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采用16S rDNA焦磷酸测序技术研究囊性纤维化患者痰液中的微生物多样性。

Microbial diversity in the sputum of a cystic fibrosis patient studied with 16S rDNA pyrosequencing.

作者信息

Armougom F, Bittar F, Stremler N, Rolain J-M, Robert C, Dubus J-C, Sarles J, Raoult D, La Scola B

机构信息

URMITE-UMR CNRS 6236, IRD 3R198, Université de la Méditerranée, 27 Boulevard Jean Moulin, 13005 Marseille, France.

出版信息

Eur J Clin Microbiol Infect Dis. 2009 Sep;28(9):1151-4. doi: 10.1007/s10096-009-0749-x. Epub 2009 May 16.

DOI:10.1007/s10096-009-0749-x
PMID:19449045
Abstract

Recent studies using 16S rRNA gene amplification followed by clonal Sanger sequencing in cystic fibrosis demonstrated that cultured microorganisms are only part of the infecting flora. The purpose of this paper was to compare pyrosequencing and clonal Sanger sequencing on sputum. The sputum of a patient with cystic fibrosis was analysed by culture, Sanger clone sequencing and pyrosequencing after 16S rRNA gene amplification. A total of 4,499 sequencing reads were obtained, which could be attributed to six consensus sequences, but the length of reads leads to fastidious data analysis. Compared to clonal Sanger sequencing and to cultivation results, pyrosequencing recovers greater species richness and gives a more reliable estimate of the relative abundance of bacterial species. The 16S pyrosequencing approach expands our knowledge of the microbial diversity of cystic fibrosis sputum. The current lack of phylogenetic resolution at the species level for the GS 20 sequencing reads will be overcome with the next generation of pyrosequencing apparatus.

摘要

近期在囊性纤维化患者中运用16S rRNA基因扩增后进行克隆桑格测序的研究表明,培养出的微生物仅是感染菌群的一部分。本文旨在比较焦磷酸测序和克隆桑格测序在痰液检测中的效果。对一名囊性纤维化患者的痰液进行培养、桑格克隆测序以及16S rRNA基因扩增后的焦磷酸测序分析。共获得4499条测序读数,可归为6个共有序列,但读数长度导致数据分析繁琐。与克隆桑格测序及培养结果相比,焦磷酸测序能发现更丰富的物种,且对细菌物种相对丰度的估计更可靠。16S焦磷酸测序方法拓展了我们对囊性纤维化痰液微生物多样性的认识。随着下一代焦磷酸测序设备的出现,目前GS 20测序读数在物种水平上缺乏系统发育分辨率的问题将得到解决。

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