By J B McFerran; M S McNulty; Commission of the European Communities. Coordination of Agricultural Research
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Additional info for Acute virus infections of poultry : a seminar in the CEC Agricultural Research Programme, held in Brussels, June 13-14, 1985
5 ~l of two inactivated influenza vaccines prepared using the virulent A/tern/S. Africa/6l (H5N2) strain were injected subcutaneously into five week old SPF chicks. HI antibody appeared faster but also waned faster after vaccination with vaccine A, in aqueous solution, than with the oil emulsion based vaccine B. This was associated with a slightly better protection against challenge with the virulent live virus by vaccine A 3 weeks after vaccination. Challenge was not followed by a significant increase of HI tines or appearance of precipitating antibody.
Andamento dell'influenza aviaria negli allevamenti di tacchini del Veneto. Riv. , 53, 5, 33-35. A. 0~1985. Simposio della Soc. It. di Patol. Aviare sull'Influenza aviare, Milano, Italia, 6/6/1985. , Cabasso, E. and Allodi, C. 1977. Alcuni aspetti e problemi legati alIa presenza di E. coli in sindromi respiratorie dei tacchini. La Clinica Vet. 100, 448-459. J. and Petek, M. 1981 Influenza A virus infections in commercial turkeys in North East Italy. , 10, 303-311. ,~inaldi, A. and Nardelli, L. 1967.
Most showed diffuse cytoplasmic staining with small inclusions (Fig. 1), occasional cells also had nuclear fluorescence. Fig. 1 Immunofluorescent staining of influenza virus antigens in tracheal impression smear. The choice of specimens to be examined by immunofluorescence is largely dictated by the presenting clinical signs and gross pathological findings. If birds are showing respiratory signs, conjunctiva, trachea and lung should obviously be examined. Any visceral organs showing gross changes should also be examined.