Microorganisms (Apr 2025)

On-Site Dual Detection of Airborne <i>Acinetobacter baumannii</i> and Its Carbapenem-Resistant Gene <i>bla</i><sub>OXA-23</sub> Using a One-Pot Visual LAMP-CRISPR/Cas12a-Based Platform

  • Huijun Lu,
  • Tong Zhang,
  • Wei Huang,
  • Jinhui Zhu,
  • Haoran Qin,
  • Xi Chen,
  • Wang Zhao,
  • Guodong Sui

DOI
https://doi.org/10.3390/microorganisms13050976
Journal volume & issue
Vol. 13, no. 5
p. 976

Abstract

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Acinetobacter baumannii (A. baumannii), a very common pathogen, poses a significant public health threat due to its antibiotic resistance and long survival in healthcare environments. Both A. baumannii and carbapenem-resistant A. baumannii (CRAB) can spread through the air, increasing infection risks. Therefore, monitoring their presence in the air is of great significance, especially in hospitals. Herein, we developed a Chelex-100-LAMP-CRISPR/Cas12a (CLC) platform including DNA release and nucleic acid test. Combined with a wet cyclone sampler, the platform can detect airborne A. baumannii and its most common carbapenem-resistant gene, blaOXA-23, within 70 min. This CLC platform has also been proven to have a detection limit of 6 × 102 CFU of CRAB per test through simulated air samples. Moreover, this platform was also used to test five actual air samples from a tertiary hospital, and the results achieved perfect concordance with sequencing data, validating the platform’s accuracy and reliability. Therefore, the CLC platform showed great potential for the rapid, on-site detection of airborne A. baumannii and its carbapenem-resistant gene blaOXA-23, offering a valuable tool for infection control in healthcare environments.

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