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Full genome based sequence and structural characterization of an unusual group A rotavirus G12P[11] isolated from neonates in Pune, western India. | LitMetric

AI Article Synopsis

  • Studies in Pune's neonatal intensive care units found early exposure to rotaviruses, specifically unique G12P[11] strains.
  • Genome sequencing of a weakened neonatal strain (NIV-1740121) showed genetic exchanges with the ROTAVAC® vaccine strain, incorporating genes from both bovine and porcine origins into a human-like framework.
  • The study enhances our understanding of how P[11] strains interact with neonates, highlighting specific changes in proteins that affect their ability to bind with glycan receptors.

Article Abstract

Studies conducted at neonatal intensive care units in Pune, western India, suggested early exposure to rotaviruses and predominance of unusual human-bovine-like G12P[11] strains. The whole genome sequencing and phylogenetic analyses of a naturally attenuated, culture adapted neonatal strain, (NIV-1740121) revealed multiple-gene reassortment events, containing ROTAVAC® vaccine strain, 116E-like VP4, VP6, NSP3, NSP5 genes, VP7 gene of G12 origin and VP3 gene of porcine ancestry in a human Wa-like backbone. Analysis of 3D structure modeling of the VP7 and VP4 proteins with respect to 116E suggested amino acid variations in the major neutralizing epitopes of VP7, contributed to a modified charge density. Visualization of receptor-glycan interaction structures of NIV-1740121 and 116E VP8* showed type I glycan binds with a similar conformation at the same active site as represented in the available crystal structure of G10P[11] VP8*. The study adds to the knowledge of age restricted tropism of P[11] strains in neonates.

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Source
http://dx.doi.org/10.1016/j.vaccine.2020.01.081DOI Listing

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