Molecular characterization of two rare human G8P[14] rotavirus strains, detected in Italy in 2012.

Infect Genet Evol

Department of Veterinary Public Health and Food Safety, Istituto Superiore di Sanità, Rome, Italy. Electronic address:

Published: October 2016

AI Article Synopsis

  • The Italian Rotavirus Surveillance Program (RotaNet-Italy) has been tracking rotavirus strains in hospitalized children since 2007, specifically focusing on one rare strain (G8P[14]) discovered in 2012 in Apulia.
  • The genetic analysis of these strains revealed a combination of genes from both animal and human origins, suggesting they were formed through reassortment events.
  • The study found significant similarities between these strains and certain sheep and human strains, highlighting concerns that current vaccines may not effectively protect against these newly emerging rotavirus strains.

Article Abstract

Since 2007, the Italian Rotavirus Surveillance Program (RotaNet-Italy) has monitored the diversity and distribution of genotypes identified in children hospitalized with rotavirus acute gastroenteritis. We report the genomic characterization of two rare human G8P[14] rotavirus strains, identified in two children hospitalized with acute gastroenteritis in the southern Italian region of Apulia during rotavirus strain surveillance in 2012. Both strains showed a G8-P[14]-I2-R2-C2-M2-A11-N2-T6-E2-H3 genomic constellation (DS-1-like genomic background). Phylogenetic analysis of each genome segment revealed a mixed configuration of genes of animal and zoonotic human origin, indicating that genetic reassortment events generated these unusual human strains. Eight out of 11 genes (VP1, VP2, VP3, VP6, VP7, NSP3, NSP4 and NSP5) of the Italian G8P[14] strains exhibited close identity with a Spanish sheep strain, whereas the remaining genes (VP4, NSP1 and NSP2) were more closely related to human strains. The amino acid sequences of the antigenic regions of outer capsid proteins VP4 and VP7 were compared with vaccine and field strains, showing high conservation between the amino acid sequences of Apulia G8P[14] strains and human and animal strains bearing G8 and/or P[14] proteins, and revealing many substitutions with respect to the RotaTeq™ and Rotarix™ vaccine strains. Conversely, the amino acid analysis of the four antigenic sites of VP6 revealed a high degree of conservation between the two Apulia strains and the human and animal strains analyzed. These results reinforce the potential role of interspecies transmission and reassortment in generating novel rotavirus strains that might not be fully contrasted by current vaccines.

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Source
http://dx.doi.org/10.1016/j.meegid.2016.07.018DOI Listing

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