期刊文献+

16SrRNA测序技术在肠道菌群检测中的研究进展 被引量:12

Research progress of 16SrRNA sequencing technology in detection of intestinal flora
下载PDF
导出
摘要 16SrRNA测序技术是最常用的高通量测序依赖的组学技术之一,由于其结构和碱基排列复杂度适中,较易于进行序列测定和分析比较。人体肠道内寄居着数量庞大、种类繁多的微生物,与宿主形成一个相互依赖且相互制约的微生态系统,在宿主营养吸收和代谢、能量供应、免疫调节和对病原体的保护中起不可替代的作用。由于16SrRNA基因是原核微生物进行系统化分类研究时最常用的分子标志物,可对肠道微生物中的所有菌种进行精确定量。因此,综述了近年来16SrRNA基因序列分析技术在肠道菌群中的应用,为今后完善16SrRNA测序技术提供帮助。 16SrRNA sequencing technology is one of the most commonly used high-throughput sequencing-dependent omics techniques. Due to the moderate complexity of structure and base alignment, it is easier to perform sequence determination and analysis comparison. A large number of large-scale microorganisms in the human intestines form an interdependent and mutually restrictive micro-ecological system with the host, which plays an irreplaceable role in host nutrient absorption and metabolism, energy supply, immune regulation and protection of pathogens. Since the 16SrRNA gene is the most commonly used molecular marker for systematic classification studies of prokaryotic microorganisms, all strains in intestinal microorganisms can be accurately quantified. In this study, the application of 16SrRNA gene sequence analysis technology in intestinal flora has been reviewed in recent years, which will help to improve 16SrRNA sequencing technology in the future.
作者 郭美薇 刘凡铭 邹伟 GUO Mei-wei;LIU Fan-ming;ZOU Wei(School of Life Science,Liaoning Normal University,Dalian 116081,China)
出处 《实验室科学》 2019年第2期1-4,8,共5页 Laboratory Science
基金 国家级大学生创新训练项目(项目编号:201810165006)
关键词 16SrRNA 肠道菌群 序列分析 16SrRNA intestinal flora sequence analysis
  • 相关文献

参考文献4

二级参考文献56

  • 1张敏,范小兵,杭晓敏,李堃宝,杨虹,沙大年,奚万艳,王一鸣.青年人肠道菌群分布及关键益生菌群落结构分析[J].微生物学报,2004,44(5):621-626. 被引量:22
  • 2许本发,王艳萍,陈莹.耐氧双歧杆菌的分离和鉴定[J].微生物学报,1994,34(1):9-13. 被引量:22
  • 3金红芝 ,范小兵 ,杭晓敏 ,李堃宝 ,杨虹 ,沈云春 .儿童肠道双歧杆菌和乳杆菌种群结构分析[J].微生物学报,2005,45(4):567-570. 被引量:9
  • 4高小亚,戈敏娟,马向华.单纯性肥胖患者血清瘦素、抵抗素和脂联素水平的研究[J].医学研究生学报,2006,19(6):544-547. 被引量:25
  • 5Satokari R M,Vaughan E E,Akkermans A,et al.Bifidobacterial diversity in human feces detected by genus-specific PCR and denaturing gradient gel electrophoresis.Appl Environ Microbiol,2001,67(2):504-513.
  • 6Matsuki T,Watanabe K,Tanaka R,et al.Distribution of bifidobacterial species in human intestinal microflora examined with 16S rRNA-gene-targeted species-specific primers.Appl Envir Microbiol,1999,65(10):4506-4512.
  • 7Langendijk P,Schut F,Jansen G J,et al.Quantitative fluorescence in situ hybridization of Bifidobacterium spp.with genus-specific 16S rRNA-targeted probes and its application in fecal samples.Appl Environ Microbiol,1995,61(8):3069-3075.
  • 8Wei G,Pan L,Du H,et al.ERIC-PCR fingerprinting-based community DNA hybridization to pinpoint genome-specific fragments as molecular markers to identify and track populations common to healthy human guts.J Microbiol Methods,2004,59(1):91-108.
  • 9Wang R F,Cao W W,Cerniglia C E.PCR detection and quantitation of predominant anaerobic bacteria in human and animal fecal samples.Appl Environ Microbiol,1996,62(4):1242-1247.
  • 10Di Cello F,Bevivino A,Chiarini L,et al.Biodiversity of a Burkholderia cepacia population isolated from the maize rhizosphere at different plant growth stages.Appl Environ Microbiol,1997,63(11):4485-4493.

共引文献30

同被引文献137

引证文献12

二级引证文献38

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