Immunodiagnosis of paramphistomosis using monoclonal antibody-based sandwich ELISA for detection of Paramphistomum gracile circulating 16 kDa antigen

被引:11
作者
Anuracpreeda, Panat [1 ,2 ]
Tepsupornkul, Kullanid [2 ]
Chawengkirttikul, Runglawan [3 ]
机构
[1] Mahidol Univ, Inst Mol Biosci, Salaya 73170, Nakorn Pathom, Thailand
[2] Mahidol Univ, Div Agr Sci, Kanchanaburi Campus, Saiyok 71150, Kanchanaburi, Thailand
[3] Mahidol Univ, Fac Sci, Dept Microbiol, Rama 6 Rd, Bangkok, Thailand
关键词
Paramphisomum gracile; paramphistomosis; 16 kDa antigen; monoclonal antibody; sandwich ELISA; immunodiagnosis; FASCIOLA-GIGANTICA; FISCHOEDERIUS-COBBOLDI; SURFACE-TOPOGRAPHY; TEGUMENT; CATTLE; CERVI; MORPHOLOGY; HISTOLOGY; PARASITE; EXTRACT;
D O I
10.1017/S003118201600264X
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
In this study, we have produced a monoclonal antibody (MoAb) against 16 kDa antigen of Paramphistomum gracile (16 kDaAgPg), and developed an accurate sandwich enzyme-linked immunosorbent assay (sandwich ELISA) for the detection of circulating 16 kDaAg in the serum and fecal samples from cattle naturally infected with P. gracile. MoAb 1D10 was immobilized on a microtitre plate, and the antigen in the samples was captured and detected with biotinylated rabbit anti-16 kDaAgPg antibody. The lower detection limit of sandwich ELISA was 3.5 pg mL(-1), and no cross-reaction with other parasite antigens was evaluated. The reliability of the assay was examined using the serum and fecal samples from cattle naturally infected with P. gracile, Fasciola gigantica, Moniezia benedeni, Trichuris sp., Strongyloides sp., strongylids and non-infected animals. The sandwich ELISA showed the sensitivity, specificity and accuracy at 98.33, 100 and 99.55% (serum samples), and 96.67, 100 and 99.09% (fecal samples). Therefore, this detection method is a rapid and excellent potential assay for the accurate diagnosis of paramphistomosis.
引用
收藏
页码:899 / 903
页数:5
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