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Evaluation of two rapid immunochromatographic tests for diagnosis of brucellosis infection in cattle

Brucellosis is a serious infectious disease that causes significant economic losses in the livestock industry. Its early diagnosis allows an adequate disease control in cattle. DAVIH Laboratories designed a lateral flow immunochromatographic assay using protein A-colloidal gold as a detector reagent...

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Autores principales: Quintero, Anitza Fragas, Herrera, Dervel Felipe Díaz, Alfonso, Dayamí Martín, Santana, Yanelis Cruz, Torres, Raisa Betancourt, Tamayo, Lucy Montano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Faculty of Veterinary Medicine, University of Tripoli and Libyan Authority for Research, Science and Technology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060728/
https://www.ncbi.nlm.nih.gov/pubmed/30057889
http://dx.doi.org/10.4314/ovj.v8i3.2
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author Quintero, Anitza Fragas
Herrera, Dervel Felipe Díaz
Alfonso, Dayamí Martín
Santana, Yanelis Cruz
Torres, Raisa Betancourt
Tamayo, Lucy Montano
author_facet Quintero, Anitza Fragas
Herrera, Dervel Felipe Díaz
Alfonso, Dayamí Martín
Santana, Yanelis Cruz
Torres, Raisa Betancourt
Tamayo, Lucy Montano
author_sort Quintero, Anitza Fragas
collection PubMed
description Brucellosis is a serious infectious disease that causes significant economic losses in the livestock industry. Its early diagnosis allows an adequate disease control in cattle. DAVIH Laboratories designed a lateral flow immunochromatographic assay using protein A-colloidal gold as a detector reagent (LFIA-PA). The objective of this work was to compare the performance of this assay using protein G-colloidal gold (LFIA-PG) with its performance using protein A-colloidal gold as the detector reagent. The assays were carried out with 20 μL of serum and 130 μL of running buffer. Interpretation of bands was by visual inspection with the naked eye at 15- 20 minutes after sample application. The tests were evaluated with 449 samples of bovine serum (111 positive and 338 negative). The diagnostic sensitivity and specificity, the positive and negative predictive values, and the efficacy of both assays were calculated, and their concordance was estimated by calculating the kappa (k) index. The estimated values of the parameters for LFIA-PG and LFPIA-PA were 100% and 95.2% of diagnostic sensitivity, 96.2% and 97.3% of diagnostic specificity, 89.5% and 92.3% for the positive predictive value, 100% and 98.5% for the negative predictive value, and 97.1% and 96.89% of efficacy, respectively. The concordance between both tests was very good (k = 0.95). It was shown the possibilities of developing a system with LFIA-PG capable of detecting antibodies against Brucella spp. The performance of the test makes possible its use as a screening method in the diagnosis of brucellosis.
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spelling pubmed-60607282018-07-27 Evaluation of two rapid immunochromatographic tests for diagnosis of brucellosis infection in cattle Quintero, Anitza Fragas Herrera, Dervel Felipe Díaz Alfonso, Dayamí Martín Santana, Yanelis Cruz Torres, Raisa Betancourt Tamayo, Lucy Montano Open Vet J Original Article Brucellosis is a serious infectious disease that causes significant economic losses in the livestock industry. Its early diagnosis allows an adequate disease control in cattle. DAVIH Laboratories designed a lateral flow immunochromatographic assay using protein A-colloidal gold as a detector reagent (LFIA-PA). The objective of this work was to compare the performance of this assay using protein G-colloidal gold (LFIA-PG) with its performance using protein A-colloidal gold as the detector reagent. The assays were carried out with 20 μL of serum and 130 μL of running buffer. Interpretation of bands was by visual inspection with the naked eye at 15- 20 minutes after sample application. The tests were evaluated with 449 samples of bovine serum (111 positive and 338 negative). The diagnostic sensitivity and specificity, the positive and negative predictive values, and the efficacy of both assays were calculated, and their concordance was estimated by calculating the kappa (k) index. The estimated values of the parameters for LFIA-PG and LFPIA-PA were 100% and 95.2% of diagnostic sensitivity, 96.2% and 97.3% of diagnostic specificity, 89.5% and 92.3% for the positive predictive value, 100% and 98.5% for the negative predictive value, and 97.1% and 96.89% of efficacy, respectively. The concordance between both tests was very good (k = 0.95). It was shown the possibilities of developing a system with LFIA-PG capable of detecting antibodies against Brucella spp. The performance of the test makes possible its use as a screening method in the diagnosis of brucellosis. Faculty of Veterinary Medicine, University of Tripoli and Libyan Authority for Research, Science and Technology 2018 2018-07-07 /pmc/articles/PMC6060728/ /pubmed/30057889 http://dx.doi.org/10.4314/ovj.v8i3.2 Text en Copyright: © Open Veterinary Journal http://creativecommons.org/licenses/by-nc-sa/4.0 Open Veterinary Journal is licensed under a Creative Commons Attribution 4.0 International License.
spellingShingle Original Article
Quintero, Anitza Fragas
Herrera, Dervel Felipe Díaz
Alfonso, Dayamí Martín
Santana, Yanelis Cruz
Torres, Raisa Betancourt
Tamayo, Lucy Montano
Evaluation of two rapid immunochromatographic tests for diagnosis of brucellosis infection in cattle
title Evaluation of two rapid immunochromatographic tests for diagnosis of brucellosis infection in cattle
title_full Evaluation of two rapid immunochromatographic tests for diagnosis of brucellosis infection in cattle
title_fullStr Evaluation of two rapid immunochromatographic tests for diagnosis of brucellosis infection in cattle
title_full_unstemmed Evaluation of two rapid immunochromatographic tests for diagnosis of brucellosis infection in cattle
title_short Evaluation of two rapid immunochromatographic tests for diagnosis of brucellosis infection in cattle
title_sort evaluation of two rapid immunochromatographic tests for diagnosis of brucellosis infection in cattle
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060728/
https://www.ncbi.nlm.nih.gov/pubmed/30057889
http://dx.doi.org/10.4314/ovj.v8i3.2
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