A rapid polymerase chain reaction (PCR) assay was developed for detecting S
almonella in faeces of horses and assessed on samples from horses admitted
to a veterinary hospital. Direct detection was achieved by amplification of
part of ompC after extraction of DNA from faeces using a spin column metho
d to reduce the amount of inhibitory substances in samples. An internal pos
itive control was included to detect false negative results. While the sens
itivity of the PCR assay was less than culture when assessed on faeces inoc
ulated with Salmonella, its sensitivity on faecal samples obtained from hor
ses was much greater than culture. Salmonella DNA was detected in 40% of fa
ecal samples using the PCR assay while Salmonella were cultured from only 2
% of the samples. The PCR assay has potential for use in either routine dia
gnosis or for detection of the carrier status in animals. (C) 2001 Elsevier
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