Abstract
Cysticercosis results from ingestion of the eggs of the tapeworm Taenia solium. Reduction of the incidence of human and swine cysticercosis requires identification and treatment of individuals who carry the adult tapeworm. T. solium and Taenia saginata eggs cannot be differentiated on the basis of morphology; thus, in order to improve existing methods for the diagnosis of taeniasis, we have developed highly sensitive, species-specific DNA probes which differentiate T. solium and T. saginata. Recombinant clones containing repetitive DNA sequences which hybridize specifically with genomic DNAs from either species were isolated and characterized. T. solium-specific DNA sequences contained complete and truncated forms of a tandemly repeated 158-bp DNA sequence. An unrelated T. saginata DNA sequence was also characterized and shown to encode a portion of the mitochondrial cytochrome c oxidase I gene. T. solium- and T. saginata-specific DNA probes did not hybridize in dot blot assays either with genomic DNA from the platyhelminths Taenia hydatigena, Taenia pisiformis, Taenia taeniaeformis, Echinococcus granulosus, and Schistosoma mansoni or with genomic DNA from other eukaryotes, including Saccharomyces cerevisiae, Candida albicans, Cryptosporidium parvum, Entamoeba histolytica, Trypanosoma gambiense, Trypanosoma brucei, and Giardia lamblia, Caenorhabditis elegans, and human DNA. By using these T. solium and T. saginata DNA probes, a rapid, highly sensitive and specific dot blot assay for the detection of T. solium eggs was developed.
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Selected References
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- Allan J. C., Avila G., Garcia Noval J., Flisser A., Craig P. S. Immunodiagnosis of taeniasis by coproantigen detection. Parasitology. 1990 Dec;101(Pt 3):473–477. doi: 10.1017/s0031182000060686. [DOI] [PubMed] [Google Scholar]
- Allan J. C., Mencos F., Garcia-Noval J., Sarti E., Flisser A., Wang Y., Liu D., Craig P. S. Dipstick dot ELISA for the detection of Taenia coproantigens in humans. Parasitology. 1993 Jul;107(Pt 1):79–85. doi: 10.1017/s0031182000079439. [DOI] [PubMed] [Google Scholar]
- Barker R. H., Jr, Banchongaksorn T., Courval J. M., Suwonkerd W., Rimwungtragoon K., Srittong N., Wirth D. F. DNA probes as epidemiological tools for surveillance of Plasmodium falciparum malaria in Thailand. Int J Epidemiol. 1994 Feb;23(1):161–168. doi: 10.1093/ije/23.1.161. [DOI] [PubMed] [Google Scholar]
- Barker R. H., Jr, Suebsaeng L., Rooney W., Alecrim G. C., Dourado H. V., Wirth D. F. Specific DNA probe for the diagnosis of Plasmodium falciparum malaria. Science. 1986 Mar 21;231(4744):1434–1436. doi: 10.1126/science.3513309. [DOI] [PubMed] [Google Scholar]
- Bowles J., Blair D., McManus D. P. Genetic variants within the genus Echinococcus identified by mitochondrial DNA sequencing. Mol Biochem Parasitol. 1992 Sep;54(2):165–173. doi: 10.1016/0166-6851(92)90109-w. [DOI] [PubMed] [Google Scholar]
- Craig P. S., Macpherson C. N., Watson-Jones D. L., Nelson G. S. Immunodetection of Echinococcus eggs from naturally infected dogs and from environmental contamination sites in settlements in Turkana, Kenya. Trans R Soc Trop Med Hyg. 1988;82(2):268–274. doi: 10.1016/0035-9203(88)90445-2. [DOI] [PubMed] [Google Scholar]
- Earnest M. P., Reller L. B., Filley C. M., Grek A. J. Neurocysticercosis in the United States: 35 cases and a review. Rev Infect Dis. 1987 Sep-Oct;9(5):961–979. doi: 10.1093/clinids/9.5.961. [DOI] [PubMed] [Google Scholar]
- Edman U., Meraz M. A., Rausser S., Agabian N., Meza I. Characterization of an immuno-dominant variable surface antigen from pathogenic and nonpathogenic Entamoeba histolytica. J Exp Med. 1990 Sep 1;172(3):879–888. doi: 10.1084/jem.172.3.879. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Erttmann K. D., Unnasch T. R., Greene B. M., Albiez E. J., Boateng J., Denke A. M., Ferraroni J. J., Karam M., Schulz-Key H., Williams P. N. A DNA sequence specific for forest form Onchocerca volvulus. Nature. 1987 Jun 4;327(6121):415–417. doi: 10.1038/327415a0. [DOI] [PubMed] [Google Scholar]
- Farahmandian I., Sahba G. H., Arfaa F., Movafagh K. A comparison of stool examination and mass-treatment for indication of the prevalence of Taenia saginata. Trop Geogr Med. 1973 Jun;25(2):171–173. [PubMed] [Google Scholar]
- Flisser A. Neurocysticercosis in Mexico. Parasitol Today. 1988 May;4(5):131–137. doi: 10.1016/0169-4758(88)90187-1. [DOI] [PubMed] [Google Scholar]
- Flisser A., Reid A., Garcia-Zepeda E., McManus D. P. Specific detection of Taenia saginata eggs by DNA hybridisation. Lancet. 1988 Dec 17;2(8625):1429–1430. doi: 10.1016/s0140-6736(88)90626-5. [DOI] [PubMed] [Google Scholar]
- Garey J. R., Wolstenholme D. R. Platyhelminth mitochondrial DNA: evidence for early evolutionary origin of a tRNA(serAGN) that contains a dihydrouridine arm replacement loop, and of serine-specifying AGA and AGG codons. J Mol Evol. 1989 May;28(5):374–387. doi: 10.1007/BF02603072. [DOI] [PubMed] [Google Scholar]
- Garfinkel L. I., Giladi M., Huber M., Gitler C., Mirelman D., Revel M., Rozenblatt S. DNA probes specific for Entamoeba histolytica possessing pathogenic and nonpathogenic zymodemes. Infect Immun. 1989 Mar;57(3):926–931. doi: 10.1128/iai.57.3.926-931.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gonzalez A., Prediger E., Huecas M. E., Nogueira N., Lizardi P. M. Minichromosomal repetitive DNA in Trypanosoma cruzi: its use in a high-sensitivity parasite detection assay. Proc Natl Acad Sci U S A. 1984 Jun;81(11):3356–3360. doi: 10.1073/pnas.81.11.3356. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Grunstein M., Hogness D. S. Colony hybridization: a method for the isolation of cloned DNAs that contain a specific gene. Proc Natl Acad Sci U S A. 1975 Oct;72(10):3961–3965. doi: 10.1073/pnas.72.10.3961. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pearson W. R., Lipman D. J. Improved tools for biological sequence comparison. Proc Natl Acad Sci U S A. 1988 Apr;85(8):2444–2448. doi: 10.1073/pnas.85.8.2444. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Samuelson J., Acuna-Soto R., Reed S., Biagi F., Wirth D. DNA hybridization probe for clinical diagnosis of Entamoeba histolytica. J Clin Microbiol. 1989 Apr;27(4):671–676. doi: 10.1128/jcm.27.4.671-676.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sarti-Gutierrez E. J., Schantz P. M., Lara-Aguilera R., Gomez Dandoy H., Flisser A. Taenia solium taeniasis and cysticercosis in a Mexican village. Trop Med Parasitol. 1988 Sep;39(3):194–198. [PubMed] [Google Scholar]
- Sarti E., Schantz P. M., Plancarte A., Wilson M., Gutierrez I. O., Lopez A. S., Roberts J., Flisser A. Prevalence and risk factors for Taenia solium taeniasis and cysticercosis in humans and pigs in a village in Morelos, Mexico. Am J Trop Med Hyg. 1992 Jun;46(6):677–685. doi: 10.4269/ajtmh.1992.46.677. [DOI] [PubMed] [Google Scholar]
- Schantz P. M., Moore A. C., Muñoz J. L., Hartman B. J., Schaefer J. A., Aron A. M., Persaud D., Sarti E., Wilson M., Flisser A. Neurocysticercosis in an Orthodox Jewish community in New York City. N Engl J Med. 1992 Sep 3;327(10):692–695. doi: 10.1056/NEJM199209033271004. [DOI] [PubMed] [Google Scholar]
- Shah J. S., Karam M., Piessens W. F., Wirth D. F. Characterization of an Onchocerca-specific DNA clone from Onchocerca volvulus. Am J Trop Med Hyg. 1987 Sep;37(2):376–384. doi: 10.4269/ajtmh.1987.37.376. [DOI] [PubMed] [Google Scholar]
- Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
- Wirth D. F., Pratt D. M. Rapid identification of Leishmania species by specific hybridization of kinetoplast DNA in cutaneous lesions. Proc Natl Acad Sci U S A. 1982 Nov;79(22):6999–7003. doi: 10.1073/pnas.79.22.6999. [DOI] [PMC free article] [PubMed] [Google Scholar]