Tuckman Margareta, Petersen Peter J, Howe Anita Y M, Orlowski Mark, Mullen Stanley, Chan Karen, Bradford Patricia A, Jones C Hal
Infectious Diseases Discovery Research, Wyeth Research, Pearl River, New York 10965, USA.
Antimicrob Agents Chemother. 2007 Sep;51(9):3205-11. doi: 10.1128/AAC.00625-07. Epub 2007 Jul 9.
Tigecycline, a member of the glycylcycline class of antibiotics, was designed to maintain the antibacterial spectrum of the tetracyclines while overcoming the classic mechanisms of tetracycline resistance. The current study was designed to monitor the prevalence of the tet(A), tet(B), tet(C), tet(D), tet(E), and tet(M) resistance determinants in Escherichia coli isolates collected during the worldwide tigecycline phase 3 clinical trials. A subset of strains were also screened for the tet(G), tet(K), tet(L), and tet(Y) genes. Of the 1,680 E. coli clinical isolates screened for resistance to classical tetracyclines, 405 (24%) were minocycline resistant (MIC > or = 8 microg/ml) and 248 (15%) were tetracycline resistant (MIC > or = 8 microg/ml) but susceptible to minocycline (MIC < or = 4 microg/ml). A total of 452 tetracycline-resistant, nonduplicate isolates were positive by PCR for at least one of the six tetracycline resistance determinants examined. Over half of the isolates encoding a single determinant were positive for tet(A) (26%) or tet(B) (32%) with tet(C), tet(D), tet(E), and tet(M), collectively, found in 4% of isolates. Approximately 33% of the isolates were positive for more than one resistance determinant, with the tet(B) plus tet(E) combination the most highly represented, found in 11% of isolates. The susceptibilities of the tetracycline-resistant strains to tigecycline (MIC(90), 0.5 microg/ml), regardless of the encoded tet determinant(s), were comparable to the tigecycline susceptibility of tetracycline-susceptible strains (MIC(90), 0.5 microg/ml). The results provide a current (2002 to 2006) picture of the distribution of common tetracycline resistance determinants encoded in a globally sourced collection of clinical E. coli strains.
替加环素是甘氨酰环素类抗生素的一员,其设计目的是在克服四环素耐药经典机制的同时保持四环素的抗菌谱。本研究旨在监测在全球替加环素3期临床试验期间收集的大肠杆菌分离株中tet(A)、tet(B)、tet(C)、tet(D)、tet(E)和tet(M)耐药决定因子的流行情况。还对一部分菌株进行了tet(G)、tet(K)、tet(L)和tet(Y)基因的筛查。在对1680株临床大肠杆菌分离株进行经典四环素耐药性筛查中,405株(24%)对米诺环素耐药(MIC≥8μg/ml),248株(15%)对四环素耐药(MIC≥8μg/ml)但对米诺环素敏感(MIC≤4μg/ml)。通过PCR检测,共有452株四环素耐药且不重复的分离株至少对所检测的六个四环素耐药决定因子中的一个呈阳性。超过一半编码单一决定因子的分离株对tet(A)(26%)或tet(B)(32%)呈阳性,tet(C)、tet(D)、tet(E)和tet(M)共同在4%的分离株中被发现。约33%的分离株对一种以上耐药决定因子呈阳性,其中tet(B)加tet(E)组合最为常见,在11%的分离株中被发现。无论编码的tet决定因子如何,四环素耐药菌株对替加环素的敏感性(MIC90,0.5μg/ml)与四环素敏感菌株对替加环素的敏感性(MIC90,0.5μg/ml)相当。这些结果提供了2002年至2006年期间在全球来源的临床大肠杆菌菌株中编码的常见四环素耐药决定因子分布情况的现状。