Genomic characterization of uncommon human G3P[6] rotavirus strains causing diarrhea in children in Italy in 2009.

Infect Genet Evol

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

Published: July 2015

AI Article Synopsis

  • Group A rotaviruses (RVA) are a leading cause of severe diarrhea in children globally, causing significant mortality, especially in developing countries.
  • In 2009, three unique G3P[6] RVA strains were discovered in hospitalized children in Southern Italy, which had not been previously documented in that region.
  • Genetic analysis showed these strains shared a rare genotype constellation and demonstrated no signs of zoonotic transfer, suggesting they have a human-specific lineage similar to RVA found in other regions like Africa and Europe.

Article Abstract

Group A rotaviruses (RVA) are the leading cause of acute gastroenteritis in young children, causing up to 450,000 deaths worldwide, mostly in developing countries. Most of RVA human infections in developed countries are related to five major G/P combinations: G1P[8], G2P[4], G3P[8], G4P[8] and G9P[8]. During the surveillance activity of RotaNet-Italy, three uncommon G3P[6] RVA strains, designated as RVA/Human-wt/ITA/NA01/2009/G3P[6], RVA/Human-wt/ITA/NA06/2009/G3P[6], and RVA/Human-wt/ITA/NA19/2009/G3P[6], were identified in the stools of children with diarrhea hospitalized in Southern Italy in 2009. Samples NA01, NA06 and NA19 were characterized as genotype G3P[6]. To investigate the three strains further, partial sequencing of the eleven genomic segments was performed. RVA strains NA01, NA06 and NA19 were found to share the rare genotype constellation: G3-P[6]-I2-R2-C2-M2-A2-N2-T2-E2-H2, which had not been reported previously in continental Italy. The phylogenetic analysis of the eleven genomic segments showed no evidence of zoonosis or inter-species reassortment at the origin of the Italian G3P[6] strains, indicating that they possessed DS-1-like genomic constellations similar to those detected previously in human cases in Africa and Europe. The analysis of the hypervariable regions of VP7 and VP4 (VP8*) revealed high amino acid identity between the Italian G3P[6] RVA strains involved in this study.

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Source
http://dx.doi.org/10.1016/j.meegid.2015.04.022DOI Listing

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