Nuevalos Guaita Marcos, Jimoh Tajudeen O, Barrall Emma B, Atanasoff Kristina E, Ehrlich Michelle E, Gandy Sam, García-Ríos Estéfani, Perez Romero Pilar, Duty J Andrew, Tortorella Domenico
National Center for Microbiology, Instituto de Salud Carlos III. Majadahonda, Madrid, Spain.
Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
J Gen Virol. 2025 Apr;106(4). doi: 10.1099/jgv.0.002096.
Human cytomegalovirus (HCMV) is a β-herpesvirus that establishes asymptomatic infections in immunocompetent individuals but can cause severe or even life-threatening symptoms in immunocompromised patients. HCMV can replicate in a wide variety of cells through the engagement of diverse cell factors with the viral envelope protein gH/gL/gO (trimer) or gH/gL/UL128/UL130/UL131a (pentamer), allowing for systemic spread within the human host. This study explores HCMV infection tropism and dynamics in human microglia, demonstrating the susceptibility of microglia to both clinical and laboratory HCMV strains, with lower efficacy for the laboratory strain, implying that both the gH/gL-trimer and -pentamer can mediate virus entry in microglia. The importance of the gH/gL pentamer for virus entry was demonstrated by the inhibition of virus infection upon pre-incubation with a soluble neuropilin-2 (NRP-2) entry factor. Further, we demonstrated that HCMV infection can be effectively inhibited by monoclonal antibodies specific for the gH/gL complexes and HCMV hyperimmunoglobulin. Lastly, we report that microglia infection can be prevented by newly characterized chemical entry inhibitors. Altogether, these findings underscore the potential of microglia as valuable models for studying HCMV neurotropism and strategies to block virus infection in cells that can impact neurological disorders.
人巨细胞病毒(HCMV)是一种β疱疹病毒,在免疫功能正常的个体中可引发无症状感染,但在免疫功能低下的患者中可导致严重甚至危及生命的症状。HCMV可通过多种细胞因子与病毒包膜蛋白gH/gL/gO(三聚体)或gH/gL/UL128/UL130/UL131a(五聚体)结合,在多种细胞中复制,从而在人类宿主内实现全身扩散。本研究探讨了HCMV在人小胶质细胞中的感染嗜性和动态变化,证明小胶质细胞对临床和实验室HCMV毒株均易感,实验室毒株的感染效率较低,这意味着gH/gL三聚体和五聚体均可介导病毒进入小胶质细胞。通过与可溶性神经纤毛蛋白-2(NRP-2)进入因子预孵育可抑制病毒感染,从而证明了gH/gL五聚体对病毒进入的重要性。此外,我们还证明,针对gH/gL复合物的单克隆抗体和HCMV高效价免疫球蛋白可有效抑制HCMV感染。最后,我们报告称,新鉴定的化学进入抑制剂可预防小胶质细胞感染。总之,这些发现强调了小胶质细胞作为研究HCMV神经嗜性以及在可能影响神经疾病的细胞中阻断病毒感染策略的有价值模型的潜力。