Previous Article | Next Article ![]()
Applied and Environmental Microbiology, September 1999, p. 3908-3914, Vol. 65, No. 9
Valio Ltd. Research and Development
Centre,
Received 10 November 1998/Accepted 27 May 1999
A total of 24 strains, biochemically identified as members of the
Lactobacillus casei group, were identified by PCR with
species-specific primers. The same set of strains was typed by randomly
amplified polymorphic DNA (RAPD) analysis, ribotyping, and pulsed-field gel electrophoresis (PFGE) in order to compare the discriminatory power
of the methods. Species-specific primers for L. rhamnosus and L. casei identified the type strain L. rhamnosus ATCC 7469 and the neotype strain L. casei
ATCC 334, respectively, but did not give any signal with the recently
revived species L. zeae, which contains the type strain
ATCC 15820 and the strain ATCC 393, which was previously classified as
L. casei. Our results are in accordance with the suggested
new classification of the L. casei group. Altogether, 21 of
the 24 strains studied were identified with the species-specific
primers. In strain typing, PFGE was the most discriminatory method,
revealing 17 genotypes for the 24 strains studied. Ribotyping and RAPD
analysis yielded 15 and 12 genotypes, respectively.
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Comparison of Ribotyping, Randomly Amplified Polymorphic DNA
Analysis, and Pulsed-Field Gel Electrophoresis in Typing of
Lactobacillus rhamnosus and L. casei
Strains
*
Corresponding author. Mailing address: Valio Ltd.
Research and Development Centre, P.O. Box 30, FIN-00039 Valio, Finland. Phone: 358 10381 3125. Fax: 358 10381 3129. E-mail:
soile.tynkkynen{at}valio.fi.
Applied and Environmental Microbiology, September 1999, p. 3908-3914, Vol. 65, No. 9
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
This article has been cited by other articles:
| J. Bacteriol. | Microbiol. Mol. Biol. Rev. | Eukaryot. Cell | All ASM Journals |
|---|