Plasma Metabolomics Reveals Distinct Biological and Diagnostic Signatures for Melioidosis

dc.contributor.authorXia L.
dc.contributor.authorHantrakun V.
dc.contributor.authorTeparrukkul P.
dc.contributor.authorWongsuvan G.
dc.contributor.authorKaewarpai T.
dc.contributor.authorDulsuk A.
dc.contributor.authorDay N.P.J.
dc.contributor.authorLemaitre R.N.
dc.contributor.authorChantratita N.
dc.contributor.authorLimmathurotsakul D.
dc.contributor.authorShojaie A.
dc.contributor.authorGharib S.A.
dc.contributor.authorWest T.E.
dc.contributor.correspondenceXia L.
dc.contributor.otherMahidol University
dc.date.accessioned2024-02-14T18:11:23Z
dc.date.available2024-02-14T18:11:23Z
dc.date.issued2024-02-01
dc.description.abstractRationale: The global burden of sepsis is greatest in low-resource settings. Melioidosis, infection with the gram-negative bacterium Burkholderia pseudomallei, is a frequent cause of fatal sepsis in endemic tropical regions such as Southeast Asia. Objectives: To investigate whether plasma metabolomics would identify biological pathways specific to melioidosis and yield clinically meaningful biomarkers. Methods: Using a comprehensive approach, differential enrichment of plasma metabolites and pathways was systematically evaluated in individuals selected from a prospective cohort of patients hospitalized in rural Thailand with infection. Statistical and bioinformatics methods were used to distinguish metabolomic features and processes specific to patients with melioidosis and between fatal and nonfatal cases. Measurements and Main Results: Metabolomic profiling and pathway enrichment analysis of plasma samples from patients with melioidosis (n = 175) and nonmelioidosis infections (n = 75) revealed a distinct immuno-metabolic state among patients with melioidosis, as suggested by excessive tryptophan catabolism in the kynurenine pathway and significantly increased levels of sphingomyelins and ceramide species. We derived a 12-metabolite classifier to distinguish melioidosis from other infections, yielding an area under the receiver operating characteristic curve of 0.87 in a second validation set of patients. Melioidosis nonsurvivors (n = 94) had a significantly disturbed metabolome compared with survivors (n = 81), with increased leucine, isoleucine, and valine metabolism, and elevated circulating free fatty acids and acylcarnitines. A limited eight-metabolite panel showed promise as an early prognosticator of mortality in melioidosis. Conclusions: Melioidosis induces a distinct metabolomic state that can be examined to distinguish underlying pathophysiological mechanisms associated with death. A 12-metabolite signature accurately differentiates melioidosis from other infections and may have diagnostic applications.
dc.identifier.citationAmerican journal of respiratory and critical care medicine Vol.209 No.3 (2024) , 288-298
dc.identifier.doi10.1164/rccm.202207-1349OC
dc.identifier.eissn15354970
dc.identifier.pmid37812796
dc.identifier.scopus2-s2.0-85184142518
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/97153
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titlePlasma Metabolomics Reveals Distinct Biological and Diagnostic Signatures for Melioidosis
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85184142518&origin=inward
oaire.citation.endPage298
oaire.citation.issue3
oaire.citation.startPage288
oaire.citation.titleAmerican journal of respiratory and critical care medicine
oaire.citation.volume209
oairecerif.author.affiliationFaculty of Tropical Medicine, Mahidol University
oairecerif.author.affiliationMahidol Oxford Tropical Medicine Research Unit
oairecerif.author.affiliationUniversity of Washington
oairecerif.author.affiliationNuffield Department of Medicine
oairecerif.author.affiliationCardiovascular Health Research Unit and
oairecerif.author.affiliationCritical Care
oairecerif.author.affiliationSunpasitthiprasong Hospital

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