Watanakunakorn C
Rev Infect Dis. 1981 Nov-Dec;3 suppl:S210-5.
Vancomycin inhibits the second stage of cell wall synthesis in susceptible bacteria. Furthermore, there is evidence that vancomycin also alters the permeability of the cell membrane and selectively inhibits ribonucleic acid synthesis. Stable L-phase variants are susceptible to vancomycin, but induction of bacterial L-phase variants with vancomycin is very difficult. Vancomycin is active against a large number of species of gram-positive cocci and bacilli, such as Staphylococcus aureus (including methicillin-resistant strains), Staphylococcus epidermidis (including multiply resistant strains). Streptococcus pneumoniae (including multiply resistant strains), Streptococcus pyogenes, Streptococcus agalactiae, Streptococcus bovis, viridans group Streptococcus, enterococcus, Clostridium species, diphtheroids, Listeria monocytogenes, Actinomyces species, and Lactobacillus species. Antimicrobial activity can be enhanced with the combination of vancomycin and an aminoglycoside against S. aureus, S. bovis, enterococcus, and viridans Streptococcus. The combination of vancomycin and rifampin also has enhanced activity against S. aureus.
万古霉素可抑制敏感细菌细胞壁合成的第二阶段。此外,有证据表明万古霉素还会改变细胞膜的通透性,并选择性地抑制核糖核酸合成。稳定的L型变体对万古霉素敏感,但用万古霉素诱导细菌L型变体非常困难。万古霉素对大量革兰氏阳性球菌和杆菌具有活性,如金黄色葡萄球菌(包括耐甲氧西林菌株)、表皮葡萄球菌(包括多重耐药菌株)、肺炎链球菌(包括多重耐药菌株)、化脓性链球菌、无乳链球菌、牛链球菌、草绿色链球菌、肠球菌、梭菌属、类白喉杆菌、单核细胞增生李斯特菌、放线菌属和乳杆菌属。万古霉素与氨基糖苷类药物联合使用时,对金黄色葡萄球菌、牛链球菌、肠球菌和草绿色链球菌的抗菌活性可增强。万古霉素与利福平联合使用时,对金黄色葡萄球菌也具有增强的活性。