The effect of an oral treatment or prevention programme, incorporating
the antibiotic tiamulin, on the development of proliferative enteropa
thy in experimentally challenged pigs was studied, Twenty weaner pigs
were challenged orally with virulent inoculum of Lawsonia intracellula
ris strain LR189/5/83, a British isolate of the causative agent of por
cine proliferative enteropathy, and seven control pigs were dosed with
a buffer solution, Seven of the 20 challenged pigs were left untreate
d; they gained less weight than the controls and three of them develop
ed mild to moderate diarrhoea two weeks after the challenge, All seven
developed lesions, six visible grossly, of proliferative enteropathy,
and numerous intracellular L intracellularis were detected in section
s of the intestines examined three weeks after the challenge, To test
a 'prevention' dosing strategy for tiamulin, six of the challenged pig
s were dosed orally with 50 ppm tiamulin, incorporated in a 2 per cent
stabilised premix, given from two days before the challenge until the
y were euthanased. To test a 'treatment' strategy, the remaining group
of seven challenged pigs were dosed orally with 150 ppm tiamulin give
n in the premix from seven days after challenge until they were euthan
ased, All the control pigs and the 13 pigs treated with tiamulin, eith
er before or after challenge, remained clinically normal and had no sp
ecific lesions of proliferative enteropathy in sections of the intesti
nes examined post mortem.