دورية أكاديمية

Metabolomic profiling reveals a finely tuned, starvation-induced metabolic switch in Trypanosoma cruzi epimastigotes.

التفاصيل البيبلوغرافية
العنوان: Metabolomic profiling reveals a finely tuned, starvation-induced metabolic switch in Trypanosoma cruzi epimastigotes.
المؤلفون: Barisón MJ; From the Laboratory of Biochemistry of Tryps-LaBTryps, Department of Parasitology, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, Brazil., Rapado LN; From the Laboratory of Biochemistry of Tryps-LaBTryps, Department of Parasitology, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, Brazil., Merino EF; the Department of Biochemistry and Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia 24061, and., Furusho Pral EM; From the Laboratory of Biochemistry of Tryps-LaBTryps, Department of Parasitology, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, Brazil., Mantilla BS; From the Laboratory of Biochemistry of Tryps-LaBTryps, Department of Parasitology, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, Brazil., Marchese L; From the Laboratory of Biochemistry of Tryps-LaBTryps, Department of Parasitology, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, Brazil., Nowicki C; the Facultad de Farmacia y Bioquímica, Instituto de Química y Fisicoquímica Biológica (IQUIFIB-CONICET), Universidad de Buenos Aires, 1113 Buenos Aires, Argentina., Silber AM; From the Laboratory of Biochemistry of Tryps-LaBTryps, Department of Parasitology, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, Brazil, asilber@usp.br., Cassera MB; the Department of Biochemistry and Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia 24061, and maria.cassera@uga.edu.
المصدر: The Journal of biological chemistry [J Biol Chem] 2017 May 26; Vol. 292 (21), pp. 8964-8977. Date of Electronic Publication: 2017 Mar 29.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
اللغة: English
بيانات الدورية: Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID: 2985121R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1083-351X (Electronic) Linking ISSN: 00219258 NLM ISO Abbreviation: J Biol Chem Subsets: MEDLINE
أسماء مطبوعة: Publication: 2021- : [New York, NY] : Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology
Original Publication: Baltimore, MD : American Society for Biochemistry and Molecular Biology
مواضيع طبية MeSH: Metabolome/*physiology , Trypanosoma cruzi/*growth & development, Life Cycle Stages/physiology ; Metabolomics
مستخلص: Trypanosoma cruzi, the etiological agent of Chagas disease, is a protozoan parasite with a complex life cycle involving a triatomine insect and mammals. Throughout its life cycle, the T. cruzi parasite faces several alternating events of cell division and cell differentiation in which exponential and stationary growth phases play key biological roles. It is well accepted that arrest of the cell division in the epimastigote stage, both in the midgut of the triatomine insect and in vitro , is required for metacyclogenesis, and it has been previously shown that the parasites change the expression profile of several proteins when entering this quiescent stage. However, little is known about the metabolic changes that epimastigotes undergo before they develop into the metacyclic trypomastigote stage. We applied targeted metabolomics to measure the metabolic intermediates in the most relevant pathways for energy metabolism and oxidative imbalance in exponentially growing and stationary growth-arrested epimastigote parasites. We show for the first time that T. cruzi epimastigotes transitioning from the exponential to the stationary phase exhibit a finely tuned adaptive metabolic mechanism that enables switching from glucose to amino acid consumption, which is more abundant in the stationary phase. This metabolic plasticity appears to be crucial for survival of the T. cruzi parasite in the myriad different environmental conditions to which it is exposed during its life cycle.
(© 2017 by The American Society for Biochemistry and Molecular Biology, Inc.)
References: Nucleic Acids Res. 2015 Jul 1;43(W1):W251-7. (PMID: 25897128)
PLoS One. 2009;4(2):e4534. (PMID: 19229347)
Essays Biochem. 2011;51:15-30. (PMID: 22023439)
Mol Biochem Parasitol. 2012 Oct;185(2):114-20. (PMID: 22898136)
Cell Microbiol. 2004 Aug;6(8):733-41. (PMID: 15236640)
J Bioenerg Biomembr. 2016 Aug;48(4):437-49. (PMID: 27222029)
Curr Pharm Des. 2011;17(20):2074-99. (PMID: 21718252)
Antimicrob Agents Chemother. 2013 Jun;57(6):2768-79. (PMID: 23571546)
Subcell Biochem. 1992;18:235-57. (PMID: 1485353)
Eur J Biochem. 1994 Dec 15;226(3):1019-27. (PMID: 7813456)
J Parasitol. 1965 Dec;51(6):922-6. (PMID: 5848818)
PLoS One. 2014 Mar 17;9(3):e92028. (PMID: 24637744)
Comp Biochem Physiol B. 1975 Nov 15;52(3):427-31. (PMID: 1183193)
J Biol Chem. 2015 Mar 20;290(12 ):7767-90. (PMID: 25623067)
J Pharm Biomed Anal. 2010 Dec 1;53(4):983-90. (PMID: 20634014)
FEBS Lett. 1999 Jul 9;454(3):192-6. (PMID: 10431805)
PLoS One. 2013 Oct 30;8(10):e77283. (PMID: 24204787)
Nucleic Acids Res. 2012 Jul;40(Web Server issue):W127-33. (PMID: 22553367)
Curr Drug Targets Infect Disord. 2005 Mar;5(1):53-64. (PMID: 15777198)
J Eukaryot Microbiol. 2002 Nov-Dec;49(6):441-6. (PMID: 12503677)
Microbiol Mol Biol Rev. 2004 Jun;68(2):187-206. (PMID: 15187181)
Mol Biochem Parasitol. 1987 Nov;26(1-2):1-10. (PMID: 3323902)
Parasitol Res. 2012 Aug;111(2):509-14. (PMID: 22648053)
Anal Chem. 2010 Jan 15;82(2):548-58. (PMID: 20038084)
Mol Biochem Parasitol. 1985 Sep;16(3):315-27. (PMID: 3903496)
Parasit Vectors. 2015 Jun 25;8:346. (PMID: 26109388)
Anal Biochem. 1976 Aug;74(2):430-40. (PMID: 962101)
J Biol Chem. 2001 Mar 2;276(9):6516-23. (PMID: 11106665)
PLoS One. 2013 Jul 22;8(7):e69419. (PMID: 23894476)
J Parasitol. 1987 Apr;73(2):438-41. (PMID: 3035158)
Int J Parasitol. 2006 Feb;36(2):157-63. (PMID: 16373069)
Proteomics. 2012 Aug;12(17):2694-703. (PMID: 22761176)
PLoS One. 2015 Feb 11;10(2):e0116712. (PMID: 25671543)
FEBS Lett. 2001 Nov 23;508(3):323-6. (PMID: 11728444)
Rev Inst Med Trop Sao Paulo. 1971 May-Jun;13(3):171-8. (PMID: 5563126)
Mol Biochem Parasitol. 1985 Sep;16(3):329-43. (PMID: 3903497)
Anal Biochem. 1976 May 7;72:248-54. (PMID: 942051)
mSphere. 2016 Apr 13;1(2):null. (PMID: 27303725)
PLoS Negl Trop Dis. 2015 Oct 23;9(10):e0004186. (PMID: 26496442)
Curr Protoc Bioinformatics. 2011 Jun;Chapter 14:Unit 14.10. (PMID: 21633943)
Adv Parasitol. 2011;75:285-305. (PMID: 21820561)
Exp Parasitol. 1967 Oct;21(2):154-9. (PMID: 6082615)
Infect Immun. 2009 Jul;77(7):3023-32. (PMID: 19433547)
J Eukaryot Microbiol. 2016 May;63(3):299-308. (PMID: 26496801)
J Mol Biol. 2015 Oct 23;427(21):3389-406. (PMID: 26156863)
J Lipid Res. 2014 Mar;55(3):592-602. (PMID: 24367045)
معلومات مُعتمدة: R01 AI108819 United States AI NIAID NIH HHS
فهرسة مساهمة: Keywords: Chagas disease; Trypanosoma cruzi; cell growth; cell metabolism; energy metabolism; epimastigotes; metabolomics; oxidative imbalance
تواريخ الأحداث: Date Created: 20170331 Date Completed: 20170609 Latest Revision: 20210205
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC5448128
DOI: 10.1074/jbc.M117.778522
PMID: 28356355
قاعدة البيانات: MEDLINE
الوصف
تدمد:1083-351X
DOI:10.1074/jbc.M117.778522