Differential molecular identification of Taeniid spp. and Sarcocystis spp. cysts isolated from infected pigs and cattle

被引:23
|
作者
Gonzalez, L. M.
Villalobos, N.
Montero, E.
Morales, J.
Sanz, R. Alamo
Muro, A.
Harrison, L. J. S.
Parkhouse, R. M. E. [1 ]
Garate, T.
机构
[1] Univ Edinburgh, Royal Dick Sch Vet Studies, Ctr Trop Vet Med, Easter Bush Vet Ctr, Roslin EH25 9RG, Midlothian, Scotland
[2] Inst Salud Carlos III, Ctr Nacl Microbiol, Serv Parasitol, Madrid 28220, Spain
[3] Natl Autonomous Univ Mexico, Fac Med Vet & Zootecn, Mexico City 04510, DF, Mexico
[4] Consejeria San, Direcc Gen Salud Publ & Asistencia, Valladolid 47071, Spain
[5] Univ Salamanca, Fac Farm, Dept Parasitol, E-37007 Salamanca, Spain
[6] Gulbenkian Inst Sci, P-2781 Oeiras, Portugal
关键词
Taenia spp; Sarcocystis spp; cyst lesions; HDP2; ITS1/ITS2; 18S rRNA; PCR; PCR-RFLP; sequencing; slaughter house;
D O I
10.1016/j.vetpar.2006.06.009
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 the present work, the species-specific identification of Taeniid spp. cysticerci and sarcocystis cysts isolated from infected pigs and cattle was achieved by PCR. In particular: (i) multiplex-PCR derived from HDP2 DNA fragment, specific for Taenia saginatal Taenia solium; (ii) PCRs and PCR-RFLPs of the rDNA internal transcribed spacers 1 and 2 (ITS1 and ITS2) for the differential diagnosis of taeniids; (iii) PCR derived from the 18S rRNA gene and sequencing, specific for Sarcoystis spp. The combined application of these three PCR protocols provided an unequivocally specific diagnosis of T saginata, T solium, T hydatigena, Sarcocystis hominis and Sarcocystis suihominis, and may have practical application in the identification of calcified degenerating or morphologically dubious cysts, for example in the slaughter house situation or in human biopsy samples. (c) 2006 Elsevier B.V. All rights reserved.
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页码:95 / 101
页数:7
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