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Development of Indirect Competitive Enzyme-Linked Immunosorbent Assay to Detect Fusarium verticillioides in Poultry Feed Samples

Fumonisins are a group of toxic secondary metabolites that are produced by Fusarium verticillioides which are associated with poultry health hazard and great economic losses. The objective of the present study was to develop an immunological method to detect F. verticillioides in poultry feed sample...

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Autores principales: Omori, Aline Myuki, Ono, Elisabete Yurie Sataque, Hirozawa, Melissa Tiemi, de Souza Suguiura, Igor Massahiro, Hirooka, Elisa Yoko, Pelegrinelli Fungaro, Maria Helena, Ono, Mario Augusto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356808/
https://www.ncbi.nlm.nih.gov/pubmed/30658385
http://dx.doi.org/10.3390/toxins11010048
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author Omori, Aline Myuki
Ono, Elisabete Yurie Sataque
Hirozawa, Melissa Tiemi
de Souza Suguiura, Igor Massahiro
Hirooka, Elisa Yoko
Pelegrinelli Fungaro, Maria Helena
Ono, Mario Augusto
author_facet Omori, Aline Myuki
Ono, Elisabete Yurie Sataque
Hirozawa, Melissa Tiemi
de Souza Suguiura, Igor Massahiro
Hirooka, Elisa Yoko
Pelegrinelli Fungaro, Maria Helena
Ono, Mario Augusto
author_sort Omori, Aline Myuki
collection PubMed
description Fumonisins are a group of toxic secondary metabolites that are produced by Fusarium verticillioides which are associated with poultry health hazard and great economic losses. The objective of the present study was to develop an immunological method to detect F. verticillioides in poultry feed samples. An indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) based on a polyclonal antibody against 67 kDa protein of the F. verticillioides 97K exoantigen was developed to detect this fungus. Antibody anti-67 kDa protein showed cross-reactivity against F. graminearum (2–7%) and F. sporotrichioides (10%), but no or low cross-reactivity against Aspergillus sp. and Penicillium sp. exoantigens. The detection limit for the 67 kDa protein of F. verticillioides was 29 ng/mL. Eighty-one poultry feed samples were analyzed for Fusarium sp. count, 67 kDa protein of F. verticillioides and fumonisin concentrations. Eighty of the 81 feed samples (98.6%) showed Fusarium sp. contamination (mean 6.2 x 10(4) CFU/g). Mean 67 kDa protein and fumonisin concentration in the poultry feed samples was 21.0 µg/g and 1.02 µg/g, respectively. The concentration of 67 kDa protein, as determined by ic-ELISA correlated positively (p < 0.05) with fumonisin levels (r = 0.76). These results suggest that this ic-ELISA has potential to detect F. verticillioides and predict fumonisin contamination in poultry feed samples.
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spelling pubmed-63568082019-02-05 Development of Indirect Competitive Enzyme-Linked Immunosorbent Assay to Detect Fusarium verticillioides in Poultry Feed Samples Omori, Aline Myuki Ono, Elisabete Yurie Sataque Hirozawa, Melissa Tiemi de Souza Suguiura, Igor Massahiro Hirooka, Elisa Yoko Pelegrinelli Fungaro, Maria Helena Ono, Mario Augusto Toxins (Basel) Article Fumonisins are a group of toxic secondary metabolites that are produced by Fusarium verticillioides which are associated with poultry health hazard and great economic losses. The objective of the present study was to develop an immunological method to detect F. verticillioides in poultry feed samples. An indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) based on a polyclonal antibody against 67 kDa protein of the F. verticillioides 97K exoantigen was developed to detect this fungus. Antibody anti-67 kDa protein showed cross-reactivity against F. graminearum (2–7%) and F. sporotrichioides (10%), but no or low cross-reactivity against Aspergillus sp. and Penicillium sp. exoantigens. The detection limit for the 67 kDa protein of F. verticillioides was 29 ng/mL. Eighty-one poultry feed samples were analyzed for Fusarium sp. count, 67 kDa protein of F. verticillioides and fumonisin concentrations. Eighty of the 81 feed samples (98.6%) showed Fusarium sp. contamination (mean 6.2 x 10(4) CFU/g). Mean 67 kDa protein and fumonisin concentration in the poultry feed samples was 21.0 µg/g and 1.02 µg/g, respectively. The concentration of 67 kDa protein, as determined by ic-ELISA correlated positively (p < 0.05) with fumonisin levels (r = 0.76). These results suggest that this ic-ELISA has potential to detect F. verticillioides and predict fumonisin contamination in poultry feed samples. MDPI 2019-01-17 /pmc/articles/PMC6356808/ /pubmed/30658385 http://dx.doi.org/10.3390/toxins11010048 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Omori, Aline Myuki
Ono, Elisabete Yurie Sataque
Hirozawa, Melissa Tiemi
de Souza Suguiura, Igor Massahiro
Hirooka, Elisa Yoko
Pelegrinelli Fungaro, Maria Helena
Ono, Mario Augusto
Development of Indirect Competitive Enzyme-Linked Immunosorbent Assay to Detect Fusarium verticillioides in Poultry Feed Samples
title Development of Indirect Competitive Enzyme-Linked Immunosorbent Assay to Detect Fusarium verticillioides in Poultry Feed Samples
title_full Development of Indirect Competitive Enzyme-Linked Immunosorbent Assay to Detect Fusarium verticillioides in Poultry Feed Samples
title_fullStr Development of Indirect Competitive Enzyme-Linked Immunosorbent Assay to Detect Fusarium verticillioides in Poultry Feed Samples
title_full_unstemmed Development of Indirect Competitive Enzyme-Linked Immunosorbent Assay to Detect Fusarium verticillioides in Poultry Feed Samples
title_short Development of Indirect Competitive Enzyme-Linked Immunosorbent Assay to Detect Fusarium verticillioides in Poultry Feed Samples
title_sort development of indirect competitive enzyme-linked immunosorbent assay to detect fusarium verticillioides in poultry feed samples
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356808/
https://www.ncbi.nlm.nih.gov/pubmed/30658385
http://dx.doi.org/10.3390/toxins11010048
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