Key result
Non-polio enteroviruses account for ~71% of aseptic meningitis cases, led by E30 and E6 genotypes.
Why the study?
Reports of non-polio enterovirus infections surged in Russia following the post-COVID era, making comprehensive genomic surveillance crucial for understanding NPEV gene evolution and predicting potential outbreaks.
The study identifies E30, E6, and CVA9 as the predominant non-polio enterovirus genotypes causing aseptic meningitis in the Ural Federal District and Western Siberia.
Supports regional NPEV surveillance in aseptic meningitis; leaves open generalizability and need for prospective validation.
Human non-polio enteroviruses (NPEVs) cause a plethora of infections in humans, ranging from mild to severe neurological diseases including aseptic meningitis. NPEVs are the leading cause of aseptic meningitis in both children and adults worldwide. In Russia, reports of NPEV infections have surged, especially in the post-COVID era starting in 2022, with elevated infection rates into 2023. A comprehensive examination of the whole genome is crucial for understanding the evolution of NPEV genes and for predicting potential outbreaks. This study focused on identifying the circulating NPEV strains in the Ural Federal District and Western Siberia, using Sanger sequencing and next-generation sequencing (NGS) methodologies. Biological samples were collected from (n = 225) patients diagnosed with aseptic meningitis. Bioinformatics analysis targeted the nucleotide sequences of the major capsid protein (partial VP1) gene fragment, and the assembly of whole NPEV genomes. A total of 159 NPEVs were characterized, representing 70.7% of the collected samples. The main capsid variants forming the predominant genotypic profile included E30 (n = 39, 24.3%), E6 (n = 31, 19.3%), and CVA9 (n = 25, 15.6%). Using NGS, we successfully assembled 13 whole genomes for E6, E30, EV-B80, CVA9, CVB5, E11, and EV-A71 and 3 partial genomes for E6 and EV-B87. This molecular-genetic analysis provides contemporary insights into the genotypic composition, circulation patterns, and evolutionary dynamics of the dominant NPEV associated with aseptic meningitis in the Ural Federal District and Western Siberia. The laboratory-based monitoring and epidemiological surveillance for genetic changes and evolutionary studies are important for improving prevention and healthcare.
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Itani et al. (2026) studied this question. In a study of 225 patients with aseptic meningitis, 70.7% had NPEVs, with E30 (24.3%), E6 (19.3%), and CVA9 (15.6%) being the most common genotypes.
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