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Serotyping and RAPD profiles of Salmonella enterica isolates from Mauritius
Author(s) -
Khoodoo M.H.R.,
Issack M.I.,
JaufeerallyFakim Y.
Publication year - 2002
Publication title -
letters in applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.698
H-Index - 110
eISSN - 1472-765X
pISSN - 0266-8254
DOI - 10.1046/j.1472-765x.2002.01151.x
Subject(s) - serotype , salmonella enterica , biology , microbiology and biotechnology , salmonella , rapd , enterobacteriaceae , bacteria , virology , escherichia coli , genetics , gene , genetic diversity , medicine , population , environmental health
Aims: The genus Salmonella is a common agent of gastroenteritis in Mauritius, generating more cases of the disease during summer than during winter. The aims of this study were to assess the genetic diversity of isolates of Salmonella enterica by RAPD fingerprinting, and to establish the relationship between human and chicken isolates. Methods: Twenty‐six isolates were obtained from hospital laboratories and commercial poultry producers locally. Results: The RAPD profiles, biochemical and serological analyses showed that two of the chicken isolates were mistakenly identified as Salmonella . The genetic diversity of the remaining 24 isolates (five chicken and 19 human), confirmed as Salmonella , was analysed using four arbitrary primers, OPA‐10, OPR‐03, OPI‐06 and OPJ‐09, chosen from an initial set of 10 decamers. Seventy RAPD markers were generated in four individual DNA profiles. Significance and Impact of the Study: Cluster analysis (UPGMA) performed using the NTSYS‐pc V 1.8 computer software, confirmed that some strains of Salmonella isolated from chicken were genetically similar to those isolated from humans. Furthermore, a 1 kbp band amplified using primer OPA‐10 was specific for the Salmonella genus as it was not amplified in any of the control bacteria.