A portable immunosensor provides sensitive and rapid detection of Borrelia burgdorferi antigen in spiked blood

Abstract There are no assays for detecting B. burgdorferi antigen in blood of infected Lyme disease individuals. Here, we provide proof-of-principle evidence that we can quantify B. burgdorferi antigen in spiked blood using a portable smartphone-based fluorescence microscope that measures immunoaggl...

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Main Authors: Sangsik Kim, Kamalika Samanta, Brandon T. Nguyen, Samantha Mata-Robles, Luciana Richer, Jeong-Yeol Yoon, Maria Gomes-Solecki
Format: Article
Language:English
Published: Nature Portfolio 2023-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-34108-9
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author Sangsik Kim
Kamalika Samanta
Brandon T. Nguyen
Samantha Mata-Robles
Luciana Richer
Jeong-Yeol Yoon
Maria Gomes-Solecki
author_facet Sangsik Kim
Kamalika Samanta
Brandon T. Nguyen
Samantha Mata-Robles
Luciana Richer
Jeong-Yeol Yoon
Maria Gomes-Solecki
author_sort Sangsik Kim
collection DOAJ
description Abstract There are no assays for detecting B. burgdorferi antigen in blood of infected Lyme disease individuals. Here, we provide proof-of-principle evidence that we can quantify B. burgdorferi antigen in spiked blood using a portable smartphone-based fluorescence microscope that measures immunoagglutination on a paper microfluidic chip. We targeted B. burgdorferi OspA to develop a working prototype and added examples of two antigens (OspC and VlsE) that have diagnostic value for discrimination of Lyme disease stage. Using an extensively validated monoclonal antibody to OspA (LA-2), detection of OspA antigen had a broad linear range up to 100 pg/mL in 1% blood and the limit of detection (LOD) was 100 fg/mL (= 10 pg/mL in undiluted blood), which was 1000 times lower than our target of 10 ng/mL. Analysis of the two other targets was done using polyclonal and monoclonal antibodies. OspC antigen was detected at LOD 100 pg/mL (= 10 ng/mL of undiluted blood) and VlsE antigen was detected at LOD 1–10 pg/mL (= 0.1–1 ng/mL of undiluted blood). The method is accurate and was performed in 20 min from sample to answer. When optimized for detecting several B. burgdorferi antigens, this assay may differentiate active from past infections and facilitate diagnosis of Lyme disease in the initial weeks of infection, when antibody presence is typically below the threshold to be detected by serologic methods.
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spelling doaj.art-d9d908b39d76464d82ed5951cd2ca52f2023-05-14T11:17:40ZengNature PortfolioScientific Reports2045-23222023-05-0113111010.1038/s41598-023-34108-9A portable immunosensor provides sensitive and rapid detection of Borrelia burgdorferi antigen in spiked bloodSangsik Kim0Kamalika Samanta1Brandon T. Nguyen2Samantha Mata-Robles3Luciana Richer4Jeong-Yeol Yoon5Maria Gomes-Solecki6Department of Biomedical Engineering, The University of ArizonaDepartment of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science CenterCollege of Medicine, The University of ArizonaDepartment of Biomedical Engineering, The University of ArizonaDepartment of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science CenterDepartment of Biomedical Engineering, The University of ArizonaDepartment of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science CenterAbstract There are no assays for detecting B. burgdorferi antigen in blood of infected Lyme disease individuals. Here, we provide proof-of-principle evidence that we can quantify B. burgdorferi antigen in spiked blood using a portable smartphone-based fluorescence microscope that measures immunoagglutination on a paper microfluidic chip. We targeted B. burgdorferi OspA to develop a working prototype and added examples of two antigens (OspC and VlsE) that have diagnostic value for discrimination of Lyme disease stage. Using an extensively validated monoclonal antibody to OspA (LA-2), detection of OspA antigen had a broad linear range up to 100 pg/mL in 1% blood and the limit of detection (LOD) was 100 fg/mL (= 10 pg/mL in undiluted blood), which was 1000 times lower than our target of 10 ng/mL. Analysis of the two other targets was done using polyclonal and monoclonal antibodies. OspC antigen was detected at LOD 100 pg/mL (= 10 ng/mL of undiluted blood) and VlsE antigen was detected at LOD 1–10 pg/mL (= 0.1–1 ng/mL of undiluted blood). The method is accurate and was performed in 20 min from sample to answer. When optimized for detecting several B. burgdorferi antigens, this assay may differentiate active from past infections and facilitate diagnosis of Lyme disease in the initial weeks of infection, when antibody presence is typically below the threshold to be detected by serologic methods.https://doi.org/10.1038/s41598-023-34108-9
spellingShingle Sangsik Kim
Kamalika Samanta
Brandon T. Nguyen
Samantha Mata-Robles
Luciana Richer
Jeong-Yeol Yoon
Maria Gomes-Solecki
A portable immunosensor provides sensitive and rapid detection of Borrelia burgdorferi antigen in spiked blood
Scientific Reports
title A portable immunosensor provides sensitive and rapid detection of Borrelia burgdorferi antigen in spiked blood
title_full A portable immunosensor provides sensitive and rapid detection of Borrelia burgdorferi antigen in spiked blood
title_fullStr A portable immunosensor provides sensitive and rapid detection of Borrelia burgdorferi antigen in spiked blood
title_full_unstemmed A portable immunosensor provides sensitive and rapid detection of Borrelia burgdorferi antigen in spiked blood
title_short A portable immunosensor provides sensitive and rapid detection of Borrelia burgdorferi antigen in spiked blood
title_sort portable immunosensor provides sensitive and rapid detection of borrelia burgdorferi antigen in spiked blood
url https://doi.org/10.1038/s41598-023-34108-9
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