头孢吡肟
头孢他啶/阿维巴坦
阿维巴坦
头孢他啶
微生物学
铜绿假单胞菌
内酰胺
化学
插入顺序
生物
他唑巴坦
立体化学
细菌
遗传学
基因
突变体
转座因子
哌拉西林
作者
Leilei Wang,Xuefei Zhang,Xun Yu Zhou,Yingwen Bi,Minggui Wang,Qinglan Guo,Fan Yang
摘要
Eleven blaPER-1-positive Pseudomonas aeruginosa clinical isolates showed variable susceptibility to ceftazidime-avibactam (CZA). The genetic contexts of blaPER-1 were identical (ISCR1-blaPER-1-gst) except for the ST697 isolate HS204 (ISCR1-ISPa1635-blaPER-1-gst). The insertion of ISPa1635 in ISCR1 upstream of blaPER-1 created a hybrid promoter, which elevated the blaPER-1 transcription level and resulted in increased resistance to CZA, ceftolozane-tazobactam, cefepime-zidebactam, and cefiderocol. Diversity in the promoter activity of blaPER-1 partially explains the variable susceptibility to CZA in PER-producing isolates.
科研通智能强力驱动
Strongly Powered by AbleSci AI