Journal of medical virology · 2026
Epidemiological and Clinical Characteristics of the Enterovirus D68 Outbreak in Spain in 2024.
СтатьяНазвание и аннотация: Перевод в очереди
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Camacho Juan, García-Ibáñez Nerea, Fernández-García María Dolores, Biya Yasmin, Ruiz de Pedro Estrella, Gutiérrez Almudena, Nieto María Carmen, Ruiz-García María Montserrat, Pastor-Fajardo María Teresa, Lagarejos Eduardo, de Leonardo Simón Carlos, Navascués Ana, Moreno-Docón Antonio, Gozalo-Marguello Mónica, Berengua Carla, Antequera Pedro, Huéscar-Pascual María Dolores, Calvo Cristina, Cabrerizo María
Аннотация
Enterovirus D68 (EV-D68) is a significant cause of respiratory and neurological disease worldwide. In 2024, Spain experienced its largest recorded EV-D68 outbreak, accounting for 37.4% of all typed EV (294/892). This study describes the epidemiological, clinical, and phylogenetic features of EV-D68 infections. Unexpectedly, EV-D68 infections as it seems were more frequent in adults than in children (57.2% vs. 42.8%, p < 0.05), particularly among individuals > 60 years (38.6%). In 84.9% of cases with an EV-D68 infection, EV-D68 was the sole pathogen detected. Respiratory pathologies predominated (91.9%), with bronchospasm/wheezing episodes and bronchiolitis in children, and pneumonia and exacerbations of chronic obstructive pulmonary disease in older adults (p < 0.05). Older patients showed a more severe clinical profile than pediatric patients, including higher hospitalization rates (79% vs. 59%), longer hospital stays (mean, 10.8 vs. 4.9 days), and more comorbidities (50% vs. 31%) (p < 0.01). Phylogenetic analysis revealed two co-circulating lineages with distinct age-related tropisms: B3.3 mainly affected children (88.5%), whereas the novel A2/D1.1 infected adults predominantly (79.6%), particularly ≥ 60 years (49.5%) (p < 0.05). This pattern may reflect lineage-specific amino acid substitutions enhancing immune evasion. Neurological disease occurred in only three patients > 60 years infected by the A2/D1.1 lineage, which contained neurovirulent substitutions (I553L, K835E, and T860N). Results support continued genomic and clinical surveillance of EV-D68.