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多利培南对具有特征性β-内酰胺酶的肠杆菌科细菌和不动杆菌属细菌的分离株、突变株及接合子的比较活性

Comparative activities of doripenem versus isolates, mutants, and transconjugants of Enterobacteriaceae and Acinetobacter spp. with characterized beta-lactamases.

作者信息

Mushtaq Shazad, Ge Yigong, Livermore David M

机构信息

Antibiotic Resistance Monitoring and Reference Laboratory, Specialist and Reference Microbiology Division, Health Protection Agency Colindale, London, NW9 5HT, United Kingdom.

出版信息

Antimicrob Agents Chemother. 2004 Apr;48(4):1313-9. doi: 10.1128/AAC.48.4.1313-1319.2004.

Abstract

Doripenem (S-4661), a new parenteral carbapenem, was tested against over 250 clinical isolates, mutants, and transconjugants of Enterobacteriaceae and Acinetobacter spp., selected or derived for their beta-lactamase expression characteristics. Imipenem, meropenem, and ertapenem were tested as comparators, along with cephalosporins and piperacillin-tazobactam, by using National Committee for Clinical Laboratory Standards agar dilution methodology. Doripenem MICs were from 0.03 to 0.25 microg/ml for Klebsiella isolates, irrespective of the presence of extended-spectrum beta-lactamases (ESBLs) or plasmid-mediated AmpC or hyperproduced K1 beta-lactamase. Similarly, MICs of doripenem for both AmpC-inducible and -derepressed Enterobacter isolates were 0.06 to 0.5 microg/ml. ESBL production did not raise the MICs of doripenem for Escherichia coli transconjugants, and studies with known expression mutants confirmed that neither inducible nor depressed AmpC beta-lactamase expression was protective in Enterobacter cloacae, Citrobacter freundii, Serratia marcescens, or Morganella morganii. In all of these respects, doripenem resembled meropenem and imipenem, whereas the MICs of ertapenem were raised (but still < or =1 microg/ml) for many ESBL-producing klebsiellas and AmpC-derepressed E. cloacae and C. freundii strains. Resistance to all carbapenems, including doripenem (MICs of mostly 16 to 64 microg/ml, compared with 0.25 to 1 microg/ml for typical strains), was seen in Acinetobacter isolates with metallo-beta-lactamases or OXA-carbapenemases. Isolates of Klebsiella and Serratia spp. with IMP, KPC, and SME beta-lactamases also were resistant to doripenem (MICs, 8 to >64 microg/ml) and to other carbapenems, although the continued apparent susceptibility (MICs, < or =0.5 microg/ml) of E. coli derivatives with cloned IMP-1 and NMC-A beta-lactamases suggested that carbapenem resistance might require other factors besides the enzymes.

摘要

多利培南(S - 4661)是一种新型肠外碳青霉烯类抗生素,对250多种肠杆菌科细菌和不动杆菌属的临床分离株、突变株及接合子进行了测试,这些菌株是根据其β - 内酰胺酶表达特性挑选或衍生而来的。采用美国国家临床实验室标准委员会的琼脂稀释法,将亚胺培南、美罗培南和厄他培南作为对照药物进行测试,同时还测试了头孢菌素类和哌拉西林 - 他唑巴坦。对于克雷伯菌属分离株,无论是否存在超广谱β - 内酰胺酶(ESBLs)、质粒介导的AmpC酶或高产K1β - 内酰胺酶,多利培南的MIC值为0.03至0.25μg/ml。同样,对于AmpC可诱导型和去阻遏型肠杆菌属分离株,多利培南的MIC值为0.06至0.5μg/ml。ESBL的产生并未提高多利培南对大肠杆菌接合子的MIC值,对已知表达突变株的研究证实,无论是诱导型还是去阻遏型AmpCβ - 内酰胺酶的表达,在阴沟肠杆菌、弗氏柠檬酸杆菌、粘质沙雷氏菌或摩根摩根菌中均无保护作用。在所有这些方面,多利培南与美罗培南和亚胺培南相似,而对于许多产ESBL的克雷伯菌属以及AmpC去阻遏型阴沟肠杆菌和弗氏柠檬酸杆菌菌株,厄他培南的MIC值升高(但仍≤1μg/ml)。在具有金属β - 内酰胺酶或OXA - 碳青霉烯酶的不动杆菌属分离株中,观察到对包括多利培南在内的所有碳青霉烯类抗生素耐药(MIC值大多为16至64μg/ml,而典型菌株为0.25至1μg/ml)。携带IMP、KPC和SMEβ - 内酰胺酶的克雷伯菌属和沙雷氏菌属分离株对多利培南(MIC值为8至>64μg/ml)和其他碳青霉烯类抗生素也耐药,不过携带克隆IMP - 1和NMC - Aβ - 内酰胺酶的大肠杆菌衍生物仍表现出明显的敏感性(MIC值≤0.5μg/ml),这表明碳青霉烯类抗生素耐药可能除了这些酶之外还需要其他因素。

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