# Genetic Diversity of the Non-Polio Enteroviruses Detected in Samples of Patients with Aseptic Meningitis in the Ural Federal District and Western Siberia

**Authors:** Tarek M. Itani, Vladislav I. Chalapa, Anastasia K. Patrusheva, Evgeniy S. Kuznetsov, Aleksandr V. Semenov

PMC · DOI: 10.3390/v18010121 · Viruses · 2026-01-16

## TL;DR

This study identifies the genetic diversity of non-polio enteroviruses causing aseptic meningitis in the Ural and Siberia regions of Russia.

## Contribution

The study provides new insights into the genotypic composition and evolution of NPEVs in a specific geographic region using Sanger and NGS sequencing.

## Key findings

- E30, E6, and CVA9 were the most prevalent NPEV strains in the study region.
- Thirteen whole NPEV genomes were assembled using next-generation sequencing.
- The study highlights the importance of genetic monitoring for public health and outbreak prediction.

## Abstract

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.

## Linked entities

- **Genes:** VP1 (pyrophosphate-energized vacuolar membrane proton pump 1) [NCBI Gene 543761]
- **Diseases:** aseptic meningitis (MONDO:0006662), polio (MONDO:0017373)

## Full-text entities

- **Diseases:** infection (MESH:D007239), Aseptic Meningitis (MESH:D008582), neurological diseases (MESH:D020271), COVID (MESH:D000086382)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12846680/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12846680/full.md

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Source: https://tomesphere.com/paper/PMC12846680