Increased gene expression and copy number of mutated bla KPC lead to high-level ceftazidime/avibactam resistance in Klebsiella pneumoniae

• Published in: BMC microbiology Vol. 21; no. 1; pp. 1 - 10
• Main Authors: Lingxiao Sun, Haibo Li, Qi Wang, Yingmei Liu, Bin Cao
• Format: Journal Article
• Language: English
• Published: BMC 01.12.2021
• Subjects: Ceftazidime/avibactam resistance; Electroporation; Minimal inhibitory concentration; Mutated bla KPC; Outer membrane protein
• ISSN: 1471-2180
• DOI: 10.1186/s12866-021-02293-0

Abstract Background Resistance to ceftazidime-avibactam was reported, and it is important to investigate the mechanisms of ceftazidime/avibactam resistance in K. pneumoniae with mutations in bla KPC. Results We report the mutated bla KPC is not the only mechanism related to CZA resistance, and investigate the role of outer porin defects, efflux pump, and relative gene expression and copy number of bla KPC and ompk35/36. Four ceftazidime/avibactam-sensitive isolates detected wild type bla KPC-2, while 4 ceftazidime/avibactam-resistant isolates detected mutated bla KPC (bla KPC-51, bla KPC-52, and bla KPC-33). Compared with other ceftazidime/avibactam-resistant isolates with the minimal inhibitory concentration of ceftazidime/avibactam ranging 128–256 mg/L, the relative gene expression and copy number of bla KPC was increased in the isolate which carried bla KPC-51 and also showed the highest minimal inhibitory concentration of ceftazidime/avibactam at 2048 mg/L. The truncated Ompk35 contributes rare to ceftazidime/avibactam resistance in our isolates. No significant difference in minimal inhibitory concentration of ceftazidime/avibactam was observed after the addition of PABN. Conclusions Increased gene expression and copy number of mutated bla KPC can cause high-level ceftazidime/avibactam resistance.