Goodwin C S, Hill J P
Antimicrob Agents Chemother. 1977 Jan;11(1):26-30. doi: 10.1128/AAC.11.1.26.
Cefoxitin, cefuroxime, and cephalothin were added to dense populations of beta-lactamase-producing enterobacteria, and the subsequent turbidity changes were monitored continuously. Viable counts and antibiotic assays were made at intervals after the addition of antibiotic, and the morphological appearances of the organisms were observed. Cephalothin caused lysis of most of the organisms tested, but even at high concentrations, after a few hours the antibiotic was destroyed and the organisms recommenced logarithmic growth. Cefoxitin produced lysis of all the strains of Escherichia coli and Klebsiella species tested, with supression of regrowth. With cephalothin and cefoxitin the viable counts after the addition of antibiotic correlated with the turbidity measurements. Cefuroxime infrequently caused lysis that suppressed multiplication, and the organisms became long and filamentous while the turbidity readings increased; the viable counts did not correlate with the turbidity measurements. Cefuroxime and cefoxitin were not destroyed by the beta-lactamases of any of the strains of enterobacteria that were studied.
将头孢西丁、头孢呋辛和头孢噻吩添加到大量产β-内酰胺酶的肠杆菌中,并持续监测随后的浊度变化。添加抗生素后每隔一段时间进行活菌计数和抗生素检测,并观察微生物的形态外观。头孢噻吩导致大多数受试微生物裂解,但即使在高浓度下,几小时后抗生素被破坏,微生物又重新开始对数生长。头孢西丁使所有受试的大肠杆菌和克雷伯菌属菌株发生裂解,并抑制其再生长。对于头孢噻吩和头孢西丁,添加抗生素后的活菌计数与浊度测量结果相关。头孢呋辛很少引起抑制增殖的裂解,微生物变长并呈丝状,而浊度读数增加;活菌计数与浊度测量结果不相关。在所研究的任何肠杆菌菌株的β-内酰胺酶作用下,头孢呋辛和头孢西丁都不会被破坏。