Potential of three-way randomly amplified polymorphic DNA analysis as a typing method for twelve Salmonella serotypes

Citation
Sm. Soto et al., Potential of three-way randomly amplified polymorphic DNA analysis as a typing method for twelve Salmonella serotypes, APPL ENVIR, 65(11), 1999, pp. 4830-4836
Citations number
22
Categorie Soggetti
Biology,Microbiology
Journal title
APPLIED AND ENVIRONMENTAL MICROBIOLOGY
ISSN journal
00992240 → ACNP
Volume
65
Issue
11
Year of publication
1999
Pages
4830 - 4836
Database
ISI
SICI code
0099-2240(199911)65:11<4830:POTRAP>2.0.ZU;2-Z
Abstract
The potential of a three-way randomly amplified polymorphic DNA (RAPD) proc edure (RAPD typing) for typing Salmonella enterica strains assigned to 12 s erotypes was analyzed. The series of organisms used included 235 strains (3 26 isolates) collected mainly from clinical samples in the Principality of Asturias and 9 reference strains. RAPD typing was performed directly with b roth cultures of bacteria by using three selected primers and optimized PCR conditions. The profiles obtained with the three primers were used to defi ne RAPD types and to evaluate the procedure as a typing method at the speci es and serotype levels. The typeability was 100%; the reproducibility and i n vitro stability could be considered good. The concordance of RAPD typing methods with serotyping methods was 100%, but some profiles obtained with t wo of the three primers were obtained with strains assigned to different se rotypes, The discrimination index (DI) within the series of organisms was 0 .94, and the DI within serotypes Typhimurium, Enteritidis, and Virchow were 0.72, 0.52, and 0.66, respectively. Within these serotypes the most common RAPD types were differentiated into phage types and vice versa; combining the types identified by the two procedures (RAPD typing and phage typing) r esulted in further discrimination (DI, 0.96, 0.74, and 0.87, respectively). The efficiency, rapidity, and flexibility of the RAPD typing method suppor t the conclusion that it can be used as a tool for identifying Salmonella o rganisms and as a typing method that is complementary to serotyping and pha ge typing methods.