Portable biosensor combining CRISPR/Cas12a and loop-mediated isothermal amplification for antibiotic resistance gene ermB in wastewater
dc.contributor.author | Mao, Kang | |
dc.contributor.author | Zhang, Hua | |
dc.contributor.author | Ran, Fang | |
dc.contributor.author | Cao, Haorui | |
dc.contributor.author | Feng, Rida | |
dc.contributor.author | Du, Wei | |
dc.contributor.author | Li, Xiqing | |
dc.contributor.author | Yang, Zhugen | |
dc.date.accessioned | 2023-10-25T09:35:37Z | |
dc.date.available | 2023-10-25T09:35:37Z | |
dc.date.freetoread | 2024-10-18 | |
dc.date.issued | 2023-10-17 | |
dc.description.abstract | Wastewater is among the main sources of antibiotic resistance genes (ARGs) in the environment, but effective methods to quickly assess ARGs on-site in wastewater are lacking. Here, using the typical ARG ermB as the target, we report a portable biosensor combining CRISPR/Cas12a and loop-mediated isothermal amplification (LAMP) for the detection of ARGs. Six primers of LAMP and the crRNA of CRISPR/Cas12a were first designed to be preamplification with LAMP and lead Cas12a to recognize the ermB via base pairing. Due to the trans-cleavage activity of CRISPR/Cas12a after amplicon recognition, ssDNA probes modified with reporter molecules were used to implement a visual assay with lateral flow test strips and fluorescence. After a simple nucleic acid extraction with magnetic beads, the constructed biosensor possesses excellent sensitivity and selectivity as low as 2.75 × 103 copies/μL using fluorescence and later flow strips in wastewater. We further evaluated the community-wide prevalence of ermB in wastewater influent and found high mass loads of ermB during different months. This user-friendly and low-cost biosensor is applicable for rapid on-site ARG detection, providing a potential point-of-use method for rapid assessments of ARG abundance in wastewater from large city areas with many wastewater treatment plants and in resource-limited rural areas. | en_UK |
dc.identifier.citation | Mao K, Zhang H, Ran F, et al., (2024) Portable biosensor combining CRISPR/Cas12a and loop-mediated isothermal amplification for antibiotic resistance gene ermB in wastewater, Journal of Hazardous Materials, Volume 462, January 2024, Article Number 132793 | en_UK |
dc.identifier.eissn | 1873-3336 | |
dc.identifier.issn | 0304-3894 | |
dc.identifier.uri | https://doi.org/10.1016/j.jhazmat.2023.132793 | |
dc.identifier.uri | https://dspace.lib.cranfield.ac.uk/handle/1826/20442 | |
dc.language.iso | en | en_UK |
dc.publisher | Elsevier | en_UK |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Antibiotic resistance gene | en_UK |
dc.subject | CRISPR/Cas12a | en_UK |
dc.subject | Loop-mediated isothermal amplification | en_UK |
dc.subject | Biosensor | en_UK |
dc.subject | Wastewater | en_UK |
dc.title | Portable biosensor combining CRISPR/Cas12a and loop-mediated isothermal amplification for antibiotic resistance gene ermB in wastewater | en_UK |
dc.type | Article | en_UK |
dcterms.dateAccepted | 2023-10-14 |
Files
Original bundle
1 - 1 of 1
Loading...
- Name:
- Antibiotic_resistance_gene_ermB_in_wastewater-2023.pdf
- Size:
- 19.33 MB
- Format:
- Adobe Portable Document Format
- Description:
License bundle
1 - 1 of 1
No Thumbnail Available
- Name:
- license.txt
- Size:
- 1.63 KB
- Format:
- Item-specific license agreed upon to submission
- Description: