Molecular approaches to malaria and Babesisosis diagnosis

The development of additional methods for detecting and identifuing Babesia and Plasmodium infections may be useful in disease monitoring, management and control efforts. To preliminarily evaluate sunthetic peptide-based serodiagnosis, a hydrophilic sequence (DDESEFDKEK)was selected from published BabR gene of B. bovis. Immunization of rabbits and cattle with the hemocyanin-conjugated peptide elicited antibody responses that specifically detected both P. falciparum and B. bovis antigens by immunofluorescence and Western blots. Using a dot-ELISA with this peptide, antisera from immunized and naturally-infected cattle, and immunized rodents, were specifically detected. Reactivity was weak and correlated with peptide immunization or infection. DNA-based detection using repetitive DNA was species-specific in dot-blot formats for B. bovis DNA, and in both dot-blot and in situ formats for P. falciparum; a streamlined enzymelinked synthetic DNA assay for P. falciparum detected 30 parasites/mm(cúbicos) from patient blood using either colorimetric (2-15 h color development) or chemiluminescent detection (0.5-6-min. exposures). Serodiagnostic and DNA hybridization methods may be complementary in the respective detection of both chronic and acute infections. However, recent improvements in the polymerase chain reaction (PCR) make feasible a more sensitive and uniform approach to the diagnosis of these and other infectious disease complexes, with appropriate primers and processing methods. An analysis of ribosomal DNA genes of Plasmodium and Toxoplasma identified Apicomplexa-conserved sequence regions. Specific and distinctive PCR profiles were obtained for primers spanning the internal transcribed spacer locus for each of several Plasmodium and Babesia species.

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Main Authors: McLaughlin,G. L., Montenegro-James,S., Vodkin,M. H., Howe,D., Toro,M., Leon,E., Armijos,R., Kakoma,I., Greenwood,B. M., Hassan-King,M., Marich,J., Ruth,J., James,M. A.
Format: Digital revista
Language:English
Published: Instituto Oswaldo Cruz, Ministério da Saúde 1992
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02761992000700007
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spelling oai:scielo:S0074-027619920007000072009-06-04Molecular approaches to malaria and Babesisosis diagnosisMcLaughlin,G. L.Montenegro-James,S.Vodkin,M. H.Howe,D.Toro,M.Leon,E.Armijos,R.Kakoma,I.Greenwood,B. M.Hassan-King,M.Marich,J.Ruth,J.James,M. A. Babesia Plasmodium diagnosis synthetic peptide serology in situ detection chemiluminescence dot-blot polymerase chain reaction internal transcribed spacer ribosomal DNA The development of additional methods for detecting and identifuing Babesia and Plasmodium infections may be useful in disease monitoring, management and control efforts. To preliminarily evaluate sunthetic peptide-based serodiagnosis, a hydrophilic sequence (DDESEFDKEK)was selected from published BabR gene of B. bovis. Immunization of rabbits and cattle with the hemocyanin-conjugated peptide elicited antibody responses that specifically detected both P. falciparum and B. bovis antigens by immunofluorescence and Western blots. Using a dot-ELISA with this peptide, antisera from immunized and naturally-infected cattle, and immunized rodents, were specifically detected. Reactivity was weak and correlated with peptide immunization or infection. DNA-based detection using repetitive DNA was species-specific in dot-blot formats for B. bovis DNA, and in both dot-blot and in situ formats for P. falciparum; a streamlined enzymelinked synthetic DNA assay for P. falciparum detected 30 parasites/mm(cúbicos) from patient blood using either colorimetric (2-15 h color development) or chemiluminescent detection (0.5-6-min. exposures). Serodiagnostic and DNA hybridization methods may be complementary in the respective detection of both chronic and acute infections. However, recent improvements in the polymerase chain reaction (PCR) make feasible a more sensitive and uniform approach to the diagnosis of these and other infectious disease complexes, with appropriate primers and processing methods. An analysis of ribosomal DNA genes of Plasmodium and Toxoplasma identified Apicomplexa-conserved sequence regions. Specific and distinctive PCR profiles were obtained for primers spanning the internal transcribed spacer locus for each of several Plasmodium and Babesia species.info:eu-repo/semantics/openAccessInstituto Oswaldo Cruz, Ministério da SaúdeMemórias do Instituto Oswaldo Cruz v.87 suppl.3 19921992-01-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02761992000700007en10.1590/S0074-02761992000700007
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language English
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author McLaughlin,G. L.
Montenegro-James,S.
Vodkin,M. H.
Howe,D.
Toro,M.
Leon,E.
Armijos,R.
Kakoma,I.
Greenwood,B. M.
Hassan-King,M.
Marich,J.
Ruth,J.
James,M. A.
spellingShingle McLaughlin,G. L.
Montenegro-James,S.
Vodkin,M. H.
Howe,D.
Toro,M.
Leon,E.
Armijos,R.
Kakoma,I.
Greenwood,B. M.
Hassan-King,M.
Marich,J.
Ruth,J.
James,M. A.
Molecular approaches to malaria and Babesisosis diagnosis
author_facet McLaughlin,G. L.
Montenegro-James,S.
Vodkin,M. H.
Howe,D.
Toro,M.
Leon,E.
Armijos,R.
Kakoma,I.
Greenwood,B. M.
Hassan-King,M.
Marich,J.
Ruth,J.
James,M. A.
author_sort McLaughlin,G. L.
title Molecular approaches to malaria and Babesisosis diagnosis
title_short Molecular approaches to malaria and Babesisosis diagnosis
title_full Molecular approaches to malaria and Babesisosis diagnosis
title_fullStr Molecular approaches to malaria and Babesisosis diagnosis
title_full_unstemmed Molecular approaches to malaria and Babesisosis diagnosis
title_sort molecular approaches to malaria and babesisosis diagnosis
description The development of additional methods for detecting and identifuing Babesia and Plasmodium infections may be useful in disease monitoring, management and control efforts. To preliminarily evaluate sunthetic peptide-based serodiagnosis, a hydrophilic sequence (DDESEFDKEK)was selected from published BabR gene of B. bovis. Immunization of rabbits and cattle with the hemocyanin-conjugated peptide elicited antibody responses that specifically detected both P. falciparum and B. bovis antigens by immunofluorescence and Western blots. Using a dot-ELISA with this peptide, antisera from immunized and naturally-infected cattle, and immunized rodents, were specifically detected. Reactivity was weak and correlated with peptide immunization or infection. DNA-based detection using repetitive DNA was species-specific in dot-blot formats for B. bovis DNA, and in both dot-blot and in situ formats for P. falciparum; a streamlined enzymelinked synthetic DNA assay for P. falciparum detected 30 parasites/mm(cúbicos) from patient blood using either colorimetric (2-15 h color development) or chemiluminescent detection (0.5-6-min. exposures). Serodiagnostic and DNA hybridization methods may be complementary in the respective detection of both chronic and acute infections. However, recent improvements in the polymerase chain reaction (PCR) make feasible a more sensitive and uniform approach to the diagnosis of these and other infectious disease complexes, with appropriate primers and processing methods. An analysis of ribosomal DNA genes of Plasmodium and Toxoplasma identified Apicomplexa-conserved sequence regions. Specific and distinctive PCR profiles were obtained for primers spanning the internal transcribed spacer locus for each of several Plasmodium and Babesia species.
publisher Instituto Oswaldo Cruz, Ministério da Saúde
publishDate 1992
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02761992000700007
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