Raposo Jéssica Vasques, Sarmento Dmitry José De Santana, Pinto Rafaela Barbosa Da Silva, Lopes Amanda Oliveira, Gallottini Marina, Tozetto-Mendoza Tânia Regina, Braz-Silva Paulo Henrique, de Paula Vanessa Salete
Instituto Oswaldo Cruz - IOC/FIOCRUZ - Fundação Oswaldo Cruz, Rio De Janeiro, Brasil.
Departamento de Estomatologia, Faculdade de Odontologia da Universidade de São Paulo - FOUSP, São Paulo, SP, Brasil.
J Oral Microbiol. 2020 Jun 30;12(1):1785801. doi: 10.1080/20002297.2020.1785801.
Roseolovirus latency and persistence in salivary glands that are frequently reactivated after renal transplantation to cause infection have been reported. However, limited information is available on the persistence and excretion of HHV-6 and HHV-7 during and after transplant.
32 renal transplant recipients were followed up before (T1) and after transplant (T2 and T3) and viral replication (via assessment of mRNA) in oral fluid samples investigated. Roseolovirus DNA was detected and quantified via multiplex qPCR. For evaluation of mRNA replication, positive samples were subjected to nested RT-PCR.
Viral replication of HHV-7 was significantly increased during T3 (72.9%), compared to the pre-transplant period T1 (25%; McNemar Test, p= 0.001). Analysis of the viral replicative to quantitative ratio disclosed ahigher number of DNA copies (>10) in positive cases of replication (p < 0.001). Astrong positive correlation (Spearman correlation coefficient = 0.781; p< 0.001) was evident between viral quantities of Roseoloviruses.
Our findings consistently suggest that the salivary gland is an important site of active and persistent infection by roseoloviruses. In view of the increasing problem of Roseoloviruses, pre- and post-transplantation, viral surveillance and monitoring of active replication are pivotal steps for effective screening and treatment of renal transplant patients.
已有报道称,玫瑰疹病毒可潜伏于唾液腺并持续存在,在肾移植后常被重新激活而引发感染。然而,关于移植期间及移植后HHV - 6和HHV - 7的持续存在及排泄情况,现有信息有限。
对32例肾移植受者在移植前(T1)、移植后(T2和T3)进行随访,并对口腔液样本中的病毒复制情况(通过评估mRNA)进行研究。通过多重定量聚合酶链反应检测并定量玫瑰疹病毒DNA。为评估mRNA复制情况,对阳性样本进行巢式逆转录聚合酶链反应。
与移植前的T1期(25%)相比,T3期HHV - 7的病毒复制显著增加(72.9%;McNemar检验,p = 0.001)。对病毒复制与定量比率的分析显示,复制阳性病例中的DNA拷贝数更多(>10)(p < 0.001)。玫瑰疹病毒的病毒量之间存在显著的正相关(Spearman相关系数 = 0.781;p < 0.001)。
我们的研究结果一致表明,唾液腺是玫瑰疹病毒活跃和持续感染的重要部位。鉴于玫瑰疹病毒问题在移植前后日益严重,病毒监测以及对活跃复制的监测是有效筛查和治疗肾移植患者的关键步骤。