首页> 外文期刊>Antimicrobial agents and chemotherapy. >Phenotypic, Biochemical, and Genetic Analysis of KPC-41, a KPC-3 Variant Conferring Resistance to Ceftazidime-Avibactam and Exhibiting Reduced Carbapenemase Activity
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Phenotypic, Biochemical, and Genetic Analysis of KPC-41, a KPC-3 Variant Conferring Resistance to Ceftazidime-Avibactam and Exhibiting Reduced Carbapenemase Activity

机译:KPC-41的表型,生化和遗传分析,KPC-3变体赋予CeTtazidime-Avibactam的耐药性,表现出降低的碳碱酶活性

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摘要

A novel KPC variant, KPC-41, was identified in a Klebsielia pneumoniae clinical isolate from Switzerland. This beta-lactamase possessed a 3-amino-acid insertion (Pro-Asn-Lys) located between amino acids 269 and 270 compared to the KPC-3 amino acid sequence. Cloning and expression of the bla(KPC-41) gene in Escherichia coli, followed by determination of MIC values and kinetic parameters, showed that KPC-41, compared to those of KPC-3, has an increased affinity to ceftazidime and a decreased sensitivity to avibactam, leading to resistance to ceftazidime-avibactam once produced in K. pneumoniae. Furthermore, KPC-41 exhibited a drastic decrease of its carbapenemase activity. This report highlights that a diversity of KPC variants conferring resistance to ceftazidime-avibactam already circulate in Europe.
机译:从瑞士的Klebsielia肺炎临床孤立中鉴定了一种新的KPC变体KPC-41。 与KPC-3氨基酸序列相比,该β-内酰胺酶具有位于氨基酸269和270之间的3-氨基酸插入(Pro-Asn-Lys)。 BLA(KPC-41)基因在大肠杆菌中的克隆和表达,随后测定MIC值和动力学参数,显示与KPC-3相比的KPC-41对头孢他啶具有增加的亲和力和降低的灵敏度 曾导致Avibactam,导致对Ceftazidime-Avibactam的抗性曾经在K.Pneumoniae中产生。 此外,KPC-41表现出其碳结构酶活性的急剧下降。 本报告突出显示赋予Ceftazidime-Avibactam的抗核磁共振变体的多样性已经在欧洲传播。

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