6533b7d9fe1ef96bd126c174

RESEARCH PRODUCT

Nucleotide variation in the VP7 gene affects PCR genotyping of G9 rotaviruses identified in Italy

Annamaria PratelliMarialaura CorrenteCanio BuonavogliaMaria TempestaSerenella AristaAntonio CiraniVito MartellaA. MadioGabriella EliaValentina Terio

subject

SerotypeRotavirusGenotypeReassortmentMolecular Sequence DataBiologymedicine.disease_causePolymerase Chain ReactionRotavirus InfectionsVirologyRotavirusGenetic variationGenotypemedicineHumansTypingChildGenotypingAntigens ViralPhylogenyDNA PrimersGeneticsBase SequenceGenetic VariationVirologyEnteritisInfectious DiseasesItalyCapsid ProteinsPrimer binding site

description

A modified (aFT9m) and a degenerate (aFT9d) version of the rotavirus G9-specific primer (aFT9) allowed strains that were previously untypable, because of point mutations accumulating at the primer binding site, to be G typed by reverse transcription-polymerase chain reaction. The strains were collected during 2001-2002 in Italy in hospitals of the Apulia region, from children affected by severe rotavirus-associated enteritis. Using a wide selection of G9 rotaviruses detected worldwide, sequencing of the G9 untypable strains, sequence comparison, and phylogenetic analysis showed that the Italian strains have strong genetic similarity (< or =99.4%) to G9 rotaviruses identified recently in many parts of the world and different from the old G9 strains identified during the 1980s (less than 90%). Genetic variation of G9 rotaviruses explains the constraints encountered in the typing assays and presumably accounts, together with genetic reassortment events, for the emergence on a global scale of the G9 serotype.

http://hdl.handle.net/10447/8916