Hostname: page-component-586b7cd67f-t8hqh Total loading time: 0 Render date: 2024-11-22T18:48:56.011Z Has data issue: false hasContentIssue false

Improved specificity of Trypanosoma cruzi identification by polymerase chain reaction using an oligonucleotide derived from the amino-terminal sequence of a Tc24 protein

Published online by Cambridge University Press:  06 April 2009

A. Taibi
Affiliation:
Centre d' Immunologie et de Biologie Parasitaire, Unité INSERM U415, Institut Pasteur, 59019 Lille cédex, France
A. Guevara-Espinoza
Affiliation:
Centre d' Immunologie et de Biologie Parasitaire, Unité INSERM U415, Institut Pasteur, 59019 Lille cédex, France
R. Schöneck
Affiliation:
Centre d' Immunologie et de Biologie Parasitaire, Unité INSERM U415, Institut Pasteur, 59019 Lille cédex, France
B. Yahiaoui
Affiliation:
Centre d' Immunologie et de Biologie Parasitaire, Unité INSERM U415, Institut Pasteur, 59019 Lille cédex, France
A. Ouaissi
Affiliation:
Centre d' Immunologie et de Biologie Parasitaire, Unité INSERM U415, Institut Pasteur, 59019 Lille cédex, France

Summary

In the present study, the diagnostic value of Trypanosoma cruzi recombinant protein (Tc24) was examined. Although antibodies against Tc24 were detected during natural and experimental T. cruzi infections, specificity studies revealed that sera from T. rangeli-infected mice also recognized to some extent Tc24 protein. In addition, sera from Tc24-immunized mice reacted against a 21 kDa polypeptide in T. rangeli extracts. Detailed analysis of the antibody response against 20—40 peptide localized in the Tc24 amino-terminal domain suggests that this sequence is not expressed by T. rangeli 21 kDa antigen. Therefore, the PCR reaction using oligonucleotides corresponding to a 20–26 peptide clearly demonstrated the specificity of the oligoprobes for T. cruzi identification. Positive signals were also found when using blood samples from T. cruzi-infected mice. Taken together, these results suggest that the PCR-based 20–26 assay may be useful in the specific diagnosis of Chagas' disease.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1995

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Affranchino, J. L., Ibanez, C. F., Luquetti, A. O., Rassi, A., Reyes, M. B., Macina, R. A., Aslund, L., Pettersson, U. & Frasch, A. C. (1989). Identification of a Trypanosoma cruzi antigen that is shed during the acute phase of Chagas' disease. Molecular and Biochemical Parasitology 34, 46–9.CrossRefGoogle ScholarPubMed
Avila, H. A., Borges, Pereira J., Thiemann, O., De Paiva, E., Degrave, W., Morel, C. M. & Simpson, L. (1993). Detection of Trypanosoma cruzi in blood specimens of chronic chagasic patients by polymerase chain reaction amplification of kinetoplast minicircle DNA: comparison with serology and xenodiagnosis. Journal of Clinical Microbiology 31, 2421–6.CrossRefGoogle ScholarPubMed
Avila, H. A., Sigman, D. S., Cohen, L. M., Millikan, R. C. & Simpson, L. (1991). Polymerase chain reaction amplification of Trypanosoma cruzi kinetoplast minicircle DNA isolated from whole blood lysates: diagnosis of chronic Chagas' disease. Molecular and Biochemical Parasitology 48, 211–22.CrossRefGoogle ScholarPubMed
Barker, R. H. Jr. (1990). DNA probe diagnosis of parasitic infections. Experimental Parasitology 70, 494–9.CrossRefGoogle ScholarPubMed
Burns, J. M., Schreffler, W. G., Rosman, D. E., Sleath, P. R., March, C. J. & Reed, S. G. (1992). Identification and synthesis of a major conserved antigenic epitope of Trypanosoma cruzi. Proceedings of the National Academy of Sciences, USA 89, 1239–43.CrossRefGoogle Scholar
Carvalho, M. R., Krieger, M. A., Almeida, E., Oelemann, W., Shikanai-Yassuda, M. A., Ferreira, A. W., Pereira, J. B., Saez-Alquezar, A., Dorlhiac, P. E., Chamone, D. F. & Goldenberg, S. (1993). Chagas' disease diagnosis: evaluation of several tests in blood screening. Transfusion 33, 830–4.CrossRefGoogle Scholar
Cetron, M. S., Hoff, R., Kahn, S., Eisen, H. & Voorhis, W. C.Van (1992). Evaluation of recombinant trypomastigote surface antigens of Trypanosoma cruzi in screening sera from a population in rural Northeastern Brazil endemic for Chagas' disease. Acta Tropica 50, 259–66.CrossRefGoogle ScholarPubMed
Chiari, E., Diaz, J. C. P., Lana, M. & Chiari, C. A. (1989). Hemocultures for the parasitological diagnosis of human chronic Chagas' disease. Revista da Sociedade Brasileira de Medicina Tropical 22, 1923.CrossRefGoogle ScholarPubMed
Corral, R. S., Orn, A. & Grinstein, S. (1992). Detection of soluble exoantigens of Trypanosoma cruzi by a dotimmunobinding assay. American Journal of Tropical Medicine and Hygiene 46, 31–8.CrossRefGoogle ScholarPubMed
Diaz, C., Nussenzweig, V. & Gonzalez, A. (1992). An improved polymerase chain reaction assay to detect Trypanosoma cruzi in blood. American Journal of Tropical Medicine and Hygiene 46, 616–23.CrossRefGoogle ScholarPubMed
Freilij, H., Muller, L. & Gonzalez, Cappa S. M. (1983). Direct micromethod for diagnosis of acute and congenital Chagas' disease. Journal of Clinical Microbiology 18, 327–30.CrossRefGoogle Scholar
Gonzalez, A., Lerner, T. J., Huecas, M., Sosa-Pineda, B., Nogueira, N. & Lizardi, P. M. (1985). Apparent generation of a segmented mRNA from two separate tandem gene families in Trypanosoma cruzi. Nucleic Acids Research 13, 5789–803.CrossRefGoogle ScholarPubMed
Gruber, A. & Zingales, B. (1993). Trypanosoma cruzi: characterization of two recombinant antigens with potential application in the diagnosis of Chagas' disease. Experimental Parasitology 76, 112.CrossRefGoogle ScholarPubMed
Krautz, G. M., Galvao, L., Cancado, L. C. M., Ouaissi, A. & Kretli, A. U. (1994). Use of a 24-kDa Trypanosoma cruzi recombinant antigen to monitor cure of human Chagas' disease. Memorias do Institute Oswaldo Cruz (Suppl 1), 89.Google Scholar
Krieger, M. A., Almeida, E., Oelemann, W., Lafaille, J. J., Borges, Pereira J., Krieger, H., Carvalho, M. R. & Goldenberg, S. (1992). Use of recombinant antigens for the accurate immunodiagnosis of Chagas' disease. American Journal of Tropical Medicine and Hygiene 46, 427–34.CrossRefGoogle ScholarPubMed
LaemmliU, K. U, K. (1970). Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature, London 227, 680–5.CrossRefGoogle ScholarPubMed
Landivar, W. H. C., Nakasa, T., Tachibana, H., Paz, K. C. & Tateno, S. (1992). Seropositivity to Trypanosoma cruzi in blood donors in Santa Cruz, Bolivia. Journal of Infectious Diseases 166, 1464–5.Google ScholarPubMed
Lorca, M., Gonzalez, A., Veloso, C., Reyes, V. & Vergara, U. (1992). Immunodetection of antibodies in sera from symptomatic and asymptomatic Chilean Chagas' disease patients with Trypanosoma cruzi recombinant antigens. American Journal of Tropical Medicine and Hygiene 46, 44–9.CrossRefGoogle ScholarPubMed
Martin, U. O., Taibi, A., Loyens, M., Maidana, C., Cornette, J., Caudioti, C., Martelleur, A., Afchain, D., Marty, B., Velge, P., Ouaissi, A. & Capron, A. (1990). Trypanosoma cruzi IgM antibodies to an 84 kDa polypeptide epitope as a possible marker of the acute phase of human Chagas' disease. Medical Sciences Research 18, 725–6.Google Scholar
Ouaissi, A., Aguirre, T., Plumas-Marty, B., Piras, M., Schöneck, R., Gras-Masse, H., Taibi, A., Loyens, M., Tartar, A., Capron, A. & Piras, R. (1992). Cloning and sequencing of 24-kDa Trypanosoma cruzi-specific antigen released in association with membrane vesicles and defined by monoclonal antibody. Biology of the CelllS, 117.Google ScholarPubMed
Ouaissi, M. A., Taibi, A., Loyens, M., Martin, U., Afchain, D., Maidana, C., Claudioti, C., Cornette, J., Martelleur, A., Velge, P., Marty, B. & Capron, A. (1991). Trypanosoma cruzi: a carbohydrate epitope defined by a monoclonal antibody as a possible marker of the acute phase of human Chagas' disease. American Journal of Tropical Medicine and Hygiene 45, 214–25.CrossRefGoogle ScholarPubMed
Rodgers, M. R., Popper, S. J. & Wirth, D. F. (1990). Amplification of kinetoplast DNA as a tool in the detection and diagnosis of Leishmania. Experimental Parasitology 71, 267–75.CrossRefGoogle ScholarPubMed
Ross, A. & Novoa-Montero, D. (1993). Comparability and reliability of ELISA, immunofluorescence, and indirect hemagglutination assays for Trypanosoma cruzi and Trypanosoma rangeli. Journal of Infectious Diseases 168, 1581–4.CrossRefGoogle ScholarPubMed
Schechter, M., Voller, A., Markinkelle, C. J., Flint, J. E., Guhl, F. & Miles, M. A. (1983). Purified Trypanosoma cruzi specific glycoprotein for discriminative serological diagnosis of South American trypanosomiasis (Chagas' disease). Lancet 22,939–41.CrossRefGoogle Scholar
Schöneck, R., Plumas-Marty, B., Taibi, A., Billaut-Mulot, O., Loyens, M., Gras-Masse, H., Capron, A. & Ouaissi, A. (1994). Trypanosoma cruzi cDNA encodes a tandemly repeated domain structure characteristic of small stress proteins and glutathione S-transferases. Biology of the Cell 80, 110.CrossRefGoogle ScholarPubMed
Smith, D. B. & Johnson, K. (1988). Single-step purification of polypeptides expressed in Escherichia coli as fusions with glutathione-S-transferase. Gene 67, 3140.CrossRefGoogle ScholarPubMed
Sturm, N. R., Degrave, W., Morel, C. & Simpsom, L. (1989). Sensitive detection and schizodeme classification of Trypanosoma cruzi cells by amplification of kinetoplast minicircle DNA sequences: use in diagnosis of Chagas' disease. Molecular and Biochemical Parasitology 33, 205–14.CrossRefGoogle ScholarPubMed
Taibi, A., Plumas-Marty, B., Guevara, Espinoza A., Schöneck, R., Pessoa, H., Loyens, M., Piras, R., Aguirre, T., Gras-Masse, H., Bossus, M., Tartar, A., Capron, A. & Ouaissi, A. (1993). Trypanosoma cruzi: immunity induced in mice and rats by trypomastigote excretory–secretory antigens and identification of a peptide sequence containing a T cell epitope with protective activity. Journal of Immunology 151, 2676–89.CrossRefGoogle Scholar
Towbin, H., Stahelin, T. & Gordon, J. (1979). Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proceedings of the National Academy of Sciences, USA 76, 4350–4.CrossRefGoogle ScholarPubMed
Vergara, U., Veloso, C., Gonzalez, A. & Lorca, M. (1992). Evaluation of an enzyme-linked immunosorbent assay for the diagnosis of Chagas' disease using synthetic peptides. American Journal of Tropical Medicine and Hygiene 46, 3943.CrossRefGoogle ScholarPubMed
Voller, A., Bartlett, A. & Bidwell, D. E. (1978). Enzyme immunoassays with special reference to ELISA techniques. Journal of Clinical Pathology 31, 507–20.CrossRefGoogle ScholarPubMed
Zicker, F., Smith, P. G., Luquetti, A. O. & Oliveira, O. S. (1990). Mass screening for Trypanosoma cruzi infections using the immunofluorescence, ELISA and haemagglutination tests on serum samples and on blood eluates from filter-paper. Bulletin of the World Health Organization 68, 465–71.Google ScholarPubMed