Characteristics of the mosaic genome of a human parechovirus type 1 strain isolated from an infant with pneumonia in China

•A whole genome of an HPeV1 strain isolated from an infant with pneumonia.•Uncoupling of phylogeny relationships between structural and non-structural gene.•A mosaic genome of strain BJ-37359 with new genomic recombination breakpoints. Human parechoviruses (HPeVs) belong to the Parechovirus genus of...

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Veröffentlicht in:Infection, genetics and evolution genetics and evolution, 2015-01, Vol.29, p.91-98
Hauptverfasser: Zhu, Runan, Luo, Lei, Zhao, Linqing, Deng, Jie, Wang, Fang, Sun, Yu, Song, Qinwei, Ding, Yaxin, Qian, Yuan
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Sprache:eng
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Zusammenfassung:•A whole genome of an HPeV1 strain isolated from an infant with pneumonia.•Uncoupling of phylogeny relationships between structural and non-structural gene.•A mosaic genome of strain BJ-37359 with new genomic recombination breakpoints. Human parechoviruses (HPeVs) belong to the Parechovirus genus of the large and growing family of Picornaviridae with a non-enveloped, single-stranded and positive-sense RNA. An HPeV strain was isolated from the nasopharyngeal aspirate specimen of a 2months old infant hospitalized with pneumonia in Beijing, China and nominated as BJ-37359 followed the code of the specimen. Strain BJ-37359 was identified as HPeV1 by whole genome sequencing. The full genome of strain BJ-37359 consisted of 7336 nucleotides (nt), excluding a poly (A) tail and contained an ORF of 6537 nt flanked by 5′UTR of 709 nt and 3′UTR of 90nt. Phylogenetic analyses revealed that strain BJ-37359 were clustered together with HPeV1 strains in the structural capsid protein region, while uncoupling in the non-structural gene regions. Analyses with Simplot and Bootscan indicated that multiple recombination events occurred in the non-structural region and VP0 region of strain BJ-37359 with other HPeV1, and other types might have contributed to the recombination, especially HPeV6 and HPeV7 strains. Recombination analyses indicated that strain BJ-37359 may have a mosaic genome with new genomic recombination breakpoints.
ISSN:1567-1348
1567-7257
DOI:10.1016/j.meegid.2014.11.006