Wu Yan-min, Yan Jie, Chen Li-li, Sun Wei-lian, Gu Zhi-yuan
Department of Stomatology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China.
J Zhejiang Univ Sci B. 2006 Nov;7(11):876-83. doi: 10.1631/jzus.2006.B0876.
To detect the infection frequencies of different genotypes of Epstein-Barr virus (EBV) in subgingival samples from chronic periodontitis (CP) patients, and to discuss the correlation between infection with EBV and clinical parameters.
Nested-PCR assay was used to detect EBV-1 and EBV-2 in subgingival samples from 65 CP patients, 65 gingivitis patients and 24 periodontally healthy individuals. The amplicons were further identified by restriction fragment length polymorphism analysis (RFLP) with endonucleases Afa I and Stu I. Clinical parameters mainly included bleeding on probing (BOP), probing depth (PD), attachment loss (AL) in six sites of the dentition.
In CP patients, gingivitis and periodontally healthy individuals, the infection frequencies were 47.7%, 24.6% and 16.7% for EBV-1, and 15.4%, 7.7% and 0% for EBV-2, respectively. In 2 out of the 65 CP patients co-infection of EBV-1 and EBV-2 was found. The positive rate of EBV-1 in chronic periodontitis patients was higher than that in gingivitis patients (P=0.01) and periodontally healthy individuals (P=0.01). But no significant difference was shown in EBV-1 frequency between gingivitis patients and healthy individuals (P>0.05) or in EBV-2 frequency among the three groups (P>0.05). In CP patients, higher mean BOP value was found in EBV-1 or EBV-2 positive patients than that in EBV negative ones (P<0.01), but with no statistical difference in the mean PD or AL value between EBV positive and negative patients (P>0.05). After initial periodontal treatment, 12 out of the 21 EBV-1 positive CP patients did not show detectable EBV-1 in subgingival samples.
nPCR plus RFLP analysis is a sensitive, specific and stable method to detect EBV-1 and EBV-2 in subgingival samples. Subgingival infection with EBV-1 is closely associated with chronic periodontitis. Infection of EBV in subgingival samples was correlated with BOP.
检测慢性牙周炎(CP)患者龈下样本中不同基因型EB病毒(EBV)的感染频率,并探讨EBV感染与临床参数之间的相关性。
采用巢式聚合酶链反应(Nested-PCR)检测65例CP患者、65例牙龈炎患者和24例牙周健康个体龈下样本中的EBV-1和EBV-2。扩增产物通过限制性片段长度多态性分析(RFLP),使用核酸内切酶Afa I和Stu I进一步鉴定。临床参数主要包括探诊出血(BOP)、探诊深度(PD)、牙列六个位点的附着丧失(AL)。
在CP患者、牙龈炎患者和牙周健康个体中,EBV-1的感染频率分别为47.7%、24.6%和16.7%,EBV-2的感染频率分别为15.4%、7.7%和0%。65例CP患者中有2例同时感染了EBV-1和EBV-2。慢性牙周炎患者中EBV-1的阳性率高于牙龈炎患者(P=0.01)和牙周健康个体(P=0.01)。但牙龈炎患者与健康个体之间的EBV-1感染频率无显著差异(P>0.05),三组之间的EBV-2感染频率也无显著差异(P>0.05)。在CP患者中,EBV-1或EBV-2阳性患者的平均BOP值高于EBV阴性患者(P<0.01),但EBV阳性和阴性患者之间的平均PD或AL值无统计学差异(P>0.05)。经过初始牙周治疗后,21例EBV-1阳性的CP患者中有12例龈下样本中未检测到EBV-1。
巢式PCR加RFLP分析是检测龈下样本中EBV-1和EBV-2的敏感、特异且稳定的方法。龈下EBV-1感染与慢性牙周炎密切相关。龈下样本中EBV感染与BOP相关。