Department of Periodontology and Oral Implantology, Temple University School of Dentistry, Philadelphia, PA 19140, USA.
J Periodontal Res. 2013 Aug;48(4):493-9. doi: 10.1111/jre.12031. Epub 2012 Nov 23.
Beta-lactam antibiotics prescribed in periodontal therapy are vulnerable to degradation by bacterial β-lactamases. This study evaluated the occurrence of β-lactamase-positive subgingival bacteria in chronic periodontitis subjects of USA origin, and assessed their in vitro resistance to metronidazole at a breakpoint concentration of 4 μg/mL.
Subgingival plaque specimens from deep periodontal pockets with bleeding on probing were removed from 564 adults with severe chronic periodontitis before treatment. The samples were transported in VMGA III and then plated onto: (i) nonselective enriched Brucella blood agar (EBBA) and incubated anaerobically for 7 d; and (ii) selective trypticase soy-bacitracin-vancomycin (TSBV) and incubated for 3 d in air + 5% CO2 . At the end of the incubation periods, the bacterial test species were identified and quantified. Specimen dilutions were also plated onto EBBA plates supplemented with 2 μg/mL of amoxicillin, a combination of 2 μg/mL of amoxicillin plus 2 μg/mL of the β-lactamase inhibitor clavulanic acid, or 4 μg/mL of metronidazole, followed by anaerobic incubation for 7 d. Bacterial test species presumptively positive for β-lactamase production were identified by growth on EBBA primary isolation plates supplemented with amoxicillin alone and no growth on EBBA primary isolation plates containing both amoxicillin plus clavulanic acid. A subset of such isolates was subjected to nitrocefin-based chromogenic disk testing to confirm the presence of β-lactamase activity. In vitro resistance to 4 μg/mL of metronidazole was noted when growth of test species occurred on metronidazole-supplemented EBBA culture plates.
Two-hundred and ninety-four (52.1%) of the study subjects yielded β-lactamase-producing subgingival bacterial test species, with Prevotella intermedia/nigrescens, Fusobacterium nucleatum and other Prevotella species most frequently identified as β-lactamase-producing organisms. Of the β-lactamase-producing bacterial test species strains recovered, 98.9% were susceptible in vitro to metronidazole at 4 μg/mL.
The occurrence of β-lactamase-positive subgingival bacterial species in more than half of the subjects with severe chronic periodontitis raises questions about the therapeutic potential of single-drug regimens with β-lactam antibiotics in periodontal therapy. The in vitro effectiveness of metronidazole against nearly all recovered β-lactamase-producing subgingival bacterial species further supports clinical periodontitis treatment strategies involving the combination of systemic amoxicillin plus metronidazole.
牙周治疗中开的β-内酰胺类抗生素容易被细菌β-内酰胺酶降解。本研究评估了美国来源的慢性牙周炎患者中β-内酰胺酶阳性的龈下细菌的发生情况,并评估了它们在 4μg/ml 截点浓度下对甲硝唑的体外耐药性。
在治疗前,从 564 名患有严重慢性牙周炎的成年人的深牙周袋中取出探诊出血的龈下菌斑标本。这些样本用 VMGA III 运输,然后接种到:(i)非选择性富集 Brucella 血琼脂(EBBA),并在厌氧条件下孵育 7 天;和(ii)选择性胰蛋白酶大豆-杆菌肽-万古霉素(TSBV),并在空气+5%CO2 下孵育 3 天。孵育期结束时,鉴定和定量细菌测试种。还将标本稀释液接种到补充有 2μg/ml 阿莫西林的 EBBA 平板上,然后进行厌氧孵育 7 天。通过在 EBBA 初步分离平板上单独添加阿莫西林生长,并且在含有阿莫西林和克拉维酸的 EBBA 初步分离平板上不生长,对推定产生β-内酰胺酶的细菌测试种进行鉴定。此类分离株的子集进行硝普基于显色盘测试以确认β-内酰胺酶活性的存在。当测试种在补充有甲硝唑的 EBBA 培养平板上生长时,注意到对 4μg/ml 甲硝唑的体外耐药性。
294 名(52.1%)研究对象产生了产β-内酰胺酶的龈下细菌测试种,中间普氏菌/黑普雷沃菌、核梭杆菌和其他普雷沃菌种最常被鉴定为产β-内酰胺酶的生物体。从回收的产β-内酰胺酶的细菌测试种菌株中,98.9%对甲硝唑在 4μg/ml 时体外敏感。
在患有严重慢性牙周炎的受试者中,超过一半的受试者存在产β-内酰胺酶的龈下细菌种,这引发了对牙周治疗中单用β-内酰胺类抗生素治疗方案的治疗潜力的质疑。甲硝唑对几乎所有回收的产β-内酰胺酶的龈下细菌种的体外有效性进一步支持了涉及全身阿莫西林加甲硝唑联合治疗的临床牙周炎治疗策略。