4.8 Article

Metal-Tagged CRISPR/Cas12a Bioassay Enables Ultrasensitive and Highly Selective Evaluation of Kanamycin Bioaccumulation in Fish Samples

Journal

ANALYTICAL CHEMISTRY
Volume 93, Issue 42, Pages 14214-14222

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.1c03094

Keywords

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Funding

  1. National Natural Science Foundation of China [22074096, 22074098]
  2. Recruitment Program of Global Experts of Sichuan Province [903]
  3. Sichuan Science and Technology Program [19CXRC0047]
  4. Fundamental Research Funds for the Central Universities

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The abuse of antibiotics in modern life and aquaculture has become a global issue, and a metal-tagged CRISPR/Cas12a bioassay has been developed to accurately evaluate antibiotics bioaccumulation in wild fish samples. This ultrasensitive and highly selective method enables fast and multiplex detection of antibiotics, showing potential for assessing bioaccumulation effects in different geographical locations of wild fish samples.
The abuse of antibiotics in modern life and aquaculture has become a worldwide problem. Trace amounts of antibiotics discharged into natural water are increased in organisms through bioaccumulation and ultimately harm human health. Herein, we report a metal-tagged CRISPR/Cas12a bioassay and apply it to an ultrasensitive and highly selective evaluation of antibiotics bioaccumulation in wild fish samples. We integrated an element-tagging report probe and collateral cleavage activity of CRISPR/Cas12a. With the recognition and capture of target kanamycin by a locked-activated system, the activator strand was subsequently released to activate the collateral cleavage activity of Cas12a, followed by the cleavage of free Tm-Rep. After SA-MB capture, the biotin terminal was modified, and the uncleaved probe of Tm-Rep was removed. The acidized supernate containing the element tag fragment could be directly detected with Tm-169 isotope monitoring by inductively coupled plasma mass spectrometry (ICPMS). With CRISPR/Cas12a biosensing and metal isotope detection by ICPMS, ultrasensitive and fast antibiotics analysis was realized with multiplex detection potential. Taking kanamycin as a modal analyte, a limit of detection as low as 4.06 pM was provided in a 30 min detection workflow. Besides, the bioaccumulation effect of kanamycin in a wild fish sample was also evaluated using the proposed strategy. We investigated the geographical distribution with Pseudorasbora parva samples collected in four different locations along a 600 km stretch of the Yangtze River. In addition, the bioaccumulation kinetics of antibiotics was evaluated in serum, muscle, and liver tissues of Pseudorasbora parva with 7 days of continuous feeding in a kanamycin-enriched environment.

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