Development of a Recombinase Polymerase Amplification-Coupled CRISPR/Cas12a Platform for Rapid Detection of Antimicrobial-Resistant Genes in Carbapenem-Resistant Enterobacterales DOI Creative Commons
Ji Yang,

Heesu Kim,

Lee-Sang Hyeon

et al.

Biosensors, Journal Year: 2024, Volume and Issue: 14(11), P. 536 - 536

Published: Nov. 5, 2024

The worldwide spread of carbapenemase-producing

Language: Английский

Leveraging CRISPR-Cas-Enhanced Isothermal Amplification Tools for Quick Identification of Pathogens Causing Livestock Diseases DOI
Ayan Mukherjee,

Sukhen Samanta,

Subhasree Das

et al.

Current Microbiology, Journal Year: 2025, Volume and Issue: 82(6)

Published: April 24, 2025

Language: Английский

Citations

0

A one-pot, one-step CRISPR-AapCas12b-based platform for sensitive and specific detection of Klebsiella pneumoniae DOI Creative Commons
Juan Zhou,

Zirong Wu,

Lei Yu

et al.

Sensing and Bio-Sensing Research, Journal Year: 2025, Volume and Issue: 48, P. 100797 - 100797

Published: April 29, 2025

Language: Английский

Citations

0

Detection of Potato Pathogen Clavibacter sepedonicus by CRISPR/Cas13a Analysis of NASBA Amplicons DOI Open Access
Svetlana A. Khmeleva, Leonid K. Kurbatov, K. G. Ptitsyn

et al.

International Journal of Molecular Sciences, Journal Year: 2024, Volume and Issue: 25(22), P. 12218 - 12218

Published: Nov. 14, 2024

The ring rot of potato caused by the bacterial pathogen Clavibacter sepedonicus is a quarantine disease posing threat to industry worldwide. sensitive and selective detection C. high importance for its effective control. Here, system reported determine viable bacteria in tubers, based on coupling CRISPR/Cas13a nuclease with NASBA (Nucleic Acid Sequence Based Amplification)—the method isothermal amplification RNA. Detection can be conducted using both instrumental non-instrumental (visual inspection test tubes under blue light) modes. When Cas13a analyses were carried out separate tubes, limit (LOD) was 1000 copies purified target 16S rRNA per reaction or about 24 colony-forming units (CFUs) 1 g tuber tissue. testing also “one-pot” format (a single tube), though lower sensitivity: LOD 10,000 RNA 100 CFU tissue visual overall time NASBA/Cas13a analysis did not exceed 2 h. developed has potential employed as routine sepedonicus, especially on-site testing.

Language: Английский

Citations

2

The current status and future prospects of CRISPR-based detection of monkeypox virus: A review DOI
Yingwei Chen, Ran Zhao, Xiaobo Hu

et al.

Analytica Chimica Acta, Journal Year: 2024, Volume and Issue: 1336, P. 343295 - 343295

Published: Oct. 1, 2024

Language: Английский

Citations

1

Development of a Recombinase Polymerase Amplification-Coupled CRISPR/Cas12a Platform for Rapid Detection of Antimicrobial-Resistant Genes in Carbapenem-Resistant Enterobacterales DOI Creative Commons
Ji Yang,

Heesu Kim,

Lee-Sang Hyeon

et al.

Biosensors, Journal Year: 2024, Volume and Issue: 14(11), P. 536 - 536

Published: Nov. 5, 2024

The worldwide spread of carbapenemase-producing

Language: Английский

Citations

0