Publication:
Comparative Metabolomics between Mycobacterium tuberculosis and the MTBVAC Vaccine Candidate.

dc.contributor.authorDíaz, Caridad
dc.contributor.authorPérez Del Palacio, José
dc.contributor.authorValero-Guillén, Pedro Luis
dc.contributor.authorMena García, Patricia
dc.contributor.authorPérez, Irene
dc.contributor.authorVicente, Francisca
dc.contributor.authorMartín, Carlos
dc.contributor.authorGenilloud, Olga
dc.contributor.authorSánchez Pozo, Antonio
dc.contributor.authorGonzalo-Asensio, Jesús
dc.date.accessioned2023-01-25T13:33:36Z
dc.date.available2023-01-25T13:33:36Z
dc.date.issued2019-05-30
dc.description.abstractMTBVAC is a live attenuated M. tuberculosis vaccine constructed by genetic deletions in the phoP and fadD26 virulence genes. The MTBVAC vaccine is currently in phase 2 clinical trials with newborns and adults in South Africa, one of the countries with the highest incidence. Although MTBVAC has been extensively characterized by genomics, transcriptomics, lipidomics, and proteomics, its metabolomic profile is yet unknown. Accordingly, in this study we aim to identify differential metabolites between M. tuberculosis and MTBVAC. To this end, an untargeted metabolomics approach based on liquid chromatography coupled to high-resolution mass spectrometry was implemented in order to explore the main metabolic differences between M. tuberculosis and MTBVAC. As an outcome, we identified a set of 34 metabolites involved in diverse bacterial biosynthetic pathways. A consistent increase in the phosphatidylinositol species was observed in the vaccine candidate relative to its parental strain. This phenotype resulted in an increased production of phosphatidylinositol mannosides, a novel PhoP-regulated phenotype in the most widespread lineages of M. tuberculosis. This study represents a step ahead in our understanding of the MTBVAC vaccine, and some of the differential metabolites identified in this work might be used as potential vaccination biomarkers.
dc.identifier.doi10.1021/acsinfecdis.9b00008
dc.identifier.essn2373-8227
dc.identifier.pmid31099236
dc.identifier.unpaywallURLhttps://pubs.acs.org/doi/pdf/10.1021/acsinfecdis.9b00008
dc.identifier.urihttp://hdl.handle.net/10668/13975
dc.issue.number8
dc.journal.titleACS infectious diseases
dc.journal.titleabbreviationACS Infect Dis
dc.language.isoen
dc.organizationFundación MEDINA (Centro de Excelencia en Investigación de Medicamentos Innovadores en Andalucía)
dc.organizationFundación MEDINA
dc.page.number1317-1326
dc.pubmedtypeComparative Study
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rights.accessRightsopen access
dc.subjectlive attenuated vaccine
dc.subjectphoP
dc.subjectphosphatidylinositol mannosides
dc.subjectvaccination biomarkers
dc.subjectvirulence
dc.subject.meshBacterial Proteins
dc.subject.meshBiosynthetic Pathways
dc.subject.meshChromatography, Liquid
dc.subject.meshMass Spectrometry
dc.subject.meshMetabolomics
dc.subject.meshMycobacterium tuberculosis
dc.subject.meshPhosphatidylinositols
dc.subject.meshTuberculosis Vaccines
dc.titleComparative Metabolomics between Mycobacterium tuberculosis and the MTBVAC Vaccine Candidate.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number5
dspace.entity.typePublication

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