AI Article Synopsis

  • - Rotavirus A (RVA), a key cause of gastroenteritis worldwide, has seen the rise of a specific strain, G3P[8], in Brazil since 2015, which was extensively studied through stool samples and genetic analysis across multiple states.
  • - Phylogenetic analysis revealed that this G3P[8] strain became dominant in Brazil by 2020, with a significant presence of equine-like variants, suggesting it originated in Asia and spread globally through various introductions between 2014 and 2017.
  • - The study highlights that while most genetic changes in the G3P[8] strain were not adaptive, ongoing genomic surveillance is crucial for tracking its evolution and informing public health strategies

Article Abstract

Rotavirus A (RVA) is a major cause of acute gastroenteritis globally that is classically genotyped by its two immunodominant outer capsid proteins, VP7 (G-) and VP4 (P-). Recent evidence suggests that the reassortant equine-like G3P[8] strain played a substantial role in RVA transmission in Brazil since 2015. To understand its global emergence and dissemination in Brazilian territory, stool samples collected from 11 Brazilian states ( = 919) were genotyped by RT-qPCR and proceeded to sequence the VP7 gene ( = 102, 79 being newly generated) of the G3P[8] samples with pronounced viral loads. Our phylogenetic genotyping showed that G3P[8] became the dominant strain in Brazil between 2017 and 2020, with equine-like variants representing 75%-100% of VP7 samples in this period. A Bayesian discrete phylogeographic analysis strongly suggests that the equine-like G3P[8] strain originated in Asia during the early 2010s and subsequently spread to Europe, the Caribbean, and South America. Multiple introductions were detected in Brazil between 2014 and 2017, resulting in five national clusters. The reconstruction of the effective population size of the largest Brazilian cluster showed an expansion until 2017, followed by a plateau phase until 2019 and subsequent contraction. Our study also supports that most mutations fixed during equine-like G3P[8] evolution were synonymous, suggesting that adaptive evolution was not an important driving force during viral dissemination in humans, potentially increasing its susceptibility to acquired immunity. This research emphasizes the need for comprehensive rotavirus genomic surveillance that allows close monitoring of its ever-shifting composition and informs more effective public health policies.IMPORTANCEOur original article demonstrated the origin and spread in a short time of equine-like G3P[8] in Brazil and the world. Due to its segmented genome, it allows numerous mechanisms including genetic drift and reassortment contribute substantially to the genetic diversity of rotavirus. Although the effectiveness and increasing implementation of vaccination have not been questioned, a matter of concern is its impact on the emergence of escape mutants or even the spread of unusual strains of zoonotic transmission that could drive epidemic patterns worldwide. This research emphasizes the need for comprehensive rotavirus genomic surveillance, which could facilitate the formulation of public policies aimed at preventing and mitigating its transmission.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10986506PMC
http://dx.doi.org/10.1128/spectrum.03709-23DOI Listing

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