Key result
Complete-genome analysis of an Echovirus 30 strain from a pediatric encephalitis case revealed six distinct non-synonymous amino acid substitutions uniquely present in the isolate PQ472410.1.
Why the study?
Echovirus 30 is linked to neurological illnesses, but complete-genome sequence data from encephalitis cases in India were lacking.
Case Report (n=1)
No
This represents the first complete-genome sequence report of Echovirus-30 from an encephalitis case in India, identifying unique mutations potentially associated with pathogenicity.
Alerts to possible regional enteroviral variants; hypothesis-generating for mutation-pathogenicity links pending validation.
Echovirus 30 (E-30), a member of the Enterovirus B species, is frequently linked to neurological illnesses such as aseptic meningitis, encephalitis, and hand, foot, and mouth disease. In this study, we present the complete-genome analysis of an Echovirus 30 strain isolated from cerebrospinal fluid (CSF) and stool samples of a pediatric encephalitis case in Kerala, India, during 2023. A comparative genomic investigation was carried out using a dataset of 111 human E-30 isolates, encompassing 116,991 mutation records. This analysis revealed six distinct non-synonymous amino acid substitutions uniquely present in the isolate PQ472410.1, which may be associated with pathogenicity and/or neurotropic behavior. To the best of our knowledge, this represents the first complete-genome sequence report of E-30 from an encephalitis case in India. These findings contribute valuable information to the understanding of E-30's molecular epidemiology and evolution and offer vital data for enhancing surveillance and response strategies against enteroviral infections.
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Waghchaure et al. (2025) conducted a case report in Encephalitis (n=1). Echovirus 30 infection vs. 111 human E-30 isolates was evaluated on Genomic mutations. Complete-genome analysis of an Echovirus 30 strain from a pediatric encephalitis case revealed six distinct non-synonymous amino acid substitutions uniquely present in the isolate PQ472410.1.
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