Roy Marlène, Lacôte Sandra, Desloire Sophie, Thiesson Adrien, Pulido Coralie, Aurine Noémie, Mathieu Cyrille, Pain Bertrand, Marianneau Philippe, Arnaud Frédérick, Ratinier Maxime
IVPC UMR754, EPHE, Université PSL, INRAE, Universite Claude Bernard Lyon 1, Lyon, France.
Laboratoire de Lyon, ANSES, Virology Unit, Lyon, France.
Virulence. 2025 Dec;16(1):2535470. doi: 10.1080/21505594.2025.2535470. Epub 2025 Jul 22.
Toscana virus (TOSV), belonging to family, is circulating in most Mediterranean countries and is transmitted to humans by infected female sand flies. While most infections are asymptomatic, TOSV is considered as a leading cause of meningitis and encephalitis in humans during summer. Three TOSV genotypes (named A, B, and C) have been identified, although no virus strain belonging to lineage C has been isolated so far. To date, the relationship between TOSV genetic diversity and viral pathogenicity or replication capacity remains unknown. This study aimed to compare two TOSV strains from either lineage A (TOSV-A) or B (TOSV-B) in several cell culture and two mouse models. We showed that TOSV-A replicated more efficiently in BSR and A549 cells, while TOSV-B had a replication advantage in human induced pluripotent stem cells differentiated in neural cells and LL-5 sand fly cells. , we were unable to detect any virus in the brains of immunocompetent C57BL/6JRj mice infected with either strain of TOSV. On the contrary, we showed that TOSV-A disseminated to the central nervous system of 129/Sv mice unlike TOSV-B, despite higher viremia of TOSV-B and a greater dissemination of this strain in other organs. The reasons for these differences are not yet known, although we showed that the presence of TOSV neutralizing antibodies in serum was slightly delayed in TOSV-A-infected mice. Altogether, the data presented in this study provide new avenues to study TOSV-induced pathogenesis and ultimately unveil molecular viral determinants modulating TOSV replication capacity.
托斯卡纳病毒(TOSV)属于[此处原文缺失病毒所属科名]科,在大多数地中海国家传播,通过受感染的雌性白蛉传播给人类。虽然大多数感染是无症状的,但TOSV被认为是夏季人类脑膜炎和脑炎的主要病因。已鉴定出三种TOSV基因型(命名为A、B和C),尽管迄今为止尚未分离到属于C谱系的病毒株。迄今为止,TOSV遗传多样性与病毒致病性或复制能力之间的关系仍不清楚。本研究旨在在几种细胞培养物和两种小鼠模型中比较来自A谱系(TOSV-A)或B谱系(TOSV-B)的两种TOSV毒株。我们发现TOSV-A在BSR和A549细胞中复制效率更高,而TOSV-B在分化为神经细胞的人诱导多能干细胞和LL-5白蛉细胞中具有复制优势。此外,我们在感染任何一种TOSV毒株的免疫活性C57BL/6JRj小鼠的脑中均未检测到任何病毒。相反,我们发现TOSV-A与TOSV-B不同,它能传播到129/Sv小鼠的中枢神经系统,尽管TOSV-B的病毒血症更高,且该毒株在其他器官中的传播范围更广。这些差异的原因尚不清楚,尽管我们发现TOSV-A感染的小鼠血清中TOSV中和抗体的出现略有延迟。总之,本研究提供的数据为研究TOSV诱导发病机制以及最终揭示调节TOSV复制能力的分子病毒决定因素提供了新途径。