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The cyanobacterial lectin, microvirin-N, enhances the specificity and sensitivity of lipoarabinomannan-based TB diagnostic tests
Tuberculosis (TB) is one of the top ten causes of death globally, despite being treatable. The eradication of TB disease requires, amongst others, diagnostic tests with high specificity and sensitivity that will work at the point of care (POC) in low-resource settings. The TB surface glycolipid anti...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8374243/ https://www.ncbi.nlm.nih.gov/pubmed/33367346 http://dx.doi.org/10.1039/d0an01725f |
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author | van der Horst, Megan Karamchand, Leshern Bauer, Westley S. Nel, Andrew J. M. Blackburn, Jonathan M. Wright, David W. |
author_facet | van der Horst, Megan Karamchand, Leshern Bauer, Westley S. Nel, Andrew J. M. Blackburn, Jonathan M. Wright, David W. |
author_sort | van der Horst, Megan |
collection | PubMed |
description | Tuberculosis (TB) is one of the top ten causes of death globally, despite being treatable. The eradication of TB disease requires, amongst others, diagnostic tests with high specificity and sensitivity that will work at the point of care (POC) in low-resource settings. The TB surface glycolipid antigen, mannose-capped lipoarabinomannan (ManLAM) currently serves as the only POC molecular diagnostic biomarker suitable for use in low cost immunoassays. Here, we demonstrate the high affinity and exceptional specificity of microvirin-N (MVN), a 14.3 kDa cyanobacterial lectin, toward H37Rv TB ManLAM and utilize it to develop a novel on-bead ELISA. MVN binds to ManLAM with sub-picomolar binding affinity, but does not bind to other variants of LAM expressed by non-pathogenic mycobacteria – a level of binding specificity and affinity that current commercially available anti-LAM antibodies cannot achieve. An on-bead ELISA was subsequently developed using MVN-functionalized magnetic beads which allows for the specific capture of ManLAM from human urine with a limit of detection (LOD) of 1.14 ng mL(−1) and no cross-reactivity when tested with PILAM, a variant of LAM found on non-pathogenic mycobacteria. |
format | Online Article Text |
id | pubmed-8374243 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-83742432021-09-01 The cyanobacterial lectin, microvirin-N, enhances the specificity and sensitivity of lipoarabinomannan-based TB diagnostic tests van der Horst, Megan Karamchand, Leshern Bauer, Westley S. Nel, Andrew J. M. Blackburn, Jonathan M. Wright, David W. Analyst Chemistry Tuberculosis (TB) is one of the top ten causes of death globally, despite being treatable. The eradication of TB disease requires, amongst others, diagnostic tests with high specificity and sensitivity that will work at the point of care (POC) in low-resource settings. The TB surface glycolipid antigen, mannose-capped lipoarabinomannan (ManLAM) currently serves as the only POC molecular diagnostic biomarker suitable for use in low cost immunoassays. Here, we demonstrate the high affinity and exceptional specificity of microvirin-N (MVN), a 14.3 kDa cyanobacterial lectin, toward H37Rv TB ManLAM and utilize it to develop a novel on-bead ELISA. MVN binds to ManLAM with sub-picomolar binding affinity, but does not bind to other variants of LAM expressed by non-pathogenic mycobacteria – a level of binding specificity and affinity that current commercially available anti-LAM antibodies cannot achieve. An on-bead ELISA was subsequently developed using MVN-functionalized magnetic beads which allows for the specific capture of ManLAM from human urine with a limit of detection (LOD) of 1.14 ng mL(−1) and no cross-reactivity when tested with PILAM, a variant of LAM found on non-pathogenic mycobacteria. The Royal Society of Chemistry 2020-12-24 /pmc/articles/PMC8374243/ /pubmed/33367346 http://dx.doi.org/10.1039/d0an01725f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry van der Horst, Megan Karamchand, Leshern Bauer, Westley S. Nel, Andrew J. M. Blackburn, Jonathan M. Wright, David W. The cyanobacterial lectin, microvirin-N, enhances the specificity and sensitivity of lipoarabinomannan-based TB diagnostic tests |
title | The cyanobacterial lectin, microvirin-N, enhances the specificity and sensitivity of lipoarabinomannan-based TB diagnostic tests |
title_full | The cyanobacterial lectin, microvirin-N, enhances the specificity and sensitivity of lipoarabinomannan-based TB diagnostic tests |
title_fullStr | The cyanobacterial lectin, microvirin-N, enhances the specificity and sensitivity of lipoarabinomannan-based TB diagnostic tests |
title_full_unstemmed | The cyanobacterial lectin, microvirin-N, enhances the specificity and sensitivity of lipoarabinomannan-based TB diagnostic tests |
title_short | The cyanobacterial lectin, microvirin-N, enhances the specificity and sensitivity of lipoarabinomannan-based TB diagnostic tests |
title_sort | cyanobacterial lectin, microvirin-n, enhances the specificity and sensitivity of lipoarabinomannan-based tb diagnostic tests |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8374243/ https://www.ncbi.nlm.nih.gov/pubmed/33367346 http://dx.doi.org/10.1039/d0an01725f |
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