Literature DB >> 6086816

Early enhanced glucose uptake in human cytomegalovirus-infected cells.

M P Landini.   

Abstract

The uptake rate of some sugars was demonstrated in human embryo fibroblasts following infection by human cytomegalovirus (HCMV) and a significant increase in glucose uptake was demonstrated. Quantitative and sequential analysis of glucose uptake during the HCMV replication cycle showed that the enhanced uptake began during the first 20 h after infection and occurred even when a high glucose level was constantly present in the medium. The increase in sugar uptake requires an active viral genome, de novo protein synthesis and seems to be dependent only on the early transcription of the viral genome, as it did occur when replication of the viral genome was limited (non-permissive cells or cells infected in the presence of DNA synthesis inhibitors).

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Year:  1984        PMID: 6086816     DOI: 10.1099/0022-1317-65-7-1229

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  39 in total

1.  Increased sugar transport in BHK cells infected with Semliki Forest virus or with herpes simplex virus.

Authors:  M A Gray; M H James; J C Booth; C A Pasternak
Journal:  Arch Virol       Date:  1986       Impact factor: 2.574

2.  Changes in membrane permeability in cells infected by human cytomegalovirus.

Authors:  M Rugolo; B Baldassarri; M P Landini
Journal:  Arch Virol       Date:  1986       Impact factor: 2.574

3.  Human cytomegalovirus major immediate-early proteins and simian virus 40 large T antigen can inhibit apoptosis through activation of the phosphatidylinositide 3'-OH kinase pathway and the cellular kinase Akt.

Authors:  Yongjun Yu; James C Alwine
Journal:  J Virol       Date:  2002-04       Impact factor: 5.103

Review 4.  Viral activation of cellular metabolism.

Authors:  Erica L Sanchez; Michael Lagunoff
Journal:  Virology       Date:  2015-03-23       Impact factor: 3.616

Review 5.  Viral effects on metabolism: changes in glucose and glutamine utilization during human cytomegalovirus infection.

Authors:  Yongjun Yu; Amy J Clippinger; James C Alwine
Journal:  Trends Microbiol       Date:  2011-05-12       Impact factor: 17.079

6.  Human Cytomegalovirus Replication Is Inhibited by the Autophagy-Inducing Compounds Trehalose and SMER28 through Distinctively Different Mechanisms.

Authors:  Alex E Clark; Maite Sabalza; Philip L S M Gordts; Deborah H Spector
Journal:  J Virol       Date:  2018-02-26       Impact factor: 5.103

Review 7.  Targeted Metabolic Reprogramming to Improve the Efficacy of Oncolytic Virus Therapy.

Authors:  Barry E Kennedy; Maryanne Sadek; Shashi A Gujar
Journal:  Mol Ther       Date:  2020-03-20       Impact factor: 11.454

8.  Systems-level metabolic flux profiling identifies fatty acid synthesis as a target for antiviral therapy.

Authors:  Joshua Munger; Bryson D Bennett; Anuraag Parikh; Xiao-Jiang Feng; Jessica McArdle; Herschel A Rabitz; Thomas Shenk; Joshua D Rabinowitz
Journal:  Nat Biotechnol       Date:  2008-09-28       Impact factor: 54.908

9.  Metabolic effects of influenza virus infection in cultured animal cells: Intra- and extracellular metabolite profiling.

Authors:  Joachim B Ritter; Aljoscha S Wahl; Susann Freund; Yvonne Genzel; Udo Reichl
Journal:  BMC Syst Biol       Date:  2010-05-13

10.  Glutamine metabolism is essential for human cytomegalovirus infection.

Authors:  Jeremy W Chambers; Tobi G Maguire; James C Alwine
Journal:  J Virol       Date:  2009-11-25       Impact factor: 5.103

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