Show simple item record

dc.contributor.authorThornton, CR
dc.contributor.authorDavies, GE
dc.contributor.authorDougherty, L
dc.date.accessioned2023-12-08T12:53:49Z
dc.date.issued2023-12-08
dc.date.updated2023-12-08T10:32:08Z
dc.description.abstractMucoromycosis is a highly aggressive angio-invasive disease of humans caused by fungi in the zygomycete order, Mucorales. While Rhizopus arrhizus is the principal agent of mucoromycosis, other Mucorales fungi including Apophysomyces, Cunninghamella, Lichtheimia, Mucor, Rhizomucor and Syncephalastrum are able to cause life-threatening rhino-orbital-cerebral, pulmonary, gastro-intestinal and necrotising cutaneous infections in humans. Diagnosis of the disease currently relies on non-specific CT, lengthy and insensitive culture from invasive biopsy, and time-consuming histopathology of tissue samples. At present, there are no rapid antigen tests that detect Mucorales-specific biomarkers of infection, and which allow point-of-care diagnosis of mucoromycosis. Here, we report the development of an IgG2b monoclonal antibody (mAb), TG11, which binds to extracellular polysaccharide (EPS) antigens of between 20 kDa and 250 kDa secreted during hyphal growth of Mucorales fungi. The mAb is Mucorales-specific and does not cross-react with other yeasts and molds of clinical importance including Aspergillus, Candida, Cryptococcus, Fusarium, Lomentospora and Scedosporium species. Using the mAb, we have developed a Competitive lateral-flow device that allows rapid (30 min) detection of the EPS biomarker in human serum and bronchoalveolar lavage (BAL), with a limit of detection (LOD) in human serum of ~100 ng/mL serum (~224.7 pmol/L serum). The LFD therefore provides a potential novel opportunity for detection of mucoromycosis caused by different Mucorales species.en_GB
dc.description.sponsorshipISCA Diagnostics Ltd.en_GB
dc.identifier.citationVol. 13, article 1305662en_GB
dc.identifier.doihttps://doi.org/10.3389/fcimb.2023.1305662
dc.identifier.urihttp://hdl.handle.net/10871/134752
dc.identifierORCID: 0000-0001-6213-3130 (Thornton, Christopher R)
dc.language.isoenen_GB
dc.publisherFrontiers Mediaen_GB
dc.rights© 2023 Thornton, Davies and Dougherty. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.en_GB
dc.subjectMucoralesen_GB
dc.subjectmucoromycosisen_GB
dc.subjectmonoclonal antibodyen_GB
dc.subjectbiomarkeren_GB
dc.subjectlateral-flow testen_GB
dc.titleDevelopment of a monoclonal antibody and a lateral-flow device for the rapid detection of a Mucorales-specific biomarkeren_GB
dc.typeArticleen_GB
dc.date.available2023-12-08T12:53:49Z
dc.identifier.issn2235-2988
exeter.article-number1305662
dc.descriptionThis is the final version. Available on open access from Frontiers Media via the DOI in this recorden_GB
dc.descriptionData availability statement: The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.en_GB
dc.identifier.journalFrontiers in Cellular and Infection Microbiologyen_GB
dc.relation.ispartofFrontiers in Cellular and Infection Microbiology, 13
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2023-11-20
dcterms.dateSubmitted2023-10-02
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2023-12-08
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2023-12-08T10:32:10Z
refterms.versionFCDAM
refterms.dateFOA2023-12-08T12:53:57Z
refterms.panelAen_GB
refterms.dateFirstOnline2023-12-08


Files in this item

This item appears in the following Collection(s)

Show simple item record

© 2023 Thornton, Davies and Dougherty.
This is an open-access article distributed
under the terms of the Creative Commons
Attribution License (CC BY). The use,
distribution or reproduction in other
forums is permitted, provided the original
author(s) and the copyright owner(s) are
credited and that the original publication in
this journal is cited, in accordance with
accepted academic practice. No use,
distribution or reproduction is permitted
which does not comply with these terms.
Except where otherwise noted, this item's licence is described as © 2023 Thornton, Davies and Dougherty. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.