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Truenat™ - micro real-time-polymerase chain reaction for rapid diagnosis of leptospirosis at minimal resource settings
BACKGROUND & OBJECTIVES: The biological spectrum of leptospirosis ranges from acute undifferentiated febrile illness to severe fatal syndrome or a combination of syndromes. Diagnosis on clinical grounds alone is difficult and depends on laboratory support. However, no confirmatory tests are avai...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8715686/ https://www.ncbi.nlm.nih.gov/pubmed/34782537 http://dx.doi.org/10.4103/ijmr.IJMR_2539_20 |
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author | Rajamani, M. Maile, Anwesh Sugunan, A.P. Vijayachari, P. |
author_facet | Rajamani, M. Maile, Anwesh Sugunan, A.P. Vijayachari, P. |
author_sort | Rajamani, M. |
collection | PubMed |
description | BACKGROUND & OBJECTIVES: The biological spectrum of leptospirosis ranges from acute undifferentiated febrile illness to severe fatal syndrome or a combination of syndromes. Diagnosis on clinical grounds alone is difficult and depends on laboratory support. However, no confirmatory tests are available, which is rapid and can be performed with minimum facilities available. The objectives of this study were to evaluate the diagnostic utility, accuracy and reproducibility of a rapid real time-PCR based method (Truenat™) for early diagnosis of leptospirosis, and its usage in low resource settings. METHODS: The Truenat™ test was performed using plasma sample collected from confirmed patients and controls. DNA was extracted from plasma samples and the reaction was performed as per the manufacturer’s instructions. Leptospiral isolates were also used to assess the performance using different serovars. RESULTS: Evaluation of the Truenat™ test with RT-PCR as the gold standard showed that Truenat™ had a sensitivity of 97.4 per cent and a specificity of 98.6 per cent. The overall agreement with RT-PCR was 98.2 per cent. INTERPRETATION & CONCLUSIONS: Our results showed that the test would be a useful tool for early diagnosis of leptospirosis in settings with minimal facilities and the test results could be obtained within an hour. This indicates that a specific therapy can be instituted during the early phase of the disease even at peripheral healthcare facilities as well during the outbreaks. |
format | Online Article Text |
id | pubmed-8715686 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-87156862022-01-14 Truenat™ - micro real-time-polymerase chain reaction for rapid diagnosis of leptospirosis at minimal resource settings Rajamani, M. Maile, Anwesh Sugunan, A.P. Vijayachari, P. Indian J Med Res Original Article BACKGROUND & OBJECTIVES: The biological spectrum of leptospirosis ranges from acute undifferentiated febrile illness to severe fatal syndrome or a combination of syndromes. Diagnosis on clinical grounds alone is difficult and depends on laboratory support. However, no confirmatory tests are available, which is rapid and can be performed with minimum facilities available. The objectives of this study were to evaluate the diagnostic utility, accuracy and reproducibility of a rapid real time-PCR based method (Truenat™) for early diagnosis of leptospirosis, and its usage in low resource settings. METHODS: The Truenat™ test was performed using plasma sample collected from confirmed patients and controls. DNA was extracted from plasma samples and the reaction was performed as per the manufacturer’s instructions. Leptospiral isolates were also used to assess the performance using different serovars. RESULTS: Evaluation of the Truenat™ test with RT-PCR as the gold standard showed that Truenat™ had a sensitivity of 97.4 per cent and a specificity of 98.6 per cent. The overall agreement with RT-PCR was 98.2 per cent. INTERPRETATION & CONCLUSIONS: Our results showed that the test would be a useful tool for early diagnosis of leptospirosis in settings with minimal facilities and the test results could be obtained within an hour. This indicates that a specific therapy can be instituted during the early phase of the disease even at peripheral healthcare facilities as well during the outbreaks. Wolters Kluwer - Medknow 2021-07 /pmc/articles/PMC8715686/ /pubmed/34782537 http://dx.doi.org/10.4103/ijmr.IJMR_2539_20 Text en Copyright: © 2021 Indian Journal of Medical Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Rajamani, M. Maile, Anwesh Sugunan, A.P. Vijayachari, P. Truenat™ - micro real-time-polymerase chain reaction for rapid diagnosis of leptospirosis at minimal resource settings |
title | Truenat™ - micro real-time-polymerase chain reaction for rapid diagnosis of leptospirosis at minimal resource settings |
title_full | Truenat™ - micro real-time-polymerase chain reaction for rapid diagnosis of leptospirosis at minimal resource settings |
title_fullStr | Truenat™ - micro real-time-polymerase chain reaction for rapid diagnosis of leptospirosis at minimal resource settings |
title_full_unstemmed | Truenat™ - micro real-time-polymerase chain reaction for rapid diagnosis of leptospirosis at minimal resource settings |
title_short | Truenat™ - micro real-time-polymerase chain reaction for rapid diagnosis of leptospirosis at minimal resource settings |
title_sort | truenat™ - micro real-time-polymerase chain reaction for rapid diagnosis of leptospirosis at minimal resource settings |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8715686/ https://www.ncbi.nlm.nih.gov/pubmed/34782537 http://dx.doi.org/10.4103/ijmr.IJMR_2539_20 |
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