Development of two immunochromatographic tests for the serodiagnosis of bovine babesiosis

被引:14
作者
Kim, Chulmin [1 ]
Alhassan, Andy [1 ]
Verdida, Rodolfo A. [1 ]
Yokoyama, Naoaki [1 ]
Xuan, Xuenan [1 ]
Fujisaki, Kozo [1 ]
Kawazu, Shin-ichiro [1 ]
Igarashi, Ikuo [1 ]
机构
[1] Obihiro Univ Agr & Vet Med, Natl Res Ctr Protozoan Dis, Obihiro, Hokkaido 0808555, Japan
基金
日本学术振兴会;
关键词
Babesia bovis; Babesia bigemina; immunochromatographic test; ELISA; IFAT;
D O I
10.1016/j.vetpar.2007.05.016
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 developed two immunochromatographic tests (ICTs), which are nitrocellulose membrane-based immunoassays for the convenient and rapid serodiagnosis of bovine babesiosis caused by Babesia bovis (BoICT) and Babesia bigemina (BiICT). The efficacy of two ICTs was evaluated using 13 positive sera from experimentally infected cattle with B. bovis or B. bigemina. Clear results showed that the BoICT and ELISA detected antibodies in sera collected from 14 to 93 days post-infection, while BiICT and ELISA detected from 13 to 274 days post-infection. In additon, non-infected cattle, Neospora caninum, and Cryptosporidium parvum were negative in two ICTs. To evaluate the field utility of the ICTs, we tested 186 field bovine sera collected from cattle living in Yanbian (China) and Mato Grosso do Sul (Brazil). The results of ICTs were compared to those of classical serodiagnostic methods, enzyme-linked immunosorbent assay (ELISA) and the indirect immunofluorescence assay (IFAT). The overall concordances of BoICT were determined as 92.5 and 90.3% when the results of ELISA and IFAT were set as the reference standards, respectively. In contrast, :hose of BiICT showed 96.8 and 92.5% relative to the results of standard ELISA and IFAT, respectively. Conventional and rapid diagnosic devices for bovine babesiosis may provide a valuable tool in clinical and field applications. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:137 / 143
页数:7
相关论文
共 34 条
[1]   Bovine piroplasms in Minorca (Balearic Islands, Spain):: a comparison of PCR-based and light microscopy detection [J].
Almeria, S ;
Castellà, J ;
Ferrer, D ;
Ortuño, A ;
Estrada-Peña, A ;
Gutiérrez, JF .
VETERINARY PARASITOLOGY, 2001, 99 (03) :249-259
[2]   Expression of C-terminal truncated and full-length Babesia bigemina rhoptry-associated protein 1 and their potential use in enzyme-linked immunosorbent assay [J].
Boonchit, S ;
Alhassan, A ;
Chan, B ;
Xuan, X ;
Yokoyama, N ;
Ooshiro, M ;
Goff, WL ;
Waghela, SD ;
Wagner, G ;
Igarashi, I .
VETERINARY PARASITOLOGY, 2006, 137 (1-2) :28-35
[3]   Improved enzyme-linked immunosorbent assay using C-terminal truncated recombinant antigens of Babesia bovis rhoptry-associated protein-1 for detection of specific antibodies [J].
Boonchit, S ;
Xuan, XN ;
Yokoyama, N ;
Goff, WL ;
Waghela, SD ;
Wagner, G ;
Igarashi, I .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (04) :1601-1604
[4]   Evaluation of an enzyme-linked immunosorbent assay with recombinant rhoptry-associated protein 1 antigen against Babesia bovis for the detection of specific antibodies in cattle [J].
Boonchit, S ;
Xuan, XN ;
Yokoyama, N ;
Goff, WL ;
Wagner, G ;
Igarashi, I .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (10) :3771-3775
[5]   CURRENT STATE AND FUTURE-TRENDS IN THE DIAGNOSIS OF BABESIOSIS [J].
BOSE, R ;
JORGENSEN, WK ;
DALGLIESH, RJ ;
FRIEDHOFF, KT ;
DEVOS, AJ .
VETERINARY PARASITOLOGY, 1995, 57 (1-3) :61-74
[6]   Serodiagnosis of Neospora caninum infection in cattle by enzyme-linked immunosorbent assay with recombinant truncated NcSAG1 [J].
Chahan, B ;
Gaturaga, I ;
Huang, XH ;
Liao, M ;
Fukumoto, S ;
Hirata, H ;
Nishikawa, Y ;
Suzuki, H ;
Sugimoto, C ;
Nagasawa, H ;
Fujisaki, K ;
Igarashi, I ;
Mikami, T ;
Xuan, XN .
VETERINARY PARASITOLOGY, 2003, 118 (3-4) :177-185
[7]  
Chan K, 2000, J MARK COMMUN, V6, P37, DOI 10.1080/135272600345543
[8]  
Chan R, 2000, J CLIN MICROBIOL, V38, P393
[9]   Dipstick enzyme immunoassay to detect Fusarium T-2 toxin in wheat [J].
DeSaeger, S ;
VanPeteghem, C .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (06) :1880-1884
[10]  
Faigel DO, 2000, AM J GASTROENTEROL, V95, P72, DOI 10.1111/j.1572-0241.2000.01702.x