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Genome-wide Mycobacterium tuberculosis variation (GMTV) database: a new tool for integrating sequence variations and epidemiology

BACKGROUND: Tuberculosis (TB) poses a worldwide threat due to advancing multidrug-resistant strains and deadly co-infections with Human immunodeficiency virus. Today large amounts of Mycobacterium tuberculosis whole genome sequencing data are being assessed broadly and yet there exists no comprehens...

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Detalles Bibliográficos
Autores principales: Chernyaeva, Ekaterina N, Shulgina, Marina V, Rotkevich, Mikhail S, Dobrynin, Pavel V, Simonov, Serguei A, Shitikov, Egor A, Ischenko, Dmitry S, Karpova, Irina Y, Kostryukova, Elena S, Ilina, Elena N, Govorun, Vadim M, Zhuravlev, Vyacheslav Y, Manicheva, Olga A, Yablonsky, Peter K, Isaeva, Yulia D, Nosova, Elena Y, Mokrousov, Igor V, Vyazovaya, Anna A, Narvskaya, Olga V, Lapidus, Alla L, O’Brien, Stephen J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234438/
https://www.ncbi.nlm.nih.gov/pubmed/24767249
http://dx.doi.org/10.1186/1471-2164-15-308
Descripción
Sumario:BACKGROUND: Tuberculosis (TB) poses a worldwide threat due to advancing multidrug-resistant strains and deadly co-infections with Human immunodeficiency virus. Today large amounts of Mycobacterium tuberculosis whole genome sequencing data are being assessed broadly and yet there exists no comprehensive online resource that connects M. tuberculosis genome variants with geographic origin, with drug resistance or with clinical outcome. DESCRIPTION: Here we describe a broadly inclusive unifying Genome-wide Mycobacterium tuberculosis Variation (GMTV) database, (http://mtb.dobzhanskycenter.org) that catalogues genome variations of M. tuberculosis strains collected across Russia. GMTV contains a broad spectrum of data derived from different sources and related to M. tuberculosis molecular biology, epidemiology, TB clinical outcome, year and place of isolation, drug resistance profiles and displays the variants across the genome using a dedicated genome browser. GMTV database, which includes 1084 genomes and over 69,000 SNP or Indel variants, can be queried about M. tuberculosis genome variation and putative associations with drug resistance, geographical origin, and clinical stages and outcomes. CONCLUSIONS: Implementation of GMTV tracks the pattern of changes of M. tuberculosis strains in different geographical areas, facilitates disease gene discoveries associated with drug resistance or different clinical sequelae, and automates comparative genomic analyses among M. tuberculosis strains.