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利用时间杀菌动力学方法评估氨苄青霉素和铋单独及联合使用对处于稳定期和对数生长期的幽门螺杆菌的杀菌活性。

Utilization of time-kill kinetic methodologies for assessing the bactericidal activities of ampicillin and bismuth, alone and in combination, against Helicobacter pylori in stationary and logarithmic growth phases.

作者信息

Coudron P E, Stratton C W

机构信息

Department of Pathology and Laboratory Medicine, McGuire Veterans Affairs Medical Center, Richmond, Virginia 23249-0001.

出版信息

Antimicrob Agents Chemother. 1995 Jan;39(1):66-9. doi: 10.1128/AAC.39.1.66.

Abstract

Assessment of in vitro susceptibility testing of Helicobacter pylori is difficult because of the fastidious, slowly growing nature of this microorganism. The high rate of relapse observed clinically and a possible subpopulation of cells that are not actively replicating suggest the potential need for bactericidal therapy in order to eradicate H. pylori. We used modified time-kill kinetic methodology in order to evaluate the bactericidal activities of ampicillin and bismuth, alone and in combination, against three strains of H. pylori in both a stationary (slow) growth phase and a logarithmic (rapid) growth phase. We found that ampicillin produced a decrease in CFU per milliliter (2 to 4 log10 units) for three strains of H. pylori when tested in logarithmic growth phases but was less inhibitory (< 1-log10-unit decrease in CFU per milliliter) when tested in a stationary growth phase. In contrast, bismuth, when tested in a logarithmic growth phase, produced little inhibitory effect, as the CFU for all strains tested increased above the inoculum. However, when tested in a stationary growth phase, bismuth produced a decrease in CFU per milliliter of < 1 to > 3 log10 units). The activities of these two agents when combined mimicked the activity of the most active drug alone for that growth phase. We conclude that the clinical use of ampicillin combined with bismuth has been more effective than that of either agent used alone because ampicillin targets replicating cells, whereas bismuth targets cells that are not actively replicating.

摘要

由于幽门螺杆菌苛求、生长缓慢的特性,对其进行体外药敏试验颇具难度。临床上观察到的高复发率以及可能存在的非活跃复制细胞亚群提示,为根除幽门螺杆菌,可能需要采用杀菌疗法。我们运用改良的时间-杀菌动力学方法,评估氨苄西林和铋剂单独及联合使用时,在稳定(缓慢)生长期和对数(快速)生长期对三株幽门螺杆菌的杀菌活性。我们发现,在对数生长期进行测试时,氨苄西林使三株幽门螺杆菌的每毫升菌落形成单位(CFU)减少(2至4个对数10单位),但在稳定生长期进行测试时,其抑制作用较小(每毫升CFU减少<1个对数10单位)。相比之下,在对数生长期进行测试时,铋剂几乎没有抑制作用,因为所有测试菌株的CFU均高于接种量。然而,在稳定生长期进行测试时,铋剂使每毫升CFU减少<1至>3个对数10单位)。这两种药物联合使用时的活性与该生长期单独使用最有效药物的活性相似。我们得出结论,氨苄西林与铋剂联合使用在临床上比单独使用任何一种药物都更有效,因为氨苄西林作用于正在复制的细胞,而铋剂作用于非活跃复制的细胞。

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Treatment strategies for Helicobacter pylori infection.
Gastroenterol Clin North Am. 1993 Mar;22(1):183-98.
2
Helicobacter pylori infection.幽门螺杆菌感染
J Antimicrob Chemother. 1993 Jul;32 Suppl A:61-8. doi: 10.1093/jac/32.suppl_a.61.
7
Susceptibility of Campylobacter pyloridis to 20 antimicrobial agents.幽门弯曲菌对20种抗菌剂的敏感性
Antimicrob Agents Chemother. 1986 Sep;30(3):510-1. doi: 10.1128/AAC.30.3.510.

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