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Immunoassay for Capsular Antigen of Bacillus anthracis Enables Rapid Diagnosis in a Rabbit Model of Inhalational Anthrax

Inhalational anthrax is a serious biothreat. Effective antibiotic treatment of inhalational anthrax requires early diagnosis; the further the disease has progressed, the less the likelihood for cure. Current means for diagnosis such as blood culture require several days to a result and require advan...

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Autores principales: Gates-Hollingsworth, Marcellene A., Perry, Mark R., Chen, Hongjing, Needham, James, Houghton, Raymond L., Raychaudhuri, Syamal, Hubbard, Mark A., Kozel, Thomas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4420260/
https://www.ncbi.nlm.nih.gov/pubmed/25942409
http://dx.doi.org/10.1371/journal.pone.0126304
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author Gates-Hollingsworth, Marcellene A.
Perry, Mark R.
Chen, Hongjing
Needham, James
Houghton, Raymond L.
Raychaudhuri, Syamal
Hubbard, Mark A.
Kozel, Thomas R.
author_facet Gates-Hollingsworth, Marcellene A.
Perry, Mark R.
Chen, Hongjing
Needham, James
Houghton, Raymond L.
Raychaudhuri, Syamal
Hubbard, Mark A.
Kozel, Thomas R.
author_sort Gates-Hollingsworth, Marcellene A.
collection PubMed
description Inhalational anthrax is a serious biothreat. Effective antibiotic treatment of inhalational anthrax requires early diagnosis; the further the disease has progressed, the less the likelihood for cure. Current means for diagnosis such as blood culture require several days to a result and require advanced laboratory infrastructure. An alternative approach to diagnosis is detection of a Bacillus anthracis antigen that is shed into blood and can be detected by rapid immunoassay. The goal of the study was to evaluate detection of poly-γ-D-glutamic acid (PGA), the capsular antigen of B. anthracis, as a biomarker surrogate for blood culture in a rabbit model of inhalational anthrax. The mean time to a positive blood culture was 26 ± 5.7 h (mean ± standard deviation), whereas the mean time to a positive ELISA was 22 ± 4.2 h; P = 0.005 in comparison with blood culture. A lateral flow immunoassay was constructed for detection of PGA in plasma at concentrations of less than 1 ng PGA/ml. Use of the lateral flow immunoassay for detection of PGA in the rabbit model found that antigen was detected somewhat earlier than the earliest time point at which the blood culture became positive. The low cost, ease of use, and rapid time to result of the lateral flow immunoassay format make an immunoassay for PGA a viable surrogate for blood culture for detection of infection in individuals who have a likelihood of exposure to B. anthracis.
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spelling pubmed-44202602015-05-12 Immunoassay for Capsular Antigen of Bacillus anthracis Enables Rapid Diagnosis in a Rabbit Model of Inhalational Anthrax Gates-Hollingsworth, Marcellene A. Perry, Mark R. Chen, Hongjing Needham, James Houghton, Raymond L. Raychaudhuri, Syamal Hubbard, Mark A. Kozel, Thomas R. PLoS One Research Article Inhalational anthrax is a serious biothreat. Effective antibiotic treatment of inhalational anthrax requires early diagnosis; the further the disease has progressed, the less the likelihood for cure. Current means for diagnosis such as blood culture require several days to a result and require advanced laboratory infrastructure. An alternative approach to diagnosis is detection of a Bacillus anthracis antigen that is shed into blood and can be detected by rapid immunoassay. The goal of the study was to evaluate detection of poly-γ-D-glutamic acid (PGA), the capsular antigen of B. anthracis, as a biomarker surrogate for blood culture in a rabbit model of inhalational anthrax. The mean time to a positive blood culture was 26 ± 5.7 h (mean ± standard deviation), whereas the mean time to a positive ELISA was 22 ± 4.2 h; P = 0.005 in comparison with blood culture. A lateral flow immunoassay was constructed for detection of PGA in plasma at concentrations of less than 1 ng PGA/ml. Use of the lateral flow immunoassay for detection of PGA in the rabbit model found that antigen was detected somewhat earlier than the earliest time point at which the blood culture became positive. The low cost, ease of use, and rapid time to result of the lateral flow immunoassay format make an immunoassay for PGA a viable surrogate for blood culture for detection of infection in individuals who have a likelihood of exposure to B. anthracis. Public Library of Science 2015-05-05 /pmc/articles/PMC4420260/ /pubmed/25942409 http://dx.doi.org/10.1371/journal.pone.0126304 Text en © 2015 Gates-Hollingsworth et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gates-Hollingsworth, Marcellene A.
Perry, Mark R.
Chen, Hongjing
Needham, James
Houghton, Raymond L.
Raychaudhuri, Syamal
Hubbard, Mark A.
Kozel, Thomas R.
Immunoassay for Capsular Antigen of Bacillus anthracis Enables Rapid Diagnosis in a Rabbit Model of Inhalational Anthrax
title Immunoassay for Capsular Antigen of Bacillus anthracis Enables Rapid Diagnosis in a Rabbit Model of Inhalational Anthrax
title_full Immunoassay for Capsular Antigen of Bacillus anthracis Enables Rapid Diagnosis in a Rabbit Model of Inhalational Anthrax
title_fullStr Immunoassay for Capsular Antigen of Bacillus anthracis Enables Rapid Diagnosis in a Rabbit Model of Inhalational Anthrax
title_full_unstemmed Immunoassay for Capsular Antigen of Bacillus anthracis Enables Rapid Diagnosis in a Rabbit Model of Inhalational Anthrax
title_short Immunoassay for Capsular Antigen of Bacillus anthracis Enables Rapid Diagnosis in a Rabbit Model of Inhalational Anthrax
title_sort immunoassay for capsular antigen of bacillus anthracis enables rapid diagnosis in a rabbit model of inhalational anthrax
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4420260/
https://www.ncbi.nlm.nih.gov/pubmed/25942409
http://dx.doi.org/10.1371/journal.pone.0126304
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