Comparative Evaluation of Four Potent <i>Neospora caninum</i> Diagnostic Antigens Using Immunochromatographic Assay for Detection of Specific Antibody in Cattle

<i>Neospora caninum</i> is an intracellular protozoan parasite responsible for numerous abortion outbreaks and neonatal abnormalities in cattle. Rapid and accurate diagnosis is critical for <i>N. caninum</i> control owing to the lack of vaccine or drug-based control strategie...

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Main Authors: Ragab M. Fereig, Hanan H. Abdelbaky, Yoshifumi Nishikawa
Format: Article
Language:English
Published: MDPI AG 2021-10-01
Series:Microorganisms
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Online Access:https://www.mdpi.com/2076-2607/9/10/2133
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author Ragab M. Fereig
Hanan H. Abdelbaky
Yoshifumi Nishikawa
author_facet Ragab M. Fereig
Hanan H. Abdelbaky
Yoshifumi Nishikawa
author_sort Ragab M. Fereig
collection DOAJ
description <i>Neospora caninum</i> is an intracellular protozoan parasite responsible for numerous abortion outbreaks and neonatal abnormalities in cattle. Rapid and accurate diagnosis is critical for <i>N. caninum</i> control owing to the lack of vaccine or drug-based control strategies. Herein, we evaluated the performance of four frequently used antigens in the diagnosis of <i>N. caninum</i> infection using immunochromatographic tests (ICTs) as a rapid, affordable, and field applicable tool. These antigens included recombinant proteins of <i>N. caninum</i> surface antigen 1 (NcSAG1), dense granule proteins 7 (NcGRA7) and 6 (NcGRA6), in addition to native <i>Neospora</i> lysate antigen (NLA). Our study revealed the utility of all antigen-based ICTs for detection of specific antibodies to <i>N. caninum</i>. However, the NcSAG1-based ICT was the best for detection of all control <i>N. caninum</i>-infected mouse or cattle sera, while NcGRA7 and NcGRA6-based ICTs exhibited specific ability to detect samples from acute and sub-acute infection in mice and cattle, respectively. Analyses of the NcSAG1-based ICT against enzyme-linked immunosorbent assays (ELISAs) of the same antigen revealed its efficiency in detection of field cattle samples as observed in high sensitivity (84.2%), specificity (93.5%), agreement (90%), and kappa value (0.78). The current knowledge provides an efficient platform for <i>N. caninum</i> control through on-site diagnosis of infected cattle.
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spelling doaj.art-daaaaa47d72e4629ae26208d244591912023-11-22T19:14:51ZengMDPI AGMicroorganisms2076-26072021-10-01910213310.3390/microorganisms9102133Comparative Evaluation of Four Potent <i>Neospora caninum</i> Diagnostic Antigens Using Immunochromatographic Assay for Detection of Specific Antibody in CattleRagab M. Fereig0Hanan H. Abdelbaky1Yoshifumi Nishikawa2National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido 080-8555, JapanNational Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido 080-8555, JapanNational Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido 080-8555, Japan<i>Neospora caninum</i> is an intracellular protozoan parasite responsible for numerous abortion outbreaks and neonatal abnormalities in cattle. Rapid and accurate diagnosis is critical for <i>N. caninum</i> control owing to the lack of vaccine or drug-based control strategies. Herein, we evaluated the performance of four frequently used antigens in the diagnosis of <i>N. caninum</i> infection using immunochromatographic tests (ICTs) as a rapid, affordable, and field applicable tool. These antigens included recombinant proteins of <i>N. caninum</i> surface antigen 1 (NcSAG1), dense granule proteins 7 (NcGRA7) and 6 (NcGRA6), in addition to native <i>Neospora</i> lysate antigen (NLA). Our study revealed the utility of all antigen-based ICTs for detection of specific antibodies to <i>N. caninum</i>. However, the NcSAG1-based ICT was the best for detection of all control <i>N. caninum</i>-infected mouse or cattle sera, while NcGRA7 and NcGRA6-based ICTs exhibited specific ability to detect samples from acute and sub-acute infection in mice and cattle, respectively. Analyses of the NcSAG1-based ICT against enzyme-linked immunosorbent assays (ELISAs) of the same antigen revealed its efficiency in detection of field cattle samples as observed in high sensitivity (84.2%), specificity (93.5%), agreement (90%), and kappa value (0.78). The current knowledge provides an efficient platform for <i>N. caninum</i> control through on-site diagnosis of infected cattle.https://www.mdpi.com/2076-2607/9/10/2133neosporosisantigenantibodyimmunochromatographycattle
spellingShingle Ragab M. Fereig
Hanan H. Abdelbaky
Yoshifumi Nishikawa
Comparative Evaluation of Four Potent <i>Neospora caninum</i> Diagnostic Antigens Using Immunochromatographic Assay for Detection of Specific Antibody in Cattle
Microorganisms
neosporosis
antigen
antibody
immunochromatography
cattle
title Comparative Evaluation of Four Potent <i>Neospora caninum</i> Diagnostic Antigens Using Immunochromatographic Assay for Detection of Specific Antibody in Cattle
title_full Comparative Evaluation of Four Potent <i>Neospora caninum</i> Diagnostic Antigens Using Immunochromatographic Assay for Detection of Specific Antibody in Cattle
title_fullStr Comparative Evaluation of Four Potent <i>Neospora caninum</i> Diagnostic Antigens Using Immunochromatographic Assay for Detection of Specific Antibody in Cattle
title_full_unstemmed Comparative Evaluation of Four Potent <i>Neospora caninum</i> Diagnostic Antigens Using Immunochromatographic Assay for Detection of Specific Antibody in Cattle
title_short Comparative Evaluation of Four Potent <i>Neospora caninum</i> Diagnostic Antigens Using Immunochromatographic Assay for Detection of Specific Antibody in Cattle
title_sort comparative evaluation of four potent i neospora caninum i diagnostic antigens using immunochromatographic assay for detection of specific antibody in cattle
topic neosporosis
antigen
antibody
immunochromatography
cattle
url https://www.mdpi.com/2076-2607/9/10/2133
work_keys_str_mv AT ragabmfereig comparativeevaluationoffourpotentineosporacaninumidiagnosticantigensusingimmunochromatographicassayfordetectionofspecificantibodyincattle
AT hananhabdelbaky comparativeevaluationoffourpotentineosporacaninumidiagnosticantigensusingimmunochromatographicassayfordetectionofspecificantibodyincattle
AT yoshifuminishikawa comparativeevaluationoffourpotentineosporacaninumidiagnosticantigensusingimmunochromatographicassayfordetectionofspecificantibodyincattle