首页> 外文期刊>Journal of immunoassay and immunochemistry >Rough lipopolysaccharide of Brucella abortus RB51 as a common antigen for serological detection of B. ovis, B. canis, and B. abortus RB51 exposure using indirect enzyme immunoassay and fluorescence polarization assay.
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Rough lipopolysaccharide of Brucella abortus RB51 as a common antigen for serological detection of B. ovis, B. canis, and B. abortus RB51 exposure using indirect enzyme immunoassay and fluorescence polarization assay.

机译:流产布鲁氏菌RB51的粗脂多糖是一种常见抗原,可通过间接酶免疫测定和荧光偏振测定法进行血清学检测。

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摘要

Rough lipopolysaccharide (RLPS) antigens were prepared from cultures of Brucella abortus RB51, B. ovis, and B. canis. The preparations were standardized by weight and tested with sera from cattle immunized with B. abortus RB51, sheep infected with B. ovis, and dogs infected with B. canis. Populations of unexposed animals of each species were also tested. The tests used were the indirect enzyme immunoassay (IELISA) using RLPS and the fluorescence polarization assay (FPA) using RLPS core fractions, labeled with fluorescein isothiocyanate. The IELISA using B. abortus RB51 RLPS antigen resulted in sensitivity and specificity values of 94.8% and 97.3%, respectively, when testing bovine sera, 98.5% and 97.8% when testing ovine sera, and 95.8% and 100% when testing dog sera. The IELISA using B. ovis RLPS antigen gave sensitivity and specificity values of 80.5% and 91.7%, respectively with bovine sera, 98.9% and 93.8% with sheep sera, and 70.8% and 79.8% with dog sera. The IELISA using B. canis RLPS antigen resulted in sensitivity and specificity values of 97.0% and 97.4%, respectively, with bovine sera, 96.2% and 96.3% with sheep sera, and 95.8% and 98.8% with dog sera. Labeling RLPS core from B. ovis and B. canis with fluorescein was not successful. B. abortus RB51 core labeled with fluorescein resulted in sensitivity and specificity values of 93.5% and 99.8%, respectively, with bovine sera and 78.1% and 99.0% with sheep sera. It was not possible to test the dog sera in the FPA.
机译:粗脂多糖(RLPS)抗原是从流产布鲁氏菌RB51,牛肝杆菌和犬双歧杆菌的培养物中制备的。将制剂按重量标准化,并用经流产双歧杆菌RB51免疫的牛,受牛双歧杆菌感染的绵羊和被犬双歧杆菌感染的狗的血清进行测试。还测试了每个物种未暴露动物的种群。使用的测试是使用RLPS的间接酶免疫测定(IELISA)和使用RLPS核心级分(用异硫氰酸荧光素标记)的荧光偏振测定(FPA)。使用流产芽孢杆菌RB51 RLPS抗原进行的IELISA检测牛血清时灵敏度和特异性分别为94.8%和97.3%,检测绵羊血清时分别为98.5%和97.8%,检测狗血清时分别为95.8%和100%。使用牛双歧杆菌RLPS抗原的IELISA对牛血清的敏感性和特异性值分别为80.5%和91.7%,对绵羊血清的敏感性和特异性值为98.9%和93.8%,对狗血清的敏感性和特异性值为70.8%和79.8%。使用犬双歧杆菌RLPS抗原的IELISA对牛血清的敏感性和特异性值分别为97.0%和97.4%,对绵羊血清的敏感性和特异性值为96.2%和96.3%,对狗血清的敏感性和特异性值为95.8%和98.8%。用荧光素标记来自B. ovis和B. canis的RLPS核心不成功。用荧光素标记的流产布鲁氏菌RB51核心对牛血清的敏感性和特异性分别为93.5%和99.8%,对绵羊血清的敏感性和特异性分别为78.1%和99.0%。无法在FPA中测试狗的血清。

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