cris.boxmetadata.label.title
Whole-genome characterization of a Peruvian alpaca rotavirus isolate expressing a novel VP4 genotype
cris.boxmetadata.label.dateissued
30 browse.startsWith.months.november 2016
cris.boxmetadata.label.accesslevel
metadata only access
cris.boxmetadata.label.resourcetype
journal article
cris.boxmetadata.label.authors
Rojas M.
Gonçalves J.L.S.
Dias H.G.
MANCHEGO SAYAN, ALBERTO GUSTAVO
PEZO CARREON, SERGIO DANILO
Santos N.
Instituto Veterinario de Investigaciones Tropicales y de Altura
cris.boxmetadata.label.publisher
Elsevier B.V.
cris.boxmetadata.label.abstract
The SA44 isolate of Rotavirus A (RVA) was identified from a neonatal Peruvian alpaca presenting with diarrhea, and the full-length genome sequence of the isolate (designated RVA/Alpaca-tc/PER/SA44/2014/G3P[40]) was determined. Phylogenetic analyses showed that the isolate possessed the genotype constellation G3-P[40]-I8-R3-C3-M3-A9-N3-T3-E3-H6, which differs considerably from those of RVA strains isolated from other species of the order Artiodactyla. Overall, the genetic constellation of the SA44 strain was quite similar to those of RVA strains isolated from a bat in Asia (MSLH14 and MYAS33). Nonetheless, phylogenetic analyses of each genome segment identified a distinct combination of genes. Several sequences were closely related to corresponding gene sequences in RVA strains from other species, including human (VP1, VP2, NSP1, and NSP2), simian (VP3 and NSP5), bat (VP6 and NSP4), and equine (NSP3). The VP7 gene sequence was closely related to RVA strains from a Peruvian alpaca (K'ayra/3368-10; 99.0% nucleotide and 99.7% amino acid identity) and from humans (RCH272; 95% nucleotide and 99.0% amino acid identity). The nucleotide sequence of the VP4 gene was distantly related to other VP4 sequences and was designated as the reference strain for the new P[40] genotype. This unique genetic makeup suggests that the SA44 strain emerged from multiple reassortment events between bat-, equine-, and human-like RVA strains.
cris.boxmetadata.label.citationstartpage
27
cris.boxmetadata.label.citationendpage
35
cris.boxmetadata.label.volume
196
cris.boxmetadata.label.language
English
cris.boxmetadata.label.ocdeknowledgeArea
Biología celular, Microbiología Ciencia veterinaria
cris.boxmetadata.label.subjects
cris.boxmetadata.label.doi
cris.boxmetadata.label.scopusidentifier
2-s2.0-84991672393
cris.boxmetadata.label.pubmedidentifier
cris.boxmetadata.label.source
Veterinary Microbiology
cris.boxmetadata.label.containerissn
03781135
cris.boxmetadata.label.sponsor
This study was supported, in part, by the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq; Nos. 471063/2012-6 and 303864/2014-1 ), the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), and the Fundação Carlos Chagas de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ; Nos. E-26/103.113/2011 and E-26/201.374/2014 ), Brazil. The funders had no role in study design, data collection, data interpretation, or the decision to submit the work for publication. We thank Soluza dos Santos Gonçalves for technical assistance.
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