应用16S rRNA基因文库技术分析土壤细菌群落的多样性

[目的]土壤微生物在菜田生态系统中具有重要的生态功能,通过16S rRNA基因克隆文库技术分析典型菜田土壤细菌群落结构的组成情况,为揭示典型的菜田土壤微生物的多样性以及土地利用变化与生态环境效应之间的关系奠定基础.[方法]采用未培养技术直接从北京和山东两地典型菜田土壤样品中提取微生物总的DNA,分别构建基于通用引物PCR扩增的土壤细菌16S rRNA基因克隆文库,通过Hinf Ⅰ和Hae Ⅲ限制性内切酶对两地土壤细菌16s rRNA基因文库中的克隆进行ARDRA(Amplified Ribosomal DNA Rstriction Analysis)分析,将所有阳性克隆分为若干个可操作分类单元(OTU).[目的]通过构建两地细菌克隆文库的系统发育树,并分析主要种群的组成表明:北京和山东菜田土壤细菌克隆文库的优势种群均为γ、β、α变形细菌亚群.两地的细菌种类组成分别包括124个OTUs和92个OTUs.[结论]北京地区和山东地区典型蔬菜地土壤细菌种群中优势种群均为变形细菌,但是土壤细菌多样性降低,这可能与典型菜田的多年连作,种植蔬菜种类单一直接相关.同时,也可能是造成菜田土壤病害普遍发生,土壤退化的一个重要原因.     

氮掺杂碳纳米颗粒对稻田根际土壤细菌群落的影响

氮掺杂碳纳米颗粒(N-CNPs)具有较高的农田氮肥增效潜力,但其对稻田根际土壤细菌群落结构和功能的影响尚不明确。本研究以连续3年施用低(1.2%,N-CNPs1)、中(6.7%,N-CNPs2)和高(9.3%,N-CNPs3)氮掺杂碳纳米颗粒的稻田根际土壤为研究对象,采用高通量测序技术和PICRUSt 功能预测方法研究其细菌群落组成和代谢功能变化。结果表明: 连续3年配施N-CNPs能提升稻田根际土壤细菌群落多样性,改变细菌群落功能;不同氮掺杂量水平间存在差异,其中以中氮掺杂量(N-CNPs2)碳纳米颗粒处理变化幅度最大。细菌群落分析结果指出,配施N-CNPs提升了根际土壤中变形菌门、酸杆菌门和疣微菌门的相对丰度,降低了浮霉菌门、绿弯菌门、硝化螺旋菌门和芽单胞菌门的相对丰度。PICRUSt 功能预测结果表明,在二级预测功能分类中,配施N-CNPs处理的氨基酸代谢、碳水化合物代谢和脂类代谢功能得到增强,而其他代谢功能则受到减弱。KEGG 直系同源基因簇丰度热图结果显示,N-CNPs2处理能提升根际土壤碳、氮代谢相关的细菌群落的相对丰度。     

16S rDNA克隆文库法探索转基因香石竹对土壤细菌群落的影响

【目的】通过研究转基因香石竹对土壤细菌群落的影响,为转基因香石竹的环境安全性评价提供依据。【方法】通过构建16S rDNA克隆文库,分析种植转基因和非转基因香石竹的土壤中细菌的群落结构组成。【结果】转基因和非转基因香石竹土壤中,共有的菌群有变形菌门(Proteobacteria)、浮霉菌门(Planctomycetes)、酸杆菌门(Acidobacteria),其中α-变形菌门、β-变形菌门、浮霉菌门为优势菌群;而在放线菌门(Actinobacteria)、疣微菌门(Verrucomicrobia)及未培养菌(Uncultured bacterium clone)等菌群存在部分差异。【结论】通过16S rDNA克隆文库方法揭示了转基因香石竹的土壤中细菌多样性十分丰富,其栽培对土壤细菌群落结构影响有限。     

竹炭对三叶草生长及土壤细菌群落的影响

研究添加不同含量(0、3%和9%)和颗粒直径(0.05、0.05～1.0和1.0～2.0 mm)竹炭对三叶草生长及土壤微生物群落结构的影响.结果表明: 竹炭对三叶草生长的促进作用前期较明显,添加9%竹炭处理略好于添加3%竹炭处理,而不同颗粒直径对三叶草生长影响差异不显著;播种后0～120 d,竹炭对三叶草生长的促进作用随着时间推移而减弱,5个月后基本消失.16S rDNA V3区片段的DGGE分析表明,添加竹炭改变了土壤细菌群落结构特征,大部分种类土壤细菌数量和细菌群落多样性指数均高于对照.定量分析表明,添加9%、细粒(D<0.05 mm)竹炭处理土壤细菌数量显著高于其他处理.同一添加含量下,细粒径竹炭对土壤细菌数量的增加效应更明显.
     

长期施肥对稻田土壤细菌、古菌多样性和群落结构的影响

稻田土壤是“迷失碳”的重要吸纳场所之一,也是温室气体(CH4和N2O等)的重要排放源.大气温室气体的动态变化与土壤碳氮转化的微生物过程紧密相关.以湖南桃江国家级稻田肥力变化长期定位试验点为平台,采用PCR-克隆测序和实时荧光定量PCR技术,研究不施肥(CK)、施氮磷钾肥(NPK)和氮磷钾肥+秸秆还田(NPKS)3种长期施肥制度(＞25 a)对稻田土壤细菌和古菌群落结构及数量的影响.细菌和古菌16S rRNA基因文库分析结果表明:稻田土壤细菌主要类群为变形菌、酸杆菌、绿弯菌,而古菌主要为泉古菌和广古菌.长期施肥导致土壤细菌和古菌种群结构产生明显差异,与CK相比,NPK和NPKS处理稻田土壤的变形菌、酸杆菌和泉古菌相对丰度增加.LIBSHUFF软件分析结果也表明,16S rRNA基因文库在CK、NPK及NPKS处理间存在显著差异.3种施肥处理的稻田土壤细菌16S rRNA基因拷贝数为每克干土0.58× 1010～1.06×1010个,古菌为每克干土1.16×106 ～ 1.72×106个.施肥(NPK和NPKS)后,细菌和古菌的多样性和数量增加,且NPKS＞NPK.说明长期施肥显著影响土壤细菌和古菌群落结构、多样性及数量.     

稻田不同水分管理方式对土壤线虫群落的影响

在下辽河平原地区就稻田不同水分管理方式对土壤线虫多度、营养类群、群落组成的影响进行了研究．结果表明,0～10cm土层不同水分管理处理的线虫总数在耙耕前和黄熟期显著低于对照,10～20cm土层各时期处理间线虫总数的差异不显著,20～30cm土层线虫总数在耙耕前和黄熟期差异极显著．北方单季稻水田试验共观察到土壤线虫16科22属．绕线属(Plectus)、垫刃属(Tylenchus)、单宫属(Monhystera)是优势属,绕线属和垫刃属对不同的水分管理比较敏感．在耙耕前和黄熟期不同水分管理方式对0～10cm土壤食细菌线虫能够产生显著影响．稻田土壤中食细菌线虫和植物寄生线虫是优势营养类群,而捕食／杂食性线虫的相对多度最低．     

秸秆覆盖免耕对土壤细菌群落区系的影响

多年连续秸秆覆盖免耕对土壤细菌群落影响很大,免耕可提高０－１０ｃｍ土层土壤细菌总数、放线菌数、棒状细菌数和贫营养细菌数量,特别是免耕土壤能使芽孢杆菌数量增多几倍。     

灌溉方式对稻田土壤微生物群落功能多样性的影响

为了探讨3种不同灌溉模式对土壤微生物群落功能多样性的影响。本研究采用Biolog-ECO板研究了双季稻田连续五年不同灌溉处理(长期灌溉,湿润灌溉,间歇灌溉)下的土壤微生物群落功能多样性。结果表明,不同灌溉方式处理的土壤微生物代谢活性强度为间歇灌溉湿润灌溉长期淹水灌溉。在不同的处理中,α-环式糊精和D-葡萄胺酸解释了主要的差异。氨基酸和糖类碳源是间歇灌溉和湿润灌溉灌溉模式下主要被利用的碳源,而酯类在长期淹水灌溉模式被利用的最多。通过评价3种灌溉方式下稻田土壤的代谢特征,证实了间歇灌溉方式有利于提高稻田土壤微生物的功能多样性,为稻田水分科学管理提供了理论依据。     

不同香蕉枯萎病区土壤细菌群落多样性

分别采集海南省临高县3个地区的香蕉枯萎病发病土壤与健康土壤样品共6份,采用常规方法测定土壤理化性质,以末端限制性片段多态性分析(T-RFLP)技术研究不同地区发病与健康土壤微生物的多样性,并分析土壤微生物群落结构与土壤因子的关系.结果表明:同一地区发病蕉园土壤的大部分理化性质指标低于健康蕉园,以pH、有效P含量的差异最显著;T-RFLP结果表明供试蕉园发病土壤的细菌多样性比健康土壤丰富;3个地区的优势种分别为片段长度为144、147与233 bp的T-RFs,通过系统发育分配工具比对,推断这3个地区的优势菌群可能属于枯草芽孢杆菌、葡萄球菌、反刍真杆菌;大部分T-RFs的分布与土壤碱解N、pH、速效K、有效P及含水量有关,且在发病土壤中的相对丰度大于健康土壤.     

基于16S rDNA测序对茶园土壤细菌群落多样性的研究

土壤细菌群落组成和多样性,对茶园土壤生态系统健康和肥力可持续性具有的重要理论意义。利用Illumina高通量测序技术测定分析16S rDNA,研究云南景迈山、布朗山和南糯山的现代茶园、古茶园(林)和森林土壤的细菌群落结构与多样性。结果表明:古茶园土壤细菌的丰度和多样性高于现代茶园及森林;研究土壤样本细菌共分属47个菌门、89个目,其中变形菌门、酸杆菌门、放线菌门、厚壁菌门与拟杆菌门是优势类群,它们在森林、现代茶园和古茶园土壤中的相对丰度累计分别达91.86%、82.48%和77.08%;伯克霍尔德氏菌目、根瘤菌目是优势菌群,其平均丰度分别达13.91%和8.17%,黄单胞菌目、红螺菌目、芽孢杆菌目、放线菌目和拟杆菌目等12个目的丰度较高,达2%以上;PCA分析表明:森林、现代茶园和古茶园土壤的细菌群落结构差异明显,除景迈山外,主要优势细菌丰度依次为:古茶园现代茶园森林,古茶园土壤细菌多样性有增强趋势。     

家蚕幼虫中肠细菌群落多样性的PCR-DGGE和16S rDNA文库序列分析

采用基于16S rDNA 的变性梯度凝胶电泳（denaturing gradient gel electrophoresis, DGGE）和16S rDNA文库序列分析的手段,研究了重要经济昆虫家蚕Bombyx mori 2个品系——专食性品系C108和广食性品系SCN2幼虫中肠内的细菌群落多样性,同时还探讨了食料对家蚕中肠内细菌群落结构的影响。文库序列分析表明,PCR 扩增得到的16S rDNA基因代表了家蚕中肠内的41种细菌系统发育型（phylotype）,大多数属于Proteobacteria,其次是Lactobacillales。此外,还有少数属于Deinococcus-Thermus、Bacillales、Clostridiales和Actinobacteria,尚有5种系统发育型不能确定其所属类型。家蚕的这2个品系中,肠球菌属Enterococcus是其中肠细菌的优势菌群,栖热菌属Thermus是次优势菌群。优势菌肠球菌属的组成在品系和不同食料喂养条件下有着一定的变化,无桑饲料喂养条件下SCN2品系中肠内还出现了新的次优势菌葡萄球菌（Staphylococcus）。DGGE图谱显示家蚕低龄幼虫和高龄幼虫肠道细菌格局存在差异,推测可能与其发育期生理状态的差异有关。本研究结果提示家蚕肠道特殊菌群的出现可能与其特殊的食性有一定的关系,食料改变、生长受阻后肠道微生态平衡也发生变化。     

Characterization of Bacterial Communities in Selected Smokeless Tobacco Products Using 16S rDNA Analysis

The bacterial communities present in smokeless tobacco (ST) products have not previously reported. In this study, we used Next Generation Sequencing to study the bacteria present in U.S.-made dry snuff, moist snuff and Sudanese toombak. Sample diversity and taxonomic abundances were investigated in these products. A total of 33 bacterial families from four phyla, Actinobacteria, Firmicutes, Proteobacteria and Bacteroidetes, were identified. U.S.-produced dry snuff products contained a diverse distribution of all four phyla. Moist snuff products were dominated by Firmicutes. Toombak samples contained mainly Actinobacteria and Firmicutes (Aerococcaceae, Enterococcaceae, and Staphylococcaceae). The program PICRUSt (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States) was used to impute the prevalence of genes encoding selected bacterial toxins, antibiotic resistance genes and other pro-inflammatory molecules. PICRUSt also predicted the presence of specific nitrate reductase genes, whose products can contribute to the formation of carcinogenic nitrosamines. Characterization of microbial community abundances and their associated genomes gives us an indication of the presence or absence of pathways of interest and can be used as a foundation for further investigation into the unique microbiological and chemical environments of smokeless tobacco products.     

红树林土壤细菌群落16S rDNA V3片段PCR产物的DGGE分析

从土壤中抽提微生物总DNA ,直接扩增 16SrDNAV3片段 ,应用变性梯度凝胶电泳 (DGGE)和分子克隆技术分析 16SrDNAV3片段的多态性 ,发现地域因素和红树品种都是影响土壤细菌群落结构的因素。通过对杯萼海桑土壤 16SrDNAV3片段PCR产物两个DGGE条带进行分子克隆、序列测定和Blast分析 ,发现每个DGGE条带包含着许多不同的 16SrDNAV3片段 ,并且其中多数为NCBI未收录的序列。这表明DGGE和克隆技术相结合的方法是研究土壤微生物群落结构的一种可行方法。     

DGGE method for analyzing 16S rDNA of methanogenic archaeal community in paddy field soil

A denaturing gradient gel electrophoresis (DGGE) method for analyzing 16S rDNA of methanogenic archaeal community in paddy field soil is presented. Five specific primers for 16S rDNA of methanogenic archaea, which were modified from the primers for archaea, were first evaluated by polymerase chain reaction and DGGE using genomic DNAs of 13 pure culture strains of methanogenic archaea. The DGGE analysis was possible with two primer pairs (0348aF-GC and 0691R; 0357F-GC and 0691R) of the five pairs tested although 16S rDNA of some non-methanogenic archaea was amplified with 0348aF-GC and 0691R. These two primer pairs were further evaluated for use in analysis of methanogenic archaeal community in Japanese paddy field soil. Good separation and quality of patterns were obtained in DGGE analysis with both primer pairs. A total of 41 DNA fragments were excised from the DGGE gels and their sequences were determined. All fragments belonged to methanogenic archaea. These results indicate that the procedure of DGGE analysis with the primer pair 0357F-GC and 0691R is suitable for investigating methanogenic archaeal community in paddy field soil.     

降解烟碱的YC-68菌株16SrDNA序列分析及鉴定

从烟叶调制过程中温度达68℃阶段的叶片上分离得到一株能降解烟碱的菌株,编号为YC-68,该菌经常规的形态、生理生化分析,确定为芽孢杆菌。根据该菌16 S rDNA恒定区的保守性设计了一对通用引物,扩增其16 S rDNA序列,将扩增的产物进行回收后进行测序,把测序后的结果提交到GenBank利用BLAST进行序列同源性分析。经过分析鉴定YC-68菌株为芽孢杆菌属的蜡状芽孢杆菌。     

东北虎粪细菌区系的16S rRNA基因序列分析

为研究东北虎粪微生物区系建立了东北虎粪细菌的16SrDNA文库。通过EcoRⅠ和HindⅢ分别对阳性克隆进行酶切分析,从东北虎的16SrDNA文库中分别获得了15个具有酶切差异的克隆。BLAST分析结果显示,在15个克隆中,10个克隆与梭菌属成员有97%以上的同源性,其中有6个序列与诺维梭菌A型(Clostridiumnovyitype A)有99%的同源性,为诺维梭菌A型;4个序列与猪粪细菌RT-18B(Swine manure bacteriumRT-18B)有97%的同源性,为消化链球菌属(Peptostreptococcus)成员。其它序列与GenBank中登录的序列同源性低于97%,为5种未培养细菌,其中4种16SrRNA基因序列分别与Clostridiumpascui、破伤风梭菌E88(ClostridiumtetaniE88)、梭菌(Clostridiumsp.)14505及产气荚膜梭菌(Clostridiumperfringens)有94%~95%的相似性。第5种与肉杆菌(Carnobacteriumsp.)R-7279株有94%的同源性。     

新疆意大利蝗不同地理种群16S rDNA序列差异研究

研究新疆东部和西部不同地理种群意大利蝗Calliptamus italicus(L.)线粒体基因中16SrDNA序列差异。结果表明:(1)意大利蝗A+T的含量(67.7%)明显高于G+C的含量(32.3%);(2)多重序列比对和UPGMA系统发育树的结果表明新疆东、西部不同地理种群的意大利蝗的遗传变异极小。     

16S rDNA克隆文库方法分析太岁样品中细菌的多样性

通过构建16S rDNA克隆文库的方法,分析太岁样品中细菌的群落结构及多样性。太岁样品中的细菌归属于4个门9个目,优势类群依次是芽胞杆菌目(Bacillales,33.01%)、柄杆菌目(Caulobacterales,32.04%)和伯克霍尔德氏菌目(Burkholderiales,12.62%);优势属为短波单胞菌属(Brevundimonas,30.10%)、葡萄球菌属(Staphylococcus,29.13%)和食酸菌属(Acidovorax,7.77%)。并且其中的5个目中含有未培养的细菌,红杆菌目(Rhodobacterales)、伯克霍尔德氏菌目和红环菌目(Rhodocyclales)的11个克隆子的细菌16S rDNA序列同源性低于97%。研究表明太岁样品中细菌多样性较丰富,且蕴藏着许多未知的微生物资源。     

16S rDNA Pyrosequencing Analysis of Bacterial Community in Heavy Metals Polluted Soils

Soil contamination with heavy metals is a widespread problem, especially prominent on grounds lying in the vicinity of mines, smelters, and other industrial facilities. Many such areas are located in Southern Poland; they are polluted mainly with Pb, Zn, Cd, or Cu, and locally also with Cr. As for now, little is known about most bacterial species thriving in such soils and even less about a core bacterial community—a set of taxa common to polluted soils. Therefore, we wanted to answer the question if such a set could be found in samples differing physicochemically and phytosociologically. To answer the question, we analyzed bacterial communities in three soil samples contaminated with Pb and Zn and two contaminated with Cr and lower levels of Pb and Zn. The communities were assessed with 16S rRNA gene fragments pyrosequencing. It was found that the samples differed significantly and Zn decreased both diversity and species richness at species and family levels, while plant species richness did not correlate with bacterial diversity. In spite of the differences between the samples, they shared many operational taxonomic units (OTUs) and it was possible to delineate the core microbiome of our sample set. The core set of OTUs comprised members of such taxa as Sphingomonas, Candidatus Solibacter, or Flexibacter showing that particular genera might be shared among sites ~40 km distant.     

Bacterial diversity in two coastal lagoons deduced from 16S rDNA PCR amplification and partial sequencing

Abstract: Amplification and sequence analysis of the 16S rRNA genes from DNA samples extracted directly from the environment allows the study of microbial diversity in natural ecosystems without the need for cultivation. In this study this methodology has been applied to two coastal lagoons. Activity and numbers of heterotrophic bacteria have indicated that, as expected, Prévost lagoon (located on the French Mediterranean coast) is more eutrophic than that of the Arcachon Bay (French Atlantic coast). Analysis of partial 16S rRNA gene sequences revealed that, in both environments, a relatively large number of clones related to Cytophaga/Flexibacter/Bacteroides as well as to α-Proteobacteria were found. One hundred percent similarity with the sequences of the data bases were not found for any of the more than a hundred clones studied, in fact for most clones maximum similarity was below 95% for the approx. 200 bases sequenced. Similarity was not higher with any of the sequences found for the 14 isolates (pure cultures) obtained from the same samples. Redundancy, i.e. number of identical sequences, was higher in the samples from Arcachon. In addition, sequences related to representatives of ten major phylogenetic branches of Bacteria were obtained from Prévost lagoon; however only five branches were represented by the data from Arcachon. These findings indicated a higher bacterial phylogenetic diversity in the Prévost lagoon.