Siqueira José F, Rôças Isabela N
Department of Endodontics, Faculty of Dentistry, Estácio de Sá University, Rio de Janeiro, RJ, Brazil.
J Endod. 2003 Nov;29(11):735-8. doi: 10.1097/00004770-200311000-00012.
A nested polymerase chain reaction (PCR)-based method was used to directly survey samples taken from primary endodontic infections for the occurrence of Pseudoramibacter alactolyticus. Identification by nested PCR was performed in root-canal samples from teeth associated with asymptomatic periradicular lesions or acute apical periodontitis, and in pus samples from acute periradicular abscesses. DNA was extracted from the samples and initially amplified using universal 16S rDNA primers. A second round of amplification used the first PCR products to detect a specific fragment of P. alactolyticus 16S rDNA. P. alactolyticus was detected in 76% of root-canal samples from teeth showing asymptomatic periradicular lesions, in 60% of samples taken from root canals associated with acute apical periodontitis, and in 32% of pus samples aspirated from acute periradicular abscesses. No significant association of this species with clinical symptoms was observed (p > 0.01). In general, P. alactolyticus occurred in 56% of samples taken from infections of endodontic origin. The high prevalence of P. alactolyticus in infections of endodontic origin as detected by nested PCR in this study, and its apparent pathogenicity, particularly in mixed infections, indicate that this bacterial species is a candidate endodontic pathogen that can participate in the etiology of different forms of periradicular diseases.
采用基于巢式聚合酶链反应(PCR)的方法,直接检测取自原发性牙髓感染的样本中解乳糖假拉米菌的存在情况。通过巢式PCR在与无症状根尖周病变或急性根尖周炎相关牙齿的根管样本以及急性根尖周脓肿的脓液样本中进行鉴定。从样本中提取DNA,首先使用通用16S rDNA引物进行扩增。第二轮扩增使用第一轮PCR产物来检测解乳糖假拉米菌16S rDNA的特定片段。在显示无症状根尖周病变的牙齿的根管样本中,76%检测到了解乳糖假拉米菌;在与急性根尖周炎相关的根管样本中,60%检测到该菌;在从急性根尖周脓肿抽吸的脓液样本中,32%检测到该菌。未观察到该菌与临床症状有显著关联(p>0.01)。总体而言,在取自牙髓源性感染的样本中,56%检测到了解乳糖假拉米菌。本研究通过巢式PCR检测到解乳糖假拉米菌在牙髓源性感染中高度流行,及其明显的致病性,尤其是在混合感染中,表明该细菌是一种可能参与不同形式根尖周疾病病因的牙髓病原体。