Development and validation of an automated, microscopy-based method for enumeration of groups of intestinal bacteria

被引:119
作者
Jansen, GJ [1 ]
Wildeboer-Veloo, ACM [1 ]
Tonk, RHJ [1 ]
Franks, AH [1 ]
Welling, G [1 ]
机构
[1] Univ Groningen, Dept Med Microbiol, NL-9713 GZ Groningen, Netherlands
关键词
gut microflora; image analysis; microscopic counting; Quantimet; 600; whole-cell hybridisation;
D O I
10.1016/S0167-7012(99)00049-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An automated microscopy-based method using fluorescently labelled 16S rRNA-targeted oligonucleotide probes directed against the predominant groups of intestinal bacteria was developed and validated. The method makes use of the Leica 600HR. image analysis system, a Kodak MegaPlus camera model 1.4 and a servo-controlled Leica DM/RXA ultra-violet microscope. Software for automated image acquisition and analysis was developed and tested. The performance of the method was validated using a set of four fluorescent oligonucleotide probes: a universal probe for the detection of all bacterial species, one probe specific for Bifidobacterium spp., a digenus-probe specific for Bacteroides spp. and Prevotella spp. and a trigenus-probe specific for Ruminococcus spp.. Clostridium spp. and Eubacterium spp. A nucleic acid stain, 4',6-diamidino-2-phenylindole (DAPI), was also included in the validation, In order to quantify the assay-error, one faecal sample was measured 20 times using each separate probe. Thereafter faecal samples of 20 different volunteers were measured following the same procedure in order to quantify the error due to individual-related differences in gut flora composition. It was concluded that the combination of automated microscopy and fluorescent whole-cell hybridisation enables distinction in gut flora-composition between volunteers at a significant level. With this method it is possible to process 48 faecal samples overnight, with coefficients of variation ranging from 0.07 to 0.30. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:215 / 221
页数:7
相关论文
共 14 条
[1]  
Eckmann Lars, 1995, Trends in Microbiology, V3, P118, DOI 10.1016/S0966-842X(00)88894-0
[2]  
Franks AH, 1998, APPL ENVIRON MICROB, V64, P3336
[3]  
GOLDIN B, 1977, CANCER, V40, P2421, DOI 10.1002/1097-0142(197711)40:5+<2421::AID-CNCR2820400905>3.0.CO
[4]  
2-I
[5]  
GORBACH SL, 1987, LANCET, V2, P1519
[6]   QUANTITATIVE FLUORESCENCE IN-SITU HYBRIDIZATION OF BIFIDOBACTERIUM SPP WITH GENUS-SPECIFIC 16S RIBOSOMAL-RNA-TARGETED PROBES AND ITS APPLICATION IN FECAL SAMPLES [J].
LANGENDIJK, PS ;
SCHUT, F ;
JANSEN, GJ ;
RAANGS, GC ;
KAMPHUIS, GR ;
WILKINSON, MHF ;
WELLING, GW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1995, 61 (08) :3069-3075
[7]  
*LEIC IM SYST LTD, 1997, LEIC QWIN US MAN, V2
[8]  
*LEIC IM SYST LTD, 1997, LEIC QWIN US MAN, V1
[9]  
*LEIC MICR SYST, 1996, LEIC DMR DAS MICR, P56
[10]   IN-SITU IDENTIFICATION OF BACTERIA IN DRINKING-WATER AND ADJOINING BIOFILMS BY HYBRIDIZATION WITH 16S-RIBOSOMAL-RNA-DIRECTED AND 23S-RIBOSOMAL-RNA-DIRECTED FLUORESCENT OLIGONUCLEOTIDE PROBES [J].
MANZ, W ;
SZEWZYK, U ;
ERICSSON, P ;
AMANN, R ;
SCHLEIFER, KH ;
STENSTROM, TA .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (07) :2293-2298