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2020, 08, v.39 3461-3467
不同DNA提取方法引起鲤鱼肠道菌群多样性分析结果的偏差
基金项目(Foundation): 国家自然科学基金项目(31272692);; 天津市企业科技特派员项目(18JCTPJC64700);; 天津市水产产业技术体系创新团队建设项目(ITTFRS2017014)共同资助
邮箱(Email): sun_jf@163.com;
DOI: 10.13417/j.gab.039.003461
摘要:

为了评价两种不同DNA提取方法引起的鲤鱼肠道菌群结构分析偏差。本研究分别以氧化锆珠破壁法(ZBC)和使用QIAamp Fast DNA Stool Mini Kit试剂盒法(QIA) 3次重复提取鲤鱼肠道总DNA,检测DNA含量、纯度,进一步采用Illumina Hi Seq测序平台,利用高通量测序技术处理,来比较分析QIA组和ZBC组的菌群种类和结构偏差。结果表明,从QIA和ZBC样品分别获得(67 045±10 777.22)条和(79 041±8 168.68)条有效序列,QIA组样品OTU (Operational taxonomic unit)数量和Shannon多样性指数均显著高于ZBC组,且QIA组样品间OTU重复性优于ZBC组样品间。鲤鱼肠道菌群在门水平上排名前十的有:变形菌门(Proteobacteria),梭杆菌门(Fusobacteria),拟杆菌门(Bacteroidetes),厚壁菌门(Firmicutes),放线菌门(Actinobacteria),芽单胞菌门(Gemmatimonadetes),绿弯菌门(Chloroflexi),浮霉菌门(Planctomycetes),异常球菌-栖热菌门(Deinococcus-thermus)和疣微菌门(Verrucomicrobia)。分析得到ZBC法提取到的DNA浓度高,特有的OTU数目多;QIA法的测序结果稳定,菌群多样性和物种丰富度均较高。高通量测序结果表明两种方法提取鲤鱼肠道微生物DNA,其菌群多样性存在偏差,但两种方法均能有效提取到鲤鱼肠道DNA,可为鲤鱼肠道菌群的研究提供参考。

Abstract:

The aim of this study was to study the biases from two DNA extraction methods of carp intestine microbiota revealed based on the Illumina HiSeq platform. We extracted the total DNA of intestinal microbiota from Cyprinus carpio L with Zirmil-beating Cell Disruption method, and the QIAamp Fast DNA Stool Mini Kit.DNA quality was evaluated based on the absorbance ratios of 260/280 nm by NanoDrop. Then Illumina HiSeq high-throughput sequencing was used to examine the intestinal bacterial communities following PCR amplification of 16S rDNA V4 region. The average sequence reads obtained from QIA and ZBC samples were 67 045±10 777.22 and 79 041±8 168.68 respectively. After resampling at the same depth of 43 979 reads, the operational taxonomic unit(OTU) number and Shannon diversity index of QIA samples were significantly higher than those of ZBC samples.By contrast, the reproducibility of OTU among QIA replicates was higher than that among ZBC replicates. The dominant phyla of ZBC and QIA samples were identical, including Proteobacteria, Fusobacteria, Bacteroidetes,Firmicutes, Actinobacteria, Gemmatimonadetes, Chloroflexi, Planctomycetes, Deinococcus-Thermus, and Verrucomicrobia. And the extracted DNA concentration of ZBC is higher, and the unique OTU numbers are large; and the sequel QIAamp Fast DNA Stool Mini Kit is stable. Significant biases on community structure of carp intestinal microbiota were detected which originated from DNA extraction. However, both methods can effectively extract the intestinal DNA of carp, and could provide reference for research intestinal flora of carp.

参考文献

Asfie M.,Yanagi H.,Okano R.,Akiyama N.,and Sugita H.,2000,The protease-producing ability of Vibrios isolated from larvae and juveniles of Japanese flounder,Aquiculture Science,48(1):139-140

Benson A.K.,Kelly S.A.,Legge R.,Ma F.,Low S.J.,Kim J.,Zhang M.,Oh P.L.,Nehrenberg D.,Hua K.J.,Kachman S.D.,Moriyama E.N.,Walter J.,Peterson D.A.,Pomp D.,and Mackay T.F.C.,2010,Individuality in gut microbiota composition is a complex polygenic trait shaped by multiple environmental and host genetic factors,Proc.Natl.Acad.Sci.USA,107(44):18933-18938

Bokulich N.A.,Subramanian S.,Faith J.J.,Gevers D.,Gordon J.I.,Knight R.,Mills D.A.,and Caporaso J.G.,2013,Quality-filtering vastly improves diversity estimates from Illumina amplicon sequencing,Nature Methods,10(1):57-59

Edgar R.C.,2013,UPARSE:highly accurate OTU sequences from microbial amplicon reads,Nature Methods,10(10):996-998

Gajardo K.,Rodiles A.,Kortner T.M.,Krogdahl魡.,Bakke A.M.,Merrifield D.L.,and S覬rum H.,2016,A high-resolution map of the gut microbiota in atlantic salmon(Salmo salar):A basis for comparative gut microbial research,Sci.Rep.,6:30893

Ganguly S.,and Prasad A.,2011,Microflora in fish digestive tract plays significant role in digestion and metabolism,Reviews in Fish Biology and Fisheries,22(1):11-16

Han Z.R.,Sun J.F.,LüA.J.,and Wang A.L.,2019,Biases from different DNA extraction methods in intestine microbiome research based on 16S r DNA sequencing:a case in the koi carp,Cyprinus carpio var.Koi,Microbiologyopen,8(1):e00626

Kashinskaya E.N.,Andree K.B.,Simonov E.P.,and Solovyev M.M.,2017,DNA extraction protocols may influence biodiversity detected in the intestinal microbiome:a case study from wild Prussian carp,Carassius gibelio,Fems Microbiology E-cology,93(2):fiw240

Liang J.H.,Yang J.Y.,Zhang H.,Zhu J.L.,Yang C.J.,and Cui G.,2010,Two methods for total DNA extraction from intestinal microorganisms,Zhongguo Weishengtaixue Zazhi(Chinese Journal of Microecology),22(5):477-478(梁金花,杨景云,张虎,朱金玲,杨春佳,崔刚,2010,两种提取肠道微生物总DNA方法的比较,中国微生态学杂志,22(5):477-478)

Lu L.D.,Jiang S.T.,and Lin Y.X.,2009,Comparison of three methods for total DNA extraction from intestinal microflora of the fowl,Zhongguo Weishengtaixue Zazhi(Chinese Journal of Microecology),21(7):588-590(卢龙娣,江胜滔,林跃鑫,2009,鸡肠道菌群总DNA三种提取方法的比较,中国微生态学杂志,21(7):588-590)

Magoc T.,and Salzberg S.L.,2011,FLASH:fast length adjustment of short reads to improve genome assemblies,Bioinformatics,27(21):2957-2963

Meng H.,Zhang Y.,Zhao L.,Zhao W.,He C.,Honaker C.F.,Zhai Z.,Sun Z.,and Siegel P.B.,2014,Body weight selection affects quantitative genetic correlated responses in gut microbiota,PLoS One,9(3):e89862

Quast C.,Pruesse E.,Yilmaz P.,Gerken J.,Schweer T.,Yarza P.,Peplies J.,and Gl觟ckner F.O.,2013,The SILVA ribosomal RNA gene database proje ct:improved data processing and web-based tools,Nucleic Acids Res.,41(D):590-596

Rao L.Y.,Li X.M.,Li X.H.,Zhu W.G.,Yu Y.H.,and Yan Q.Y.,2018,Comparison between the intestinal bacterial communities of the transgenic common CARP and the controls,Shuisheng Shengwu Xuebao(Acta Hydrobiologica Sinica),42(2):349-355(饶刘瑜,李学梅,李星浩,朱文根,余育和,颜庆云,2018,转基因鲤鱼与对照鲤肠道微生物群落差异研究,水生生物学报,42(2):349-355)

Smriga S.,Sandin S.A.,and Azam F.,2010,Abundance,diversity,and activity of microbial assemblages associated with coral reef fish guts and feces,Fems Microbiology Ecology,73(1):31-42

Sullam K.E.,Essinger S.D.,Lozupone C.A.,O'Connor M.P.,Rosen G.L.,Knight R.,Kilham S.S.,and Russell J.A.,2012,Environmental and ecological factors that shape the gut bacterial communities of fish:a meta-analysis,Molecular Ecology,21(13):3363-3378

Wang Q.,Garrity G.M.,Tiedje J.M.,and Cole J.R.,2007,Naive Bayesian classifier for rapid assignment of r RNA sequences into the new bacterial taxonomy,Appl.Environ.Microbiol.,73(16):5261-5267

Wei J.,Yang H.L.,Xu Z.L.,Deng X.P.,Lin Y.H.,Xiong Q.,Wang G.,Bai Y.X.,LüS.B.,and Tan X.B.,2017,Influence of different intercropping patterns of flue-cured tobacco on soil properties and fungal community structure,Turang Tongbao(Chinese Journal of Soil Science),48(3):631-638(韦俊,杨焕文,徐照丽,邓小鹏,林云红,熊茜,王戈,白羽祥,吕世保,谭小兵,2017,烤烟不同套作模式对土壤理化性质和真菌群落结构的影响,土壤通报,48(3):631-638)

Wen C.,He Y.,Xue M.,Liang H.,and Dong J.,2016,Biases on community structure during DNA extraction of shrimp intestinal microbiota revealed by high-throughput sequencing,Acta Microbiologica Sinica,56(1):130-142

Wen C.Q.,He Y.Y.,Xue M.,Liang H.F.,and Dong J.D.,2016,Biases on community structure during DNA extraction of shrimp intestinal microbiota revealed by high-throughput sequencing,Weishengwu Xuebao(Acta microbiologica Sinica),56(1):130-142(温崇庆,何瑶瑶,薛明,梁华芳,董俊德,2016,高通量测序分析DNA提取引起的对虾肠道菌群结构偏差,微生物学报,56(1):130-142)

Xiong J.,Wang K.,Wu J.F.,Qiu Q.L.,Yang K.J.,Qian Y.X.,and Zhang D.M.,2015,Changes in intestinal bacterial communities are closely associated with shrimp disease severity,Appl.Microbiol.Biotechnol.,99(16):6911-6919

Ye L.,Amberg J.,Chapman D.,Gaikowski M.,and Liu W.T.,2014,Fish gut microbiota analysis differentiates physiology and behavior of invasive Asian carp and indigenous American fish,ISME J.,8(3):541-551

Zhang N.,Li J.,Song J.,Mao X.C.,Wang Y.M.,Wang J.F.,and Tang Q.J.,2017,Fructo-oligosaccharides protect mice against exhaustive exercise-induced dyslipidemia by modulating gut microbial composition and function,Xiandai Shipin Keji(Modern Food Science and Technology),33(5):7-13(张娜,李晶,宋佳,毛相朝,王玉明,王静凤,唐庆娟,2017,低聚果糖靶向调节肠道菌群缓解力竭运动导致的脂质代谢紊乱,现代食品科技,33(5):7-13)

Zheng Y.,Zhang J.C.,Guo Z.,and Zhang H.P.,2014,Research progress on high-throughput sequencing to analysis the diversity of gut microbiota and its influence factors,Zhongguo Shipin Xuebao(Journal of Chinese Institute of Food Science and Technology),14(11):157-164(郑艺,张家超,郭壮,张和平,2014,基于高通量测序技术分析肠道菌群及其影响因素的研究进展,中国食品学报,14(11):157-164)

Zhou J.Z.,Wu L.Y.,Deng Y.,Zhi X.,Jiang Y.H.,Tu Q.,Xie J.,Van Nostrand J.D.,He Z.,and Yang Y.,2011,Reproducibility and quantitation of amplicon sequencing-based detection,ISME J.,5(8):1303-1313

Zoetendal E.G.,Heilig H.G.,Klaassens E.S.,Booijink C.C.,Kleerebezem M.,Smidt H.,and Willem M.V.,2006,Isolation of DNA from bacterial samples of the human gastrointestinal tract,Nature Protocols,1(2):870-873

基本信息:

DOI:10.13417/j.gab.039.003461

中图分类号:S917.4

引用信息:

[1]王浩伊,江博赟,孙敬锋,等.不同DNA提取方法引起鲤鱼肠道菌群多样性分析结果的偏差[J].基因组学与应用生物学,2020,39(08):3461-3467.DOI:10.13417/j.gab.039.003461.

基金信息:

国家自然科学基金项目(31272692);; 天津市企业科技特派员项目(18JCTPJC64700);; 天津市水产产业技术体系创新团队建设项目(ITTFRS2017014)共同资助

发布时间:

2020-08-25

出版时间:

2020-08-25

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