Your browser doesn't support javascript.
loading
Integrating standardized whole genome sequence analysis with a global Mycobacterium tuberculosis antibiotic resistance knowledgebase.
Ezewudo, Matthew; Borens, Amanda; Chiner-Oms, Álvaro; Miotto, Paolo; Chindelevitch, Leonid; Starks, Angela M; Hanna, Debra; Liwski, Richard; Zignol, Matteo; Gilpin, Christopher; Niemann, Stefan; Kohl, Thomas Andreas; Warren, Robin M; Crook, Derrick; Gagneux, Sebastien; Hoffner, Sven; Rodrigues, Camilla; Comas, Iñaki; Engelthaler, David M; Alland, David; Rigouts, Leen; Lange, Christoph; Dheda, Keertan; Hasan, Rumina; McNerney, Ruth; Cirillo, Daniela M; Schito, Marco; Rodwell, Timothy C; Posey, James.
Afiliação
  • Ezewudo M; Critical Path Institute, 1730 E River Rd., Tucson, AZ, 85718, USA.
  • Borens A; Critical Path Institute, 1730 E River Rd., Tucson, AZ, 85718, USA.
  • Chiner-Oms Á; Joint unit Infection and Public Health FISABIO-CSISP/University of Valencia, Institute of integrative Systems Biology, Valencia, Spain.
  • Miotto P; Emerging Bacterial Pathogens Unit, IRCCS San Raffaele Scientific Institute, via Olgettina 58, 20132, Milano, Italy.
  • Chindelevitch L; School of Computing Science, Simon Fraser University, 8888 University Ave, Burnaby, BC, V5A 1S6, Canada.
  • Starks AM; Division of Tuberculosis Elimination, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, 1600 Clifton Road MS F08, Atlanta, GA, 30329, USA.
  • Hanna D; Critical Path Institute, 1730 E River Rd., Tucson, AZ, 85718, USA.
  • Liwski R; Critical Path Institute, 1730 E River Rd., Tucson, AZ, 85718, USA.
  • Zignol M; Global Tuberculosis Program, World Health Organization, Geneva, Switzerland.
  • Gilpin C; Global Tuberculosis Program, World Health Organization, Geneva, Switzerland.
  • Niemann S; German Center for Infection Research, Partner Site Borstel, Borstel, Germany.
  • Kohl TA; Molecular and Experimental Mycobacteriology, Priority area Infections, Research Center Borstel, Borstel, Germany.
  • Warren RM; DST/NRF Centre of Excellence for Biomedical Tuberculosis Research/SAMRC Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Stellenbosch, South Africa.
  • Crook D; Nuffield Department of Medicine, John Radcliffe Hospital, University of Oxford, Oxford, OX3 9DU, United Kingdom.
  • Gagneux S; Swiss Tropical and Public Health Institute, Basel, Switzerland.
  • Hoffner S; Department of Public Health Sciences, Karolinska institute, Stockholm, Sweden.
  • Rodrigues C; Hinduja Hospital, Veer Savarkar Marg, Mahim, Mumbai, India.
  • Comas I; Tuberculosis Genomics Unit, Biomedicine Institute of Valencia (IBV-CSIC), Street Jaime Roig 11. P.O., 4010, Valencia, Spain.
  • Engelthaler DM; Translational Genomics Research Institute, 3051 W. Shamrell Blvd. Ste 106, Flagstaff, AZ, 86005, USA.
  • Alland D; Center for Emerging Pathogens, Rutgers-New Jersey Medical School, 185 South Orange Avenue, Newark, NJ, 07103, USA.
  • Rigouts L; Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
  • Lange C; Division of Clinical Infectious Diseases and German Center for Infection Research Tuberculosis Unit, Research Center Borstel, Borstel, Germany.
  • Dheda K; Lung Infection and Immunity Unit, Department of Medicine, Division of Pulmonology and UCT Lung Institute, University of Cape Town, Old Main Building, Groote Schuur Hospital, Observatory, Cape Town, South Africa.
  • Hasan R; Department of Pathology and Laboratory Medicine, Aga Khan University, Stadium Road, Karachi, Pakistan.
  • McNerney R; Department of Medicine, Division of Pulmonology, University of Cape Town, Groote Schuur Hospital, Cape Town, South Africa.
  • Cirillo DM; Emerging Bacterial Pathogens Unit, IRCCS San Raffaele Scientific Institute, via Olgettina 58, 20132, Milano, Italy.
  • Schito M; Critical Path Institute, 1730 E River Rd., Tucson, AZ, 85718, USA.
  • Rodwell TC; Department of Medicine, University of California, San Diego, CA, USA.
  • Posey J; The Foundation for Innovative New Diagnostics, Geneva, Switzerland.
Sci Rep ; 8(1): 15382, 2018 10 18.
Article em En | MEDLINE | ID: mdl-30337678
Drug-resistant tuberculosis poses a persistent public health threat. The ReSeqTB platform is a collaborative, curated knowledgebase, designed to standardize and aggregate global Mycobacterium tuberculosis complex (MTBC) variant data from whole genome sequencing (WGS) with phenotypic drug susceptibility testing (DST) and clinical data. We developed a unified analysis variant pipeline (UVP) ( https://github.com/CPTR-ReSeqTB/UVP ) to identify variants and assign lineage from MTBC sequence data. Stringent thresholds and quality control measures were incorporated in this open source tool. The pipeline was validated using a well-characterized dataset of 90 diverse MTBC isolates with conventional DST and DNA Sanger sequencing data. The UVP exhibited 98.9% agreement with the variants identified using Sanger sequencing and was 100% concordant with conventional methods of assigning lineage. We analyzed 4636 publicly available MTBC isolates in the ReSeqTB platform representing all seven major MTBC lineages. The variants detected have an above 94% accuracy of predicting drug based on the accompanying DST results in the platform. The aggregation of variants over time in the platform will establish confidence-graded mutations statistically associated with phenotypic drug resistance. These tools serve as critical reference standards for future molecular diagnostic assay developers, researchers, public health agencies and clinicians working towards the control of drug-resistant tuberculosis.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Tuberculose Resistente a Múltiplos Medicamentos / Farmacorresistência Bacteriana Múltipla / Sequenciamento Completo do Genoma / Mutação / Mycobacterium tuberculosis Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Tuberculose Resistente a Múltiplos Medicamentos / Farmacorresistência Bacteriana Múltipla / Sequenciamento Completo do Genoma / Mutação / Mycobacterium tuberculosis Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos