Bierer B W, Derieux W T
Poult Sci. 1976 Jan;55(1):209-12. doi: 10.3382/ps.0550209.
Five groups of turkeys received C.U. strain Pasteurella multocida vaccine in the drinking water for one day. One group received the 0.1% level of sulfaquinoxaline feed medication at the time of vaccination, while 4 other groups received the feed medication 1, 2, 3 and 4 days after vaccination, respectively. Two weeks after vaccination all groups were exposed to a virulent P-1059 strain of P. multocida by the drinking water route. The results suggest that turkeys on the feed medication at the time of vaccination and possibly those receiving the initial fed medication the next day, failed to experience a satisfactory immunologic response. The possible ill effects of the sulfaquinoxaline feed medication on the duration of the immunity was not determined. A schedule and level of feed medication approved by the Food and Drug Administration was used; namely, 2 days on the 0.1% level, 3 days on a normal ration, and then 2 additional days on the 0.05% level of sulfaquinoxaline feed medication.
五组火鸡通过饮水方式接种禽霍乱(C.U.株)多杀性巴氏杆菌疫苗,为期一天。一组在接种疫苗时接受0.1%水平的磺胺喹恶啉饲料药物治疗,而其他四组分别在接种疫苗后的第1、2、3和4天接受饲料药物治疗。接种疫苗两周后,所有组通过饮水途径接触强毒P-1059株多杀性巴氏杆菌。结果表明,接种疫苗时接受饲料药物治疗的火鸡,以及可能第二天接受初始饲料药物治疗的火鸡,未能产生令人满意的免疫反应。磺胺喹恶啉饲料药物对免疫持续时间可能产生的不良影响尚未确定。使用了食品药品监督管理局批准的饲料药物治疗方案和水平;即0.1%水平用药2天,正常日粮3天,然后再用0.05%水平的磺胺喹恶啉饲料药物治疗2天。