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Highly sensitive and rapid point-of-care testing for HIV-1 infection based on CRISPR-Cas13a system

BACKGROUND: Human immunodeficiency virus type one (HIV-1) is the leading cause of acquired immunodeficiency syndrome (AIDS). AIDS remains a global public health concern but can be effectively suppressed by life-long administration of combination antiretroviral therapy. Early detection and diagnosis...

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Autores principales: Li, Xiaohui, Su, Bin, Yang, Lan, Kou, Zhihua, Wu, Hao, Zhang, Tong, Liu, Lifeng, Han, Yao, Niu, Mengwei, Sun, Yansong, Li, Hao, Jiang, Taiyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518925/
https://www.ncbi.nlm.nih.gov/pubmed/37749486
http://dx.doi.org/10.1186/s12879-023-08492-6
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author Li, Xiaohui
Su, Bin
Yang, Lan
Kou, Zhihua
Wu, Hao
Zhang, Tong
Liu, Lifeng
Han, Yao
Niu, Mengwei
Sun, Yansong
Li, Hao
Jiang, Taiyi
author_facet Li, Xiaohui
Su, Bin
Yang, Lan
Kou, Zhihua
Wu, Hao
Zhang, Tong
Liu, Lifeng
Han, Yao
Niu, Mengwei
Sun, Yansong
Li, Hao
Jiang, Taiyi
author_sort Li, Xiaohui
collection PubMed
description BACKGROUND: Human immunodeficiency virus type one (HIV-1) is the leading cause of acquired immunodeficiency syndrome (AIDS). AIDS remains a global public health concern but can be effectively suppressed by life-long administration of combination antiretroviral therapy. Early detection and diagnosis are two key strategies for the prevention and control of HIV/AIDS. Rapid and accurate point-of-care testing (POCT) provides critical tools for managing HIV-1 epidemic in high-risk areas and populations. METHODS: In this study, a POCT for HIV-1 RNA was developed by CRISPR-Cas13a lateral flow strip combined with reverse transcriptase recombinase-aided amplification (RT-RAA) technology, the results can be directly observed by naked eyes. RESULTS: Moreover, with the degenerate base-binding CRISPR-Cas13a system was introduced into the RT-RAA primer designing, the technology developed in this study can be used to test majority of HIV-1 RNA with limit of detection (LOD) 1 copy/μL, while no obvious cross-reaction with other pathogens. We evaluated this method for detecting HIV-1 RNA of clinical samples, the results showed that the sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and accuracy were 91.81% (85.03- 96.19%), 100% (92.60–100%), 100% (96.41–100%), 39.14% (25.59–54.60%) and 92.22% (86.89–95.88%), respectively. The lowest viral load detectable by this method was 112copies/mL. CONCLUSION: Above all, this method provides a point-of-care detection of HIV-1 RNA, which is stable, simple and with good sensitivity and specificity. This method has potential to be developed for promoting early diagnosis and treatment effect monitoring of HIV patients in clinical. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08492-6.
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spelling pubmed-105189252023-09-26 Highly sensitive and rapid point-of-care testing for HIV-1 infection based on CRISPR-Cas13a system Li, Xiaohui Su, Bin Yang, Lan Kou, Zhihua Wu, Hao Zhang, Tong Liu, Lifeng Han, Yao Niu, Mengwei Sun, Yansong Li, Hao Jiang, Taiyi BMC Infect Dis Research BACKGROUND: Human immunodeficiency virus type one (HIV-1) is the leading cause of acquired immunodeficiency syndrome (AIDS). AIDS remains a global public health concern but can be effectively suppressed by life-long administration of combination antiretroviral therapy. Early detection and diagnosis are two key strategies for the prevention and control of HIV/AIDS. Rapid and accurate point-of-care testing (POCT) provides critical tools for managing HIV-1 epidemic in high-risk areas and populations. METHODS: In this study, a POCT for HIV-1 RNA was developed by CRISPR-Cas13a lateral flow strip combined with reverse transcriptase recombinase-aided amplification (RT-RAA) technology, the results can be directly observed by naked eyes. RESULTS: Moreover, with the degenerate base-binding CRISPR-Cas13a system was introduced into the RT-RAA primer designing, the technology developed in this study can be used to test majority of HIV-1 RNA with limit of detection (LOD) 1 copy/μL, while no obvious cross-reaction with other pathogens. We evaluated this method for detecting HIV-1 RNA of clinical samples, the results showed that the sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and accuracy were 91.81% (85.03- 96.19%), 100% (92.60–100%), 100% (96.41–100%), 39.14% (25.59–54.60%) and 92.22% (86.89–95.88%), respectively. The lowest viral load detectable by this method was 112copies/mL. CONCLUSION: Above all, this method provides a point-of-care detection of HIV-1 RNA, which is stable, simple and with good sensitivity and specificity. This method has potential to be developed for promoting early diagnosis and treatment effect monitoring of HIV patients in clinical. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08492-6. BioMed Central 2023-09-25 /pmc/articles/PMC10518925/ /pubmed/37749486 http://dx.doi.org/10.1186/s12879-023-08492-6 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Li, Xiaohui
Su, Bin
Yang, Lan
Kou, Zhihua
Wu, Hao
Zhang, Tong
Liu, Lifeng
Han, Yao
Niu, Mengwei
Sun, Yansong
Li, Hao
Jiang, Taiyi
Highly sensitive and rapid point-of-care testing for HIV-1 infection based on CRISPR-Cas13a system
title Highly sensitive and rapid point-of-care testing for HIV-1 infection based on CRISPR-Cas13a system
title_full Highly sensitive and rapid point-of-care testing for HIV-1 infection based on CRISPR-Cas13a system
title_fullStr Highly sensitive and rapid point-of-care testing for HIV-1 infection based on CRISPR-Cas13a system
title_full_unstemmed Highly sensitive and rapid point-of-care testing for HIV-1 infection based on CRISPR-Cas13a system
title_short Highly sensitive and rapid point-of-care testing for HIV-1 infection based on CRISPR-Cas13a system
title_sort highly sensitive and rapid point-of-care testing for hiv-1 infection based on crispr-cas13a system
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518925/
https://www.ncbi.nlm.nih.gov/pubmed/37749486
http://dx.doi.org/10.1186/s12879-023-08492-6
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