Literature DB >> 9645841

Increased excretion of aromatic amino acid catabolites in animals infected with Trypanosoma brucei evansi.

A El Sawalhy1, J R Seed, J E Hall, H El Attar.   

Abstract

Aromatic amino acid catabolism by Trypanosoma brucei evansi was investigated in vivo using C3HeB/FeJ mice. The major catabolites detected by gas chromatography in the urines of infected animals were phenylpyruvic acid, 4-hydroxyphenylpyruvic acid, and indole-3-pyruvic acid. Identity of each compound was confirmed by gas chromatography-mass spectrometry. Concentrations of catabolites in urine of infected mice were correlated with parasitemia and returned to normal following suramin treatment. Other aromatic amino acid metabolites, including indole-3-acetic acid, indole-3-lactic acid, and 4-hydroxyphenyllactic acid, were detected in urine from infected animals by gas chromatography mass spectrometry, although quantities were too low to be quantified reproducibly. Both phenylpyruvic acid and 4-hydroxyphenylpyruvic acid were also detected in urine of dogs and donkeys experimentally infected in Egypt with a recent field isolate of T. b. evansi. Tryptophan metabolites could not be assayed in dog and urine samples because formalin, which degraded the indole acids, had to be added before the samples could be imported into the U.S. Finally, concentrations of urinary catabolites during infection were correlated with the tyrosine aminotransferase activity in infected mouse sera.

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Year:  1998        PMID: 9645841

Source DB:  PubMed          Journal:  J Parasitol        ISSN: 0022-3395            Impact factor:   1.276


  7 in total

1.  Crystal structure of Trypanosoma cruzi tyrosine aminotransferase: substrate specificity is influenced by cofactor binding mode.

Authors:  W Blankenfeldt; C Nowicki; M Montemartini-Kalisz; H M Kalisz; H J Hecht
Journal:  Protein Sci       Date:  1999-11       Impact factor: 6.725

2.  Trypanosoma brucei metabolite indolepyruvate decreases HIF-1α and glycolysis in macrophages as a mechanism of innate immune evasion.

Authors:  Anne F McGettrick; Sarah E Corcoran; Paul J G Barry; Jennifer McFarland; Cécile Crès; Anne M Curtis; Edward Franklin; Sinéad C Corr; K Hun Mok; Eoin P Cummins; Cormac T Taylor; Luke A J O'Neill; Derek P Nolan
Journal:  Proc Natl Acad Sci U S A       Date:  2016-11-15       Impact factor: 11.205

3.  Metabonomic investigation of single and multiple strain Trypanosoma brucei brucei infections.

Authors:  Jia V Li; Jasmina Saric; Yulan Wang; Jürg Utzinger; Elaine Holmes; Oliver Balmer
Journal:  Am J Trop Med Hyg       Date:  2011-01       Impact factor: 2.345

4.  Liver Metabolic Alterations and Changes in Host Intercompartmental Metabolic Correlation during Progression of Malaria.

Authors:  Arjun Sengupta; Angika Basant; Soumita Ghosh; Shobhona Sharma; Haripalsingh M Sonawat
Journal:  J Parasitol Res       Date:  2011-05-29

5.  Trypanosoma brucei Secreted Aromatic Ketoacids Activate the Nrf2/HO-1 Pathway and Suppress Pro-inflammatory Responses in Primary Murine Glia and Macrophages.

Authors:  Nicole K Campbell; David G Williams; Hannah K Fitzgerald; Paul J Barry; Clare C Cunningham; Derek P Nolan; Aisling Dunne
Journal:  Front Immunol       Date:  2019-09-11       Impact factor: 7.561

Review 6.  The Uptake and Metabolism of Amino Acids, and Their Unique Role in the Biology of Pathogenic Trypanosomatids.

Authors:  Letícia Marchese; Janaina de Freitas Nascimento; Flávia Silva Damasceno; Frédéric Bringaud; Paul A M Michels; Ariel Mariano Silber
Journal:  Pathogens       Date:  2018-04-01

7.  The Trypanosoma brucei-Derived Ketoacids, Indole Pyruvate and Hydroxyphenylpyruvate, Induce HO-1 Expression and Suppress Inflammatory Responses in Human Dendritic Cells.

Authors:  Hannah K Fitzgerald; Sinead A O'Rourke; Eva Desmond; Nuno G B Neto; Michael G Monaghan; Miriam Tosetto; Jayne Doherty; Elizabeth J Ryan; Glen A Doherty; Derek P Nolan; Jean M Fletcher; Aisling Dunne
Journal:  Antioxidants (Basel)       Date:  2022-01-15
  7 in total

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