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CRISPR/Cas12a powered air-displacement enhanced evanescent wave fluorescence fiber-embedded microfluidic biochip for nucleic acid amplification-free detection of Escherichia coli O157:H7.
Han, Xiangzhi; Song, Dan; Xu, Wenjuan; Lu, Laiya; Zhu, Anna; Long, Feng.
Afiliação
  • Han X; School of Environment and Natural Resources, Renmin University of China, Beijing 100872, China.
  • Song D; School of Environment and Natural Resources, Renmin University of China, Beijing 100872, China.
  • Xu W; School of Environment and Natural Resources, Renmin University of China, Beijing 100872, China.
  • Lu L; School of Environment and Natural Resources, Renmin University of China, Beijing 100872, China; State Key Laboratory of NBC Protection for Civilian, Beijing 102205, China.
  • Zhu A; School of Environment and Natural Resources, Renmin University of China, Beijing 100872, China; State Key Laboratory of NBC Protection for Civilian, Beijing 102205, China.
  • Long F; School of Environment and Natural Resources, Renmin University of China, Beijing 100872, China. Electronic address: longf04@ruc.edu.cn.
J Hazard Mater ; 469: 134037, 2024 May 05.
Article em En | MEDLINE | ID: mdl-38521032
ABSTRACT
Simple yet ultrasensitive and contamination-free quantification of environmental pathogenic bacteria is in high demand. In this study, we present a portable clustered regularly interspaced short palindromic repeats-associated protein 12a (CRISPR/Cas12a) powered Air-displacement enhanced Evanescent wave fluorescence Fiber-embedded microfluidic Biochip (AEFB) for the high-frequency and nucleic acid amplification-free ultrasensitive detection of Escherichia coli O157H7. The performance of AEFB was dramatically enhanced upon employing a simple air-solution displacement process. Theoretical assays demonstrated that air-solution displacement significantly enhances evanescent wave field intensity on the fiber biosensor surface and increases the V-number in tapered fiber biosensors. Consequently, light-matter interaction is strengthened, and fluorescence coupling and collection efficiency are improved, considerably enhancing sensitivity. By integrating the CRISPR biosensing mechanism, AEFB facilitated rapid, accurate, nucleic acid amplification-free detection of E.coli O157H7 with polymerase chain reaction (PCR)-level sensitivity (176 cfu/mL). To validate its practicality, AEFB was used to detect E.coli O157H7 in surface water and wastewater. Comparison with RT-PCR showed a strong linear relationship (R2 = 0.9871), indicating the excellent accuracy and reliability of this technology in real applications. AEFB is highly versatile and can be easily extended to detect other pathogenic bacteria, which will significantly promote the high-frequency assessment and early-warning of bacterial contamination in aquatic environments.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácidos Nucleicos / Técnicas Biossensoriais / Escherichia coli O157 Idioma: En Revista: J Hazard Mater Assunto da revista: SAUDE AMBIENTAL Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácidos Nucleicos / Técnicas Biossensoriais / Escherichia coli O157 Idioma: En Revista: J Hazard Mater Assunto da revista: SAUDE AMBIENTAL Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Holanda