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Four thermostatic steps: A novel CRISPR-Cas12-based system for the rapid at-home detection of respiratory pathogens

ABSTRACT: The outbreak of coronavirus disease 2019 (COVID-19) in 2019 has severely damaged the world's economy and public health and made people pay more attention to respiratory infectious diseases. However, traditional quantitative real-time polymerase chain reaction (qRT-PCR) nucleic acid de...

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Autores principales: Fang, Jianhua, Liu, Jing, Cheng, Na, Kang, Xiuhua, Huang, Zhanchao, Wang, Guoyu, Xiong, Xiaofeng, Lu, Tian, Gong, Zhenghua, Huang, Zhigang, Che, Jun, Xiang, Tianxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173909/
https://www.ncbi.nlm.nih.gov/pubmed/37166482
http://dx.doi.org/10.1007/s00253-023-12568-3
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author Fang, Jianhua
Liu, Jing
Cheng, Na
Kang, Xiuhua
Huang, Zhanchao
Wang, Guoyu
Xiong, Xiaofeng
Lu, Tian
Gong, Zhenghua
Huang, Zhigang
Che, Jun
Xiang, Tianxin
author_facet Fang, Jianhua
Liu, Jing
Cheng, Na
Kang, Xiuhua
Huang, Zhanchao
Wang, Guoyu
Xiong, Xiaofeng
Lu, Tian
Gong, Zhenghua
Huang, Zhigang
Che, Jun
Xiang, Tianxin
author_sort Fang, Jianhua
collection PubMed
description ABSTRACT: The outbreak of coronavirus disease 2019 (COVID-19) in 2019 has severely damaged the world's economy and public health and made people pay more attention to respiratory infectious diseases. However, traditional quantitative real-time polymerase chain reaction (qRT-PCR) nucleic acid detection kits require RNA extraction, reverse transcription, and amplification, as well as the support of large-scale equipment to enrich and purify nucleic acids and precise temperature control. Therefore, novel, fast, convenient, sensitive and specific detection methods are urgently being developed and moving to proof of concept test. In this study, we developed a new nucleic acid detection system, referred to as 4 Thermostatic steps (4TS), which innovatively allows all the detection processes to be completed in a constant temperature device, which performs extraction, amplification, cutting of targets, and detection within 40 min. The assay can specifically and sensitively detect five respiratory pathogens, namely SARS-CoV-2, Mycoplasma felis (MF), Chlamydia felis (CF), Feline calicivirus (FCV), and Feline herpes virus (FHV). In addition, a cost-effective and practical small-scale reaction device was designed and developed to maintain stable reaction conditions. The results of the detection of the five viruses show that the sensitivity of the system is greater than 94%, and specificity is 100%. The 4TS system does not require complex equipment, which makes it convenient and fast to operate, and allows immediate testing for suspected infectious agents at home or in small clinics. Therefore, the assay system has diagnostic value and significant potential for further reducing the cost of early screening of infectious diseases and expanding its application. KEY POINTS: • The 4TS system enables the accurate and specific detection of nucleic acid of pathogens at 37 °C in four simple steps , and the whole process only takes 40 min. •A simple alkali solution can be used to extract nucleic acid. • A small portable device simple to operate is developed for home diagnosis and detection of respiratory pathogens. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-023-12568-3.
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spelling pubmed-101739092023-05-14 Four thermostatic steps: A novel CRISPR-Cas12-based system for the rapid at-home detection of respiratory pathogens Fang, Jianhua Liu, Jing Cheng, Na Kang, Xiuhua Huang, Zhanchao Wang, Guoyu Xiong, Xiaofeng Lu, Tian Gong, Zhenghua Huang, Zhigang Che, Jun Xiang, Tianxin Appl Microbiol Biotechnol Applied Genetics and Molecular Biotechnology ABSTRACT: The outbreak of coronavirus disease 2019 (COVID-19) in 2019 has severely damaged the world's economy and public health and made people pay more attention to respiratory infectious diseases. However, traditional quantitative real-time polymerase chain reaction (qRT-PCR) nucleic acid detection kits require RNA extraction, reverse transcription, and amplification, as well as the support of large-scale equipment to enrich and purify nucleic acids and precise temperature control. Therefore, novel, fast, convenient, sensitive and specific detection methods are urgently being developed and moving to proof of concept test. In this study, we developed a new nucleic acid detection system, referred to as 4 Thermostatic steps (4TS), which innovatively allows all the detection processes to be completed in a constant temperature device, which performs extraction, amplification, cutting of targets, and detection within 40 min. The assay can specifically and sensitively detect five respiratory pathogens, namely SARS-CoV-2, Mycoplasma felis (MF), Chlamydia felis (CF), Feline calicivirus (FCV), and Feline herpes virus (FHV). In addition, a cost-effective and practical small-scale reaction device was designed and developed to maintain stable reaction conditions. The results of the detection of the five viruses show that the sensitivity of the system is greater than 94%, and specificity is 100%. The 4TS system does not require complex equipment, which makes it convenient and fast to operate, and allows immediate testing for suspected infectious agents at home or in small clinics. Therefore, the assay system has diagnostic value and significant potential for further reducing the cost of early screening of infectious diseases and expanding its application. KEY POINTS: • The 4TS system enables the accurate and specific detection of nucleic acid of pathogens at 37 °C in four simple steps , and the whole process only takes 40 min. •A simple alkali solution can be used to extract nucleic acid. • A small portable device simple to operate is developed for home diagnosis and detection of respiratory pathogens. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-023-12568-3. Springer Berlin Heidelberg 2023-05-11 2023 /pmc/articles/PMC10173909/ /pubmed/37166482 http://dx.doi.org/10.1007/s00253-023-12568-3 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Applied Genetics and Molecular Biotechnology
Fang, Jianhua
Liu, Jing
Cheng, Na
Kang, Xiuhua
Huang, Zhanchao
Wang, Guoyu
Xiong, Xiaofeng
Lu, Tian
Gong, Zhenghua
Huang, Zhigang
Che, Jun
Xiang, Tianxin
Four thermostatic steps: A novel CRISPR-Cas12-based system for the rapid at-home detection of respiratory pathogens
title Four thermostatic steps: A novel CRISPR-Cas12-based system for the rapid at-home detection of respiratory pathogens
title_full Four thermostatic steps: A novel CRISPR-Cas12-based system for the rapid at-home detection of respiratory pathogens
title_fullStr Four thermostatic steps: A novel CRISPR-Cas12-based system for the rapid at-home detection of respiratory pathogens
title_full_unstemmed Four thermostatic steps: A novel CRISPR-Cas12-based system for the rapid at-home detection of respiratory pathogens
title_short Four thermostatic steps: A novel CRISPR-Cas12-based system for the rapid at-home detection of respiratory pathogens
title_sort four thermostatic steps: a novel crispr-cas12-based system for the rapid at-home detection of respiratory pathogens
topic Applied Genetics and Molecular Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173909/
https://www.ncbi.nlm.nih.gov/pubmed/37166482
http://dx.doi.org/10.1007/s00253-023-12568-3
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