期刊文献+

基于16SrDNA高通量测序方法检测猪舍空气微生物多样性 被引量:19

Microbial Diversity of Piggery Air Detected by 16S rDNA High-throughput Sequencing
原文传递
导出
摘要 采用16SrDNA高通量测序方法研究猪舍空气微生物的多样性。实验采用Illumina MiSeq 2×250系统,对细菌16S rDNA(V4)区进行测序;采用QIIME软件对数据进行分析。结果表明:猪舍空气微生物多样性丰富,基于97%的相似规律来确定OTU(operational taxonomical unit),其中,有16种门、115种科、217种属被鉴定;在属水平上,10种优势菌群是Pseudomonas、Acinetobacter、Streptococcus、Lactococcus、Enhydrobacter、Lactobacillus、Chryseobacterium、Wautersiella、Flavobacterium、Leuconostoc,其中,6种被报道为病原微生物。实验结果表明,了解猪舍空气微生物的多样性、丰度及优势菌群的病原性对猪舍疾病防控有一定指导意义。 Using 16S rDNA high-throughput sequencing to explore the microbial divers ity of the piggery air. Air samples were collected from 5 types of hoggeries in QiongLai. The V4 viriable region of 16s rDNA was amplified by PCR and sequenced with Illumina MiSeq 2×250 platform. QIIME software was used to analyze data. We observed high microbial diversity in piggery air. OTU (operational taxonomical unit) were identified based on the 97% similarity rule, which corresponds to, 16 bacteria Phylum, 115 Families and 217 Genus when balsted to known taxa from GreenGene data base. At Genus level, 10 abundant genus are Pseudomonas, Acinetobacter, Streptococcus, Lactococcus, Enhydrobacter, Lactobacillus, Chryseobacterium, Wautersiella, Flavobacterium, Leuconostoc, 6 of which among the top 10 were reported to be pathogenic. Study on the piggery air microbial diversity can provide a new guidance for animal disease prevention.
出处 《中国畜牧杂志》 CAS 北大核心 2015年第3期81-84,共4页 Chinese Journal of Animal Science
基金 生猪产业技术体系四川创新团队建设项目(SZCXTD-2) 教育部长江学者和创新团队发展计划(RT13083)
关键词 16SrDNA高通量测序 猪舍 空气微生物 多样性 16S rDNA high-throughput sequencing piggery air microorganism diversity
  • 相关文献

参考文献17

  • 1孙广力,孙刚,李书华,魏萍,郭昭林,杨本.黑龙江省规模化养猪场大肠杆菌病血清型流行病学调查[J].黑龙江畜牧兽医,2004(7):90-91. 被引量:27
  • 2Elliott L F, McCalla T M, Deshazer J A. Bacteria in the air of housed swine units[J]. App Environ Microb, 1976, 32(2): 270- 273.
  • 3Masclaux F G, Sakwinska O, Charrire N, et ol. Concentration of Airbome Staphylococcus aureus (MRSA and MSSA), Total Bacteria, and Endotoxins in Pig Farms [J]. Ann Occup Hyg,2013, 57(5): 550-557.
  • 4Nehme B, Gilbert Y, Letourneau V, et al. Culture-independent characterization of archaeal biodiversity in swine confinement building bioaerosols [J]. App Environ Microb, 2009, 75 (17): 5445-5450.
  • 5Kristiansen A, Pedersen K H, Nielsen P H, et ol. Bacterial community structure of a full-scale biofilter treating pig house exhaust air[J]. Syst Appl Microbiol, 2011, 34(5): 344-352.
  • 6Caporaso J G, Kuczynski J, Stombaugh J, et al. QIIME allows analysis of high-throughput community sequencing data [J]. Nat Methods, 2010, 7(5): 335-336.
  • 7Smyth R P, Schlub T E, Grimm A, et a!. Reducing chimera formation during PCR amplification to ensure accurate genotyping[J]. Gene, 2010, 469(1): 45-51.
  • 8Hardie K R, Pommier S, Wilhelm S. The secreted proteins of Pseudomonas aeruginosa: their export machineries, and how they contribute to pathogenesis [J]. Horizon Bioscience, 2009, ISBN 978-904455-42-4.
  • 9Hanski I, von Hertzen L, Fyhrquist N, et cd. Environmental biodiversity, human mierobiota, and allergy are interrelated[J]. Proc National Acad Sci, 2012, 109(21): 8334-8339.
  • 10Hertzen E, Johansson L, Kansal R, et d. Intraeellular Streptococcus pyogenes in human macrophages display an altered gene expression profile[J]. PloS One, 2012, 7(4): e35218.

共引文献26

同被引文献155

引证文献19

二级引证文献50

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部