Molecular epidemiology of Campylobacter jejuni in broiler flocks using randomly amplified polymorphic DNA-PCR and 23S rRNA-PCR and role of litter in its transmission
Re. Payne et al., Molecular epidemiology of Campylobacter jejuni in broiler flocks using randomly amplified polymorphic DNA-PCR and 23S rRNA-PCR and role of litter in its transmission, APPL ENVIR, 65(1), 1999, pp. 260-263
Poultry has long been cited as a reservoir for Campylobacter spp,, and litt
er has been implicated as a vehicle in their transmission. Chicks were rais
ed on litter removed front a broiler house positive for Campylobacter jejun
i, Litter was removed from the house on days 0, 3, and 9 after birds were r
emoved for slaughter. Chicks were raised on these three litters under contr
olled conditions in flocks of 25, None of these birds yielded C, jejuni in
their cecal droppings through 7 weeks. Two successive flocks from the same
Campylobacter-positive broiler house were monitored for Campylobacter colon
ization. Campylobacter jejuni prevalence rates were determined for each flo
ck. Randomly amplified polymorphic DNA (RAPD)-PCR and 23S rRNA-PCR typing m
ethods were used to group isolates. A high prevalence (60%) of C. jejuni in
flock 1 coincided with the presence of an RAPD profile not appearing in fl
ock 2, which had a lower rate of prevalence (28%). A 23S rRNA-PCR typing me
thod was used to determine if strains with different RAPD profiles and diff
erent prevalence rates contained different 23S sequences. RAPD profiles det
ected with higher prevalence rates contained a spacer in the 23S rRNA regio
n 100% of the time, while RAPD profiles found with lower prevalence rates c
ontained an intervening sequence less than 2% of the time. Data suggest var
ying colonizing potentials of different RAPD profiles and a source other th
an previously used litter as a means of transmission of C,jejuni, These mol
ecular typing methods demonstrate their usefulness, when used together, in
this epidemiologic investigation.