Qi Zhenhua, Pei Guangsheng, Chen Lei, Zhang Weiwen
1] Laboratory of Synthetic Microbiology, School of Chemical Engineering &Technology, Tianjin University, Tianjin 300072, P.R. China [2] Key Laboratory of Systems Bioengineering (Ministry of Education), Tianjin University, Tianjin 300072, P.R. China [3] SynBio Research Platform, Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), 300072, P.R. China.
Sci Rep. 2014 Dec 15;4:7478. doi: 10.1038/srep07478.
Microbial syntrophic metabolism has been well accepted as the heart of how methanogenic and other anaerobic microbial communities function. In this work, we applied a single-cell RT-qPCR approach to reveal gene-expression heterogeneity in a model syntrophic system of Desulfovibrio vulgaris and Methanosarcina barkeri, as compared with the D. vulgaris monoculture. Using the optimized primers and single-cell analytical protocol, we quantitatively determine gene-expression levels of 6 selected target genes in each of the 120 single cells of D. vulgaris isolated from its monoculture and dual-culture with M. barkeri. The results demonstrated very significant cell-to-cell gene-expression heterogeneity for the selected D. vulgaris genes in both the monoculture and the syntrophic dual-culture. Interestingly, no obvious increase in gene-expression heterogeneity for the selected genes was observed for the syntrophic dual-culture when compared with its monoculture, although the community structure and cell-cell interactions have become more complicated in the syntrophic dual-culture. In addition, the single-cell RT-qPCR analysis also provided further evidence that the gene cluster (DVU0148-DVU0150) may be involved syntrophic metabolism between D. vulgaris and M. barkeri. Finally, the study validated that single-cell RT-qPCR analysis could be a valuable tool in deciphering gene functions and metabolism in mixed-cultured microbial communities.
微生物互营代谢已被广泛认为是产甲烷和其他厌氧微生物群落功能的核心。在这项工作中,我们应用单细胞逆转录定量聚合酶链反应(RT-qPCR)方法,揭示了与普通脱硫弧菌单培养相比,普通脱硫弧菌和巴氏甲烷八叠球菌模型互营系统中的基因表达异质性。使用优化的引物和单细胞分析方案,我们定量测定了从普通脱硫弧菌单培养及其与巴氏甲烷八叠球菌的共培养中分离出的120个单细胞中6个选定靶基因的基因表达水平。结果表明,在单培养和互营共培养中,选定的普通脱硫弧菌基因在细胞间存在非常显著的基因表达异质性。有趣的是,与单培养相比,互营共培养中选定基因的基因表达异质性没有明显增加,尽管在互营共培养中群落结构和细胞间相互作用变得更加复杂。此外,单细胞RT-qPCR分析还进一步证明了基因簇(DVU0148-DVU0150)可能参与普通脱硫弧菌和巴氏甲烷八叠球菌之间的互营代谢。最后,该研究验证了单细胞RT-qPCR分析可能是解读混合培养微生物群落中基因功能和代谢的有价值工具。