Olsvik B, Flynn M J, Tenover F C, Slots J, Olsen I
University of Oslo, Norway.
Oral Microbiol Immunol. 1996 Oct;11(5):304-8. doi: 10.1111/j.1399-302x.1996.tb00186.x.
Tetracycline-resistance in gram-negative periodontal bacteria is often due to the presence of the tet(Q) gene. In the present study the polymerase chain reaction (PCR) was used to examine 54 isolates of gram-negative anaerobic rods (Prevotella intermedia, Prevotella nigrescens and related or Bacteroides-like species) for the presence of the tet(Q) gene. The isolates were recovered from 42 patients with periodontal disease living in northern Europe and North America. An 814 base-pair segment of the tet(Q) gene was amplified from all 41 isolates resistant to tetracycline with minimal inhibitory concentrations of 4 micrograms/ml and above. The presence of the tet(Q) gene was verified using hybridization with a specific oligonucleotide internal to the amplified region and restriction endonuclease digestion with DdeI. A PCR product of the same size was also amplified from one tetracycline susceptible isolate (minimal inhibitory concentration = 0.5 microgram/ml). However, this isolate and the one isolate that was resistant to tetracycline at 4 micrograms/ml showed a weaker signal than the remaining isolates when hybridized with the internal probe. Typing of the PCR products using restriction endonuclease digests with AluI and HpaII revealed two clusters of distinct electrophoresis patterns, indicating that two different subtypes of the tet(Q) gene were present in this material. A control strain containing the tet(Q) gene from Bacteroides thetaiotaomicron had a different electrophoresis pattern for AluI. This study indicated that subtypes of the tet(Q) gene in tetracycline-resistant gram-negative periodontal bacteria exist both within the same patient and within the same species.
革兰氏阴性牙周细菌中的四环素抗性通常归因于tet(Q)基因的存在。在本研究中,聚合酶链反应(PCR)用于检测54株革兰氏阴性厌氧杆菌(中间普氏菌、变黑普氏菌及相关或类拟杆菌属物种)中tet(Q)基因的存在情况。这些分离株取自生活在北欧和北美的42例牙周病患者。从所有41株对四环素耐药且最低抑菌浓度为4微克/毫升及以上的分离株中扩增出了tet(Q)基因的一个814个碱基对的片段。通过与扩增区域内部的特异性寡核苷酸杂交以及用DdeI进行限制性内切酶消化来验证tet(Q)基因的存在。从一株四环素敏感分离株(最低抑菌浓度 = 0.5微克/毫升)中也扩增出了大小相同的PCR产物。然而,当与内部探针杂交时,该分离株和一株对4微克/毫升四环素耐药的分离株显示出比其余分离株更弱的信号。用AluI和HpaII进行限制性内切酶消化对PCR产物进行分型,结果显示出两组不同的电泳图谱,表明该材料中存在两种不同亚型的tet(Q)基因。一株含有来自嗜热栖热放线杆菌的tet(Q)基因的对照菌株,其AluI的电泳图谱不同。本研究表明,四环素耐药革兰氏阴性牙周细菌中的tet(Q)基因亚型在同一患者体内和同一物种内均存在。