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

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dc.contributor.author Williams, Aurelia Alvina
dc.contributor.author Kgoadi, Khanyisile
dc.contributor.author Steffens, Francois E.
dc.contributor.author Steenkamp, Paul
dc.contributor.author Meyer, Debra
dc.date.accessioned 2017-02-09T08:30:24Z
dc.date.available 2017-02-09T08:30:24Z
dc.date.issued 2014
dc.description.abstract Immune 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.department Biochemistry en_ZA
dc.description.department Statistics en_ZA
dc.description.librarian hb2017 en_ZA
dc.description.sponsorship The Medical Research Council (MRC), Technology Innovation Agency (TIA) and the National Research Foundation (NRF) of South Africa. en_ZA
dc.description.uri http://benthamscience.com/journal/index.php?journalID=cmb en_ZA
dc.identifier.citation Williams, 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.issn 2213-235X (print)
dc.identifier.issn 2213-2368 (online)
dc.identifier.other 10.2174/2213235X02666140214201251
dc.identifier.uri http://hdl.handle.net/2263/58946
dc.language.iso en en_ZA
dc.publisher Bentham Science en_ZA
dc.rights © 2014 Bentham Science Publishers en_ZA
dc.subject Biofluid en_ZA
dc.subject Biomarker en_ZA
dc.subject Metabonomics en_ZA
dc.subject Ostro™ plates en_ZA
dc.subject Human immunodeficiency virus (HIV) en_ZA
dc.subject Highly active antiretroviral therapy (HAART) en_ZA
dc.subject Linear discriminant analysis (LDA) en_ZA
dc.subject Solid phase extraction (SPE) en_ZA
dc.subject Ultra-performance liquid chromatography mass spectrometry (UPLC-MS) en_ZA
dc.title UPLC-MS metabonomics reveals perturbed metabolites in HIV-infected sera en_ZA
dc.type Postprint Article en_ZA


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