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新型β-内酰胺类药物头孢比普对耐甲氧西林金黄色葡萄球菌的体外活性研究

In-vitro profile of a new beta-lactam, ceftobiprole, with activity against methicillin-resistant Staphylococcus aureus.

作者信息

Jones M E

机构信息

Eurofins Medinet (Anti-Infective Services) Inc., 13665 Dulles Technology Drive, Herndon, VA 20171, USA.

出版信息

Clin Microbiol Infect. 2007 Jun;13 Suppl 2:17-24. doi: 10.1111/j.1469-0691.2007.01722.x.

Abstract

Ceftobiprole is a novel, broad-spectrum cephalosporin with in-vitro activity against common Gram-positive and Gram-negative organisms. It forms a stable inhibitory complex with Staphylococcus aureus penicillin-binding protein (PBP) 2' (2a), resulting in enhanced activity against methicillin-resistant S. aureus (MRSA). In recent studies of methicillin-susceptible S. aureus, the ceftobiprole MIC(90) value was most frequently < or =1.0 mg/L (MIC range < or =0.25-1.0 mg/L). For MRSA, MIC(90) values were generally 2.0 mg/L (MIC range < or =0.06-4.0 mg/L). MICs for all streptococcal species, except penicillin-resistant Streptococcus viridans but including penicillin-resistant Streptococcus pneumoniae, ranged from < or =0.008 to 2.0 mg/L. Ceftobiprole is active against Enterococcus faecalis (MIC(90) = 4 mg/L), but not generally active against Enterococcus faecium (MIC(90) > 16 mg/L). Ceftobiprole displayed bactericidal activity against Gram-negative pathogens comparable to that of cefepime, ceftazidime or piperacillin-tazobactam in early studies. However, recent data show activity against Pseudomonas aeruginosa similar to that of cefepime but less than that of ceftazidime. Ceftobiprole, like cefepime, is stable in the presence of most class A non-extended spectrum beta-lactamases and inducible class C beta-lactamases. Ceftobiprole is a poor inducer of AmpC beta-lactamase and a poor substrate for hydrolysis by AmpC beta-lactamase. Studies of ceftobiprole in several animal models have demonstrated potent in-vivo efficacy against infections caused by MRSA, including strains intermediately resistant to vancomycin. It was also efficacious in murine infections caused by Gram-negative bacteria with MIC values < or =2 mg/L. The broad spectrum of activity demonstrated by ceftobiprole in vitro and in vivo suggests that it may have potential for empirical treatment of suspected Gram-negative and Gram-positive infections, including those caused by MRSA.

摘要

头孢比普是一种新型广谱头孢菌素,对常见革兰氏阳性菌和革兰氏阴性菌具有体外活性。它与金黄色葡萄球菌青霉素结合蛋白(PBP)2'(2a)形成稳定的抑制复合物,从而增强了对耐甲氧西林金黄色葡萄球菌(MRSA)的活性。在最近对甲氧西林敏感金黄色葡萄球菌的研究中,头孢比普的MIC(90)值大多≤1.0mg/L(MIC范围≤0.25 - 1.0mg/L)。对于MRSA,MIC(90)值一般为2.0mg/L(MIC范围≤0.06 - 4.0mg/L)。除耐青霉素的草绿色链球菌外,所有链球菌属(包括耐青霉素的肺炎链球菌)的MIC值范围为≤0.008至2.0mg/L。头孢比普对粪肠球菌有活性(MIC(90) = 4mg/L),但对屎肠球菌一般无活性(MIC(90)> 16mg/L)。在早期研究中,头孢比普对革兰氏阴性病原体显示出与头孢吡肟、头孢他啶或哌拉西林 - 他唑巴坦相当的杀菌活性。然而,最近的数据表明,它对铜绿假单胞菌的活性与头孢吡肟相似,但低于头孢他啶。与头孢吡肟一样,头孢比普在大多数A类非超广谱β - 内酰胺酶和可诱导的C类β - 内酰胺酶存在时稳定。头孢比普是AmpCβ - 内酰胺酶的弱诱导剂,也是AmpCβ - 内酰胺酶水解的差底物。在多个动物模型中对头孢比普的研究表明,它对由MRSA引起的感染具有强大的体内疗效,包括对万古霉素中度耐药的菌株。它对MIC值≤2mg/L的革兰氏阴性菌引起的小鼠感染也有效。头孢比普在体外和体内显示出的广泛活性表明,它可能有潜力用于经验性治疗疑似革兰氏阴性和革兰氏阳性感染,包括由MRSA引起的感染。

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