Discrimination of Neospora caninum from Toxoplasma gondii and other apicomplexan parasites by hybridization and PCR

被引:66
作者
Kaufmann, H
Yamage, M
Roditi, I
Dobbelaere, D
Dubey, JP
Holmdahl, OJM
Trees, A
Gottstein, B
机构
[1] UNIV BERN,FAC MED,INST PARASITOL,CH-3001 BERN,SWITZERLAND
[2] UNIV BERN,INST GEN MICROBIOL,CH-3012 BERN,SWITZERLAND
[3] USDA ARS,BELTSVILLE AGR RES CTR,LPSI,PARASITE BIOL & EPIDEMIOL LAB,BELTSVILLE,MD 20705
[4] SWEDISH UNIV AGR SCI,DEPT PARASITOL,S-75007 UPPSALA,SWEDEN
[5] UNIV LIVERPOOL,LIVERPOOL SCH TROP MED,LIVERPOOL L3 5QA,MERSEYSIDE,ENGLAND
关键词
Neospora caninum; Toxoplasma gondii; Sarcocystis; Apicomplexa; DNA probe; PCR;
D O I
10.1006/mcpr.1996.0038
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Neospora caninum is a protozoan parasite which causes neurological problems in dogs and abortion in cattle. As N. caninum is difficult to distinguish morphologically from Toxoplasma gondii, we developed a molecular tool capable of discriminating between the two parasites. Genomic DNA was isolated from in vitro cultured N. caninum tachyzoites and cloned into a plasmid vector. Resulting colonies were subsequently screened by differential hybridization using N. caninum and T. gondii DNA. Two clones were characterized in detail: one clone, termed pNc5, was found to be specific for N. caninum whereas the second clone, pNc1, hybridized with DNA from both parasites. The sequence of pNc5 was determined and different oligonucleotide primers were designed for use in the polymerase chain reaction (PCR). A 944 bp fragment was specifically amplified from N. caninum DNA, but not from DNA extracted from T. gondii or different Sarcocystis species. Positive signals in PCR were obtained with as little as 100 pg parasite template DNA. In addition, dual PCR with primer pairs specific for N. caninum and T. gondii allowed the detection of either parasite in mixed samples. (C) 1996 Academic Press Limited
引用
收藏
页码:289 / 297
页数:9
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