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ORIGINAL RESEARCH article

Front. Microbiol.

Sec. Infectious Agents and Disease

Volume 16 - 2025 | doi: 10.3389/fmicb.2025.1669811

This article is part of the Research TopicRapid and Efficient Analytical Technologies for Pathogen DetectionView all 18 articles

Rapid identification of Acinetobacter baumannii using novel specific molecular targets derived from pan-genome analysis and its clinical application

Provisionally accepted
  • 1The First Affiliated Hospital of Henan University of Science and Technology, Luoyang, China
  • 2Huaiyin Normal University, Huai'an, China
  • 3Fujian Medical University, Fuzhou, China

The final, formatted version of the article will be published soon.

Acinetobacter baumannii is a pathogen capable of causing severe hospital-acquired infections such as ventilator-associated pneumonia and bacteremia, accounting for over 80% of nosocomial infections. Current nucleic acid tests (NATs) for A. baumannii suffer from limitations in specificity and sensitivity due to reliance on suboptimal targets. Therefore, this study aimed to identify novel, highly specific molecular targets for A. baumannii NATs using pan-genome analysis. A total of 9 specific molecular targets for A. baumsmpB and ppaX. These specific species targets have been verified by BLAST and PCR of non-target strains to have 100% specificity for A. baumannii. The specificity of the 9 target genes was verified by PCR, and 3 pairs of different PCR primers were designed for each target gene to determine the best sensitivity of PCR method for each target. Corresponding qPCR detection methods of 9 targets was also established and that of ureE was screened with the lowest detection limit of 10-7 ng/µL. The qPCR method based on the ureE gene can achieve rapid, sensitive and accurate detection of A. baumannii in actual samples with interference from non-target bacteria. After verification of 23 samples, the qPCR method based on the mined target met the requirements in sensitivity, specificity and efficiency, and was consistent with the national verification method. These results confirm that novel pan-genome targets with excellent generalizability among A. baumannii strains enhance detection accuracy in hospital environments, bringing hope for rapid clinical identification, timely interventions, and reduced mortality.

Keywords: Acinetobacter baumannii, novel specific molecular targets, pan-genome analysis, PCR, Nucleic acid testing

Received: 20 Jul 2025; Accepted: 13 Oct 2025.

Copyright: © 2025 Chen, Wang, Ju, Zhang, Ren, Chen, Yi, Zhang, Zhang and Xiang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Jianying Zhang, zhangyingjian@haust.edu.cn
Shenghang Zhang, fzzyyzsh@126.com
Xinran Xiang, xiangxr2022@163.com

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