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Detection of Staphylococcus Enterotoxin B (SEB) Using an Immunochromatographic Test Strip

BACKGROUND: Staphylococcus aureus is one of the most important microorganisms that causes various human diseases by secreting virulence factors known as staphylococcal super antigens (SAgs). Staphylococcal Enterotoxin B (SEB) is a bacterial antigen that is responsible for food poisoning in humans. A...

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Autores principales: Gholamzad, Mehrdad, Khatami, Mohammad Reza, Ghassemi, Soheil, Vaise Malekshahi, Ziba, Shooshtari, Mohammad Barat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4609312/
https://www.ncbi.nlm.nih.gov/pubmed/26495113
http://dx.doi.org/10.5812/jjm.26793
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author Gholamzad, Mehrdad
Khatami, Mohammad Reza
Ghassemi, Soheil
Vaise Malekshahi, Ziba
Shooshtari, Mohammad Barat
author_facet Gholamzad, Mehrdad
Khatami, Mohammad Reza
Ghassemi, Soheil
Vaise Malekshahi, Ziba
Shooshtari, Mohammad Barat
author_sort Gholamzad, Mehrdad
collection PubMed
description BACKGROUND: Staphylococcus aureus is one of the most important microorganisms that causes various human diseases by secreting virulence factors known as staphylococcal super antigens (SAgs). Staphylococcal Enterotoxin B (SEB) is a bacterial antigen that is responsible for food poisoning in humans. Among SEB detection methods, a lateral flow device (LFD) is ideal for rapid immunochromatographic tests because it is easy to use, requires minimal time to produce results, and does not require personnel training. OBJECTIVES: In our laboratory, the production of an immunochromatographic test strip, for the detection of SEB using a sandwich assay and a competitive method, was described; the test can detect SEB with high sensitivity. MATERIALS AND METHODS: The strip assays were compared with PCR, a valid method for detection. For PCR, a specific sequence for SEB production was detected using primers designed according to GenBank sequences. RESULTS: In total, 80 food samples suspected of SEB contamination were assessed using the two methods. Fifty-four samples were contaminated based on the PCR technique and twenty-six of those were confirmed using the strip assay. CONCLUSIONS: The sensitivity of the sandwich method was approximately 10 ng/mL and that of the competitive method was approximately 250 ng/mL. In the LFD, a highly specific monoclonal antibody used for both the sandwich and competitive methods resulted in an increased sensitivity and accuracy for the detection of a minimal SEB concentration.
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spelling pubmed-46093122015-10-22 Detection of Staphylococcus Enterotoxin B (SEB) Using an Immunochromatographic Test Strip Gholamzad, Mehrdad Khatami, Mohammad Reza Ghassemi, Soheil Vaise Malekshahi, Ziba Shooshtari, Mohammad Barat Jundishapur J Microbiol Research Article BACKGROUND: Staphylococcus aureus is one of the most important microorganisms that causes various human diseases by secreting virulence factors known as staphylococcal super antigens (SAgs). Staphylococcal Enterotoxin B (SEB) is a bacterial antigen that is responsible for food poisoning in humans. Among SEB detection methods, a lateral flow device (LFD) is ideal for rapid immunochromatographic tests because it is easy to use, requires minimal time to produce results, and does not require personnel training. OBJECTIVES: In our laboratory, the production of an immunochromatographic test strip, for the detection of SEB using a sandwich assay and a competitive method, was described; the test can detect SEB with high sensitivity. MATERIALS AND METHODS: The strip assays were compared with PCR, a valid method for detection. For PCR, a specific sequence for SEB production was detected using primers designed according to GenBank sequences. RESULTS: In total, 80 food samples suspected of SEB contamination were assessed using the two methods. Fifty-four samples were contaminated based on the PCR technique and twenty-six of those were confirmed using the strip assay. CONCLUSIONS: The sensitivity of the sandwich method was approximately 10 ng/mL and that of the competitive method was approximately 250 ng/mL. In the LFD, a highly specific monoclonal antibody used for both the sandwich and competitive methods resulted in an increased sensitivity and accuracy for the detection of a minimal SEB concentration. Kowsar 2015-09-08 /pmc/articles/PMC4609312/ /pubmed/26495113 http://dx.doi.org/10.5812/jjm.26793 Text en Copyright © 2015, Ahvaz Jundishapur University of Medical Sciences. http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Research Article
Gholamzad, Mehrdad
Khatami, Mohammad Reza
Ghassemi, Soheil
Vaise Malekshahi, Ziba
Shooshtari, Mohammad Barat
Detection of Staphylococcus Enterotoxin B (SEB) Using an Immunochromatographic Test Strip
title Detection of Staphylococcus Enterotoxin B (SEB) Using an Immunochromatographic Test Strip
title_full Detection of Staphylococcus Enterotoxin B (SEB) Using an Immunochromatographic Test Strip
title_fullStr Detection of Staphylococcus Enterotoxin B (SEB) Using an Immunochromatographic Test Strip
title_full_unstemmed Detection of Staphylococcus Enterotoxin B (SEB) Using an Immunochromatographic Test Strip
title_short Detection of Staphylococcus Enterotoxin B (SEB) Using an Immunochromatographic Test Strip
title_sort detection of staphylococcus enterotoxin b (seb) using an immunochromatographic test strip
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4609312/
https://www.ncbi.nlm.nih.gov/pubmed/26495113
http://dx.doi.org/10.5812/jjm.26793
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