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金黄色葡萄球菌和铜绿假单胞菌接种量对氟喹诺酮类和碳青霉烯类药物体外活性及体内疗效的影响。

Influence of inoculum size of Staphylococcus aureus and Pseudomonas aeruginosa on in vitro activities and in vivo efficacy of fluoroquinolones and carbapenems.

作者信息

Mizunaga Shingo, Kamiyama Tomoko, Fukuda Yoshiko, Takahata Masahiro, Mitsuyama Junichi

机构信息

Research Laboratories, Toyama Chemical Co. Ltd, Japan.

出版信息

J Antimicrob Chemother. 2005 Jul;56(1):91-6. doi: 10.1093/jac/dki163. Epub 2005 May 12.

Abstract

OBJECTIVES

We investigated the effect of inoculum size on MIC, bactericidal activity and the post-antibiotic effect (PAE) of carbapenems (imipenem, panipenem and meropenem) and injectable quinolones (pazufloxacin and ciprofloxacin) against Staphylococcus aureus and Pseudomonas aeruginosa, and also the relationship between in vivo systemic infection by changing the inoculum size injected in mice.

RESULTS

Increasing the bacterial inoculum (10(5)-10(8) cfu/mL) had no significant effect on the MIC of any of the tested antimicrobial agents. With the standard inocula (10(6) cfu/mL) of both test strains, all the antimicrobial agents showed bactericidal activity; however, increasing the inoculum size to >10(8) cfu/mL resulted in a reduction in bactericidal activity of all the antimicrobial agents against S. aureus Smith. In contrast, increasing the inoculum size of P. aeruginosa exerted only a minimal influence on the bactericidal activity of fluoroquinolones, but resulted in a reduction in the bactericidal activity of carbapenems. With the standard inoculum size of S. aureus Smith, pre-incubation with fluoroquinolones and carbapenems, except for meropenem, was sufficient to produce PAEs. When the inoculum was increased, the duration of the PAEs of these antimicrobial agents was reduced; however, those of fluoroquinolones were longer than carbapenems. Inoculum size had a greater influence on the in vivo efficacy of carbapenems than that of fluoroquinolones.

CONCLUSIONS

Our results suggest that decreased bactericidal activity, or the in vitro PAE of carbapenems and fluoroquinolones, is related to the reduced in vivo protective effect against infection caused by high inoculum with S. aureus or P. aeruginosa.

摘要

目的

我们研究了接种量对碳青霉烯类抗生素(亚胺培南、帕尼培南和美罗培南)及注射用喹诺酮类抗生素(帕珠沙星和环丙沙星)针对金黄色葡萄球菌和铜绿假单胞菌的最低抑菌浓度(MIC)、杀菌活性及抗生素后效应(PAE)的影响,同时还研究了通过改变小鼠体内注射的接种量与体内全身感染之间的关系。

结果

增加细菌接种量(10⁵ - 10⁸ cfu/mL)对任何一种受试抗菌药物的MIC均无显著影响。对于两种受试菌株的标准接种量(10⁶ cfu/mL),所有抗菌药物均表现出杀菌活性;然而,将接种量增加至>10⁸ cfu/mL会导致所有抗菌药物对金黄色葡萄球菌史密斯菌株的杀菌活性降低。相比之下,增加铜绿假单胞菌的接种量对氟喹诺酮类药物的杀菌活性影响极小,但会导致碳青霉烯类药物的杀菌活性降低。对于金黄色葡萄球菌史密斯菌株的标准接种量,除美罗培南外,用氟喹诺酮类和碳青霉烯类药物进行预孵育足以产生PAE。当接种量增加时,这些抗菌药物的PAE持续时间缩短;然而,氟喹诺酮类药物的PAE持续时间比碳青霉烯类药物长。接种量对碳青霉烯类药物体内疗效的影响大于氟喹诺酮类药物。

结论

我们的结果表明,碳青霉烯类和氟喹诺酮类药物杀菌活性降低或体外PAE与针对由高接种量金黄色葡萄球菌或铜绿假单胞菌引起的感染的体内保护作用降低有关。

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