Ultrasensitive CRISPR/Cas12a-Based System for Detection of <i>Bla</i><sub>OXA-1</sub> Gene in Antibiotic-Resistant Microorganisms
Marina Tyumentseva | Aleksandr Tyumentsev | Anna Prelovskaya | Andrey Akinin | Yulia Mikhailova | Andrey Shelenkov | Anna Panevina | Vasiliy Akimkin
The <i>bla</i><sub>OXA-1</sub> gene encodes an oxacillin-hydrolyzing beta-lactamase of extended-spectrum beta-lactamase (ESBL)-producing microorganisms. The <i>bla</i><sub>OXA-1</sub> gene is found in the resistomes of some <i>Enterobacteriaceae</i>, <i>Morganellaceae</i>, <i>Pasteurellaceae</i>, <i>Moraxellaceae</i>, <i>Aeromonadaceae</i>, <i>Pseudomonadaceae</i>, <i>Yersiniaceae</i>, and <i>Vibrionaceae</i>. Most ESBL detection methods, including those to detect OXA-1-producing microorganisms, are time-consuming, and require specialized equipment and qualified personnel. Here, we report a new CRISPR(Clustered Regularly Interspaced Short Palindromic Repeats)/Cas12a-based detection assay coupled with polymerase chain reaction (PCR) to sensitively detect OXA-1-bearing microorganisms. The PCR-coupled CRISPR/Cas12a-based fluorescence assay includes (i) a pre-amplification step and (ii) a nucleic acid detection step. The pre-amplification step is based on a commonly used PCR, and the detection step is based on the CRISPR/Cas12a property to nonspecifically hydrolyze single-stranded DNA fluorescent reporter molecules. The pre-amplification step takes 65 min, and the detection step is shortened and takes only 5 min. The developed assay can easily detect single (1.25) copies of the <i>bla</i><sub>OXA-1</sub> gene in a reaction and is efficient not only in the detection of a <i>bla</i><sub>OXA-1</sub> model matrix but also in the detection of <i>bla</i><sub>OXA-1</sub>-positive microorganisms. We hope that our assay has the potential to improve the monitoring of OXA-1-producing microorganisms and therefore contribute to mitigating the deadly global threat of antibiotic-resistant microorganisms.
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