The campylobacter infection of 10 sows and their piglets was monitored. These pigs werekept on two multiplier farms. Rectal faeces samples were taken from the sows shortly beforelittering and at different intervals after littering. Swab samples of rectal content were taken fromsix piglets per sow at different intervals after birth. Nine sows were shown to be infected withcampylobacter before litter and all sows after litter, with an average colony count of 4·1in log N g–1 of faeces. Half of the piglets became infected withcampylobacter during the first week of life and 85%, after four weeks. Two genetic subtypingmethods (ERIC‐PCR and RFLP) were used to study the relationships between campylobacterisolates from sows and piglets. A large diversity of campylobacter subtypes was found.Nevertheless, piglets and their mothers often harboured campylobacter isolates with identicalgenetic subtyping profiles, suggesting that piglets become infected via their mothers. However,observed similarities in genetic subtyping profiles between campylobacters isolated on differentfarms made this difficult to prove.

The effects of proline and caffeic acid on the survival of Shiga toxin-producing Escherichia coli (STEC) O157:H7 strain ATCC 43895 in a model apple juice medium were studied. It is hypothesized that the inhibitory effect of caffeic acid may explain why almost all outbreaks of STEC O157:H7 infections linked to apple juice or cider have occurred in October or November.

Numerous epidemiological reports implicate foods of animal origin as vehicles of human campylobacteriosis. Pigs are probably an important reservoir of campylobacter and a potential source of human infection. In order to improve our knowledge of the epidemiology of campylobacter in pigs, the prevalence of campylobacter and its contamination of feed were monitored in eight pig farms. Faeces samples of pigs aged 11 and 22 weeks, and samples of rectal, ileal and gastric content at a slaughterhouse were collected for bacteriological examination. On 5 farms, subsequent groups of pigs housed in the same stalls was sampled, too. A selection of the campylobacter isolates was characterized with a genetic typing method (RFLP). More than 85% of the sampled porkers were shown to be intestinal carriers of campylobacter at all stages of fattening. Subsequent groups of pigs housed in the same stalls were all carriers, too. The level of campylobacters in the faeces tended to decrease as the pigs got older. There was no difference in the frequency and level of infection with campylobacter between porkers on different farms. The feeding system (wet feed versus dry pellets) did not seem to influence the prevalence of campylobacter although wet feed gave lower counts of Enterobacteriaceae in the faeces. RFLP-typing showed a high diversity of campylobacter strains at each sampling on the farm. Similarities were seen between strains isolated during two subsequent samplings of the same group of pigs, but not between strains isolated on the same farm from subsequent groups of pigs housed in the same stall. This suggests that the piglets were already infected at a young age on the breeding farm.

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