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粪便样本在储存期间肠道细菌微生物群的体外变化。

In vitro alterations of intestinal bacterial microbiota in fecal samples during storage.

作者信息

Ott Stephan J, Musfeldt Meike, Timmis Kenneth N, Hampe Jochen, Wenderoth Dirk F, Schreiber Stefan

机构信息

Department of General Internal Medicine, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.

出版信息

Diagn Microbiol Infect Dis. 2004 Dec;50(4):237-45. doi: 10.1016/j.diagmicrobio.2004.08.012.

Abstract

The human gastrointestinal tract harbors an extremely diverse and complex microbial ecosystem. Most of the existent data about the enteric microflora have been generated using stool samples, but the collection and storage of fecal samples are often problematic. The influence of the storage of stool samples on the bacterial diversity and the degradation of bacterial DNA was analysed in this study. Stool samples from 5 healthy volunteers were exposed to different storage temperatures and durations. The bacterial diversity and the amount of intact bacterial DNA were analysed by single-stranded conformation polymorphism analysis (SSCP) and real-time polymerase chain reaction (PCR), both using a 16S rDNA approach. Additionally, biopsy specimens were taken from 3 of the 5 individuals to compare fecal and mucosal flora. The bacterial diversity of the fecal flora and the total number of bacteria were significantly reduced after 8 and 24 hours at both room temperature and 4 degrees C. The mucosa-associated bacterial microflora showed substantial differences compared with the fecal flora. The observed alterations of fecal flora during storage point to the difficulty of the molecular analysis of the bacterial diversity and the enumeration of bacterial cells in fecal samples.

摘要

人类胃肠道拥有极其多样和复杂的微生物生态系统。目前关于肠道微生物群的大多数现有数据都是通过粪便样本获得的,但粪便样本的采集和储存往往存在问题。本研究分析了粪便样本储存对细菌多样性和细菌DNA降解的影响。采集了5名健康志愿者的粪便样本,使其暴露于不同的储存温度和时长下。采用单链构象多态性分析(SSCP)和实时聚合酶链反应(PCR),均使用16S rDNA方法,分析细菌多样性和完整细菌DNA的量。此外,从5名个体中的3人身上采集了活检标本,以比较粪便菌群和黏膜菌群。在室温及4℃条件下,8小时和24小时后,粪便菌群的细菌多样性和细菌总数均显著降低。与粪便菌群相比,黏膜相关细菌微生物群存在显著差异。粪便菌群在储存过程中观察到的变化表明,粪便样本中细菌多样性的分子分析和细菌细胞计数存在困难。

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