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NTIS 바로가기Comparative immunology, microbiology and infectious diseases, v.23 no.4, 2000년, pp.239 - 252
Rodrı́guez, S.D (Centro Nacional de Investigaciones Disciplinarias en Parasitologı́) , Garcı́a Ortiz, M.A (a Veterinaria, INIFAP, SAGAR, Mexico) , Hernández Salgado, G (Centro Nacional de Investigaciones Disciplinarias en Parasitologı́) , Santos Cerda, N.A (a Veterinaria, INIFAP, SAGAR, Mexico) , Aboytes Torres, R (Centro Nacional de Investigaciones Disciplinarias en Parasitologı́) , Cantó (a Veterinaria, INIFAP, SAGAR, Mexico) , Alarcón, G.J (Facultad de Ciencias Naturales, Universidad Autó)
AbstractThe present study was performed to dose-titrate an Anaplasma marginale experimental immunogen derived from partially purified initial bodies from three geographically different Mexican strains. Three five-bovine groups were inoculated twice on days zero and 21 with A. marginale initial bodie...
RésuméLe but de l’étude était de définir la meilleure dose d’un immunogen expérimental contre l’Anaplasmose bovine. L’immunogen était dérivé des corps initiaux de trois isolats mexicains géographiquement différents. Trois groupes de cinq bovins ont été inoculés deux fois, les jours zéro et vingt et un, avec des corps initiaux équivalents à 1.5×1010 (groupe I), 3×1010 (groupe II) et 6×1010 (groupe III) érythrocytes infectés et mélangés avec l’adjuvant STDCM®. Un groupe semblable de cinq bovins a servi de témoin non vaccinés. Le jour quatre-vingt-sept, les quatre groupes ont été éprouvés avec une dose de 1×108 érythrocytes infectés à l’aide de la souche MEX-15-099-01 d’A. marginale. La période avant l’épreuve était très semblable pour chacun des quatre groupes. Les cinq bovins témoins ont présentés un syndrôme aigu typique d’Anaplasmose atteignant une rickettsemie moyen de 30.9% et une perte de 73.4% de volume cellulaire agglomér, deux d’entre eux sont morts. Parmi les bovins des groupes vaccinés, seul un d’entre eux (groupe II) a présenté un tableau clinique aigu et il est mort. Par ailleurs, aucun des autres animaux vaccinés a présenté de signe clinique, ils ont présenté des rickettsémies très basses (3.2, 3.8, et 4.3%) et des pertes de PCV de 49.9, 47.8 et 49.3% respectivement. Les poids de départ étaient très semblables parmi les quatre groupes avant l’épreuve, après celle-ci, tous les animaux ont perdu poids, cependant les pertes pour les groupes I et II ont été moindre en comparaison avec celles du groupe IV (P<0.01). Bien qu’il n’y ait eu aucune différence significative parmi les groupes vaccinés, le groupe III était légèrement plus affecté. Globalement, ces résultats montrent une protection totale de 93.3% par groupe, 100% pour les groupes I et III et de 80% pour le groupe II.
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