Open AccessDevelopment of an oligonucleotide microarray method for Salmonella serotyping
Author(s) -
TankouoSandjong B.,
Sessitsch A.,
StralisPavese N.,
Liebana E.,
Kornschober C.,
Allerberger F.,
Hächler H.,
Bodrossy L.
Publication year - 2008
Publication title -
microbial biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.287
H-Index - 74
ISSN - 1751-7915
DOI - 10.1111/j.1751-7915.2008.00053.x
Subject(s) - salmonella enterica , serotype , salmonella , microbiology and biotechnology , typing , biology , housekeeping gene , virulence , microarray , virology , bacteria , gene , genetics , gene expression
Summary Adequate identification of Salmonella enterica serovars is a prerequisite for any epidemiological investigation. This is traditionally obtained via a combination of biochemical and serological typing. However, primary strain isolation and traditional serotyping is time‐consuming and faster methods would be desirable. A microarray, based on two housekeeping and two virulence marker genes ( atpD , gyrB , fliC and fljB ), has been developed for the detection and identification of the two species of Salmonella ( S. enterica and S. bongori ), the five subspecies of S. enterica (II, IIIa, IIIb, IV, VI) and 43 S. enterica ssp. enterica serovars (covering the most prevalent ones in Austria and the UK). A comprehensive set of probes ( n = 240), forming 119 probe units, was developed based on the corresponding sequences of 148 Salmonella strains, successfully validated with 57 Salmonella strains and subsequently evaluated with 35 blind samples including isolated serotypes and mixtures of different serotypes. Results demonstrated a strong discriminatory ability of the microarray among Salmonella serovars. Threshold for detection was 1 colony forming unit per 25 g of food sample following overnight (14 h) enrichment.