JDS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Journal of Dairy Science Vol. 80 No. 7 1254-1259
© 1997 by American Dairy Science Association ®
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kaneko, T.
Right arrow Articles by Kurihara, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kaneko, T.
Right arrow Articles by Kurihara, H.

Digoxigenin-Labeled Deoxyribonucleic Acid Probes for the Enumeration of Bifidobacteria in Fecal Samples

Tsutomu Kaneko 1 and Hiroko Kurihara 1

1 Central Research Institute, Meiji Milk Products Co., 1-21-3 Sakae-cho, Higashimurayama, Tokyo 189, Japan

The numbers of bifidobacteria in fecal samples were specifically determined by colony hybridization with the mixture of digoxigenin-labeled DNA probes that were prepared from whole chromosomal DNA of Bifidobacterium longum 6001 and Bifidobacterium adolescentis 6003. These DNA probes strongly hybridized with DNA of B. longum, B. adolescentis, Bifidobacterium breve, Bifidobacterium suis, Bifidobacterium infantis, Bifidobacterium bifidum, Bifidobacterium angulatum, and Bifidobacterium animalis. Detectable positive signals with DNA of Bifidobacterium pseudolongum ssp. pseudolongum, Bifidobacterium catenulatum, and Bifidobacterium thermophilum were also found after hybridization. When dotblot hybridization was performed with whole cells of 47 reference strains containing 11 species (16 strains) of bifidobacteria, all of the bifidobacteria tested could be specifically detected by using these DNA probes; Lactobacillus fermentum JCM 1173, however, showed a slight nonspecific signal. The counts of bifidobacteria by colony hybridization in the fecal samples of four of the five subjects were the same as the counts that were obtained by the conventional method using BL agar medium. Furthermore, no significant difference existed in the number of bifidobacteria that were determined by either method.

Key Words: bifidobacteria • deoxyribonucleic acid probe • digoxigenin

Submitted on February 7, 1996
Accepted on November 18, 1996




This article has been cited by other articles:


Home page
Appl. Environ. Microbiol.Home page
X. Bonjoch, E. Balleste, and A. R. Blanch
Multiplex PCR with 16S rRNA Gene-Targeted Primers of Bifidobacterium spp. To Identify Sources of Fecal Pollution
Appl. Envir. Microbiol., May 1, 2004; 70(5): 3171 - 3175.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
Y. Nebra, X. Bonjoch, and A. R. Blanch
Use of Bifidobacterium dentium as an Indicator of the Origin of Fecal Water Pollution
Appl. Envir. Microbiol., May 1, 2003; 69(5): 2651 - 2656.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
A. Schwiertz, G. Le Blay, and M. Blaut
Quantification of Different Eubacterium spp. in Human Fecal Samples with Species-Specific 16S rRNA-Targeted Oligonucleotide Probes
Appl. Envir. Microbiol., January 1, 2000; 66(1): 375 - 382.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1997 by the American Dairy Science Association ®.