Marcus Vinicius Canário Viana

Dr. Marcus Vinicius Canário Viana

orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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11 June 2015 in Current Genomics
Verified
Journal Article
Open access
PDF file
LGLuis Carlos Guimaraes
Luis Carlos Guimaraes
LJLeandro Benevides de Jesus
Leandro Benevides de Jesus
MVMarcus Vinicius Canário Viana
Marcus Vinicius Canário Viana
ASArtur Silva
Artur Silva
RRRommel Thiago Juca Ramos
Rommel Thiago Juca Ramos
VAVasco Azevedo
Vasco Azevedo
The number of genomes that have been deposited in databases has increased exponentially after the advent of Next-Generation Sequencing (NGS), which produces high-throughput sequence data; this circumstance has demanded the development of new bioinformatics software and the creation of new areas, such as comparative genomics. In comparative genomics, the genetic content of an organism is compared against other organisms, which helps in the prediction of gene function and coding region sequences, identification of evolutionary events and determination of phylogenetic relationships. However, expanding comparative genomics to a large number of related bacteria, we can infer their lifestyles, gene repertoires and minimal genome size. In this context, a powerful approach called Pan-genome has been initiated and developed. This approach involves the genomic comparison of different strains of the same species, or even genus. Its main goal is to establish the total number of non-redundant genes that are present in a determined dataset. Pan-genome consists of three parts: core genome; accessory or dispensable genome; and species-specific or strain-specific genes. Furthermore, pan-genome is considered to be “open” as long as new genes are added significantly to the total repertoire for each new additional genome and “closed” when the newly added genomes cannot be inferred to significantly increase the total repertoire of the genes. To perform all of the required calculations, a substantial amount of software has been developed, based on orthologous and paralogous gene identification.

18 August 2017 in Scientific Reports
Verified
Journal Article
Open access
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Madangchanok ImchenMadangchanok Imchen
Madangchanok Imchen
Ranjith KumavathRanjith Kumavath
Ranjith Kumavath
Debmalya BarhDebmalya Barh
Debmalya Barh
VAVasco Azevedo
Vasco Azevedo
PGPreetam Ghosh
Preetam Ghosh
AWAlice R. Wattam
Alice R. Wattam
In this study, we categorize the microbial community in mangrove sediment samples from four different locations within a vast mangrove system in Kerala, India. We compared this data to other samples taken from the other known mangrove data, a tropical rainforest, and ocean sediment. An examination of the microbial communities from a large mangrove forest that stretches across southwestern India showed strong similarities across the higher taxonomic levels. When ocean sediment and a single isolate from a tropical rain forest were included in the analysis, a strong pattern emerged with Bacteria from the phylum Proteobacteria being the prominent taxon among the forest samples. The ocean samples were predominantly Archaea, with Euryarchaeota as the dominant phylum. Principal component and functional analyses grouped the samples isolated from forests, including those from disparate mangrove forests and the tropical rain forest, from the ocean. Our findings show similar patterns in samples were isolated from forests, and these were distinct from the ocean sediment isolates. The taxonomic structure was maintained to the level of class, and functional analysis of the genes present also displayed these similarities. Our report for the first time shows the richness of microbial diversity in the Kerala coast and its differences with tropical rain forest and ocean microbiome.

1 February 2020 in Gene
Verified
Journal Article
Closed access
FMFrancielly Morais-Rodrigues
Francielly Morais-Rodrigues
RSRita Silv́eRio-Machado
Rita Silv́eRio-Machado
Rodrigo KatoRodrigo Kato
Rodrigo Kato
DRDiego Lucas Neres Rodrigues
Diego Lucas Neres Rodrigues
JVJuan Valdez-Baez
Juan Valdez-Baez
MSMarcos A. dos Santos
Marcos A. dos Santos

19 October 2017 in PLOS ONE
Verified
Journal Article
Open access
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SJSyed Babar Jamal
Syed Babar Jamal
Syed Shah HassanSyed Shah Hassan
Syed Shah Hassan
Sandeep TiwariSandeep Tiwari
Sandeep Tiwari
MVMarcus Vinicius Canário Viana
Marcus Vinicius Canário Viana
LBLeandro De Jesus Benevides
Leandro De Jesus Benevides
Vasco AzevedoVasco Azevedo
Vasco Azevedo
Corynebacterium diphtheriae (Cd) is a Gram-positive human pathogen responsible for diphtheria infection and once regarded for high mortalities worldwide. The fatality gradually decreased with improved living standards and further alleviated when many immunization programs were introduced. However, numerous drug-resistant strains emerged recently that consequently decreased the efficacy of current therapeutics and vaccines, thereby obliging the scientific community to start investigating new therapeutic targets in pathogenic microorganisms. In this study, our contributions include the prediction of modelome of 13 C. diphtheriae strains, using the MHOLline workflow. A set of 463 conserved proteins were identified by combining the results of pangenomics based core-genome and core-modelome analyses. Further, using subtractive proteomics and modelomics approaches for target identification, a set of 23 proteins was selected as essential for the bacteria. Considering human as a host, eight of these proteins (glpX, nusB, rpsH, hisE, smpB, bioB, DIP1084, and DIP0983) were considered as essential and non-host homologs, and have been subjected to virtual screening using four different compound libraries (extracted from the ZINC database, plant-derived natural compounds and Di-terpenoid Iso-steviol derivatives). The proposed ligand molecules showed favorable interactions, lowered energy values and high complementarity with the predicted targets. Our proposed approach expedites the selection of C. diphtheriae putative proteins for broad-spectrum development of novel drugs and vaccines, owing to the fact that some of these targets have already been identified and validated in other organisms.

1 September 2018 in Gene
Verified
Journal Article
Closed access
RHRaquel Hurtado
Raquel Hurtado
DCDennis Carhuaricra
Dennis Carhuaricra
Siomar SoaresSiomar Soares
Siomar Soares
MVMarcus Vinicius Canário Viana
Marcus Vinicius Canário Viana
VAVasco Azevedo
Vasco Azevedo
Flavia AburjaileFlavia Aburjaile
Flavia Aburjaile

26 January 2017 in PLOS ONE
Verified
Journal Article
Open access
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RBRafael Baraúna
Rafael Baraúna
RRRommel T J Ramos
Rommel T J Ramos
AVAdonney Veras
Adonney Veras
KPKenny C Pinheiro
Kenny C Pinheiro
LBLeandro J Benevides
Leandro J Benevides
ASArtur Silva
Artur Silva
Seven genomes of Corynebacterium pseudotuberculosis biovar equi were sequenced on the Ion Torrent PGM platform, generating high-quality scaffolds over 2.35 Mbp. This bacterium is the causative agent of disease known as “pigeon fever” which commonly affects horses worldwide. The pangenome of biovar equi was calculated and two phylogenomic approaches were used to identify clustering patterns within Corynebacterium genus. Furthermore, other comparative analyses were performed including the prediction of genomic islands and prophages, and SNP-based phylogeny. In the phylogenomic tree, C. pseudotuberculosis was divided into two distinct clades, one formed by nitrate non-reducing species (biovar ovis) and another formed by nitrate-reducing species (biovar equi). In the latter group, the strains isolated from California were more related to each other, while the strains CIP 52.97 and 1/06-A formed the outermost clade of the biovar equi. A total of 1,355 core genes were identified, corresponding to 42.5% of the pangenome. This pangenome has one of the smallest core genomes described in the literature, suggesting a high genetic variability of biovar equi of C. pseudotuberculosis. The analysis of the similarity between the resistance islands identified a higher proximity between the strains that caused more severe infectious conditions (infection in the internal organs). Pathogenicity islands were largely conserved between strains. Several genes that modulate the pathogenicity of C. pseudotuberculosis were described including peptidases, recombination enzymes, micoside synthesis enzymes, bacteriocins with antimicrobial activity and several others. Finally, no genotypic differences were observed between the strains that caused the three different types of infection (external abscess formation, infection with abscess formation in the internal organs, and ulcerative lymphangitis). Instead, it was noted that there is a higher phenetic correlation between strains isolated at California compared to the other strains. Additionally, high variability of resistance islands suggests gene acquisition through several events of horizontal gene transfer.