Abstract

Mycolic acids are attractive diagnostic markers for tuberculosis (TB) infection because they are bacteria-derived, contain information about bacterial species, modulate host–pathogen interactions and are chemically inert. Here, we present a novel approach based on mass spectrometry. Quantification of specific precursor → fragment transitions of approximately 2000 individual mycolic acids (MAs) resulted in high analytical sensitivity and specificity. We next used this tool in a retrospective case–control study of patients with pulmonary TB with varying disease burdens from South Korea, Vietnam, Uganda and South Africa. MAs were extracted from small volume sputum (200 µl) and analysed without the requirement for derivatization. Infected patients (70, 19 of whom were HIV+) could be separated from controls (40, 20 of whom were HIV+) with a sensitivity and specificity of 94 and 93%, respectively. Furthermore, we quantified MA species in lung tissue of TB-infected mice and demonstrated effective clearance of MA levels following curative rifampicin treatment. Thus, our results demonstrate for the first time the feasibility and clinical relevance of direct detection of mycobacterial lipids as biomarkers of TB infection.

Highlights

  • The number of mycobacterial infections has increased dramatically over the past two decades due to, among other factors, the HIV/AIDS epidemic (Harries & Dye, 2006; Iademarco & Castro, 2003; Saltini, 2006)

  • We show that quantification of mycolic acids (MAs) from sputum, in particular C26 a-MAs, leads to diagnostic performances comparable to or better than conventional acid-fast bacillus (AFB) smear staining

  • For example fragmentation of m/z 1164, which corresponds to an a-MA with a molecular composition of C80H156O3 which is present in many species of mycobacteria including Mycobacterium tuberculosis (MTB), yielded product ions corresponding to alpha-branch fatty acids with different chain lengths: trace amounts of m/z 339 (C22:0), m/z 367 (C24:0) and m/z 395 (C26:0) as the predominant acyl species (Fig 1B)

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Summary

Introduction

The number of mycobacterial infections has increased dramatically over the past two decades due to, among other factors, the HIV/AIDS epidemic (Harries & Dye, 2006; Iademarco & Castro, 2003; Saltini, 2006). Infection with Mycobacterium tuberculosis (MTB) remains a major global health threat, with over nine million new cases and close to two million deaths annually. Detection of active tuberculosis (TB) remains a serious problem in areas where TB is present and in preclinical and clinical trials. Prior to the introduction of sequence-based techniques, one clinically useful method for mycobacterial speciation was high-performance liquid chromatography (HPLC) analysis of unique mycolic acids (MAs) (Butler & Guthertz, 2001). MAs, which are categorized according to the functional groups www.embomolmed.org

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