4.5 Article

Eastern Equine Encephalitis Virus Diversity in Massachusetts Patients, 1938-2020

Journal

AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE
Volume 109, Issue 2, Pages 387-396

Publisher

AMER SOC TROP MED & HYGIENE
DOI: 10.4269/ajtmh.23-0047

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Eastern equine encephalitis virus (EEEV) is an alphavirus that can cause severe viral encephalitis in humans. This study investigated the evolutionary patterns of EEEV within human hosts by analyzing viral genomes from contemporary and historical samples. The results revealed clustering of sequences from the same region and minimal changes within brain regions, as well as the presence of compartmentalized mutations. These findings contribute to our understanding of EEEV infection in humans.
Eastern equine encephalitis virus (EEEV) is a relatively little-studied alphavirus that can cause devastating viral encephalitis, potentially leading to severe neurological sequelae or death. Although case numbers have historically been low, outbreaks have been increasing in frequency and scale since the 2000 s. It is critical to investigate EEEV evolu-tionary patterns, especially within human hosts, to understand patterns of emergence, host adaptation, and within-host evolution. To this end, we obtained formalin-fixed paraffin-embedded tissue blocks from discrete brain regions from five contemporary (2004-2020) patients from Massachusetts, confirmed the presence of EEEV RNA by in situ hybridization (ISH) staining, and sequenced viral genomes. We additionally sequenced RNA from scrapings of historical slides made from brain sections of a patient in the first documented EEE outbreak in humans in 1938. ISH staining revealed the pres-ence of RNA in all contemporary samples, and quantification loosely correlated with the proportion of EEEV reads in samples. Consensus EEEV sequences were generated for all six patients, including the sample from 1938; phylogenetic analysis using additional publicly available sequences revealed clustering of each study sample with like sequences from a similar region, whereas an intrahost comparison of consensus sequences between discrete brain regions revealed min-imal changes. Intrahost single nucleotide variant (iSNV) analysis of four samples from two patients revealed the presence of tightly compartmentalized, mostly nonsynonymous iSNVs. This study contributes critical primary human EEEV sequences, including a historic sequence as well as novel intrahost evolution findings, contributing substantially to our understanding of the natural history of EEEV infection in humans.

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