Pérez-de-Mora Alfredo, Lacourt Anna, McMaster Michaye L, Liang Xiaoming, Dworatzek Sandra M, Edwards Elizabeth A
Department of Chemical Engineering & Applied Chemistry, University of Toronto, Toronto, ON, Canada.
Research Unit Analytical Biogeochemistry, Department of Environmental Sciences, Helmholtz Zentrum München, Neuherberg, Germany.
Front Microbiol. 2018 May 17;9:812. doi: 10.3389/fmicb.2018.00812. eCollection 2018.
() strains differ primarily from one another by the number and identity of the reductive dehalogenase homologous catalytic subunit A () genes within their respective genomes. While multiple genes have been sequenced, the activity of the corresponding proteins has been identified in only a few cases. Examples include the enzymes whose substrates are groundwater contaminants such as trichloroethene (TCE), -dichloroethene (cDCE) and vinyl chloride (VC). The associated genes, namely , and , along with the 16S rRNA gene are often used as biomarkers of growth in field samples. In this study, we monitored an additional 12 uncharacterized sequences identified in the metagenome in the mixed -containing culture KB-1 to monitor population shifts in more detail. Quantitative PCR (qPCR) assays were developed for 15 genes and used to measure population diversity in 11 different sub-cultures of KB-1, each enriched on different chlorinated ethenes and ethanes. The proportion of gene copies relative to 16S rRNA gene copies revealed the presence of multiple distinct strains in each culture, many more than the two strains inferred from 16S rRNA analysis. The specific electron acceptor amended to each culture had a major influence on the distribution of strains and their associated genes. We also surveyed the abundance of genes in samples from two bioaugmented field sites (Canada and United Kingdom). Growth of the dominant strain in KB-1 was detected at the United Kingdom site. At both field sites, the measurement of relative abundances revealed population shifts over time as dechlorination progressed from TCE through cDCE to VC and ethene. These shifts indicate a selective pressure of the most abundant chlorinated electron acceptor, as was also observed in lab cultures. These results also suggest that reductive dechlorination at contaminated sites is brought about by multiple strains of whether or not the site is bioaugmented. Understanding the driving forces behind population selection and activity is improving predictability of remediation performance at chlorinated solvent contaminated sites.
不同的()菌株主要区别在于其各自基因组中还原性脱卤酶同源催化亚基A()基因的数量和特性。虽然多个基因已被测序,但仅在少数情况下鉴定出了相应蛋白质的活性。实例包括其底物为地下水污染物(如三氯乙烯(TCE)、-二氯乙烯(cDCE)和氯乙烯(VC))的酶。相关的基因,即、和,连同16S rRNA基因,常被用作野外样品中生长的生物标志物。在本研究中,我们监测了在含混合培养物KB-1的宏基因组中鉴定出的另外12个未表征的序列,以更详细地监测种群变化。针对15个基因开发了定量PCR(qPCR)检测方法,并用于测量KB-1的11种不同亚培养物中的种群多样性,每种亚培养物在不同的氯代乙烯和乙烷上富集。基因拷贝相对于16S rRNA基因拷贝的比例表明每种培养物中存在多个不同的菌株,比从16S rRNA分析推断出的两种菌株多得多。添加到每种培养物中的特定电子受体对菌株及其相关基因的分布有重大影响。我们还调查了来自两个生物强化野外场地(加拿大和英国)的样品中基因的丰度。在英国场地检测到了KB-1中优势菌株的生长。在两个野外场地,随着脱氯从TCE经cDCE进展到VC和乙烯,相对丰度的测量显示种群随时间发生了变化。这些变化表明了最丰富的氯代电子受体的选择压力,这在实验室培养物中也观察到了。这些结果还表明,无论场地是否进行了生物强化,污染场地的还原性脱氯都是由多种菌株引起的。了解种群选择和活性背后的驱动力正在提高对氯代溶剂污染场地修复性能的可预测性。