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基于高通量测序的石斑鱼循环水养殖生物滤池微生物群落分析
引用本文:黄志涛,宋协法,李勋,万荣,董登攀,石蓉蓉,翟介明.基于高通量测序的石斑鱼循环水养殖生物滤池微生物群落分析[J].农业工程学报,2016,32(Z1):242-247.
作者姓名:黄志涛  宋协法  李勋  万荣  董登攀  石蓉蓉  翟介明
作者单位:1. 中国海洋大学水产学院海洋渔业系,青岛,266003;2. 青岛市黄岛区海洋与渔业局,青岛,266555;3. 山东莱州明波水产公司,烟台,264000
基金项目:国家自然科学基金项目(31502212);山东省博士后创新项目专项资金(201302025);中央高校基本科研业务费专项(201413062)
摘    要:为了解循环水养殖系统生物过滤器内微生物群落结构,明确其内部微生物的多样性。该文采用Illumina-Mi Seq高通量测序技术对石斑鱼循环水养殖系统3级浸没式生物滤池内微生物群落结构及多样性进行分析。研究结果表明:3个浸没式生物滤池的样品分别获得712,635,865个Operational Taxonomic Unit(OTU),共同包含的OTU为488个,其中3号滤池的微生物群落丰富度和多样性高于1号和2号生物滤池,且1号生物滤池和2号生物滤池内微生物群落结构相似度较高。在门的水平,3个滤池以变形菌门Proteobacteria、拟杆菌门Bacteroidetes为优势菌;在属的水平,发现3个滤池中起硝化作用的细菌主要是亚硝化单胞菌Nitrosomonas和硝化螺菌Nitrospira。该试验为揭开生物滤池这个"黑匣子"提供数据基础,对研究海水循环水养殖生物滤池的构建及其脱氮效率具有重要的指导意义。

关 键 词:养殖  微生物  污染  循环水养殖  浸没式生物滤池  微生物群落  高通量测序
收稿时间:2015/4/21 0:00:00
修稿时间:2015/11/5 0:00:00

Analysis of microbial diversity of submerged biofilters in recirculating aquaculture system for grouper based on high-throughput DNA sequencing
Huang Zhitao,Song Xief,Li Xun,Wan Rong,Dong Dengpan,Shi Rongrong and Zhai Jieming.Analysis of microbial diversity of submerged biofilters in recirculating aquaculture system for grouper based on high-throughput DNA sequencing[J].Transactions of the Chinese Society of Agricultural Engineering,2016,32(Z1):242-247.
Authors:Huang Zhitao  Song Xief  Li Xun  Wan Rong  Dong Dengpan  Shi Rongrong and Zhai Jieming
Institution:1. Department of Fisheries, College of Fisheries, Ocean University of China, Qingdao 266003, China,1. Department of Fisheries, College of Fisheries, Ocean University of China, Qingdao 266003, China,2. Huangdao Ocean and Fisheries Bureau of Qingdao, Qingdao 266555, China,1. Department of Fisheries, College of Fisheries, Ocean University of China, Qingdao 266003, China,1. Department of Fisheries, College of Fisheries, Ocean University of China, Qingdao 266003, China,1. Department of Fisheries, College of Fisheries, Ocean University of China, Qingdao 266003, China and 3. Laizhou MingBo Aquatic CO., LTD, Yantai 264000, China
Abstract:Abstract: Nitrification biofilters were widely used to remove ammonia and other metabolic waste products in recirculating aquaculture systems, in which the biofilms played a crucial role in the biotransformation of contaminants. The functional dynamics of the microbial communities were not thoroughly characterized, which provided the impetus for efforts to characterize their species composition and activity. Microbial communities in various biofilters have been intensively studied by various molecular methods, such as polymerase chain reaction - denaturing gradient gel electrophoresis (PCR-DGGE), terminal restriction fragment length polymorphism (T-RFLP), sequencing of clones in DNA libraries and fluorescent in situ hybridization (FISH). However, these tools tend to underestimate the microbial diversity of the biofilter. So-called metagenomic studies use either "shotgun" or PCR-directed sequencing to characterize largely unbiased samples of genes from all the members of sampled communities. Compared to traditional methods, application of the metagenomics approach - in combination with next-generation DNA sequencing, which can generate millions of DNA sequence reads with an average length of over 400 bp - can provide insights of unprecedented depth into microbial community composition and diversity. Against this background, we applied polymerase chain reaction-mediated amplification of the 16S rRNA gene and high-throughput Illumina-MiSeq sequencing to seek insights into the microbial community composition of a series of submerged biofilters in commercial recirculating aquaculture systems for grouper (Epinehelus moara). Our results demonstrated the usefulness of the approach for elucidating bacterial community structure in the series of biofilter; we detected a mean of 27,737 usable DNA sequence reads and 737 operational taxonomic units (OTU) for each of the 3 submerged biofilters and 488 OTUs were shared among the series of submerged biofilters. Rarefaction curves indicated that further sequencing would not result in identification many more OTUs within each sample. Biofilter 3 had the highest microbial diversity than biofilter 1 and biofilter 2 based on the value of Chao1 index and Simpson index. Bacterial community compositions were characterized at the phylum and genus levels, respectively. Among the 14 most frequently observed phyla, the most dominant was Proteobacteria, representing about 50% of reads in the overall data set for a given filter. The other dominant phyla were Bacteroidetes (23.3%-35.4%), Verrucomicrobia (2.0%-8.8%), Chloroflexi (2.5%-3.5%), Planctomycetes (1.6%-6.3%), Actinobacteria (2.0%-2.7%) and Nitrospirae (0.2%-7.1%), which were similar with the previous study. At the genus level of taxonomic classification, more than eighty taxa were observed, including 2 genera which were important to the process of nitrification. The nitrite-oxidizing genus Nitrospira was abundant in biofilter 3 (7%) and less abundant in biofilter 2 (0.8%) and biofilter 1 (0.2%). The ammonia-oxidizing genus Nitrosomonas varied ranging from 0.1 % to 2.3%. These results suggested that Nitrosomonas and Nitrospira played important role in nitrification in the series of submerged biofilters. The UPGMAM dendrogram created by hierarchical cluster analysis of our results showed the biofilter1 and biofilter 2 closely clustered. The results showed that high-throughput DNA sequencing technology could provide unprecedented depth into microbial community and the findings in this work would data and theoretical basis for design and optimization of series of submerged biofilters in recirculating aquaculture system.
Keywords:aquaculture  microbiology  pollution  recirculating aquaculture system (RAS)  submerged biofilters  bacterial community  high-throughput DNA sequencing
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