Multiplex PCR using 16S rRNA gene-targeted primers for the identification of bifidobacteria from human origin

被引:50
作者
Mullié, C
Odou, MF
Singer, E
Romond, MB
Izard, D
机构
[1] Fac Pharm, F-80037 Amiens 1, France
[2] Fac Sci Pharmaceut & Biol, F-59006 Lille, France
关键词
Bifidobacteriurn; species identification; human; multiplex polymerase chain reaction; 16S rDNA;
D O I
10.1016/S0378-1097(03)00245-3
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Three multiplex polymerase chain reactions (PCRs) targeted on Bifidobacterium and related species were designed to identify human species. The selected primers yielded amplified products of various sizes, each specific for a species. Three to four pairs were gathered in one PCR reaction and their specificity under multiplex conditions was confirmed using DNA from 26 reference strains. Using this technique on unidentified faecal strains, B. bifidum, B. longum and B. breve species were commonly recovered in infants while B. adolescentis, B. catenulatum/B. pseudocatenulatum continuum and B. longum species were predominant in adults. Thus, a single PCR can provide the assignment of a strain to one these species, reducing the number of PCR reactions and hands-on time for the identification of human isolates of bifidobacteria. Moreover, this technique is also applicable for the in situ detection of bifidobacteria in DNA extracts from human stools. (C) 2003 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:129 / 136
页数:8
相关论文
共 19 条
[1]   PHENOTYPIC AND GENOMIC ANALYSES OF HUMAN STRAINS BELONGING OR RELATED TO BIFIDOBACTERIUM-LONGUM, BIFIDOBACTERIUM-INFANTIS, AND BIFIDOBACTERIUM-BREVE [J].
BAHAKA, D ;
NEUT, C ;
KHATTABI, A ;
MONGET, D ;
GAVINI, F .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1993, 43 (03) :565-573
[2]  
BIAVATI B, 1984, MICROBIOLOGICA, V7, P341
[3]   Bifidobacterium inopinatum sp nov and Bifidobacterium denticolens sp nov, two new species isolated from human dental caries [J].
Crociani, F ;
Biavati, B ;
Alessandrini, A ;
Chiarini, C ;
Scardovi, V .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1996, 46 (02) :564-571
[4]   Detection of fructose-6-phosphate phosphoketolase (F6PPK), a key enzyme of the bifid-shunt, in Gardnerella vaginalis [J].
Gavini, F ;
VanEsbroeck, M ;
Touzel, JP ;
Fourment, A ;
Goossens, H .
ANAEROBE, 1996, 2 (03) :191-193
[5]  
Hoyles L, 2002, INT J SYST EVOL MICR, V52, P995, DOI [10.1099/ijs.0.02065-0, 10.1099/00207713-52-3-995]
[6]  
Jian WY, 2002, INT J SYST EVOL MICR, V52, P809, DOI [10.1099/ijs.0.02054-0, 10.1099/00207713-52-3-809]
[7]   Evaluation of using a short region of the recA gene for rapid and sensitive speciation of dominant bifidobacteria in the human large intestine [J].
Kullen, MJ ;
Brady, LJ ;
OSullivan, DJ .
FEMS MICROBIOLOGY LETTERS, 1997, 154 (02) :377-383
[8]  
LAUER E, 1983, SYST APPL MICROBIOL, V4, P42, DOI 10.1016/S0723-2020(83)80033-2
[9]   16S rRNA and 16S to 23S internal transcribed spacer sequence analyses reveal inter- and intraspecific Bifidobacterium phylogeny [J].
LeblondBourget, N ;
Philippe, H ;
Mangin, I ;
Decaris, B .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1996, 46 (01) :102-111
[10]  
Matsuki T, 1998, FEMS MICROBIOL LETT, V167, P113, DOI 10.1111/j.1574-6968.1998.tb13216.x