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1.
Microbiol Resour Announc ; 8(30)2019 Jul 25.
Article in English | MEDLINE | ID: mdl-31346013

ABSTRACT

The fungus Mucor irregularis is a causative agent of mucormycosis. The transcriptome analysis of the isolated M. irregularis strain C3B revealed the presence of an RNA polymerase domain of a negative-polarity RNA virus. In this work, we describe the gene ontology-based annotation of the Mucor irregularis transcriptome, which includes a putative RNA mycovirus.

2.
Genome Announc ; 3(2)2015 Mar 19.
Article in English | MEDLINE | ID: mdl-25792052

ABSTRACT

The complete genome was determined for 12 viruses isolated from 8 different pools of mosquitoes (Culex sp. and Psorophora ferox) collected at Brejeira farm, Canaan dos Carajas, Para state in northern Brazil. Eight of the viruses were distantly related to Piura virus, hereafter designated as Brejeira virus; the other 4 were similar to Wallerfield virus.

3.
J Gen Virol ; 95(Pt 10): 2251-2259, 2014 Oct.
Article in English | MEDLINE | ID: mdl-24986085

ABSTRACT

The genus Orbivirus of the family Reoviridae comprises 22 virus species including the Changuinola virus (CGLV) serogroup. The complete genome sequences of 13 CGLV serotypes isolated between 1961 and 1988 from distinct geographical areas of the Brazilian Amazon region were obtained. All viral sequences were obtained from single-passaged CGLV strains grown in Vero cells. CGLVs are the only orbiviruses known to be transmitted by phlebotomine sandflies. Ultrastructure and molecular analysis by electron microscopy and gel electrophoresis, respectively, revealed viral particles with typical orbivirus size and morphology, as well as the presence of a segmented genome with 10 segments. Full-length nucleotide sequencing of each of the ten RNA segments of the 13 CGLV serotypes provided basic information regarding the genome organization, encoded proteins and genetic traits. Segment 2 (encoding VP2) of the CGLV is uncommonly larger in comparison to those found in other orbiviruses and shows varying sizes even among different CGLV serotypes. Phylogenetic analysis support previous serological findings, which indicate that CGLV constitutes a separate serogroup within the genus Orbivirus. In addition, six out of 13 analysed CGLV serotypes showed reassortment of their genome segments.


Subject(s)
Genome, Viral , Orbivirus/genetics , Orbivirus/physiology , RNA, Viral/genetics , Sequence Analysis, DNA , Animals , Brazil , Cluster Analysis , Electrophoresis , Gene Order , Humans , Insecta , Microscopy, Electron , Molecular Sequence Data , Orbivirus/chemistry , Orbivirus/ultrastructure , Phylogeny , Viral Structural Proteins/analysis , Virion/ultrastructure
4.
FEMS Microbiol Lett ; 298(2): 241-8, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19659744

ABSTRACT

The PhoB/PhoR-dependent response to inorganic phosphate (Pi)-starvation in Vibrio cholerae O1 includes the expression of vc0719 for the response regulator PhoB, vca0033 for an alkaline phosphatase and vca1008 for an outer membrane protein (OMP). Sequences with high identity to these genes have been found in the genome of clinical and environmental strains, suggesting that the Pi-starvation response in V. cholerae is well conserved. VCA1008, an uncharacterized OMP involved in V. cholerae pathogenicity, presents sequence similarity to porins of Gram-negative bacteria such as phosphoporin PhoE from Escherichia coli. A three-dimensional model shows that VCA1008 is a 16-stranded pore-forming beta-barrel protein that shares three of the four conserved lysine residues responsible for PhoE anionic specificity with PhoE. VCA1008 beta-barrel apparently forms trimers that collapse into monomers by heating. Properties such as heat modifiability and resistance to denaturation by sodium dodecyl sulfate at lower temperatures permitted us to suggest that VCA1008 is a classical porin, more precisely, a phosphoporin due to its Pi starvation-induced PhoB-dependent expression, demonstrated by electrophoretic mobility shift assay and promoter fusion-lacZ assays.


Subject(s)
Porins/genetics , Porins/metabolism , Vibrio cholerae O1/genetics , Vibrio cholerae O1/metabolism , Amino Acid Sequence , Artificial Gene Fusion , Bacterial Proteins/metabolism , DNA, Bacterial/metabolism , Electrophoretic Mobility Shift Assay , Gene Expression Regulation, Bacterial , Genes, Reporter , Hot Temperature , Models, Molecular , Molecular Sequence Data , Phosphates/metabolism , Porins/chemistry , Protein Binding , Protein Multimerization , Protein Stability , Protein Structure, Tertiary , Sequence Homology, Amino Acid , beta-Galactosidase/genetics , beta-Galactosidase/metabolism
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