4.7 Article

Development and application of Cas13a-based diagnostic assay for Neisseria gonorrhoeae detection and azithromycin resistance identification

Journal

JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
Volume 77, Issue 3, Pages 656-664

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jac/dkab447

Keywords

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Funding

  1. Overseas Famous Teacher Project of Guangdong Provincial Department of Science and Technology [2020A1414010136]
  2. Medical Science and Technology Research Foundation of Guangdong Province [A2019010, A2021139]
  3. Guangdong Traditional Chinese Medicine Research Project [20191230, 20211277]
  4. Guangdong Provincial Medical Research Fund [B2020149]
  5. Scientific Research Initiative Project of Southern Medical University (Project of Youth Science and Technology Personnel Training) [PY2018N100]
  6. key scientific research platforms and research projects of colleges and universities in Guangdong Province [2018KQNCX025]

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The development of a Cas13a-based assay for rapid detection of Neisseria gonorrhoeae and identification of azithromycin resistance is a promising method for application in clinical practice.
Background Gonorrhoea, caused by Neisseria gonorrhoeae, has spread worldwide. Strains resistant to most antibiotics, including ceftriaxone and azithromycin, have emerged to an alarming level. Rapid testing for N. gonorrhoeae and its antimicrobial resistance will therefore contribute to clinical decision making for early diagnosis and rational drug use. Methods A Cas13a-based assay (specific high-sensitivity enzymatic reporter unlocking; SHERLOCK) was developed for N. gonorrhoeae detection (porA gene) and azithromycin resistance identification (A2059G, C2611T). Assays were evaluated for sensitivity with purified dsDNA and specificity with 17 non-gonococcal strains. Performance of SHERLOCK (porA) was compared with Roche Cobas 4800 using 43 urine samples. Identification of azithromycin resistance mutations (A2059G, C2611T) was evaluated using a total of 84 clinical isolates and 18 urine samples. Lateral flow was tested for this assay as a readout tool. Moreover, we directly assayed 27 urethral swabs from patients with urethritis to evaluate their status in terms of N. gonorrhoeae infection and azithromycin resistance. Results The SHERLOCK assay was successfully developed with a sensitivity of 10 copies/reaction, except 100 copies/reaction for A2059G, and no cross-reaction with other species. Comparison of the SHERLOCK assay with the Cobas 4800 revealed 100% concordance within 18 positive and 25 negative urine samples. Of the 84 isolates, 21 strains with azithromycin resistance mutations were distinguished and further verified by sequencing and MIC determination. In addition, 62.96% (17/27) strains from swab samples were detected with no mutant strains confirmed by sequencing. Conclusions The SHERLOCK assay for rapid N. gonorrhoeae detection combined with azithromycin resistance testing is a promising method for application in clinical practice.

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