Literature DB >> 31099236

Comparative Metabolomics between Mycobacterium tuberculosis and the MTBVAC Vaccine Candidate.

Caridad Díaz1, José Pérez Del Palacio1, Pedro Luis Valero-Guillén2, Patricia Mena García1, Irene Pérez3,4, Francisca Vicente1, Carlos Martín3,4,5, Olga Genilloud1, Antonio Sánchez Pozo6, Jesús Gonzalo-Asensio3,4,7.   

Abstract

MTBVAC 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.

Entities:  

Keywords:  live attenuated vaccine; phoP; phosphatidylinositol mannosides; vaccination biomarkers; virulence

Year:  2019        PMID: 31099236     DOI: 10.1021/acsinfecdis.9b00008

Source DB:  PubMed          Journal:  ACS Infect Dis        ISSN: 2373-8227            Impact factor:   5.084


  5 in total

1.  Development of small-molecule inhibitors of fatty acyl-AMP and fatty acyl-CoA ligases in Mycobacterium tuberculosis.

Authors:  Marzena Baran; Kimberly D Grimes; Paul A Sibbald; Peng Fu; Helena I M Boshoff; Daniel J Wilson; Courtney C Aldrich
Journal:  Eur J Med Chem       Date:  2020-06-13       Impact factor: 6.514

2.  Untargeted Metabolomics by Liquid Chromatography-Mass Spectrometry in Biomedical Research.

Authors:  Caridad Díaz; Carmen González-Olmedo
Journal:  Methods Mol Biol       Date:  2023

3.  Live attenuated TB vaccines representing the three modern Mycobacterium tuberculosis lineages reveal that the Euro-American genetic background confers optimal vaccine potential.

Authors:  Irene Pérez; Santiago Uranga; Fadel Sayes; Wafa Frigui; Sofía Samper; Ainhoa Arbués; Nacho Aguiló; Roland Brosch; Carlos Martín; Jesús Gonzalo-Asensio
Journal:  EBioMedicine       Date:  2020-04-28       Impact factor: 8.143

4.  Human Plasma Metabolomics for Biomarker Discovery: Targeting the Molecular Subtypes in Breast Cancer.

Authors:  Leticia Díaz-Beltrán; Carmen González-Olmedo; Natalia Luque-Caro; Caridad Díaz; Ariadna Martín-Blázquez; Mónica Fernández-Navarro; Ana Laura Ortega-Granados; Fernando Gálvez-Montosa; Francisca Vicente; José Pérez Del Palacio; Pedro Sánchez-Rovira
Journal:  Cancers (Basel)       Date:  2021-01-05       Impact factor: 6.639

Review 5.  Metabolic Versatility of Mycobacterium tuberculosis during Infection and Dormancy.

Authors:  Dorothy Pei Shan Chang; Xue Li Guan
Journal:  Metabolites       Date:  2021-02-02
  5 in total

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