Author Correction: Genome-wide analysis of multi- and extensively drug-resistant Mycobacterium tuberculosis
Autor: | Susana Campino, Theolis Costa Barbosa Bessa, Nora Mocillo, Miguel Viveiros, Dang Minh Ha, Grant A. Hill-Cawthorne, Abdallah O Ahmed, Anirvan Chatterjee, Arnab Pain, Louis Grandjean, Julian Parkhill, Erivelton de Oliveira Sousa, Maxine Caws, Keertan Dheda, Abdallah M. Abdallah, Saad Alghamdi, João Perdigão, Elizabeth M. Streicher, Yaa Oppong, Nicholas Furnham, Stefan Panaiotov, Adriana Alves, Mridul Nair, Moses Joloba, Mona Alsomali, Edward C. Jones-López, Jaime Robledo, Nashwa Talaat Shesha, Zineb Rchiad, Martin L. Hibberd, Ruth McNerney, F. A. Sirgel, Stephanie Portelli, Robert M Warren, Carlos Penha, Christophe Sola, Isabel Portugal, Zahra Hasan, Amelia C. Crampin, Jody Phelan, Shahjahan Ali, Judith R. Glynn, Tomoshige Matsumoto, Rumina Hasan, Francesc Coll, Anabela Miranda, Kim Mallard, Paul D. van Helden, Taane G. Clark, David Moore, Patricia Sheen |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
biology Published Erratum Genome wide analysis MEDLINE Drug resistance Computational biology biology.organism_classification Genome-wide association studies Mycobacterium tuberculosis 03 medical and health sciences 030104 developmental biology ComputingMethodologies_DOCUMENTANDTEXTPROCESSING Genetics Tuberculosis Microbial genetics |
Zdroj: | Repositório Científico de Acesso Aberto de Portugal Repositório Científico de Acesso Aberto de Portugal (RCAAP) instacron:RCAAP |
ISSN: | 1546-1718 |
Popis: | This deposit is composed by a publication in which the IGC's authors have had the role of collaboration (it's a collaboration publication). This type of deposit in ARCA is in restrictedAccess (it can't be in open access to the public), and can only be accessed by two ways: either by requesting a legal copy from the author (the email contact present in this deposit) or by visiting the following link: https://www.nature.com/articles/s41588-018-0074-3 This publication hasn't any creative commons license associated. This deposit is composed simultaneously by the original published article and also by the "correction" for the published article (erratum). The link for the original article: https://www.nature.com/articles/s41588-017-0029-0#Ack1 This deposit is composed by the main article plus the supplementary materials of the publication. In the version of this article initially published, the URL listed for TubercuList was incorrect. The correct URL is https://mycobrowser.epfl.ch/. The error has been corrected in the HTML and PDF versions of the article. To characterize the genetic determinants of resistance to antituberculosis drugs, we performed a genome-wide association study (GWAS) of 6,465 Mycobacterium tuberculosis clinical isolates from more than 30 countries. A GWAS approach within a mixed-regression framework was followed by a phylogenetics-based test for independent mutations. In addition to mutations in established and recently described resistance-associated genes, novel mutations were discovered for resistance to cycloserine, ethionamide and para-aminosalicylic acid. The capacity to detect mutations associated with resistance to ethionamide, pyrazinamide, capreomycin, cycloserine and para-aminosalicylic acid was enhanced by inclusion of insertions and deletions. Odds ratios for mutations within candidate genes were found to reflect levels of resistance. New epistatic relationships between candidate drug-resistance-associated genes were identified. Findings also suggest the involvement of efflux pumps (drrA and Rv2688c) in the emergence of resistance. This study will inform the design of new diagnostic tests and expedite the investigation of resistance and compensatory epistatic mechanisms. The project was supported by the KAUST faculty baseline research fund (BAS/1/1020-01-01) to A.P. The authors wish to thank members of the KAUST Bioscience Core laboratory who sequenced samples. We thank the Wellcome Trust Sanger Institute core and pathogen sequencing and informatics teams who were involved in the Malawi and Uganda studies. The work was funded in part by the Wellcome Trust (grant numbers WT096249/Z/11/B, WT088559MA, WT081814/Z/06/Z and WT098051) and the Wellcome Trust–Burroughs Wellcome Fund Infectious Diseases Initiative grant (number 063410/ABC/00/Z). F.C. was the recipient of a Bloomsbury College PhD Studentship and was supported by the Wellcome Trust (201344/Z/16/Z); J. Perdigão received a Fundação para a Ciência e a Tecnologia (Portugal) postdoctoral fellowship fund (SFRH/BPD/95406/2013). The Calouste Gulbenkian Foundation, the Institute Gulbenkian in Lisbon and the European Society of Clinical Microbiology and Infectious Diseases supported the research of C.P., J. Perdigão, I.P. and M.V. J. Phelan is funded by a BBSRC PhD studentship. T.G.C. is funded by the Medical Research Council UK (grant numbers MR/K000551/1, MR/M01360X/1, MR/N010469/1 and MC_PC_15103). N.F. is funded by the Medical Research Council UK (grant number MR/K020420/1). T.M. is supported by the Ministry of Health, Labor and Welfare of Japan (H21-Shinkou-Ippan-008 and H24-Shinkou-Ippan-010). info:eu-repo/semantics/publishedVersion |
Databáze: | OpenAIRE |
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