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Development of a promising antigenic cocktail for the global detection of Babesia caballi in horse by ELISA
In this study, we designed novel truncated Babesia caballi (B. caballi) recombinant proteins from the previously used B. caballi proteins; 134-Kilodalton Protein (rBC134) and Merozoite Rhoptry 48 Protein (rBC48). Then, we evaluated the diagnostic performance of the newly designed proteins when used...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104287/ https://www.ncbi.nlm.nih.gov/pubmed/37058508 http://dx.doi.org/10.1371/journal.pone.0284535 |
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author | El-Sayed, Shimaa Abd El-Salam Rizk, Mohamed Abdo Baghdadi, Hanadi B. Ringo, Aaron Edmond Sambuu, Gantuya Nugraha, Arifin Budiman Igarashi, Ikuo |
author_facet | El-Sayed, Shimaa Abd El-Salam Rizk, Mohamed Abdo Baghdadi, Hanadi B. Ringo, Aaron Edmond Sambuu, Gantuya Nugraha, Arifin Budiman Igarashi, Ikuo |
author_sort | El-Sayed, Shimaa Abd El-Salam |
collection | PubMed |
description | In this study, we designed novel truncated Babesia caballi (B. caballi) recombinant proteins from the previously used B. caballi proteins; 134-Kilodalton Protein (rBC134) and Merozoite Rhoptry 48 Protein (rBC48). Then, we evaluated the diagnostic performance of the newly designed proteins when used as a single antigen or when used as cocktail antigen consists of rBC134 full length (rBC134f) + newly designed rBC48 (rBC48t) or newly designed rBC134 (rBC134t) + rBC48t for the detection of B. caballi infection in horse using indirect enzyme-linked immunosorbent assay (iELISA). We used one dose and a half of each antigen in the cocktail formulas. The serum samples were collected from different endemic areas in addition to the sera collected from horses experimentally infected with B. caballi were used in the present study. Cocktail antigen in full dose of (rBC134f + rBC48t) exhibited the highest optical density (OD) values with B. caballi–infected sera and showed the lowest OD values with normal equine sera or B. caballi, and Theileria equi mixed infected sera in comparison with the single antigen. Interestingly, the same cocktail antigen exhibited the highest concordance rate (76.74%) and kappa value (0.79) in the screening of 200 field serum samples collected from five B. caballi endemic countries, including South Africa (n = 40), Ghana (n = 40), Mongolia (n = 40), Thailand (n = 40), and China (n = 40) using iELISA and the results were compared to those of indirect fluorescent antibody test (IFAT) as a reference. Moreover, the identified promising cocktail full dose antigen (rBC134f + rBC48t) showed that it can detect the infection as early as the 4(th) day post-infection in sera collected from experimentally infected horses. The obtained results revealed the reliability of the rBC134f + rBC48t cocktail antigen when used in full dose for the detection of specific antibodies to B. caballi in horses which will be useful for epidemiological surveys and control of equine babesiosis. |
format | Online Article Text |
id | pubmed-10104287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-101042872023-04-15 Development of a promising antigenic cocktail for the global detection of Babesia caballi in horse by ELISA El-Sayed, Shimaa Abd El-Salam Rizk, Mohamed Abdo Baghdadi, Hanadi B. Ringo, Aaron Edmond Sambuu, Gantuya Nugraha, Arifin Budiman Igarashi, Ikuo PLoS One Research Article In this study, we designed novel truncated Babesia caballi (B. caballi) recombinant proteins from the previously used B. caballi proteins; 134-Kilodalton Protein (rBC134) and Merozoite Rhoptry 48 Protein (rBC48). Then, we evaluated the diagnostic performance of the newly designed proteins when used as a single antigen or when used as cocktail antigen consists of rBC134 full length (rBC134f) + newly designed rBC48 (rBC48t) or newly designed rBC134 (rBC134t) + rBC48t for the detection of B. caballi infection in horse using indirect enzyme-linked immunosorbent assay (iELISA). We used one dose and a half of each antigen in the cocktail formulas. The serum samples were collected from different endemic areas in addition to the sera collected from horses experimentally infected with B. caballi were used in the present study. Cocktail antigen in full dose of (rBC134f + rBC48t) exhibited the highest optical density (OD) values with B. caballi–infected sera and showed the lowest OD values with normal equine sera or B. caballi, and Theileria equi mixed infected sera in comparison with the single antigen. Interestingly, the same cocktail antigen exhibited the highest concordance rate (76.74%) and kappa value (0.79) in the screening of 200 field serum samples collected from five B. caballi endemic countries, including South Africa (n = 40), Ghana (n = 40), Mongolia (n = 40), Thailand (n = 40), and China (n = 40) using iELISA and the results were compared to those of indirect fluorescent antibody test (IFAT) as a reference. Moreover, the identified promising cocktail full dose antigen (rBC134f + rBC48t) showed that it can detect the infection as early as the 4(th) day post-infection in sera collected from experimentally infected horses. The obtained results revealed the reliability of the rBC134f + rBC48t cocktail antigen when used in full dose for the detection of specific antibodies to B. caballi in horses which will be useful for epidemiological surveys and control of equine babesiosis. Public Library of Science 2023-04-14 /pmc/articles/PMC10104287/ /pubmed/37058508 http://dx.doi.org/10.1371/journal.pone.0284535 Text en © 2023 El-Sayed et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article El-Sayed, Shimaa Abd El-Salam Rizk, Mohamed Abdo Baghdadi, Hanadi B. Ringo, Aaron Edmond Sambuu, Gantuya Nugraha, Arifin Budiman Igarashi, Ikuo Development of a promising antigenic cocktail for the global detection of Babesia caballi in horse by ELISA |
title | Development of a promising antigenic cocktail for the global detection of Babesia caballi in horse by ELISA |
title_full | Development of a promising antigenic cocktail for the global detection of Babesia caballi in horse by ELISA |
title_fullStr | Development of a promising antigenic cocktail for the global detection of Babesia caballi in horse by ELISA |
title_full_unstemmed | Development of a promising antigenic cocktail for the global detection of Babesia caballi in horse by ELISA |
title_short | Development of a promising antigenic cocktail for the global detection of Babesia caballi in horse by ELISA |
title_sort | development of a promising antigenic cocktail for the global detection of babesia caballi in horse by elisa |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104287/ https://www.ncbi.nlm.nih.gov/pubmed/37058508 http://dx.doi.org/10.1371/journal.pone.0284535 |
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