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A CRISPR/Cas12a-assisted rapid detection platform by biosensing the apxIVA of Actinobacillus pleuropneumoniae

Actinobacillus pleuropneumoniae is an important respiratory pig pathogen that causes substantial losses in the worldwide swine industry. Chronic or subclinical infection with no apparent clinical symptoms poses a challenge for preventing transmission between herds. Rapid diagnostics is important for...

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Autores principales: Luan, Tian, Wang, Lu, Zhao, Jiyu, Luan, Hui, Zhang, Yueling, Wang, Chunlai, Langford, Paul R., Liu, Siguo, Zhang, Wanjiang, Li, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9493679/
https://www.ncbi.nlm.nih.gov/pubmed/36160205
http://dx.doi.org/10.3389/fmicb.2022.928307
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author Luan, Tian
Wang, Lu
Zhao, Jiyu
Luan, Hui
Zhang, Yueling
Wang, Chunlai
Langford, Paul R.
Liu, Siguo
Zhang, Wanjiang
Li, Gang
author_facet Luan, Tian
Wang, Lu
Zhao, Jiyu
Luan, Hui
Zhang, Yueling
Wang, Chunlai
Langford, Paul R.
Liu, Siguo
Zhang, Wanjiang
Li, Gang
author_sort Luan, Tian
collection PubMed
description Actinobacillus pleuropneumoniae is an important respiratory pig pathogen that causes substantial losses in the worldwide swine industry. Chronic or subclinical infection with no apparent clinical symptoms poses a challenge for preventing transmission between herds. Rapid diagnostics is important for the control of epidemic diseases. In this study, we formulated an A. pleuropneumoniae species-specific apxIVA-based CRISPR/Cas12a-assisted rapid detection platform (Card) that combines recombinase polymerase amplification (RPA) of target DNA and subsequent Cas12a ssDNase activation. Card has a detection limit of 10 CFUs of A. pleuropneumoniae, and there is no cross-reactivity with other common swine pathogens. The detection process can be completed in 1 h, and there was 100% agreement between the conventional apxIVA-based PCR and Card in detecting A. pleuropneumoniae in lung samples. Microplate fluorescence readout enables high-throughput use in diagnostic laboratories, and naked eye and lateral flow test readouts enable use at the point of care. We conclude that Card is a versatile, rapid, accurate molecular diagnostic platform suitable for use in both laboratory and low-resource settings.
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spelling pubmed-94936792022-09-23 A CRISPR/Cas12a-assisted rapid detection platform by biosensing the apxIVA of Actinobacillus pleuropneumoniae Luan, Tian Wang, Lu Zhao, Jiyu Luan, Hui Zhang, Yueling Wang, Chunlai Langford, Paul R. Liu, Siguo Zhang, Wanjiang Li, Gang Front Microbiol Microbiology Actinobacillus pleuropneumoniae is an important respiratory pig pathogen that causes substantial losses in the worldwide swine industry. Chronic or subclinical infection with no apparent clinical symptoms poses a challenge for preventing transmission between herds. Rapid diagnostics is important for the control of epidemic diseases. In this study, we formulated an A. pleuropneumoniae species-specific apxIVA-based CRISPR/Cas12a-assisted rapid detection platform (Card) that combines recombinase polymerase amplification (RPA) of target DNA and subsequent Cas12a ssDNase activation. Card has a detection limit of 10 CFUs of A. pleuropneumoniae, and there is no cross-reactivity with other common swine pathogens. The detection process can be completed in 1 h, and there was 100% agreement between the conventional apxIVA-based PCR and Card in detecting A. pleuropneumoniae in lung samples. Microplate fluorescence readout enables high-throughput use in diagnostic laboratories, and naked eye and lateral flow test readouts enable use at the point of care. We conclude that Card is a versatile, rapid, accurate molecular diagnostic platform suitable for use in both laboratory and low-resource settings. Frontiers Media S.A. 2022-09-09 /pmc/articles/PMC9493679/ /pubmed/36160205 http://dx.doi.org/10.3389/fmicb.2022.928307 Text en Copyright © 2022 Luan, Wang, Zhao, Luan, Zhang, Wang, Langford, Liu, Zhang and Li. https://creativecommons.org/licenses/by/4.0/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.
spellingShingle Microbiology
Luan, Tian
Wang, Lu
Zhao, Jiyu
Luan, Hui
Zhang, Yueling
Wang, Chunlai
Langford, Paul R.
Liu, Siguo
Zhang, Wanjiang
Li, Gang
A CRISPR/Cas12a-assisted rapid detection platform by biosensing the apxIVA of Actinobacillus pleuropneumoniae
title A CRISPR/Cas12a-assisted rapid detection platform by biosensing the apxIVA of Actinobacillus pleuropneumoniae
title_full A CRISPR/Cas12a-assisted rapid detection platform by biosensing the apxIVA of Actinobacillus pleuropneumoniae
title_fullStr A CRISPR/Cas12a-assisted rapid detection platform by biosensing the apxIVA of Actinobacillus pleuropneumoniae
title_full_unstemmed A CRISPR/Cas12a-assisted rapid detection platform by biosensing the apxIVA of Actinobacillus pleuropneumoniae
title_short A CRISPR/Cas12a-assisted rapid detection platform by biosensing the apxIVA of Actinobacillus pleuropneumoniae
title_sort crispr/cas12a-assisted rapid detection platform by biosensing the apxiva of actinobacillus pleuropneumoniae
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9493679/
https://www.ncbi.nlm.nih.gov/pubmed/36160205
http://dx.doi.org/10.3389/fmicb.2022.928307
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