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Development and Evaluation of a Latex Agglutination Test for the Identification of Francisella tularensis Subspecies Pathogenic for Human
Francisella tularensis are highly infectious bacteria causing a zoonotic disease called tularemia. Identification of this bacterium is based on antigen detection or PCR. The paper presents a latex agglutination test (LAT) for rapid identification of clinically relevant F. tularensis subspecies. The...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Exeley Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7256844/ https://www.ncbi.nlm.nih.gov/pubmed/30015465 http://dx.doi.org/10.21307/pjm-2018-030 |
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author | RASTAWICKI, WALDEMAR FORMIŃSKA, KAMILA ZASADA, ALEKSANDRA A. |
author_facet | RASTAWICKI, WALDEMAR FORMIŃSKA, KAMILA ZASADA, ALEKSANDRA A. |
author_sort | RASTAWICKI, WALDEMAR |
collection | PubMed |
description | Francisella tularensis are highly infectious bacteria causing a zoonotic disease called tularemia. Identification of this bacterium is based on antigen detection or PCR. The paper presents a latex agglutination test (LAT) for rapid identification of clinically relevant F. tularensis subspecies. The test can be performed within three minutes with live or inactivated bacteria. The possibility to test the inactivated samples reduces the risk of laboratory acquired infection and allows performing the test under BSL-2 conditions. |
format | Online Article Text |
id | pubmed-7256844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Exeley Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72568442020-06-03 Development and Evaluation of a Latex Agglutination Test for the Identification of Francisella tularensis Subspecies Pathogenic for Human RASTAWICKI, WALDEMAR FORMIŃSKA, KAMILA ZASADA, ALEKSANDRA A. Pol J Microbiol Microbiology Francisella tularensis are highly infectious bacteria causing a zoonotic disease called tularemia. Identification of this bacterium is based on antigen detection or PCR. The paper presents a latex agglutination test (LAT) for rapid identification of clinically relevant F. tularensis subspecies. The test can be performed within three minutes with live or inactivated bacteria. The possibility to test the inactivated samples reduces the risk of laboratory acquired infection and allows performing the test under BSL-2 conditions. Exeley Inc. 2018-06 2018-06-30 /pmc/articles/PMC7256844/ /pubmed/30015465 http://dx.doi.org/10.21307/pjm-2018-030 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Microbiology RASTAWICKI, WALDEMAR FORMIŃSKA, KAMILA ZASADA, ALEKSANDRA A. Development and Evaluation of a Latex Agglutination Test for the Identification of Francisella tularensis Subspecies Pathogenic for Human |
title | Development and Evaluation of a Latex Agglutination Test for the Identification of Francisella tularensis Subspecies Pathogenic for Human |
title_full | Development and Evaluation of a Latex Agglutination Test for the Identification of Francisella tularensis Subspecies Pathogenic for Human |
title_fullStr | Development and Evaluation of a Latex Agglutination Test for the Identification of Francisella tularensis Subspecies Pathogenic for Human |
title_full_unstemmed | Development and Evaluation of a Latex Agglutination Test for the Identification of Francisella tularensis Subspecies Pathogenic for Human |
title_short | Development and Evaluation of a Latex Agglutination Test for the Identification of Francisella tularensis Subspecies Pathogenic for Human |
title_sort | development and evaluation of a latex agglutination test for the identification of francisella tularensis subspecies pathogenic for human |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7256844/ https://www.ncbi.nlm.nih.gov/pubmed/30015465 http://dx.doi.org/10.21307/pjm-2018-030 |
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