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Optimizing the microscopic agglutination test (MAT) panel for the diagnosis of Leptospirosis in a low resource, hyper-endemic setting with varied microgeographic variation in reactivity
The microscopic agglutination test (MAT) is the standard serological reference test for the diagnosis of leptospirosis, despite being a technically demanding and laborious procedure. The use of a locally optimised MAT panel is considered essential for proper performance and interpretation of results...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8279374/ https://www.ncbi.nlm.nih.gov/pubmed/34197457 http://dx.doi.org/10.1371/journal.pntd.0009565 |
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author | Jayasundara, Dinesha Gamage, Chandika Senavirathna, Indika Warnasekara, Janith Matthias, Michael A. Vinetz, Joseph M. Agampodi, Suneth |
author_facet | Jayasundara, Dinesha Gamage, Chandika Senavirathna, Indika Warnasekara, Janith Matthias, Michael A. Vinetz, Joseph M. Agampodi, Suneth |
author_sort | Jayasundara, Dinesha |
collection | PubMed |
description | The microscopic agglutination test (MAT) is the standard serological reference test for the diagnosis of leptospirosis, despite being a technically demanding and laborious procedure. The use of a locally optimised MAT panel is considered essential for proper performance and interpretation of results. This paper describes the procedure of selecting such an optimised panel for Sri Lanka, a country hyper-endemic for leptospirosis. MAT was performed using 24 strains on 1132 serum samples collected from patients presenting with acute undifferentiated fever. Of 24 strains, 15 were selected as the optimised panel, while only 11% of serum samples showed positivity. A geographical variation in predominantly reactive serovars was observed, whereas reactivity was low with the saprophytic strain Patoc. Testing with paired sera yielded a higher sensitivity but provided only a retrospective diagnosis. Serological tests based on ELISA with complementary molecular diagnosis using PCR are a feasible and robust alternative approach to diagnose leptospirosis in countries having a higher burden of the disease. |
format | Online Article Text |
id | pubmed-8279374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-82793742021-07-26 Optimizing the microscopic agglutination test (MAT) panel for the diagnosis of Leptospirosis in a low resource, hyper-endemic setting with varied microgeographic variation in reactivity Jayasundara, Dinesha Gamage, Chandika Senavirathna, Indika Warnasekara, Janith Matthias, Michael A. Vinetz, Joseph M. Agampodi, Suneth PLoS Negl Trop Dis Research Article The microscopic agglutination test (MAT) is the standard serological reference test for the diagnosis of leptospirosis, despite being a technically demanding and laborious procedure. The use of a locally optimised MAT panel is considered essential for proper performance and interpretation of results. This paper describes the procedure of selecting such an optimised panel for Sri Lanka, a country hyper-endemic for leptospirosis. MAT was performed using 24 strains on 1132 serum samples collected from patients presenting with acute undifferentiated fever. Of 24 strains, 15 were selected as the optimised panel, while only 11% of serum samples showed positivity. A geographical variation in predominantly reactive serovars was observed, whereas reactivity was low with the saprophytic strain Patoc. Testing with paired sera yielded a higher sensitivity but provided only a retrospective diagnosis. Serological tests based on ELISA with complementary molecular diagnosis using PCR are a feasible and robust alternative approach to diagnose leptospirosis in countries having a higher burden of the disease. Public Library of Science 2021-07-01 /pmc/articles/PMC8279374/ /pubmed/34197457 http://dx.doi.org/10.1371/journal.pntd.0009565 Text en © 2021 Jayasundara et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Jayasundara, Dinesha Gamage, Chandika Senavirathna, Indika Warnasekara, Janith Matthias, Michael A. Vinetz, Joseph M. Agampodi, Suneth Optimizing the microscopic agglutination test (MAT) panel for the diagnosis of Leptospirosis in a low resource, hyper-endemic setting with varied microgeographic variation in reactivity |
title | Optimizing the microscopic agglutination test (MAT) panel for the diagnosis of Leptospirosis in a low resource, hyper-endemic setting with varied microgeographic variation in reactivity |
title_full | Optimizing the microscopic agglutination test (MAT) panel for the diagnosis of Leptospirosis in a low resource, hyper-endemic setting with varied microgeographic variation in reactivity |
title_fullStr | Optimizing the microscopic agglutination test (MAT) panel for the diagnosis of Leptospirosis in a low resource, hyper-endemic setting with varied microgeographic variation in reactivity |
title_full_unstemmed | Optimizing the microscopic agglutination test (MAT) panel for the diagnosis of Leptospirosis in a low resource, hyper-endemic setting with varied microgeographic variation in reactivity |
title_short | Optimizing the microscopic agglutination test (MAT) panel for the diagnosis of Leptospirosis in a low resource, hyper-endemic setting with varied microgeographic variation in reactivity |
title_sort | optimizing the microscopic agglutination test (mat) panel for the diagnosis of leptospirosis in a low resource, hyper-endemic setting with varied microgeographic variation in reactivity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8279374/ https://www.ncbi.nlm.nih.gov/pubmed/34197457 http://dx.doi.org/10.1371/journal.pntd.0009565 |
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