Kobayashi F, Saino Y, Koshi T, Hattori Y, Nakayama M, Iwasaki A, Mori T, Mitsuhashi S
Antimicrob Agents Chemother. 1982 Apr;21(4):536-44. doi: 10.1128/AAC.21.4.536.
Carpetimycins A and B showed widely broad spectra and potent activity against gram-positive and gram-negative bacteria, including various species of anaerobic bacteria. The antimicrobial activity of carpetimycin A was 8 to 64 times greater than that of carpetimycin B and 4 to 128 times greater than that of cefoxitin. The inhibitory concentration of carpetimycin A required to inhibit more than 90% of clinical isolates was 0.39 micrograms/ml for Escherichia coli and klebsiella and 1.56 microgram/ml for Proteus and Staphylococcus aureus. At a concentration of 3.13 micrograms/ml, carpetimycin A inhibited almost all clinical isolates of Enterobacter and Citrobacter, which showed resistance to many clinically used beta-lactam antibiotics. Carpetimycins A and B furthermore were shown to have potent inhibitory activities against several kinds of beta-lactamases produced by beta-lactam-resistant strains; they inhibited not only penicillinase-type beta-lactamases but also cephalosporinase-type beta-lactamases, which were insensitive to clavulanic acid. In combination with beta-lactam antibiotics such as ampicillin, carbenicillin, and cefazolin, carpetimycins A and B showed synergistic activities against beta-lactam-resistant bacteria.
卡培霉素A和B显示出广泛的光谱以及对革兰氏阳性和革兰氏阴性细菌,包括各种厌氧菌的强效活性。卡培霉素A的抗菌活性比卡培霉素B高8至64倍,比头孢西丁高4至128倍。抑制超过90%临床分离株所需的卡培霉素A的抑制浓度,对于大肠杆菌和克雷伯菌属为0.39微克/毫升,对于变形杆菌和金黄色葡萄球菌为1.56微克/毫升。在3.13微克/毫升的浓度下,卡培霉素A几乎抑制了所有对许多临床使用的β-内酰胺抗生素耐药的阴沟肠杆菌和柠檬酸杆菌的临床分离株。此外,卡培霉素A和B对β-内酰胺耐药菌株产生的几种β-内酰胺酶显示出强效抑制活性;它们不仅抑制青霉素酶型β-内酰胺酶,还抑制对克拉维酸不敏感的头孢菌素酶型β-内酰胺酶。与氨苄西林、羧苄西林和头孢唑林等β-内酰胺抗生素联合使用时,卡培霉素A和B对β-内酰胺耐药细菌显示出协同活性。