首页> 外文期刊>Journal of periodontal research >Real-time polymerase chain reaction quantification of human cytomegalovirus and Epstein-Barr virus in periodontal pockets and the adjacent gingiva of periodontitis lesions.
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Real-time polymerase chain reaction quantification of human cytomegalovirus and Epstein-Barr virus in periodontal pockets and the adjacent gingiva of periodontitis lesions.

机译:实时聚合酶链反应定量的人类巨细胞病毒和爱泼斯坦-巴尔病毒在牙周袋和牙周炎病变附近的牙龈。

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BACKGROUND: Genomic sequences of human cytomegalovirus (HCMV) and Epstein-Barr virus (EBV), two herpesviruses, can frequently be detected in periodontal pockets of progressive periodontitis lesions, but the prevalence and load of the two viruses in gingival tissue are unknown. This study determined levels of HCMV and EBV DNA in the periodontal pocket and in the adjacent gingiva of periodontitis lesions using a real-time polymerase chain reaction (PCR) assay. MATERIAL AND METHODS: A total of 20 systemically healthy periodontitis patients participated in the study. Nine patients below 35 years of age were tentatively diagnosed as having aggressive (early onset) periodontitis, and 11 patients 36-56 years of age as having chronic (adult) periodontitis. Clinical parameters were evaluated using established methods. Using periodontal curettes, specimens were harvested from 6-10 mm periodontal pockets and from the adjacent inflamed periodontal pocket wall. A 5'-nuclease (TaqMan) real-time PCR assay was used toidentify and quantify genomic copies of periodontal HCMV and EBV. RESULTS: HCMV DNA was detected in 78% of subgingival and 33% of gingival tissue samples from aggressive periodontitis lesions, but only in 46% of subgingival and 9% of gingival tissue samples from chronic periodontitis lesions. In aggressive periodontitis, HCMV subgingival and gingival tissue counts were positively correlated with periodontal pocket depth and probing attachment loss at sample sites (p6 mm, but none of 14 patients having mean pocket depth at sample teeth
机译:背景:人类巨细胞病毒(HCMV)和爱泼斯坦-巴尔病毒(EBV)(两种疱疹病毒)的基因组序列可以在进行性牙周炎病变的牙周袋中频繁检测到,但是这两种病毒在牙龈组织中的流行和负荷尚不清楚。这项研究使用实时聚合酶链反应(PCR)测定法测定了牙周炎病变的牙周袋和邻近牙龈中的HCMV和EBV DNA水平。材料与方法:共有20名全身健康的牙周炎患者参加了该研究。初步诊断出9名35岁以下的患者患有侵袭性(早发)牙周炎,11名36-56岁的患者患有慢性(成人)牙周炎。使用既定方法评估临床参数。使用牙周刮匙,从6-10 mm的牙周袋和相邻的发炎的牙周袋壁中采集标本。使用5'核酸酶(TaqMan)实时PCR分析来鉴定和定量牙周HCMV和EBV的基因组拷贝。结果:在侵袭性牙周炎病变中78%的龈下和33%的牙龈组织样本中检测到HCMV DNA,但在慢性牙周炎病变中仅46%的龈下和9%的牙龈组织样本中检测到HCMV DNA。在侵袭性牙周炎中,HCMV龈下和牙龈组织计数与牙周袋深度和样本部位探查附着丢失呈正相关(p <或= 0.03; Spearman秩相关系数检验)。在侵略性牙周炎病变中有89%的龈下和78%的牙龈组织样品中发现了EBV DNA,但在慢性牙周炎病变中的龈下和牙龈组织样品中只有46%鉴定出EBV DNA。在侵袭性牙周炎中,样本部位的EBV龈下计数和牙周袋深度呈正相关(p = 0.04; Spearman相关),EBV龈组织计数与全口平均牙龈指数呈正相关(p = 0.04; Spearman相关)。在慢性牙周炎中,统计学意义仅在样本部位的EBV龈下计数与牙周袋深度之间发现(p = 0.04; Spearman相关性)。 HCMV-EBV合并感染在78%的侵袭性牙周炎病变中显示,但仅在27%的慢性牙周炎病变中显示(p = 0.03;卡方检验)。另外,在9名侵略性牙周炎患者中有7名,但在11名慢性牙周炎患者中只有3名在牙龈下或牙龈组织样本中发现了10,000多个HCMV或EBV拷贝(p = 0.03;卡方检验)。在六例样本牙齿中平均牙周袋深度(每颗牙齿四个研究部位)> 6 mm的患者中有四名,但在样本牙齿平均口袋深度小于或等于6 mm的14名患者中,没有一个发现HCMV或EBV拷贝超过100,000牙龈下或牙龈样品(p = 0.001;卡方检验)。在成对的龈下和齿龈组织样本中显示疱疹病毒的牙周炎病变中,组织样本显示四分之三的患者中HCMV拷贝数较高,八分之六的患者中EBV拷贝数较高。结论:相对于慢性牙周炎病变,在侵袭性牙周炎病变的牙周袋和牙龈组织中HCMV和EBV DNA拷贝的发生率升高,并且疱疹病毒计数随牙周炎严重程度的增加而增加,这为两者的牙周病作用提供了实质性支持病毒。牙周部位疱疹病毒DNA的实时PCR测定可能成为监测破坏性牙周疾病进程的有前途的标志。疱疹病毒和细菌,目前大多是单独研究的,可能在牙周炎的发展中协同配合,在以后的牙周感染研究中应被视为病原体。

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