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Ultrasensitive electrochemical genosensors for species-specific diagnosis of malaria
The absence of reliable species-specific diagnostic tools for malaria at point-of-care (POC) remains a major setback towards effective disease management. This is partly due to the limited sensitivity and specificity of the current malaria POC diagnostic kits especially in cases of low-density paras...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pergamon Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472471/ https://www.ncbi.nlm.nih.gov/pubmed/36225971 http://dx.doi.org/10.1016/j.electacta.2022.140988 |
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author | Ansah, Felix Krampa, Francis Donkor, Jacob K. Owusu-Appiah, Caleb Ashitei, Sarah Kornu, Victor E. Danku, Reinhard K. Chirawurah, Jersley D. Awandare, Gordon A. Aniweh, Yaw Kanyong, Prosper |
author_facet | Ansah, Felix Krampa, Francis Donkor, Jacob K. Owusu-Appiah, Caleb Ashitei, Sarah Kornu, Victor E. Danku, Reinhard K. Chirawurah, Jersley D. Awandare, Gordon A. Aniweh, Yaw Kanyong, Prosper |
author_sort | Ansah, Felix |
collection | PubMed |
description | The absence of reliable species-specific diagnostic tools for malaria at point-of-care (POC) remains a major setback towards effective disease management. This is partly due to the limited sensitivity and specificity of the current malaria POC diagnostic kits especially in cases of low-density parasitaemia and mixed species infections. In this study, we describe the first label-free DNA-based genosensors based on electrochemical impedance spectroscopy (EIS) for species-specific detection of P. falciparum, P. malariae and P. ovale. The limits of detection (LOD) for the three species-specific genosensors were down in attomolar concentrations ranging from 18.7 aM to 43.6 aM, which is below the detection limits of previously reported malaria genosensors. More importantly, the diagnostic performance of the three genosensors were compared to quantitative real-time polymerase chain reaction (qPCR) assays using purified genomic DNA and the paired whole blood lysates from clinical samples. Remarkably, all the qPCR-positive purified genomic DNA samples were correctly identified by the genosensors indicating 100% sensitivity for each of the three malaria species. The specificities of the three genosensors ranged from 66.7% to 100.0% with a Therapeutic Turnaround Time (TTAT) within 30 min, which is comparable to the TTAT of current POC diagnostic tools for malaria. This work represents a significant step towards the development of accurate and rapid species-specific nucleic acid-based toolkits for the diagnosis of malaria at the POC. |
format | Online Article Text |
id | pubmed-9472471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Pergamon Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-94724712022-10-10 Ultrasensitive electrochemical genosensors for species-specific diagnosis of malaria Ansah, Felix Krampa, Francis Donkor, Jacob K. Owusu-Appiah, Caleb Ashitei, Sarah Kornu, Victor E. Danku, Reinhard K. Chirawurah, Jersley D. Awandare, Gordon A. Aniweh, Yaw Kanyong, Prosper Electrochim Acta Article The absence of reliable species-specific diagnostic tools for malaria at point-of-care (POC) remains a major setback towards effective disease management. This is partly due to the limited sensitivity and specificity of the current malaria POC diagnostic kits especially in cases of low-density parasitaemia and mixed species infections. In this study, we describe the first label-free DNA-based genosensors based on electrochemical impedance spectroscopy (EIS) for species-specific detection of P. falciparum, P. malariae and P. ovale. The limits of detection (LOD) for the three species-specific genosensors were down in attomolar concentrations ranging from 18.7 aM to 43.6 aM, which is below the detection limits of previously reported malaria genosensors. More importantly, the diagnostic performance of the three genosensors were compared to quantitative real-time polymerase chain reaction (qPCR) assays using purified genomic DNA and the paired whole blood lysates from clinical samples. Remarkably, all the qPCR-positive purified genomic DNA samples were correctly identified by the genosensors indicating 100% sensitivity for each of the three malaria species. The specificities of the three genosensors ranged from 66.7% to 100.0% with a Therapeutic Turnaround Time (TTAT) within 30 min, which is comparable to the TTAT of current POC diagnostic tools for malaria. This work represents a significant step towards the development of accurate and rapid species-specific nucleic acid-based toolkits for the diagnosis of malaria at the POC. Pergamon Press 2022-10-10 /pmc/articles/PMC9472471/ /pubmed/36225971 http://dx.doi.org/10.1016/j.electacta.2022.140988 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ansah, Felix Krampa, Francis Donkor, Jacob K. Owusu-Appiah, Caleb Ashitei, Sarah Kornu, Victor E. Danku, Reinhard K. Chirawurah, Jersley D. Awandare, Gordon A. Aniweh, Yaw Kanyong, Prosper Ultrasensitive electrochemical genosensors for species-specific diagnosis of malaria |
title | Ultrasensitive electrochemical genosensors for species-specific diagnosis of malaria |
title_full | Ultrasensitive electrochemical genosensors for species-specific diagnosis of malaria |
title_fullStr | Ultrasensitive electrochemical genosensors for species-specific diagnosis of malaria |
title_full_unstemmed | Ultrasensitive electrochemical genosensors for species-specific diagnosis of malaria |
title_short | Ultrasensitive electrochemical genosensors for species-specific diagnosis of malaria |
title_sort | ultrasensitive electrochemical genosensors for species-specific diagnosis of malaria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472471/ https://www.ncbi.nlm.nih.gov/pubmed/36225971 http://dx.doi.org/10.1016/j.electacta.2022.140988 |
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