Clermont D, Chesneau O, De Cespédès G, Horaud T
Laboratoire des Staphylocoques et des Streptocoques, Institut Pasteur, Paris, France.
Antimicrob Agents Chemother. 1997 Jan;41(1):112-6. doi: 10.1128/AAC.41.1.112.
An approach based on PCR has been developed to identify new members of the tet gene family in streptococci resistant to tetracycline and minocycline. Degenerate primers, corresponding to portions of the conserved domains of the proteins Tet(M), Tet(O), TeTB(P), Tet(Q), and Tet(S), all specifying the tetracycline-minocycline resistance phenotype, were used to selectively amplify DNA fragments within the coding sequences. Nine streptococcal strains which do not carry the genes tet(M), tet(O), tetB(P), tet(Q), or tet(S) were investigated. Four of them gave no detectable PCR products. The five remaining strains each yielded a PCR product of 1.1 kbp. DNA hybridization experiments showed that these putative Tet determinants fell into four new hybridization classes, of which one, Tet T, was further analyzed. The gene tet(T) was isolated from Streptococcus pyogenes A498, and the nucleotide sequence that was necessary and sufficient for the expression of tetracycline resistance in Escherichia coli was determined. The deduced Tet(T) protein consists of 651 amino acids. The protein most closely related to Tet(T) was Tet(Q), which has 49% identical amino acid residues. A phylogenetic analysis revealed that Tet T represents a novel branching order among the Tet determinants so far described.
已开发出一种基于聚合酶链反应(PCR)的方法,用于在对四环素和米诺环素耐药的链球菌中鉴定tet基因家族的新成员。使用与Tet(M)、Tet(O)、TeTB(P)、Tet(Q)和Tet(S)蛋白保守结构域部分相对应的简并引物,这些蛋白均赋予四环素-米诺环素耐药表型,用于选择性扩增编码序列内的DNA片段。研究了9株不携带tet(M)、tet(O)、tetB(P)、tet(Q)或tet(S)基因的链球菌菌株。其中4株未检测到PCR产物。其余5株菌株均产生了1.1 kbp的PCR产物。DNA杂交实验表明,这些假定的Tet决定簇分为四个新的杂交类别,其中一个类别Tet T被进一步分析。从化脓性链球菌A498中分离出tet(T)基因,并确定了在大肠杆菌中表达四环素抗性所必需且足够的核苷酸序列。推导的Tet(T)蛋白由651个氨基酸组成。与Tet(T)关系最密切的蛋白是Tet(Q),其氨基酸残基有49%相同。系统发育分析表明,Tet T代表了迄今为止所描述的Tet决定簇中的一个新的分支顺序。