关键词: Acinetobacter baumannii ISAba36 OXA-72 carbapenem resistance cefiderocol sulbactam-durlobactam

Mesh : Acinetobacter baumannii / drug effects genetics Cefiderocol Anti-Bacterial Agents / pharmacology Humans Cephalosporins / pharmacology Acinetobacter Infections / drug therapy microbiology Microbial Sensitivity Tests Carbapenems / pharmacology Receptors, Cell Surface / genetics metabolism Sulbactam / pharmacology Male Drug Resistance, Multiple, Bacterial / genetics Azabicyclo Compounds / pharmacology DNA Transposable Elements / genetics Bacterial Outer Membrane Proteins

来  源:   DOI:10.1128/aac.00290-24   PDF(Pubmed)

Abstract:
We report the emergence of cefiderocol resistance in a blaOXA-72 carbapenem-resistant Acinetobacter baumannii isolate from a sacral decubitus ulcer. Cefiderocol was initially used; however, a newly approved sulbactam-durlobactam therapy with source control and flap coverage was successful in treating the infection. Laboratory investigation revealed cefiderocol resistance mediated by ISAba36 insertion into the siderophore receptor pirA.
摘要:
我们报告了从骶褥疮溃疡中分离出的对blaOXA-72碳青霉烯耐药的鲍曼不动杆菌对头孢地洛的耐药性。最初使用头孢地洛;然而,新批准的舒巴坦-durlobactam治疗与源控制和皮瓣覆盖成功治疗感染。实验室研究显示,通过将ISAba36插入铁载体受体pirA介导的头孢地洛耐药性。
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