6533b7d8fe1ef96bd126a51e

RESEARCH PRODUCT

Genetic heterogeneity in the VP7 of group C rotaviruses.

P. MoschidouMarialaura CorrenteNicola DecaroMax CiarletVito MartellaAnna Lucia BellaciccoCostantina DesarioAntonio LavazzaSerenella AristaKrisztián BányaiCanio BuonavogliaMaria TempestaGrazia GrecoEleonora Lorusso

subject

RotavirusGenotypeSequence analysisSwinevirusesMolecular Sequence DataBiologymedicine.disease_causeEvolution MolecularZoonosisGenetic HeterogeneityPhylogeneticsRotavirusVirologyGenotypemedicineAnimalsHumansAmino Acid SequencePeptide sequenceAntigens ViralPhylogenyGeneticsSequence Homology Amino AcidGenetic heterogeneityStrain (biology)Zoonosisvirus diseasesmedicine.diseaseVirologyEnteritisPigsCapsid ProteinsGroup C rotavirusSequence Analysis

description

AbstractEvidence for a possible zoonotic role of group C rotaviruses (GCRVs) has been recently provided. To gain information on the genetic relationships between human and animal GCRVs, we sequenced the VP7 gene of 10 porcine strains detected during a large surveillance study from different outbreaks of gastroenteritis in piglets. Four GCRV strains were genetically related to the prototype GCRV porcine Cowden strain. A completely new VP7 genotype included 4 strains (344/04-7-like) that shared 92.5% to 97.0% aa identity to each other, but <83% to human GCRVs and <79% to other porcine and bovine GCRVs. A unique 4-aa insertion (SSSV or SSTI), within a variable region at the carboxy-terminus of VP7, represented a distinctive feature for these 4 unique strains. An additional strain, 134/04-18, was clearly different from all human and animal GCRVs (<85% aa identity) and likely accounts for a distinct VP7 genotype. The VP7 of a unique strain, 42/05-21, shared similar ranges of aa sequence identities with porcine and human strains (88.0–90.7% to porcine GCRVs and 85.2–88.2% to human GCRVs). Plotting the VP7 gene of strain 42/05-21 against the VP7 of human and porcine strains revealed discontinuous evolution rates throughout the VP7 molecule, suggesting different mutational pressure or a remote intragenic recombination event. These findings provide the need for future epidemiological surveys and warrant studies to investigate the pathogenic potential of these novel GCRVs in pigs.

10.1016/j.virol.2007.05.039https://pubmed.ncbi.nlm.nih.gov/17614111