Abstract

IntroductionSeveral studies have observed serum lipid changes during malaria infection in humans. All of them were focused at analysis of lipoproteins, not specific lipid molecules. The aim of our study was to identify novel patterns of lipid species in malaria infected patients using lipidomics profiling, to enhance diagnosis of malaria and to evaluate biochemical pathways activated during parasite infection.MethodsUsing a multivariate characterization approach, 60 samples were representatively selected, 20 from each category (mild, severe and controls) of the 690 study participants between age of 0.5–6 years. Lipids from patient’s plasma were extracted with chloroform/methanol mixture and subjected to lipid profiling with application of the LCMS-QTOF method.ResultsWe observed a structured plasma lipid response among the malaria-infected patients as compared to healthy controls, demonstrated by higher levels of a majority of plasma lipids with the exception of even-chain length lysophosphatidylcholines and triglycerides with lower mass and higher saturation of the fatty acid chains. An inverse lipid profile relationship was observed when plasma lipids were correlated to parasitaemia.ConclusionsThis study demonstrates how mapping the full physiological lipid response in plasma from malaria-infected individuals can be used to understand biochemical processes during infection. It also gives insights to how the levels of these molecules relate to acute immune responses.

Highlights

  • Several studies have observed serum lipid changes during malaria infection in humans

  • It is known that hyperlipidaemia in infection arises because of an increase of very low density lipoproteins (VLDL) levels due to increased de novo fatty acid (FA) synthesis and suppressed fatty acid oxidation

  • In a recent study we have found increased levels of fatty acids in malaria patients compared with controls, which could differentiate between mild and severe cases and were positively correlated with parasitaemia values (Surowiec et al 2015)

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Summary

Introduction

Several studies have observed serum lipid changes during malaria infection in humans. Lipids and lipoprotein metabolism in humans have been the focus of intense study and are extensively described in many books and reviews (Vance and Vance 2008; Brown and Marnett 2011). It is known that hyperlipidaemia in infection arises because of an increase of very low density lipoproteins (VLDL) levels due to increased de novo fatty acid (FA) synthesis and suppressed fatty acid oxidation. This results in increased hepatic production of VLDL, suppression of VLDL lipolysis by inhibition of lipoprotein lipase and increased adipose tissue lipolysis. One of the integral components of VLDL, cholesterol, is necessary for the internalization of eukaryotic pathogens into host cells (Bansal et al 2005)

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