Pw. Burkhalter et al., DETECTION OF SALMONELLA SPP IN EGGS - DNA ANALYSES, CULTURE TECHNIQUES, AND SEROLOGY, Journal of AOAC International, 78(6), 1995, pp. 1531-1537
A polymerase chain reaction (PCR) method for direct detection of Salmo
nella spp, in whole-shell eggs is described, The method does not requi
re isolating strains, Preenrichment, rapid DNA isolation, and a nested
PCR system targeting the invA gene enabled detection of the genus Sal
monella, The specific nested PCR product of 283 base pairs was formed
from all 21 serovars, including 43 Salmonella strains tested. No PCR p
roduct was formed from 56 non-Salmonella enterobacteriacea and other b
acterial strains tested, Experiments with artificially contaminated eg
gs showed a detection limit of about 10(3)-10(4) colony-forming units
(cfu)/egg before and about 1-10 cfu/egg after preenrichment, In analys
is of 180 single eggs from 4 flocks and 36 pools of 5 eggs each from a
nother 4 flocks from the same producer, Salmonella spp, were detected
in 5 of 90 eggs from 2 different flocks. Determination of anti-Salmone
lla antibodies in eggs yielded positive results for 2 additional and t
he 2 PCR-positive flocks, In contrast, classical selective culture det
ected Salmonella spp. in only 1 of 100 eggs in one flock when Inn eggs
from each flock were analyzed.