Post weaning multisystemic wasting syndrome: clinical and histopathological findings in a follow up of sick animals isolated in a lazaret

Citation
P. Gambade et al., Post weaning multisystemic wasting syndrome: clinical and histopathological findings in a follow up of sick animals isolated in a lazaret, REV MED VET, 151(4), 2000, pp. 351-360
Citations number
14
Categorie Soggetti
Veterinary Medicine/Animal Health
Journal title
REVUE DE MEDECINE VETERINAIRE
ISSN journal
00351555 → ACNP
Volume
151
Issue
4
Year of publication
2000
Pages
351 - 360
Database
ISI
SICI code
0035-1555(200004)151:4<351:PWMWSC>2.0.ZU;2-Y
Abstract
Post weaning multisystemic wasting syndrome is a new infectious disease com plex of swine wasting of growing pigs is the major clinical sign associated with a tremendous increase of the mortality rate. PCV2 is at the moment re cognised as the main agent of the disease. In a 200 sows farrow to finish u nit where the disease exists for 2 years, in a batch of 300 piglets 2 six w eeks old not sick yet are euthanasied and are considered as negative contro l. 3 weeks later 9 sick pigs of the same batch are isolated and identified in a confortable lazaret on the farm. At do all the 9 pigs are bled and 2 a re euthanasied for post mortem examinations. Between d0 and d42 Living pigs are bled at d21 and d42 and the 3 living pigs are euthanasied on d42. (Pig s numbers 1, 2 and 7). Post mortem and lab examinations are : gross lesions , histology in situ hybridization (ISH) on sera urea, transaminases activit ies, hemograms, free aminoacid concentrations, creatinine and bilirubin. PR SS and experimental Ploufragan PCV2 serology tests are done on the last blo od sample of the pig. All the signs described in the previous references ar e found on these pigs : wasting, dyspenea, cough, icterus, pale and ulcers. Surviving pigs at d21 (n degrees 1, 2, 7) have completely physically recov er at d42. Considering the gross and histological lesions what ever the day of the death, looking of the piglet are still the same : intersticial pneu monia, lymphoid cuffing and lymphoid depletion, lymphoid node enlargement, icterus, kidney enlargement with nephrititis. Pancreas lesions are frequent . ISH positive tests decreased with the living of sick piglets, and is negati ve on piglets sacrified at d42 in spite of gross and histological lesions. Biochemistry on transaminases, bilirubin urea, seems to be of a limited val ue. Hemograms are more interesting, with an inversion on sick pigs with a d eep lymphopenia. For the surviving pigs with a normal look, we have noticed and increase of beta and gama globulins, and a slight sere conversion on P RSS and PCV2. In conclusion this study shows that sick piglets isolated in a lazaret can recover a physical normal look in 40 % of cases, in spite of specific lesio ns still present on euthanasied pigs. ISH is a useful tool on early diagnos is on the opposite PCV2 Elisa test is late and not complete. Deep lymphopen ia is a bad pronostic, but when the number is above 8000 lymphocits/mm(3) p ronostic is good. Are the pigs at d42 negative on ISH carriers of the virus ? What are the mechanisms which save apparently the pig ? These questions need to be deepened in a further study.