Comparative Metabolomics between Mycobacterium tuberculosis and the MTBVAC Vaccine Candidate.
Caridad DíazJosé Pérez Del PalacioPedro Luis Valero-GuillénPatricia Mena GarcíaIrene PérezFrancisca VicenteCarlos MartínOlga GenilloudAntonio Sánchez PozoJesus Gonzalo-AsensioPublished in: ACS infectious diseases (2019)
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.
Keyphrases
- mycobacterium tuberculosis
- liquid chromatography
- mass spectrometry
- high resolution mass spectrometry
- pulmonary tuberculosis
- clinical trial
- south africa
- ms ms
- hiv aids
- tandem mass spectrometry
- gas chromatography
- genome wide
- ultra high performance liquid chromatography
- escherichia coli
- staphylococcus aureus
- transcription factor
- pseudomonas aeruginosa
- risk factors
- dna methylation
- adverse drug
- randomized controlled trial
- high resolution
- multidrug resistant
- emergency department
- climate change
- simultaneous determination
- open label
- biofilm formation
- hiv positive
- gas chromatography mass spectrometry
- human health
- gestational age