Hohhot, China.
Front Microbiol. 2018 Aug 31;9:2045. doi: 10.3389/fmicb.2018.02045. eCollection 2018.
Lactic acid bacteria (LAB) are important for human health. However, the relative abundance of LAB in complex samples, such as fecal samples, is low and their presence and diversity (at the species level) is understudied. Therefore, we designed LAB-specific primer pairs based on 16S rRNA gene consensus sequences from 443 species of LAB from seven genera. The LAB strains selected were genetically similar and known to play a role in human health. Prior to primer design, we obtained consistent sequences for the primer-binding sites by comparing the 16S rRNA gene sequences, manually identifying single-stranded primers and modifying these primers using degenerate bases. We assembled primer pairs with product sizes of >400 bp. Optimal LAB-specific primers were screened using three methods: PCR amplification, agarose gel electrophoresis and single-molecule real-time (SMRT) sequencing analysis. During the SMRT analysis procedure, we focused on sequence reads and diversity at the species level of target LAB in three fecal samples, using the universal bacterium primer 27f/1492r as a reference control. We created a phylogenetic tree to confirm the ability of the best candidate primer pair to differentiate amongst species. The results revealed that LAB-specific primer L5, with a product size of 750 bp, could generate 3222, 2552, and 3405 sequence reads from fecal Samples 1, 2, and 3. This represented 14, 13 and 10% of all target LAB sequence reads, respectively, compared with 2, 0.8, and 0.8% using the 27f/1492r primer. In addition, L5 detected LAB that were in low abundance and could not be detected using the 27f/1492r primer. The phylogenetic tree based on the alignments between the forward and reverse primer of L5 showed that species within the seven target LAB genera could be distinguished from each other, confirming L5 is a powerful tool for inferring phylogenetic relationships amongst LAB species. In conclusion, L5 is a LAB-specific primer that can be used for high-throughput sequencing and identification of taxa to the species level, especially in complex samples with relatively low LAB content. This enables further research on LAB population diversity in complex ecosystem, and on relationships between LAB and their hosts.
乳酸菌(LAB)对人类健康至关重要。然而,在粪便样本等复杂样本中,乳酸菌的相对丰度较低,而且它们的存在情况和多样性(在物种水平上)尚未得到充分研究。因此,我们基于来自七个属的443种乳酸菌的16S rRNA基因共有序列设计了乳酸菌特异性引物对。所选的乳酸菌菌株在基因上相似,并且已知在人类健康中发挥作用。在引物设计之前,我们通过比较16S rRNA基因序列,手动识别单链引物并使用简并碱基修饰这些引物,从而获得了引物结合位点的一致序列。我们组装了产物大小大于400 bp的引物对。使用三种方法筛选最佳的乳酸菌特异性引物:PCR扩增、琼脂糖凝胶电泳和单分子实时(SMRT)测序分析。在SMRT分析过程中,我们以通用细菌引物27f/1492r作为参考对照,重点关注三个粪便样本中目标乳酸菌在物种水平上的序列读数和多样性。我们创建了一个系统发育树,以确认最佳候选引物对区分不同物种的能力。结果表明,产物大小为750 bp的乳酸菌特异性引物L5,可从粪便样本1、2和3中分别产生3222、2552和3405个序列读数。这分别占所有目标乳酸菌序列读数的14%、13%和10%,而使用27f/1492r引物时分别为2%、0.8%和0.8%。此外,L5检测到了低丰度的乳酸菌,而使用27f/1492r引物无法检测到这些乳酸菌。基于L5正向和反向引物之间比对构建的系统发育树表明,七个目标乳酸菌属内的物种可以相互区分,这证实了L5是推断乳酸菌物种间系统发育关系的有力工具。总之,L5是一种乳酸菌特异性引物,可用于高通量测序和物种水平的分类群鉴定,特别是在乳酸菌含量相对较低的复杂样本中。这有助于进一步研究复杂生态系统中乳酸菌种群的多样性,以及乳酸菌与其宿主之间的关系。