Laksono Brigitta M, Bergsma Atze J, Iuliano Alessandro, Veldhoen Dominique Y, van Nieuwkoop Stefan, Boter Marjan, Leijten Lonneke, Bauer Lisa, Oude Munnink Bas B, Pijnappel Wwm Pim, van Riel Debby
Department of Viroscience, Erasmus MC, Rotterdam, The Netherlands.
Department of Paediatrics, Erasmus MC, Rotterdam, The Netherlands.
Life Sci Alliance. 2025 Sep 5;8(11). doi: 10.26508/lsa.202503372. Print 2025 Nov.
Enterovirus D68 (EV-D68) is an emerging respiratory virus associated with extra-respiratory complications, especially acute flaccid myelitis. However, the pathogenesis of acute flaccid myelitis is not fully understood. It is hypothesised that through infection of skeletal muscles, the virus further infects motor neurons via the neuromuscular junction. We hypothesise that EV-D68 infection of human skeletal muscles can impair muscle function directly, thereby contributing to the development of EV-D68-associated muscle weakness. Here, we inoculated human induced pluripotent stem cell-derived skeletal muscle myotubes grown in 2D and 3D with different EV-D68 isolates, which resulted in a productive infection and cell death. We showed through neuraminidase treatment that sialic acids facilitate infection of these cells. EV-D68 infection of the 3D model led to tissue damage, reduction of contractile force, and hampered muscle regeneration. Altogether, we showed that human skeletal muscle can act as an extra-respiratory replication site and infection of skeletal muscles may contribute to EV-D68-associated muscle weakness.
肠道病毒D68(EV-D68)是一种新出现的呼吸道病毒,与呼吸道外并发症有关,尤其是急性弛缓性脊髓炎。然而,急性弛缓性脊髓炎的发病机制尚未完全明确。据推测,该病毒通过感染骨骼肌,经神经肌肉接头进一步感染运动神经元。我们推测,EV-D68感染人类骨骼肌可直接损害肌肉功能,进而导致与EV-D68相关的肌无力。在此,我们用不同的EV-D68分离株接种在二维和三维环境中生长的人诱导多能干细胞衍生的骨骼肌肌管,引发了有效感染和细胞死亡。我们通过神经氨酸酶处理表明,唾液酸促进这些细胞的感染。EV-D68感染三维模型导致组织损伤、收缩力降低和肌肉再生受阻。总之,我们证明了人类骨骼肌可作为呼吸道外的复制位点,骨骼肌感染可能导致与EV-D68相关的肌无力。