Shurley J F, Legendre A M, Scalarone G M
Department of Biological Sciences, Idaho State University, Pocatello, 83209, USA.
Mycopathologia. 2005 Sep;160(2):137-42. doi: 10.1007/s11046-005-3153-9.
A competitive binding inhibition enzyme linked immunosorbent assay (ELISA) was used to detect Blastomyces dermatitidis antigens in urine specimens from dogs with blastomycosis. Sera from rabbits immunized with B. dermatitidis killed whole yeast cells were used as the primary antibody in the competitive ELISA. This initial study was performed to determine if B. dermatitidis antigen detection was possible and to test the efficacy of the rabbit sera as a primary antibody. An indirect ELISA was also performed to compare antigen detection in urine to antibody detection in the sera of the infected dogs. The results indicate 100% (36/36 specimens) detection of both antigen and antibody. Cross reactivity with Histoplasma capsulatum, as well as non-specific binding with the normal urine specimens, was observed with the competitive binding inhibition ELISA.
采用竞争性结合抑制酶联免疫吸附测定(ELISA)检测患有芽生菌病犬尿液标本中的皮炎芽生菌抗原。用经皮炎芽生菌灭活全酵母细胞免疫的兔血清作为竞争性ELISA的一抗。开展这项初步研究是为了确定是否能够检测到皮炎芽生菌抗原,并测试兔血清作为一抗的有效性。还进行了间接ELISA,以比较尿液中的抗原检测与感染犬血清中的抗体检测。结果表明抗原和抗体的检测率均为100%(36/36份标本)。在竞争性结合抑制ELISA中观察到与荚膜组织胞浆菌的交叉反应以及与正常尿液标本的非特异性结合。