S. Mcorist et al., ORAL-ADMINISTRATION OF TYLOSIN PHOSPHATE FOR TREATMENT AND PREVENTIONOF PROLIFERATIVE ENTEROPATHY IN PIGS, American journal of veterinary research, 58(2), 1997, pp. 136-139
Objective-To evaluate the efficacy of orally administered tylosin phos
phate for prevention and treatment proliferative enteropathy (PE) in p
igs. Animals-Crossbred pigs weaned at 24 days of age. Procedure-Pigs w
ere challenge exposed with an inoculum of Lawsonia intracellularis str
ain LR189/5/83. Seven control pigs received buffer solution. Of 33 of
challenge-exposed pigs, 8 were untreated. Two groups of challenge-expo
sed pigs were dosed orally with tylosin phosphate via a 2% stabilized
premix, starting with 100 or 40 ppm 4 days before challenge exposure a
nd continuing for 16 days, when the dose was reduced to 40 or 20 ppm,
respectively, which was continued for 12 more days, Another group of c
hallenge-exposed pigs was dosed orally with 100 ppm of tylosin phospha
te commencing 7 days after challenge exposure and continuing for 21 da
ys. Pigs were euthanatized and necropsied 4 weeks after challenge expo
sure. Results-The 8 untreated pigs had reduced weight gain; 3 of them
had moderate diarrhea 8 weeks after challenge exposure, Five pigs had
gross lesions of PE at necropsy. Seven pigs had histologic lesions of
PE with numerous L intracellularis organisms. None of the pigs in the
control, nonchallenge-exposed, or the 3 groups given tylosin phosphate
before or after challenge exposure had clinical signs or lesions of P
E. Conclusion and Clinical Implications-Tylosin phosphate can be effec
tive for prevention and for treatment of PE, using reported dosing sch
edules. We can experimentally induce PE, using the pure culture challe
nge-exposure model, for use in testing of treatments.