Yang Y, Bhachech N, Bradford P A, Jett B D, Sahm D F, Bush K
Wyeth-Ayerst Research, Pearl River, New York 10965, USA.
Antimicrob Agents Chemother. 1998 Jul;42(7):1671-6. doi: 10.1128/AAC.42.7.1671.
Ceftazidime-resistant Escherichia coli and Klebsiella pneumoniae (49 and 102 isolates, respectively) were collected from Barnes-Jewish Hospital, St. Louis, Mo., from 1992 to 1996. They were uniformly resistant to ceftazidime, generally resistant to aztreonam, and variably susceptible to cefotaxime. Four representative E. coli strains and 15 Klebsiella strains were examined. From one to four beta-lactamases were produced per strain, with three possible enzymes related to ceftazidime resistance: enzymes with pI values of 5.6, 6.1, or 7.6. By pulsed-field gel electrophoresis there were at least 13 different Klebsiella strain types and 3 different E. coli strain types, indicating that the outbreak was not clonal. After cloning and sequencing of the beta-lactamase-encoding genes, the enzyme with a pI of 5.6 was identified as TEM-10. The enzyme with a pI of 6.1 was a novel TEM variant (TEM-43) with Lys at 104, His at 164, and Thr at 182. TEM-43 showed broad-spectrum hydrolytic activity against all penicillins, with the highest hydrolysis rate for ceftazidime compared to those for the other expanded-spectrum cephalosporins. Aztreonam was also a good substrate for TEM-43, with hydrolytic activity similar to that of ceftazidime and affinity higher than that of ceftazidime. The TEM-43 beta-lactamase was well inhibited by clavulanic acid and tazobactam at concentrations of < 10 nM. Sulbactam was less effective than the other inhibitors. The Thr182 mutation previously reported in an inhibitor-resistant beta-lactamase did not cause the TEM-43 enzyme to become resistant to any of the inhibitors.
1992年至1996年期间,从密苏里州圣路易斯市的巴恩斯犹太医院收集了对头孢他啶耐药的大肠杆菌和肺炎克雷伯菌(分别为49株和102株)。它们对头孢他啶均耐药,对氨曲南普遍耐药,对头孢噻肟的敏感性各不相同。检测了4株代表性大肠杆菌菌株和15株克雷伯菌菌株。每株菌产生1至4种β-内酰胺酶,有3种可能与头孢他啶耐药相关的酶:pI值为5.6、6.1或7.6的酶。通过脉冲场凝胶电泳,至少有13种不同的克雷伯菌菌株类型和3种不同的大肠杆菌菌株类型,表明此次暴发不是克隆性的。对编码β-内酰胺酶的基因进行克隆和测序后,pI为5.6的酶被鉴定为TEM-10。pI为6.1的酶是一种新型TEM变体(TEM-43),第104位为赖氨酸,第164位为组氨酸,第182位为苏氨酸。TEM-43对所有青霉素均表现出广谱水解活性,与其他广谱头孢菌素相比,对头孢他啶的水解率最高。氨曲南也是TEM-43的良好底物,其水解活性与头孢他啶相似,亲和力高于头孢他啶。克拉维酸和他唑巴坦在浓度<10 nM时能很好地抑制TEM-43β-内酰胺酶。舒巴坦的效果不如其他抑制剂。先前在一种耐抑制剂β-内酰胺酶中报道的第182位苏氨酸突变并未导致TEM-43酶对任何一种抑制剂产生耐药性。