Diego C. B. Mariano
Universidade Federal de Minas Gerais
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Featured researches published by Diego C. B. Mariano.
Genome Announcements | 2014
Letícia de Castro Oliveira; Tessália Diniz Luerce Saraiva; Siomar de Castro Soares; Rommel Thiago Jucá Ramos; Pablo H. C. Sá; Adriana Ribeiro Carneiro; Fábio Miranda; Matheus Freire; Wendel Renan; Alberto Fernandes de Oliveira Junior; Anderson Rodrigues dos Santos; Anne Cybelle Pinto; Bianca Mendes Souza; Camila Prósperi De Castro; Carlos Augusto Almeida Diniz; Clarissa Santos Rocha; Diego C. B. Mariano; Edgar L. Aguiar; Edson L. Folador; Eudes Barbosa; Flávia Aburjaile; Lucas Amorim Gonçalves; Luis Carlos Guimarães; Marcela de Azevedo; Pamela Mancha Agresti; Renata F. Silva; Sandeep Tiwari; Sintia Almeida; Syed Shah Hassan; Vanessa Bastos Pereira
ABSTRACT Lactococcus lactis subsp. lactis NCDO 2118 is a nondairy lactic acid bacterium, a xylose fermenter, and a gamma-aminobutyric acid (GABA) producer isolated from frozen peas. Here, we report the complete genome sequence of L. lactis NCDO 2118, a strain with probiotic potential activity.
Bioinformation | 2015
Diego C. B. Mariano; Felipe L. Pereira; Preetam Ghosh; Debmalya Barh; Henrique Cp Figueiredo; Artur M. S. Silva; Rommel Tj Ramos; Vasco Azevedo
The newest technologies for DNA sequencing have led to the determination of the primary structure of the genomes of organisms, mainly prokaryotes, with high efficiency and at lower costs. However, the presence of regions with repetitive sequences, in addition to the short reads produced by the Next-Generation Sequencing (NGS) platforms, created a lot of difficulty in reconstructing the original genome in silico. Thus, even today, genome assembly continues to be one of the major challenges in bioinformatics specifically when repetitive sequences are considered. In this paper, we present an approach to assemble repetitive regions in prokaryotic genomes. Our methodology enables (i) the identification of these regions through visual tools, (ii) the characterization of sequences on the extremities of gaps and (iii) the extraction of consensus sequences based on mapping of raw data to a reference genome. We also present a case study on the assembly of regions that encode ribosomal RNAs (rRNA) in the genome of Corynebacterium ulcerans FRC11, in order to show the efficiency of the strategies presented here. The proposed methods and tools will help in finishing genome assemblies, besides reducing the running time and associated costs. Availability All scripts are available at http://github.com/dcbmariano/maprepeat
Standards in Genomic Sciences | 2016
Sintia Almeida; Sandeep Tiwari; Diego C. B. Mariano; Flávia Souza; Syed Babar Jamal; Nilson Coimbra; Roberto Tadeu Raittz; Fernanda Alves Dorella; Alex de Carvalho; Felipe L. Pereira; Siomar de Castro Soares; Carlos Augusto Gomes Leal; Debmalya Barh; Preetam Ghosh; Henrique César Pereira Figueiredo; Lilia F. Moura-Costa; Ricardo Wagner Portela; Roberto Meyer; Artur Silva; Vasco Azevedo
Corynebacterium pseudotuberculosis strain VD57 (Cp_VD57), a highly virulent, nonmotile, non-sporulating, and a mesophilic bacterium, was isolated from a goat’s granulomatous lesion in the municipality of Juazeiro, Bahia State, Brazil. Here, we describe a set of features of the strain, together with the details of its complete genome sequence and annotation. The genome comprises of a 2.5 Mbp long, single circular genome with 2,101 protein-coding genes, 12 rRNA, 49 tRNA and 47 pseudogenes and a G + C content of 52.85 %. Genetic variation was detected in Cp_VD57 using C. pseudotuberculosis strain 1002 as reference, wherein small genomic insertions and deletions were identified. The comparative analysis of the genome sequence provides means to better understand the host pathogen interactions of this strain and can also help us to understand the molecular and genetic basis of virulence of this bacterium.
BMC Genomics | 2015
Vinicius Augusto Carvalho de Abreu; Sintia Almeida; Sandeep Tiwari; Syed Shah Hassan; Diego C. B. Mariano; Artur Silva; Jan Baumbach; Vasco Azevedo; Richard Röttger
BackgroundOrganisms utilize a multitude of mechanisms for responding to changing environmental conditions, maintaining their functional homeostasis and to overcome stress situations. One of the most important mechanisms is transcriptional gene regulation. In-depth study of the transcriptional gene regulatory network can lead to various practical applications, creating a greater understanding of how organisms control their cellular behavior.DescriptionIn this work, we present a new database, CMRegNet for the gene regulatory networks of Corynebacterium glutamicum ATCC 13032 and Mycobacterium tuberculosis H37Rv. We furthermore transferred the known networks of these model organisms to 18 other non-model but phylogenetically close species (target organisms) of the CMNR group. In comparison to other network transfers, for the first time we utilized two model organisms resulting into a more diverse and complete network of the target organisms.ConclusionCMRegNet provides easy access to a total of 3,103 known regulations in C. glutamicum ATCC 13032 and M. tuberculosis H37Rv and to 38,940 evolutionary conserved interactions for 18 non-model species of the CMNR group. This makes CMRegNet to date the most comprehensive database of regulatory interactions of CMNR bacteria. The content of CMRegNet is publicly available online via a web interface found at http://lgcm.icb.ufmg.br/cmregnet.
Genome Announcements | 2015
Thiago J. Sousa; Diego C. B. Mariano; Doglas Parise; Mariana T D Parise; Marcus Vinicius Canário Viana; Luis Carlos Guimarães; Leandro J. Benevides; Flávia Souza Rocha; Priscilla Bagano; Rommel Thiago Jucá Ramos; Artur Silva; Henrique César Pereira Figueiredo; Sintia Almeida; Vasco Azevedo
ABSTRACT We present here the complete genome sequence of Corynebacterium pseudotuberculosis strain 12C, isolated from a sheep abscess in the Brazil. The sequencing was performed with the Ion Torrent Personal Genome Machine (PGM) system, a fragment library, and a coverage of ~48-fold. The genome presented is a circular chromosome with 2,337,451 bp in length, 2,119 coding sequences, 12 rRNAs, 49 tRNAs, and a G+C content of 52.83%.
BMC Bioinformatics | 2016
Diego C. B. Mariano; Felipe L. Pereira; Edgar L. Aguiar; Letícia de Castro Oliveira; Leandro J. Benevides; Luis Carlos Guimarães; Edson L. Folador; Thiago J. Sousa; Preetam Ghosh; Debmalya Barh; Henrique César Pereira Figueiredo; Artur Silva; Rommel Thiago Jucá Ramos; Vasco Azevedo
BackgroundThe evolution of Next-Generation Sequencing (NGS) has considerably reduced the cost per sequenced-base, allowing a significant rise of sequencing projects, mainly in prokaryotes. However, the range of available NGS platforms requires different strategies and software to correctly assemble genomes. Different strategies are necessary to properly complete an assembly project, in addition to the installation or modification of various software. This requires users to have significant expertise in these software and command line scripting experience on Unix platforms, besides possessing the basic expertise on methodologies and techniques for genome assembly. These difficulties often delay the complete genome assembly projects.ResultsIn order to overcome this, we developed SIMBA (SImple Manager for Bacterial Assemblies), a freely available web tool that integrates several component tools for assembling and finishing bacterial genomes. SIMBA provides a friendly and intuitive user interface so bioinformaticians, even with low computational expertise, can work under a centralized administrative control system of assemblies managed by the assembly center head. SIMBA guides the users to execute assembly process through simple and interactive pages. SIMBA workflow was divided in three modules: (i) projects: allows a general vision of genome sequencing projects, in addition to data quality analysis and data format conversions; (ii) assemblies: allows de novo assemblies with the software Mira, Minia, Newbler and SPAdes, also assembly quality validations using QUAST software; and (iii) curation: presents methods to finishing assemblies through tools for scaffolding contigs and close gaps. We also presented a case study that validated the efficacy of SIMBA to manage bacterial assemblies projects sequenced using Ion Torrent PGM.ConclusionBesides to be a web tool for genome assembly, SIMBA is a complete genome assemblies project management system, which can be useful for managing of several projects in laboratories. SIMBA source code is available to download and install in local webservers at http://ufmg-simba.sourceforge.net.
Journal of Genomics | 2017
Raquel Hurtado; Flávia Aburjaile; Diego C. B. Mariano; Marcus Vinicius Canário; Leandro J. Benevides; Daniel Antonio Fernandez; Nataly Olivia Allasi; Rocío Rímac; Julio Eduardo Juscamayta; Jorge Maximiliano; Raúl Rosadio; Vasco Azevedo; Lenin Maturrano
Pasteurella multocida is one of the most frequently isolated bacteria in acute pneumonia cases, being responsible for high mortality rates in Peruvian young alpacas, with consequent social and economic costs. Here we report the genome sequence of P. multocida strain UNMSM, isolated from the lung of an alpaca diagnosed with pneumonia, in Peru. The genome consists of 2,439,814 base pairs assembled into 82 contigs and 2,252 protein encoding genes, revealing the presence of known virulence-associated genes (ompH, ompA, tonB, tbpA, nanA, nanB, nanH, sodA, sodC, plpB and toxA). Further analysis could provide insights about bacterial pathogenesis and control strategies of this disease in Peruvian alpacas.
Genome Announcements | 2016
Sintia Almeida; Dan Loureiro; Ricardo W. Portela; Diego C. B. Mariano; Thiago J. Sousa; Felipe L. Pereira; Fernanda Alves Dorella; Alex F. Carvalho; Lilia F. Moura-Costa; Carlos Augusto Gomes Leal; Henrique César Pereira Figueiredo; Roberto Meyer; Vasco Azevedo
ABSTRACT We present here the genome sequence of the attenuated Corynebacterium pseudotuberculosis strain T1. The sequencing was performed with an Ion Torrent Personal Genome Machine platform. The genome is a circular chromosome of 2,337,201 bp, with a G+C content of 52.85% and a total of 2,125 coding sequences (CDSs), 12 rRNAs, 49 tRNAs, and 24 pseudogenes.
Gene | 2018
Anne Cybelle Pinto Gomide; Izabela Coimbra Ibraim; Jorianne T. C. Alves; Pablo H.C.G. de Sá; Yuri Rafael de Oliveira Silva; Mariana Passos Santana; Wanderson M. Silva; Edson L. Folador; Diego C. B. Mariano; Thiago Luiz de Paula Castro; Silvanira Barbosa; Fernanda Alves Dorella; Alex F. Carvalho; Felipe L. Pereira; Carlos Augusto Gomes Leal; Henrique César Pereira Figueiredo; Vasco Azevedo; Artur Silva; Adriana Ribeiro Carneiro Folador
Corynebacterium pseudotuberculosis has been widely studied in an effort to understand its biological evolution. Transcriptomics has revealed possible candidates for virulence and pathogenicity factors of strain 1002 (biovar Ovis). Because C. pseudotuberculosis is classified into two biovars, Ovis and Equi, it was interesting to assess the transcriptional profile of biovar Equi strain 258, the causative agent of ulcerative lymphangitis. The genome of this strain was re-sequenced; the reassembly was completed using optical mapping technology, and the sequence was subsequently re-annotated. Two growth conditions that occur during the host infection process were simulated for the transcriptome: the osmotic and acid medium. Genes that may be associated with the microorganisms resilience under unfavorable conditions were identified through RNAseq, including genes present in pathogenicity islands. The RT-qPCR was performed to confirm the results in biological triplicate for each condition for some genes. The results extend our knowledge of the factors associated with the spread and persistence of C. pseudotuberculosis during the infection process and suggest possible avenues for studies related to the development of vaccines, diagnosis, and therapies that might help minimize damage to agribusinesses.
Genome Announcements | 2016
Sandeep Tiwari; Syed Babar Jamal; Letícia de Castro Oliveira; Dominique Clermont; Chantal Bizet; Diego C. B. Mariano; Paulo Vinícius Sanches Daltro de Carvalho; Flávia Souza; Felipe L. Pereira; Siomar de Castro Soares; Luis Carlos Guimarães; Fernanda Alves Dorella; Alex F. Carvalho; Carlos Augusto Gomes Leal; Debmalya Barh; Henrique César Pereira Figueiredo; Syed Shah Hassan; Vasco Azevedo; Artur Silva
ABSTRACT In this work, we describe a set of features of Corynebacterium auriscanis CIP 106629 and details of the draft genome sequence and annotation. The genome comprises a 2.5-Mbp-long single circular genome with 1,797 protein-coding genes, 5 rRNA, 50 tRNA, and 403 pseudogenes, with a G+C content of 58.50%.