1H Nuclear Magnetic Resonance Metabolomics of Plasma Unveils Liver Dysfunction in Dengue Patients

被引:25
作者
El-Bacha, Tatiana [1 ,6 ]
Struchiner, Claudio J. [2 ]
Cordeiro, Marli Tenorio [3 ]
Almeida, Fabio C. L. [1 ,4 ]
Marques, Ernesto Torres, Jr. [3 ,5 ]
Da Poian, Andrea T. [1 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Bioquim Med Leopoldo de Meis, Rio De Janeiro, RJ, Brazil
[2] Fundacao Oswaldo Cruz, Dept Doencas Endem Samuel Pessoa, Rio De Janeiro, RJ, Brazil
[3] Fiocruz MS, Aggeu Magalhaes Res Ctr, Virol & Expt Therapy Lab, Recife, PE, Brazil
[4] Univ Fed Rio de Janeiro, Ctr Nacl Biol Estrutural & Bioimagem, Rio De Janeiro, RJ, Brazil
[5] Univ Pittsburgh, Ctr Vaccine Res, Pittsburgh, PA USA
[6] Univ Fed Rio de Janeiro, Inst Nutr Josue de Castro, Rio De Janeiro, RJ, Brazil
关键词
NMR-SPECTROSCOPY; HUMAN-BLOOD; AMINO-ACID; SERUM; INFECTION; GLUTAMINE; URINE;
D O I
10.1128/JVI.00187-16
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Dengue, due to its global burden, is the most important arthropod-borne flavivirus disease, and early detection lowers fatality rates to below 1%. Since the metabolic resources crucial for viral replication are provided by host cells, detection of changes in the metabolic profile associated with disease pathogenesis could help with the identification of markers of prognostic and diagnostic importance. We applied H-1 nuclear magnetic resonance exploratory metabolomics to study longitudinal changes in plasma metabolites in a cohort in Recife, Brazil. To gain statistical power, we used innovative paired multivariate analyses to discriminate individuals with primary and secondary infection presenting as dengue fever (DF; mild) and dengue hemorrhagic fever (DHF; severe) and subjects with a nonspecific nondengue (ND) illness (ND subjects). Our results showed that a decrease in plasma low-density lipoprotein (LDL) and very-low-density lipoprotein (VLDL) discriminated dengue virus (DENV)-infected subjects from ND subjects, and also, subjects with severe infection even presented a decrease in lipoprotein concentrations compared to the concentrations in subjects with mild infection. These results add to the ongoing discussion that the manipulation of lipid metabolism is crucial for DENV replication and infection. In addition, a decrease in plasma glutamine content was characteristic of DENV infection and disease severity, and an increase in plasma acetate levels discriminated subjects with DF and DHF from ND subjects. Several other metabolites shown to be altered in DENV infection and the implications of these alterations are discussed. We hypothesize that these changes in the plasma metabolome are suggestive of liver dysfunction, could provide insights into the underlying molecular mechanisms of dengue virus pathogenesis, and could help to discriminate individuals at risk of the development of severe infection and predict disease outcome. IMPORTANCE Dengue, due to its global burden, is the most important mosquito-borne viral disease. There is no specific treatment for dengue disease, and early detection lowers fatality rates to below 1%. In this study, we observed the effects of dengue virus infection on the profile of small molecules in the blood of patients with mild and severe infection. Variations in the profiles of these small molecules reflected the replication of dengue virus in different tissues and the extent of tissue damage during infection. The results of this study showed that the molecules that changed the most were VLDL, LDL, and amino acids. We propose that these changes reflect liver dysfunction and also that they can be used to discriminate subjects with mild dengue from those with severe dengue.
引用
收藏
页码:7429 / 7443
页数:15
相关论文
共 51 条
[1]   Two-Dimensional Difference Gel Electrophoresis (DiGE) Analysis of Plasmas from Dengue Fever Patients [J].
Albuquerque, Lidiane M. ;
Trugilho, Monique R. O. ;
Chapeaurouge, Alex ;
Jurgilas, Patricia B. ;
Bozza, Patricia T. ;
Bozza, Fernando A. ;
Perales, Jonas ;
Neves-Ferreira, Ana G. C. .
JOURNAL OF PROTEOME RESEARCH, 2009, 8 (12) :5431-5441
[2]   Metabolic profiling, metabolomic and metabonomic procedures for NMR spectroscopy of urine, plasma, serum and tissue extracts [J].
Beckonert, Olaf ;
Keun, Hector C. ;
Ebbels, Timothy M. D. ;
Bundy, Jacob G. ;
Holmes, Elaine ;
Lindon, John C. ;
Nicholson, Jeremy K. .
NATURE PROTOCOLS, 2007, 2 (11) :2692-2703
[3]   ASSIGNMENT OF RESONANCES FOR ACUTE-PHASE GLYCOPROTEINS IN HIGH-RESOLUTION PROTON NMR-SPECTRA OF HUMAN-BLOOD PLASMA [J].
BELL, JD ;
BROWN, JCC ;
NICHOLSON, JK ;
SADLER, PJ .
FEBS LETTERS, 1987, 215 (02) :311-315
[4]   The global distribution and burden of dengue [J].
Bhatt, Samir ;
Gething, Peter W. ;
Brady, Oliver J. ;
Messina, Jane P. ;
Farlow, Andrew W. ;
Moyes, Catherine L. ;
Drake, John M. ;
Brownstein, John S. ;
Hoen, Anne G. ;
Sankoh, Osman ;
Myers, Monica F. ;
George, Dylan B. ;
Jaenisch, Thomas ;
Wint, G. R. William ;
Simmons, Cameron P. ;
Scott, Thomas W. ;
Farrar, Jeremy J. ;
Hay, Simon I. .
NATURE, 2013, 496 (7446) :504-507
[5]   Metabolomics Approach for Investigation of Effects of Dengue Virus Infection Using the EA hy926 Cell Line [J].
Birungi, Grace ;
Chen, Sheryl Meijie ;
Loy, Boon Pheng ;
Ng, Mah Lee ;
Li, Sam Fong Yau .
JOURNAL OF PROTEOME RESEARCH, 2010, 9 (12) :6523-6534
[6]   Lower Low-Density Lipoprotein Cholesterol Levels Are Associated with Severe Dengue Outcome [J].
Biswas, Hope H. ;
Gordon, Aubree ;
Nunez, Andrea ;
Perez, Maria Angeles ;
Balmaseda, Angel ;
Harris, Eva .
PLOS NEGLECTED TROPICAL DISEASES, 2015, 9 (09)
[7]   Molecular classification of outcomes from dengue virus-3 infections [J].
Brasier, Allan R. ;
Zhao, Yingxin ;
Wiktorowicz, John E. ;
Spratt, Heidi M. ;
Nascimento, Eduardo J. M. ;
Cordeiro, Marli T. ;
Soman, Kizhake V. ;
Ju, Hyunsu ;
Recinos, Adrian, III ;
Stafford, Susan ;
Wu, Zheng ;
Marques, Ernesto T. A., Jr. ;
Vasilakis, Nikos .
JOURNAL OF CLINICAL VIROLOGY, 2015, 64 :97-106
[8]  
Brazil Ministry of Health, 2015, B EPIDEMIOLOGICO, V48
[9]   Plasma metabolomics identifies lipid abnormalities linked to markers of inflammation, microbial translocation, and hepatic function in HIV patients receiving protease inhibitors [J].
Cassol, Edana ;
Misra, Vikas ;
Holman, Alexander ;
Kamat, Anupa ;
Morgello, Susan ;
Gabuzda, Dana .
BMC INFECTIOUS DISEASES, 2013, 13
[10]   Glutamine Metabolism Is Essential for Human Cytomegalovirus Infection [J].
Chambers, Jeremy W. ;
Maguire, Tobi G. ;
Alwine, James C. .
JOURNAL OF VIROLOGY, 2010, 84 (04) :1867-1873