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J. Med. Microbiol. -- Vol. 49 (2000), 63-71
© 2000 Society for General Microbiology
ISSN 0022-2615


MOLECULAR IDENTIFICATION AND TYPING

Identification of mutans and other oral streptococci by random amplified polymorphic DNA analysis

T.L. TRUONG, C. MÉNARD*, C. MOUTON and L. TRAHAN

Groupe de Recherche en Écologie Buccale, Faculté de Médecine Dentaire, Université Laval, Québec G1K 7P4 and *Centre de Recherche en Infectiologie de l'Université Laval, CHUQ, Building CHUL, 2705 Blvd Laurier, Ste-Foy G1V 4G2, Canada

Corresponding author: Dr L. Trahan (e-mail: Luc.Trahan{at}greb.ulaval.ca).

Received 4 May 1999 revised version received 15 July 1999; accepted 19 July 1999.

Abstract

The identification and classification of the non-haemolytic or viridans group of streptococci have long been recognised as difficult and unsatisfactory. Phenotypic and genotypic heterogeneity have resulted in ambiguous speciation, particularly with mutans streptococci and other oral streptococci. This study was done to determine whether random amplified polymorphic DNA (RAPD) analysis is useful to identify and even classify oral and other streptococci. DNA was prepared and purified from 25 strains of mutans streptococci including 11 reference strains of Streptococcus mutans, seven of S. sobrinus, three of S. rattus and one each of the four other species of the mutans group, together with 20 other reference species, mostly streptococci, and from 49 fresh isolates of mutans streptococci and of S. mutans from human saliva and dental plaque. DNA amplification was primed with each of three arbitrarily selected primers nine or 10 nucleotides in length. The amplified DNA fragments (amplicons) obtained were compared by agarose gel electrophoresis. Species- and strain-specific RAPD fingerprints were obtained not only from pure genomic DNA, but also from the supernates of crude cellular or colony extracts. Pending the analysis of numerous other strains, the data suggest that RAPD may be of value: (i) to distinguish the species S. mutans and S. sobrinus from each other and potentially from other species of oral streptococci, (ii) to differentiate and possibly classify oral streptococci and (iii) as a valuable tool in mutans streptococci epidemiology and transmission studies, by virtue of its rapidity, efficiency and reproducibility in generating genetic fingerprints of streptococcal isolates.




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