Tang Gaoyan, Samaranayake Lakshman P, Yip Hak-Kong, Chu Frederick C S, Tsang Peter C S, Cheung Becky P K
Oral Bio-Sciences, Faculty of Dentistry, The University of Hong Kong, Hong Kong SAR, China.
J Dent. 2003 Nov;31(8):559-68. doi: 10.1016/s0300-5712(03)00112-x.
The poor sensitivity of phenotypic identification techniques has hampered the taxonomic differentiation of Actinomyces. Hence we developed a sensitive and specific, PCR-based oligonucleotide-DNA hybridization technique to detect Actinomyces spp. and, used this method to detect these organisms in samples directly obtained from infected root canals.
A total of 32 samples from 28 Chinese patients, with primary root canal infections, aseptically exposed at the first patient visit, were studied. Whole bacterial genomic DNA was isolated directly from paper point samples. The variable regions of 16S ribosomal DNA of bacteria were amplified and labeled with digoxigenin for further hybridization and detection. A total of seven oligonucleotide probes specific for A. bovis, A. gerencseriae, A. israelii, A. meyeri, catalase-negative A. naeslundii (genospecies 1 and 2), catalase-positive A. naeslundii genospecies 2 and A. odontolyticus were used.
16 of the 32 teeth were infected with one or more Actinomyces species. The prevalence rates of the examined species were: A. odontolyticus 31.3%, A. meyeri 9.4%, A. naeslundii 9.4%, A. israelii 6.3% and A. gerencseriae 3.1%; no A. bovis was detected in any of the canals. Furthermore, A. odontolyticus was isolated more frequently from root canals with caries or a history of caries (Fisher's exact test: P=0.0496; Odds ratio=9.00, 95% confidence interval: 0.97-83.63), and A. naeslundii was significantly associated with traumatized teeth (Fisher's exact test: P=0.0121; Odds ratio=57.00, 95% confidence interval: 2.10-1546.90). However, no significant correlation was found between Actinomyces spp. and clinical symptoms and signs, such as pain, swelling, percussion to tenderness, sinus and periapical radiolucency.
Actinomyces spp. may be important pathogens of root canal infections. A. naeslundii in particular may be related with traumatized teeth. A. odontolyticus appears to be involved in infections related to caries, exposure of dentinal tubules during cavity preparation and/or leaking restoration, but further clarification with large samples is necessary.
表型鉴定技术的低敏感性阻碍了放线菌的分类鉴别。因此,我们开发了一种灵敏且特异的基于聚合酶链反应(PCR)的寡核苷酸 - DNA杂交技术来检测放线菌属,并使用该方法直接检测从感染根管获取的样本中的这些微生物。
对28例中国患者的32个样本进行了研究,这些样本来自初次就诊时无菌暴露的原发性根管感染。直接从纸尖样本中分离全细菌基因组DNA。扩增细菌16S核糖体DNA的可变区,并用洋地黄毒苷标记,用于进一步杂交和检测。总共使用了七种寡核苷酸探针,分别针对牛放线菌、杰氏放线菌、衣氏放线菌、迈氏放线菌、过氧化氢酶阴性的内氏放线菌(基因型1和2)、过氧化氢酶阳性的内氏放线菌基因型2和溶牙放线菌。
32颗牙齿中有16颗感染了一种或多种放线菌。所检测菌种的患病率分别为:溶牙放线菌31.3%、迈氏放线菌9.4%、内氏放线菌9.4%、衣氏放线菌6.3%和杰氏放线菌3.1%;在任何根管中均未检测到牛放线菌。此外,溶牙放线菌更频繁地从有龋齿或有龋齿病史的根管中分离出来(Fisher精确检验:P = 0.0496;优势比 = 9.00,95%置信区间:0.97 - 83.63),而内氏放线菌与外伤牙显著相关(Fisher精确检验:P = 0.0121;优势比 = 57.00,95%置信区间:2.10 - 1546.90)。然而,未发现放线菌与临床症状和体征(如疼痛、肿胀、叩痛、窦道和根尖周透射区)之间存在显著相关性。
放线菌可能是根管感染的重要病原菌。特别是内氏放线菌可能与外伤牙有关。溶牙放线菌似乎参与了与龋齿、窝洞制备过程中牙本质小管暴露和/或修复体渗漏相关的感染,但需要大样本进一步阐明。