covid
Buscar en
Brazilian Journal of Microbiology
Toda la web
Inicio Brazilian Journal of Microbiology Rio Negro virophage: Sequencing of the near complete genome and transmission ele...
Información de la revista
Vol. 49. Núm. S1.
Páginas 260-261 (noviembre 2018)
Compartir
Compartir
Descargar PDF
Más opciones de artículo
Vol. 49. Núm. S1.
Páginas 260-261 (noviembre 2018)
Bacterial, Fungal and Virus Molecular Biology
Open Access
Rio Negro virophage: Sequencing of the near complete genome and transmission electron microscopy of viral factories and particles
Visitas
1286
Iara Apolinário Borges, Felipe Lopes de Assis, Ludmila Karen dos Santos Silva, Jônatas Abrahão
Autor para correspondencia
jonatas.abrahao@gmail.com

Corresponding author at: Jônatas Abrahão, Laboratório de Vírus, Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos 6627, 31270-901 Belo Horizonte, MG, Brazil. Tel.: +55 3134093002.
Universidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Departamento de Microbiologia, Laboratório de Vírus, Belo Horizonte, MG, Brazil
Este artículo ha recibido

Under a Creative Commons license
Información del artículo
Resumen
Texto completo
Bibliografía
Descargar PDF
Estadísticas
Figuras (1)
Abstract

Rio Negro virophage (RNV) was co-isolated with a strain of mimivirus named sambavirus, from Brazilian Amazon. We report the near complete genome sequence of RNV, the first virophage isolated in Brazil. We also present new microscopical data demonstrating that RNV particles have similar dimensions to that described to sputnik virophages.

Texto completo

Rio Negro virophage (RNV) was co-isolated in 2011 with a strain of mimivirus lineage A named sambavirus, from Rio Negro river, Brazilian Amazon.1 Phylogenetic analyses based on RNV capsid gene revealed the clustering of RNV with sputnik virophages.1 Hereby describe the nearly complete genome of RNV.

Sambavirus and RNV were co-cultured in A. castellanii monolayers at a multiplicity of infection of 0.01 during four days. The lysate was collected and centrifuged at 1400g for 10min. The resultant supernatant was consecutively passed through 0.8 and 0.2μm filters and ultracentifuged at 90,000g for 2h in a sucrose cushion of 38%. The genome was extracted from the purified RNV sample and sequenced by Illumina MiSeq instrument (Illumina Inc., San Diego, CA, USA) with the paired end application and assembled de novo using SPADES v. 3.5.0, followed by manual annotation based on genomes of Sputniks 1, 2 and 3 (GenBank, NCBI: EU606015.1, JN603369.1 and JN603370.1, respectively). Localizations within RNV genome mentioned in this work are therefore based on its alignment with these three sequences by Clustal W, MEGA 7.0.26.

RNV genome is a double-stranded DNA molecule of 18,145bp encoding 20 putative open reading frames ranging from 330 to 2340bp. This information added to the analyses of RNV genome, corroborate its close relationship with sputnik strains. The RNV and sputinik 2 strains present a highly similar gene content and genome synteny despite SNPs and insertions observed in both coding and non-coding regions. RNV presents a 49bp insertion at position 11,841 leading to a longer intergenic region between ORFs 14 and 15. This sequence is a repetition of the preceding 49 nucleotides except for a SNP at the 22nd position, where a C was replaced by a G. There are also SNPs at positions 16,075, 18,141 and a deletion at 18,145. At the position 18,016 there is the insertion of 3 guanines. Compared to other sputinik genomes, the last 244bp of RNV genome are missing. The successful amplification of a PCR targeting this region in RNV indicates that it also presents this last fragment (data not shown). Since the best hit of RNV genome is sputnik 2, RNV was deposited in GenBank as Sputnik virophage 2 isolate Rio Negro (accession number MG676470).

Transmission electron microscopy of RNV purified particles showed 50–70nm particles, as observed to other sputnik viruses (Fig. 1A). This is consistent with that expected, since RNV capsid gene is very similar to sputnik virophages orthologs. In addition to that demonstrated in our previous work,1 it was possible to visualize RNV particles being formed inside sambavirus viral factories, as demonstrated elsewhere2,3 (Fig. 1B).

Fig. 1.

Transmission electron microscopy of RNV in Acanthamoeba cells co-infected with sambavirus. (A) RNV particle inside a vesicle at time 8h post infection. (B) Sambavirus viral factory (asterisk) producing both sambavirus particles and RNV particles (arrow).

(0.27MB).

In summary, RNV is a sputnik-like virophage isolated from Brazilian Amazon, with genomic and morphological characteristics very similar to those described to sputnik virophage group.

Acknowledgements

We are grateful to our colleagues from Laboratório de Vírus of Universidade Federal de Minas Gerais. In addition, this work was supported by Pro-Reitoria de Pesquisa da Universidade Federal de Minas Gerais (PRPq-UFMG) and by the agencies Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Coordenação de Aperfeiçoamento de Pessoal de Nivel Superior (CAPES) and Fundação de Amparo Pesquisa do estado de Minas Gerais (FAPEMIG). We also thank Dr. Matthias Fischer for his comments regarding RNV genome.

References
[1]
R.K. Campos, P.V. Boratto, F.L. Assis, et al.
Samba virus: a novel mimivirus from a giant rain forest, the Brazilian Amazon.
[2]
B. La Scola, C. Desnues, I. Pagnier, et al.
The virophage as a unique parasite of the giant mimivirus.
Nature, 455 (2008), pp. 100-104
[3]
C. Desnues, B. La Scola, N. Yutin, et al.
Provirophages and transpovirons as the diverse mobilome of giant viruses.
Proc Natl Acad Sci U S A, 109 (2012), pp. 18078-18083
[Epub 2012 Oct 15]
Copyright © 2018. Sociedade Brasileira de Microbiologia
Descargar PDF
Opciones de artículo