Lactobacillus plantarum is a species of considerable industrial and medical interest. To date, the
lack of reliable molecular methods for definite identification at strain level has hindered studies of the
population biology of this organism. Here, a multilocus sequence typing (MLST) system for this
organism is described, which exploits the genetic variation present in six housekeeping loci to
determine the genetic relationship among isolates. The MLST system was established using 16
L. plantarum strains that were also characterized by ribotyping and restriction fragment length
polymorphism (RFLP) analysis of the PCR-amplified 16S–23S rDNA intergenic spacer region
(ISR). Ribotyping grouped the strains into four groups; however, RFLP analysis of the ISRs showed
no differences in the strains analysed. In contrast, MLST had a good discriminatory ability. The
sequence analysis of the six genes showed 14 different allelic combinations, with 12 of them
represented by only one strain. By using this MLST approach we were able to confirm the identity of
two strains deposited in the Spanish Type Culture Collection as different strains. Phylogenetic
analysis indicated a panmictic population structure of L. plantarum and split decomposition analysis
indicated that recombination plays a role in creating genetic heterogeneity in L. plantarum. As
MLST allows precise identification, and easy comparison and exchange of results obtained in
different laboratories, the future application of this new molecular method could be useful for the
identification of valuable L. plantarum strainsThis work has been supported by grants AGL2005-00470 and RM03-
002. We thank R. Gonza´lez and E. Garcı´a for their critical reading of
the manuscript. The technical assistance of M. V. Santamarı´a is greatly
appreciated. We also thank A. Hexter for correcting the English
version. B. de las Rivas is a recipient of a postdoctoral fellowship
and A. Marcobal of a predoctoral fellowship both from the Comunidad
de Madrid.Peer reviewe