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blaOXA-101 和 blaOXA-573 在广泛耐药/全耐药(XDR/PDR)铜绿假单胞菌对头孢他啶-阿维巴坦耐药性中的作用
Authors Kang Y, Cui J
Received 16 December 2024
Accepted for publication 18 April 2025
Published 16 May 2025 Volume 2025:18 Pages 2547—2555
DOI http://doi.org/10.2147/IDR.S506452
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Zhi Ruan
Yixin Kang,1,2 Junchang Cui1,2
1Nankai University, Tianjin, People’s Republic of China; 2College of Pulmonary & Critical Care Medicine, The Eighth Medical Center, Chinese PLA General Hospital, Beijing, People’s Republic of China
Correspondence: Junchang Cui, College of Pulmonary & Critical Care Medicine, The Eighth Medical Center, Chinese PLA General Hospital, 17A Heishanhu Road, Haidian District, Beijing, 100091, People’s Republic of China, Email guoguoyoumeng@163.com
Objective: To explore the association of the resistance of extensively drug-resistant/ pan-drug-resistant Pseudomonas aeruginosa (XDR/PDR-PA) to ceftazidime-avibactam (CZA) with various class D β-lactamase genes.
Methods: Twofold dilution was used to determine the minimum inhibitory concentration (MIC) of CZA against XDR/PDR-PA. Whole genome sequencing and bioinformatics analysis were used to determine the drug-resistant genes of each isolate. Pearson correlation coefficient and statistical analysis were used to assess the association of the resistance of XDR/PDR-PA to CZA and various class D β-lactamase genes.
Results: ST244 was the predominant type (34/68, 50%) among the 68 XDR/PDR-PA strains. Subsequently, ST357 was the second most prevalent type (5/68, 7.4%) strain. blaOXA-101 and blaOXA-573 genes were associated with resistance to CZA (p-value was 0.029 and 0.021, respectively) in the 68 XDR/PDR-PA isolates tested.
Conclusion: Our work found that blaOXA-101 and blaOXA-847 play a role in XDR/PDR-PA resistance to CZA.
Keywords: P. aeruginosa, β-lactamases, ceftazidime–avibactam