PCR-ELISA for diagnosis of Trypanosoma evansi in animals and vector

被引:18
作者
Chansiri, K
Khuchareontaworn, S
Sarataphan, N
机构
[1] Srinakharinwirot Univ, Fac Med, Dept Biochem, Bangkok 10110, Thailand
[2] Minist Agr & Cooperat, Dept Livestock Dev, Natl Inst Anim Hlth, Parasitol Sect, Bangkok 10900, Thailand
关键词
PCR; ELISA; Trypanosoma evansi; Babesia; Anaplasma; Theileria;
D O I
10.1006/mcpr.2002.0412
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A highly sensitive and specific polymerase chain reaction (PCR) based assay for the detection of Trypanosoma evansi present in the blood of different animals and vector was developed. A simple lysis method was used to remove of the red blood cells to facilitate direct input of samples into the PCR reactions. The primer set was designed and synthesized to amplify a single band of 257 bp PCR product that was subsequently examined by enzyme-linked immunosorbent assay (ELISA). The sensitivity limit of PCR-ELISA was 0.01 pg that was corresponded to 1 parasite/ml of blood. No cross-reactivity of the assay was observed against Babesia bovis, B. bigemina, Anaplasma marginale, Theileria sp. and host DNA. The PCR-ELISA was shown to detect 33 samples of T. evansi infected blood of animals and 10 mosquitoes from different geographical area in Thailand. The results were corresponded to those of the PCR and mouse inoculation. This implies that the technique of PCR-ELISA is not only beneficial for diagnosis of the parasite but also useful for epidemiological study and designing rational trypanosomiasis control program. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:173 / 177
页数:5
相关论文
共 17 条
[1]  
BOONYAWONG T, 1975, THAI J VET MED, V5, P665
[2]  
CHAICHANAPUNPOL I, 1985, KASETSART VET, V6, P1
[3]   Anaplasma marginale: Detection of carrier cattle by PCR-ELISA [J].
Gale, KR ;
Dimmock, CM ;
Gartside, M ;
Leatch, G .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 1996, 26 (10) :1103-1109
[4]   Camel trypanosomosis in the Canary islands:: assessment of seroprevalence and infection rates using the card agglutination test (CATT/T-evansi) and parasite detection tests [J].
Gutierrez, C ;
Juste, MC ;
Corbera, JA ;
Magnus, E ;
Verloo, D ;
Montoya, JA .
VETERINARY PARASITOLOGY, 2000, 90 (1-2) :155-159
[5]   Comparative studies on the sensitivity of polymerase chain reaction and microscopic examination for the detection of Trypanosoma evansi in experimentally infected mice [J].
Ijaz, MK ;
Nur-E-Kamal, MSA ;
Mohamed, AIA ;
Dar, FK .
COMPARATIVE IMMUNOLOGY MICROBIOLOGY AND INFECTIOUS DISEASES, 1998, 21 (03) :215-223
[6]  
INDRAKAMHANG P, 1982, 20 ANN C KAS U 4 5 F, P45
[7]   TRYPANOSOMA-EVANSI INFECTION IN BUFFALOS IN NORTHEAST THAILAND .1. FIELD INVESTIGATIONS [J].
LOHR, KF ;
POHLPARK, S ;
SRIKITJAKARN, L ;
THABORAN, P ;
BETTERMANN, G ;
STAAK, C .
TROPICAL ANIMAL HEALTH AND PRODUCTION, 1985, 17 (02) :121-125
[8]  
MATTHIAS AG, 1980, J VET MED, V10, P47
[9]   Direct and sensitive detection of Trypanosoma evansi by polymerase chain reaction [J].
Omanwar, S ;
Rao, JR ;
Basagoudanavar, SH ;
Singh, RK ;
Butchaiah, G .
ACTA VETERINARIA HUNGARICA, 1999, 47 (03) :351-359
[10]   A possible role for Rusa deer (Cervus timorensis russa) and wild pigs in spread of Trypanosoma evansi from Indonesia to Papua New Guinea [J].
Reid, SA ;
Husein, A ;
Hutchinson, GW ;
Copeman, DB .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 1999, 94 (02) :195-197