首页> 外文会议>Annual Meeting of the American Association of Swine Practitioners >Efficacy of Erysipelothrix rhusiopathiae bacterin administered in two different adjuvants against virulent challenge of pigs 20 weeks after vaccination
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Efficacy of Erysipelothrix rhusiopathiae bacterin administered in two different adjuvants against virulent challenge of pigs 20 weeks after vaccination

机译:在疫苗接种后20周施用两种不同佐剂中患者患有两种不同佐剂的毒素攻击的疗效

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The purpose of this study was to evaluate protection against virulent Erysipelothrix rhusiopathiae challenge in pigs that had been vaccinated 20 weeks earlier with a vaccine containing 1 of 2 adjuvants. Pigs were randomly allotted to 1 of 3 groups: group A (Amphigen~(TM) adjuvant, n=20); group B (adjuvant B, n=10); group C (nonvaccinated controls, n=10). Pigs in groups A and B were vaccinated when approximately 3 and 6 weeks old. Blood samples were obtained for serologic analysis. Twenty weeks after the date of the second vaccination, all pigs were challenged with a virulent culture of E. rhusiopathiae, and then monitored daily for clinical signs of disease. Pigs were considered positive for disease: (1) if they were febrile (rectal temperature > 40.3C or > 40.9C for vaccinated and nonvaccinated pigs, respectively) for 2 consecutive days; (2) if they were febrile for 1 day and had other signs of disease (eg, recumbency, lethargy, metastatic skin lesions); or (3) if they had clinical signs of disease and E. rhusiopathiae was isolated. Vaccination with the Amphigen adjuvanted bacterin induced a substantial serologic response that peaked 2 weeks after the second vaccination. Nine of 10 (90%) control pigs were determined to be positive for infection following challenge. Fifteen of 20 (75%) pigs in group A were protected against challenge, whereas only 1 of 10 (10%) pigs in group B were protected. Results indicated that vaccination of pigs with E. rhusiopathiae bacterin vaccine with Amphigen provided significant (P (0.05) protection from challenge 20 weeks after vaccination.
机译:本研究的目的是评估对20周早些时候接种疫苗的猪的毒性红细胞素挑战的保护,含有2个佐剂的疫苗。将猪随机分配给3组中的1个:A组(Amphigen〜(TM)佐剂,n = 20); B组(佐剂B,N = 10); C组(非疫苗控制,n = 10)。 A和B组中的猪在大约3和6周龄时接种疫苗。获得血液样品进行血清学分析。第二十几周在第二次疫苗接种日期后,所有猪都挑战了一种毒性培养的E. Rhusiopathiae,然后每天监测疾病的临床症状。猪被认为是疾病阳性的:(1)如果连续2天将它们分别是发热(直肠温度> 40.3℃或> 40.9c次接种的疫苗和非疫苗猪; (2)如果它们是发热1天,并且具有其他疾病迹象(例如,斜倚,嗜睡,转移性皮肤病变);或(3)如果他们患有疾病的临床迹象,并且被分离出Rhusiopathiae。用Amphigen辅助细菌疫苗接种诱导大量血清响应,其在第二次疫苗接种后2周达到峰值。在攻击后,确定九个(90%)对照猪被确定为阳性感染。 A组中的20只(75%)猪受到保护免受挑战,而B组只有10名(10%)猪的猪受到保护。结果表明,猪与E. Rhusiopathiae细菌疫苗接种具有Amphigen的母猪提供显着(P(0.05)疫苗后20周保护。

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