Validation of fluorescent in situ hybridization combined with flow cytometry for assessing interindividual variation in the composition of human fecal microflora during long-term storage of samples

被引:34
作者
Rochet, V [1 ]
Rigottier-Gois, L [1 ]
Rabot, S [1 ]
Doré, J [1 ]
机构
[1] INRA, Unite Ecol & Physiol Syst Digest, F-78352 Jouy En Josas, France
关键词
fecal microflora; long-term storage; fluorescent in situ hybridization; flow cytometry;
D O I
10.1016/j.mimet.2004.07.012
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This work was conducted to assess the accuracy of in situ hybridization to slow difference, in human microflora composition between volunteers and to optimize the storage of fecal samples to allow delayed analysis of gut microflora composition in humans. Fecal samples from 25 healthy subjects (14 women, 11 men aged 24-51) were collected. The samples were fixed in 4% Paraformaldehyde (PFA) solution at 4 degreesC overnight and stored at -70 degreesC. Twenty samples were analysed to quantify the variation due to interindividual differences in the composition of fecal microflora. The five remaining samples were stored either after PFA fixation or directly frozen at -70 degreesC and were monitored on a 12-month period. The fecal microflora was analysed by in situ hybridization combined with flow cytometry detection. Ribosomal RNA-targeted probes were used to assess the relative proportions of four phylogenetic, groups: Clostridium coccoides-Eubacterium rectale (Erec 482), Bacteroides (Bac 303), Faecalibacterium prausnitzii (Fprau 645) and Bifidobacterium (Bif 164). Our results demonstrated that the method used is adapted to detect significant differences in fecal microflora composition in humans. Moreover, samples stored in PFA solution demonstrated a stable composition even after 8 months of storage. Conversely, frozen samples were less stable as the Bifidobacterium and C. coccoides-E. rectale groups showed significant differences after 2 months of storage. In conclusion, the fecal microflora composition can be analysed up to 8 months after 4% PFA fixation and storage at -70 degreesC. It represents an extended time compared with the 2-month period currently recommended. This will give more flexibility for applying this technology in epidemiological studies including a large number of samples. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:263 / 270
页数:8
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