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首页> 外文期刊>New Zealand Veterinary Journal >Development of an enzyme-linked immunosorbent assay for the serological detection of exposure of poultry in New Zealand to Erysipelothrix rhusiopathiae and their serological response to vaccination.
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Development of an enzyme-linked immunosorbent assay for the serological detection of exposure of poultry in New Zealand to Erysipelothrix rhusiopathiae and their serological response to vaccination.

机译:酶联免疫吸附测定技术的开发,用于血清学检测新西兰家禽暴露于 Erysipelothrix rhusiopathiae 及其对疫苗的血清学应答。

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AIMS: To modify and validate an existing swine erysipelas ELISA for use with poultry serum and to assess the safety of a swine erysipelas vaccine for use in New Zealand layer birds. METHODS: An existing swine erysipelas ELISA was modified for use in domestic poultry and was validated using sera from birds injected with either 2 mL of a commercially available killed swine erysipelas vaccine (low-dose; n=12 birds), 4 mL of vaccine (high-dose; n=11 birds), or 2 mL saline (control; n=11 birds) on Day 0 and again on Day 21. Blood samples were collected on Days 0, 21, 42, and 63, and safety of the vaccine for use in layer birds was determined by assessing cloacal temperature and injection site reactions in birds at 0, 4, 24, 48, 72 and 96 h post-vaccination. RESULTS: The ELISA that was developed had a diagnostic sensitivity and specificity of 93% and 98%, respectively, after being optimised for a positive cut-off at an optical density (OD) >=1.50 read at 450-nm wavelength. OD readings were higher on Days 21, 42, and 63 than Day 0 in both the low-dose and high-dose groups (p<0.05), and differed amongst the three groups on Days 21, 42, and 63 (p<0.05), suggesting that vaccination using either dose induced detectable levels of antibody, even after a single dose. In addition, the high-dose protocol induced higher levels of antibody production than the low-dose protocol. No local or systemic reactions to the vaccine were observed and cloacal temperatures remained in the normal biological range after vaccination. CONCLUSIONS: The ELISA that was developed had satisfactory diagnostic performance characteristics and the vaccine appeared to be safe for use in layer birds. However, the study design did not permit an assessment of the vaccine's efficacy to protect birds from clinical erysipelas. CLINICAL RELEVANCE: A diagnostic ELISA has been developed for determining the exposure of layer birds to E. rhusiopathiae. The test will be useful for monitoring flock-level erysipelas, response to vaccination, and in epidemiological studies designed to identify risk factors for exposure to the disease.Digital Object Identifier http://dx.doi.org/10.1080/00480169.2011.639057
机译:目的:修改和验证现有的与家禽血清一起使用的猪丹毒ELISA,并评估在新西兰产禽中使用的猪丹毒疫苗的安全性。方法:对现有的猪丹毒ELISA进行了修改以用于家禽,并使用注射了2毫升市售灭活猪丹毒疫苗(低剂量; n = 12禽),4毫升疫苗(高剂量; n = 11只禽)或2 mL生理盐水(对照组; n = 11只禽)在第0天,然后在第21天再次采集。在第0、21、42和63天收集血液样本,以确保安全。通过评估疫苗接种后0、4、24、48、72和96 h家禽的泄殖腔温度和注射部位反应,确定用于禽类的疫苗。结果:开发的ELISA经过优化,可在450 nm波长读取的光密度(OD)> = 1.50时用于阳性截止值,诊断灵敏度和特异性分别为93%和98%。在低剂量和高剂量组中,第21、42和63天的OD读数均高于第0天(p <0.05),并且在第21、42和63天的三组之间差异(p <0.05) ),这表明即使使用单剂疫苗,使用任何一种剂量的疫苗接种也会诱导可检测水平的抗体。另外,高剂量方案比低剂量方案诱导更高水平的抗体产生。疫苗接种后未观察到疫苗的局部或全身反应,泄殖腔温度保持在正常生物学范围内。结论:所开发的ELISA具有令人满意的诊断性能特征,该疫苗似乎可安全用于禽类。但是,该研究设计不允许评估该疫苗保护鸟类免受临床丹毒的功效。临床相关性:已经开发了一种诊断性ELISA,用于确定禽类对E的暴露。风湿病。该测试将有助于监测鸡群级别的丹毒,对疫苗的反应以及旨在确定暴露于该疾病的危险因素的流行病学研究。数字对象标识符http://dx.doi.org/10.1080/00480169.2011.639057

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