Kitzis M D, Billot-Klein D, Goldstein F W, Williamson R, Tran Van Nhieu G, Carlet J, Acar J F, Gutmann L
Laboratoire de Microbiologie Médicale, Hôpital Saint-Joseph, Paris, France.
Antimicrob Agents Chemother. 1988 Jan;32(1):9-14. doi: 10.1128/AAC.32.1.9.
The novel beta-lactamase CTX-1 (pI 6.3) encoded on a transferable 84-kilobase plasmid was found in six different bacterial species. It was responsible for a significant decrease in susceptibility towards most penicillins and cephalosporins, except imipenem, temocillin, and cephalosporins which have a 7-alpha-methoxy substituent. Synergy between either ampicillin, piperacillin, cefotaxime, ceftazidime, or aztreonam and three beta-lactamase inhibitors (clavulanic acid, sulbactam, and YTR 830) was generally found for different strains harboring CTX-1. This enzyme may be related to or derived from the TEM enzyme, since an intragenic probe of the TEM-1 gene hybridized with a fragment of the plasmid carrying CTX-1.
在一项可转移的84千碱基质粒上编码的新型β - 内酰胺酶CTX - 1(pI 6.3)在六种不同细菌物种中被发现。它导致对大多数青霉素和头孢菌素的敏感性显著降低,但对亚胺培南、替莫西林以及具有7 - α - 甲氧基取代基的头孢菌素除外。对于携带CTX - 1的不同菌株,通常发现氨苄西林、哌拉西林、头孢噻肟、头孢他啶或氨曲南与三种β - 内酰胺酶抑制剂(克拉维酸、舒巴坦和YTR 830)之间存在协同作用。这种酶可能与TEM酶相关或源自TEM酶,因为TEM - 1基因的基因内探针与携带CTX - 1的质粒片段杂交。