TY - JOUR
T1 - Phylogenetic and genome-wide deep-sequencing analyses of Canine parvovirus reveal co-infection with field variants and emergence of a recent recombinant strain
AU - Rez, Ruben Pé
AU - Calleros, Lucía
AU - Marandino, Ana
AU - Sarute, Nicolás
AU - Iraola, Gregorio
AU - Grecco, Sofia
AU - Blanc, Hervé
AU - Vignuzzi, Marco
AU - Isakov, Ofer
AU - Shomron, Noam
AU - Carrau, Lucía
AU - Hernández, Martín
AU - Francia, Lourdes
AU - Sosa, Katia
AU - Tomás, Gonzalo
AU - Panzera, Yanina
N1 - Publisher Copyright:
© 2014 Pérez et al.
PY - 2014/11/3
Y1 - 2014/11/3
N2 - Canine parvovirus (CPV), a fast-evolving single-stranded DNA virus, comprises three antigenic variants (2a, 2b, and 2c) with different frequencies and genetic variability among countries. The contribution of co-infection and recombination to the genetic variability of CPV is far from being fully elucidated. Here we took advantage of a natural CPV population, recently formed by the convergence of divergent CPV-2c and CPV-2a strains, to study co-infection and recombination. Complete sequences of the viral coding region of CPV-2a and CPV-2c strains from 40 samples were generated and analyzed using phylogenetic tools. Two samples showed co-infection and were further analyzed by deep sequencing. The sequence profile of one of the samples revealed the presence of CPV-2c and CPV-2a strains that differed at 29 nucleotides. The other sample included a minor CPV-2a strain (13. 3% of the viral population) and a major recombinant strain (86. 7%). The recombinant strain arose from inter-genotypic recombination between CPV-2c and CPV-2a strains within the VP1/VP2 gene boundary. Our findings highlight the importance of deep-sequencing analysis to provide a better understanding of CPV molecular diversity.
AB - Canine parvovirus (CPV), a fast-evolving single-stranded DNA virus, comprises three antigenic variants (2a, 2b, and 2c) with different frequencies and genetic variability among countries. The contribution of co-infection and recombination to the genetic variability of CPV is far from being fully elucidated. Here we took advantage of a natural CPV population, recently formed by the convergence of divergent CPV-2c and CPV-2a strains, to study co-infection and recombination. Complete sequences of the viral coding region of CPV-2a and CPV-2c strains from 40 samples were generated and analyzed using phylogenetic tools. Two samples showed co-infection and were further analyzed by deep sequencing. The sequence profile of one of the samples revealed the presence of CPV-2c and CPV-2a strains that differed at 29 nucleotides. The other sample included a minor CPV-2a strain (13. 3% of the viral population) and a major recombinant strain (86. 7%). The recombinant strain arose from inter-genotypic recombination between CPV-2c and CPV-2a strains within the VP1/VP2 gene boundary. Our findings highlight the importance of deep-sequencing analysis to provide a better understanding of CPV molecular diversity.
UR - http://www.scopus.com/inward/record.url?scp=84909606663&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0111779
DO - 10.1371/journal.pone.0111779
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C2 - 25365348
AN - SCOPUS:84909606663
SN - 1932-6203
VL - 9
JO - PLoS ONE
JF - PLoS ONE
IS - 11
M1 - e111779
ER -