UPLC-MS metabonomics reveals perturbed metabolites in HIV-infected sera

dc.contributor.authorWilliams, Aurelia Alvina
dc.contributor.authorKgoadi, Khanyisile
dc.contributor.authorSteffens, Francois E.
dc.contributor.authorSteenkamp, Paul
dc.contributor.authorMeyer, Debra
dc.contributor.emaildebra.meyer@up.ac.zaen_ZA
dc.date.accessioned2017-02-09T08:30:24Z
dc.date.available2017-02-09T08:30:24Z
dc.date.issued2014
dc.description.abstractImmune responses to infection by the human immunodeficiency virus (HIV) and the use of highly active antiretroviral therapy (HAART) to treat HIV infection, contributes to metabolic irregularities in the host. Current methods for the extraction and identification of metabolites in biofluids generally make use of laborious, time-consuming protocols. Here, 96-well Ostro™ plates and filtration under positive pressure was used to facilitate the simultaneous, reproducible extraction of metabolites from multiple serum samples which were then analyzed by ultra-performance liquid chromatography mass spectrometry (UPLC-MS). The easy to use solid phase extraction (SPE) protocol eliminated numerous potential contaminants while the UPLC-MS detection of metabolites produced visibly different chromatograms for HIV negative (n=16), HIV+ (n=13) and HIV+HAART+ (n=15) serum samples. Linear discriminant analysis (LDA) amplified these differences, classified the groups with 100% accuracy and identified biomarkers explaining the greatest variances between the groups. The 21 metabolites altered by HIV and/or HAART primarily represented those linked to lipid and energy pathways which is where known metabolic changes associated with HIV infection occur. This work demonstrated for the first time that OstroTM plates and UPLC-MS metabonomics was able to successfully identify distinct differences between the experimental groups and detected metabolites related to HAART and other drugs used in the treatment of HIV-associated conditions. The findings of this approach suggests a possible role for this methodology in disease prognosis as well as in the monitoring of treatment success or failure and linking treatment to metabolic complications.en_ZA
dc.description.departmentBiochemistryen_ZA
dc.description.departmentStatisticsen_ZA
dc.description.librarianhb2017en_ZA
dc.description.sponsorshipThe Medical Research Council (MRC), Technology Innovation Agency (TIA) and the National Research Foundation (NRF) of South Africa.en_ZA
dc.description.urihttp://benthamscience.com/journal/index.php?journalID=cmben_ZA
dc.identifier.citationWilliams, A, Kgoadi, K, Steffens, F, Steenkamp, P & Meyer, D 2014, 'UPLC-MS metabonomics reveals perturbed metabolites in HIV-infected sera', Current Metabolomics, vol. 2, no. 1, pp. 37-52.en_ZA
dc.identifier.issn2213-235X (print)
dc.identifier.issn2213-2368 (online)
dc.identifier.other10.2174/2213235X02666140214201251
dc.identifier.urihttp://hdl.handle.net/2263/58946
dc.language.isoenen_ZA
dc.publisherBentham Scienceen_ZA
dc.rights© 2014 Bentham Science Publishersen_ZA
dc.subjectBiofluiden_ZA
dc.subjectBiomarkeren_ZA
dc.subjectMetabonomicsen_ZA
dc.subjectOstro™ platesen_ZA
dc.subjectHuman immunodeficiency virus (HIV)en_ZA
dc.subjectHighly active antiretroviral therapy (HAART)en_ZA
dc.subjectLinear discriminant analysis (LDA)en_ZA
dc.subjectSolid phase extraction (SPE)en_ZA
dc.subjectUltra-performance liquid chromatography mass spectrometry (UPLC-MS)en_ZA
dc.titleUPLC-MS metabonomics reveals perturbed metabolites in HIV-infected seraen_ZA
dc.typePostprint Articleen_ZA

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