Department of Endodontics, School of Dentistry, Nihon University, Tokyo, Japan.
Division of Advanced Dental Treatment, Dental Research Centre, School of Dentistry, Nihon University, Tokyo, Japan.
Int Endod J. 2020 Apr;53(4):492-505. doi: 10.1111/iej.13255. Epub 2019 Dec 15.
To assess whether Epstein-Barr virus (EBV) reactivation is triggered by persistent apical periodontitis-related microbes using in vitro and ex vivo methodologies.
Surgically removed human periapical granulomas (n = 50) and healthy gingival tissues (n = 10) were analysed to determine the presence of EBV and seven persistent apical periodontitis-related microbes. In addition, real-time polymerase chain reaction was used to detect the mRNA expression of BZLF-1, an immediate-early gene of EBV. Expression of latent membrane protein (LMP)-1 and ZEBRA, an early lytic protein of EBV encoded by BZLF-1, was also examined using triple-colour immunofluorescence staining. n-Butyric acid produced by the microbes was quantified, and luciferase assays were performed in association with bacterial lysates. In addition, Daudi cells were cultured with bacterial lysates, and the expression levels of BZLF-1 mRNA and ZEBRA protein were determined.
EBV DNA and BZLF-1 mRNA were detected in 47 out of 50 periapical granulomas, but not in healthy gingival tissues. The EBV DNA copy number and the number of Fusobacterium nucleatum were significantly positively correlated with BZLF-1 expression in periapical granulomas. The number of Prevotella intermedia was slightly correlated with BZLF-1 expression; however, the other microbes were not. CD79a-positive B cells in periapical granulomas, but not those in healthy gingival tissues, expressed both LMP-1 and ZEBRA. n-Butyric acid production was the highest in F. nucleatum and the lowest in P. intermedia. Enterococcus faecalis, Candida albicans and the other tested microbes did not produce n-butyric acid. An F. nucleatum lysate exhibited significantly increased BZLF-1-luciferase activity in the same manner of commercial butyric acid, whereas P. intermedia did not. F. nucleatum also induced the expression of BZLF-1 mRNA and ZEBRA protein by Daudi cells, indicating that EBV reactivation was induced.
Among the persistent apical periodontitis-related bacteria that were tested, F. nucleatum most strongly reactivated latent EBV, whereas E. faecalis and C. albicans as well as the other microbes did not.
使用体外和离体方法评估是否 Epstein-Barr 病毒(EBV)的再激活是由持续的根尖周炎相关微生物触发的。
分析手术切除的人根尖肉芽肿(n=50)和健康牙龈组织(n=10),以确定 EBV 和七种持续的根尖周炎相关微生物的存在。此外,还使用实时聚合酶链反应检测 EBV 的早期基因 BZLF-1 的 mRNA 表达。使用三色免疫荧光染色还检查了潜伏膜蛋白(LMP)-1 和 EBV 由 BZLF-1 编码的早期裂解蛋白 ZEBRA 的表达。量化微生物产生的正丁酸,并与细菌裂解物一起进行荧光素酶测定。此外,用细菌裂解物培养 Daudi 细胞,并确定 BZLF-1 mRNA 和 ZEBRA 蛋白的表达水平。
在 50 个根尖肉芽肿中有 47 个检测到 EBV DNA 和 BZLF-1 mRNA,但在健康牙龈组织中未检测到。根尖肉芽肿中 EBV DNA 拷贝数和核梭杆菌数量与 BZLF-1 表达呈显著正相关。中间普氏菌与 BZLF-1 表达略有相关,但其他微生物没有。根尖肉芽肿中的 CD79a 阳性 B 细胞,但不是健康牙龈组织中的 B 细胞,表达 LMP-1 和 ZEBRA。核梭杆菌产生的正丁酸最多,中间普氏菌产生的最少。粪肠球菌、白色念珠菌和其他测试的微生物均不产生正丁酸。核梭杆菌裂解物表现出与商业正丁酸相同的方式显著增加 BZLF-1 荧光素酶活性,而中间普氏菌则没有。核梭杆菌还通过 Daudi 细胞诱导 BZLF-1 mRNA 和 ZEBRA 蛋白的表达,表明 EBV 被激活。
在所测试的持续的根尖周炎相关细菌中,核梭杆菌最强地重新激活潜伏的 EBV,而粪肠球菌、白色念珠菌和其他微生物则没有。