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首页> 外文期刊>Canadian Journal of Veterinary Research >Serodiagnosis of pleuropneumonia using enzyme-linked immunosorbent assay with capsular polysaccharide antigens of Actinobacillus pleuropneumoniae serotypes 1, 2, 5 and 7.
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Serodiagnosis of pleuropneumonia using enzyme-linked immunosorbent assay with capsular polysaccharide antigens of Actinobacillus pleuropneumoniae serotypes 1, 2, 5 and 7.

机译:使用酶联免疫吸附法对胸膜肺炎放线杆菌血清型1、2、5和7的荚膜多糖抗原进行血清学诊断。

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摘要

Capsular polysaccharide antigens of serotypes 1, 2, 5 and 7 of Actinobacillus pleuropneumoniae were used in enzyme-linked immunosorbent assays (ELISAs) to test sera from experimentally infected and field pigs. Specific reactions were found in sera of experimental pigs with antigens of serotypes 1, 5 and 7 whereas the serotype 2 antigen was cross-reactive. A 1:200 serum dilution was used for testing of 300 sera from 21 swine herds in southern Ontario. Cases of pleuropneumonia had occurred in 11 of these herds, but not in the others. The negative cut-off value was the mean optical density at 405 nm (OD405) + three standard deviations (SD) for 16 negative reference sera. Sera from four pigs naturally infected with Actinobacillus suis were tested and found to react to varying degrees with each of the antigens. Therefore a second cut-off value was determined as the mean OD405 + 2 SD for the A. suis sera. Sera which, in the ELISA produced OD readings above the latter cut-off were considered positive for antibodies to A. pleuropneumoniae; those which were lower than the former cut-off were considered negative. Readings between the two cut-off values may have been due to low positive titers or cross-reactivity, possibly with A. suis, and could not be used to predict pleuropneumonia. Of the pleuropneumonia-free herds, none had positive reactors to serotypes 5 or 7, whereas one and two herds had positive reactors to serotypes 1 and 2, respectively. Of the pleuropneumonia positive herds, six had positive reactors to serotype 1, one to serotype 2, four to serotype 5, and eight to serotype 7.
机译:胸膜肺炎放线杆菌血清型1、2、5和7的荚膜多糖抗原被用于酶联免疫吸附试验(ELISA)中,以检测实验感染和田间猪的血清。在实验猪的血清中发现了特异性反应,这些血清具有血清型1、5和7,而血清型2抗原具有交叉反应性。 1:200的血清稀释液用于检测安大略省南部21个猪群的300份血清。其中有11例发生了胸膜肺炎的病例,而其他病例则没有。负截止值是16个阴性参照血清在405 nm处的平均光密度(OD405)+三个标准差(SD)。测试了四只自然感染了猪放线杆菌的猪的血清,发现它们与每种抗原有不同程度的反应。因此,第二个截断值被确定为猪链球菌血清的平均OD405 + 2 SD。在ELISA中产生的OD读数高于后者的血清被认为对胸膜肺炎链球菌抗体呈阳性。低于前一个临界值的那些被认为是负面的。两个临界值之间的读数可能是由于阳性滴度低或交叉反应性(可能与猪链球菌有关),不能用于预测胸膜肺炎。在无胸膜肺炎的牛群中,没有一个对5或7血清型呈阳性反应器,而一个和两个牛群对1和2血清型呈阳性反应器。在胸膜肺炎阳性猪群中,有六个对血清型1有阳性反应器,一个对血清型2有反应器,四个对血清型5有反应器,而对7型血清有8个阳性反应器。

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