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Development of multiplex gold nanoparticles biosensors for ultrasensitive detection and genotyping of equine herpes viruses

Gold nanoparticles (GNPs) biosensors can detect low viral loads and differentiate between viruses types, enabling early diagnosis and effective disease management. In the present study, we developed GNPs biosensors with two different capping agent, citrate-GNPs biosensors and polyvinylpyrrolidone (P...

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Autores principales: Ghoniem, Shimaa M., ElZorkany, Heba E., Hagag, Naglaa M., El-Deeb, Ayman H., Shahein, Momtaz A., Hussein, Hussein A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10500010/
https://www.ncbi.nlm.nih.gov/pubmed/37704638
http://dx.doi.org/10.1038/s41598-023-41918-4
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author Ghoniem, Shimaa M.
ElZorkany, Heba E.
Hagag, Naglaa M.
El-Deeb, Ayman H.
Shahein, Momtaz A.
Hussein, Hussein A.
author_facet Ghoniem, Shimaa M.
ElZorkany, Heba E.
Hagag, Naglaa M.
El-Deeb, Ayman H.
Shahein, Momtaz A.
Hussein, Hussein A.
author_sort Ghoniem, Shimaa M.
collection PubMed
description Gold nanoparticles (GNPs) biosensors can detect low viral loads and differentiate between viruses types, enabling early diagnosis and effective disease management. In the present study, we developed GNPs biosensors with two different capping agent, citrate-GNPs biosensors and polyvinylpyrrolidone (PVP)-GNPs biosensors for detection of EHV-1 and EHV-4 in multiplex real time PCR (rPCR). Citrate-GNPs and PVP-GNPs biosensors can detect dilution 10(10) of EHV-1 with mean Cycle threshold (Ct) 11.7 and 9.6, respectively and one copy as limit of detection, while citrate-GNPs and PVP-GNPs biosensors can detect dilution 10(10) of EHV-4 with mean Ct 10.5 and 9.2, respectively and one copy as limit of detection. These findings were confirmed by testing 87 different clinical samples, 4 more samples were positive with multiplex GNPs biosensors rPCR than multiplex rPCR. Multiplex citrate-GNPs and PVP-GNPs biosensors for EHV-1 and EHV-4 are a significant breakthrough in the diagnosis of these virus types. These biosensors offer high sensitivity and specificity, allowing for the accurate detection of the target viruses at very low concentrations and improve the early detection of EHV-1 and EHV-4, leading to faster control of infected animals to prevent the spread of these viruses.
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spelling pubmed-105000102023-09-15 Development of multiplex gold nanoparticles biosensors for ultrasensitive detection and genotyping of equine herpes viruses Ghoniem, Shimaa M. ElZorkany, Heba E. Hagag, Naglaa M. El-Deeb, Ayman H. Shahein, Momtaz A. Hussein, Hussein A. Sci Rep Article Gold nanoparticles (GNPs) biosensors can detect low viral loads and differentiate between viruses types, enabling early diagnosis and effective disease management. In the present study, we developed GNPs biosensors with two different capping agent, citrate-GNPs biosensors and polyvinylpyrrolidone (PVP)-GNPs biosensors for detection of EHV-1 and EHV-4 in multiplex real time PCR (rPCR). Citrate-GNPs and PVP-GNPs biosensors can detect dilution 10(10) of EHV-1 with mean Cycle threshold (Ct) 11.7 and 9.6, respectively and one copy as limit of detection, while citrate-GNPs and PVP-GNPs biosensors can detect dilution 10(10) of EHV-4 with mean Ct 10.5 and 9.2, respectively and one copy as limit of detection. These findings were confirmed by testing 87 different clinical samples, 4 more samples were positive with multiplex GNPs biosensors rPCR than multiplex rPCR. Multiplex citrate-GNPs and PVP-GNPs biosensors for EHV-1 and EHV-4 are a significant breakthrough in the diagnosis of these virus types. These biosensors offer high sensitivity and specificity, allowing for the accurate detection of the target viruses at very low concentrations and improve the early detection of EHV-1 and EHV-4, leading to faster control of infected animals to prevent the spread of these viruses. Nature Publishing Group UK 2023-09-13 /pmc/articles/PMC10500010/ /pubmed/37704638 http://dx.doi.org/10.1038/s41598-023-41918-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ghoniem, Shimaa M.
ElZorkany, Heba E.
Hagag, Naglaa M.
El-Deeb, Ayman H.
Shahein, Momtaz A.
Hussein, Hussein A.
Development of multiplex gold nanoparticles biosensors for ultrasensitive detection and genotyping of equine herpes viruses
title Development of multiplex gold nanoparticles biosensors for ultrasensitive detection and genotyping of equine herpes viruses
title_full Development of multiplex gold nanoparticles biosensors for ultrasensitive detection and genotyping of equine herpes viruses
title_fullStr Development of multiplex gold nanoparticles biosensors for ultrasensitive detection and genotyping of equine herpes viruses
title_full_unstemmed Development of multiplex gold nanoparticles biosensors for ultrasensitive detection and genotyping of equine herpes viruses
title_short Development of multiplex gold nanoparticles biosensors for ultrasensitive detection and genotyping of equine herpes viruses
title_sort development of multiplex gold nanoparticles biosensors for ultrasensitive detection and genotyping of equine herpes viruses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10500010/
https://www.ncbi.nlm.nih.gov/pubmed/37704638
http://dx.doi.org/10.1038/s41598-023-41918-4
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