College of Resources and Environment, University of Chinese Academy of Sciences, 19A Yuquan Road, Beijing, 100049, China.
Microb Ecol. 2014 Aug;68(2):360-9. doi: 10.1007/s00248-014-0415-4. Epub 2014 Apr 10.
Permafrost wetlands are important methane emission sources and fragile ecosystems sensitive to climate change. Presently, there remains a lack of knowledge regarding bacterial communities, especially methanotrophs in vast areas of permafrost on the Tibetan Plateau in Northwest China and the Sanjiang Plain (SJ) in Northeast China. In this study, 16S rRNA-based quantitative PCR (qPCR) and 454 pyrosequencing were used to identify bacterial communities in soils sampled from a littoral wetland of Lake Namco on the Tibetan Plateau (NMC) and an alluvial wetland on the SJ. Additionally, methanotroph-specific primers targeting particulate methane monooxygenase subunit A gene (pmoA) were used for qPCR and pyrosequencing analysis of methanotrophic community structure in NMC soils. qPCR analysis revealed the presence of 10(10) 16S rRNA gene copies per gram of wet soil in both wetlands, with 10(8) pmoA copies per gram of wet soil in NMC. The two permafrost wetlands showed similar bacterial community compositions, which differed from those reported in other cold environments. Proteobacteria, Actinobacteria , and Chloroflexi were the most abundant phyla in both wetlands, whereas Acidobacteria was prevalent in the acidic wetland SJ only. These four phyla constituted more than 80 % of total bacterial community diversity in permafrost wetland soils, and Methylobacter of type I methanotrophs was overwhelmingly dominant in NMC soils. This study is the first major bacterial sequencing effort of permafrost in the NMC and SJ wetlands, which provides fundamental data for further studies of microbial function in extreme ecosystems under climate change scenarios.
多年冻土湿地是重要的甲烷排放源和对气候变化敏感的脆弱生态系统。目前,对于中国西北青藏高原和东北三江平原(SJ)广大多年冻土区的细菌群落,特别是甲烷氧化菌,我们的了解仍然有限。在这项研究中,我们使用基于 16S rRNA 的定量 PCR(qPCR)和 454 焦磷酸测序技术,对青藏高原纳木错湖滨湿地(NMC)和 SJ 冲积湿地土壤中的细菌群落进行了分析。此外,我们还使用了针对颗粒态甲烷单加氧酶亚单位 A 基因(pmoA)的甲烷氧化菌特异性引物,对 NMC 土壤中的甲烷氧化菌群落结构进行了 qPCR 和焦磷酸测序分析。qPCR 分析表明,两个湿地土壤中每克湿土的 16S rRNA 基因拷贝数均为 10(10),NMC 土壤中每克湿土的 pmoA 拷贝数为 10(8)。这两个多年冻土湿地的细菌群落组成相似,但与其他寒冷环境中的报道不同。变形菌门、放线菌门和绿弯菌门是两个湿地中最丰富的门,而 SJ 酸性湿地中则以酸杆菌门为主。这四个门构成了多年冻土湿地土壤中总细菌群落多样性的 80%以上,并且 I 型甲烷氧化菌中的甲基杆菌在 NMC 土壤中占绝对优势。本研究是 NMC 和 SJ 湿地多年冻土的首次主要细菌测序工作,为进一步研究气候变化背景下极端生态系统中的微生物功能提供了基础数据。