scholarly journals AMP-Activated Kinase Restricts Rift Valley Fever Virus Infection by Inhibiting Fatty Acid Synthesis

2012 ◽  
Vol 8 (4) ◽  
pp. e1002661 ◽  
Author(s):  
Theresa S. Moser ◽  
Daniel Schieffer ◽  
Sara Cherry
2018 ◽  
Vol 218 (11) ◽  
pp. 1847-1851 ◽  
Author(s):  
Anita K McElroy ◽  
Jessica R Harmon ◽  
Timothy Flietstra ◽  
Stuart T Nichol ◽  
Christina F Spiropoulou

2019 ◽  
Vol 40 (4) ◽  
pp. 367-377 ◽  
Author(s):  
Adewale Victor Opayele ◽  
Linda Amarachi Ndiana ◽  
Georgina Njideka Odaibo ◽  
David Olufemi Olaleye

2014 ◽  
Vol 109 ◽  
pp. 64-67 ◽  
Author(s):  
Gema Lorenzo ◽  
Miguel Rodríguez-Pulido ◽  
Elena López-Gil ◽  
Francisco Sobrino ◽  
Belén Borrego ◽  
...  

2017 ◽  
Vol 11 (10) ◽  
pp. e0006050 ◽  
Author(s):  
Brittany L. Dodson ◽  
Elizabeth S. Andrews ◽  
Michael J. Turell ◽  
Jason L. Rasgon

2012 ◽  
Vol 6 (2) ◽  
pp. e1529 ◽  
Author(s):  
Kimberly K. Gray ◽  
Melissa N. Worthy ◽  
Terry L. Juelich ◽  
Stacy L. Agar ◽  
Allison Poussard ◽  
...  

2012 ◽  
Vol 163 (2) ◽  
pp. 417-423 ◽  
Author(s):  
Ted M. Ross ◽  
Nitin Bhardwaj ◽  
Stephanie J. Bissel ◽  
Amy L. Hartman ◽  
Darci R. Smith

Author(s):  
Vincent Mastrodomenico ◽  
Jeremy J. Esin ◽  
Shefah Qazi ◽  
Oreoluwa S. Omoba ◽  
Brittany L. Fung ◽  
...  

AbstractViruses require host cell metabolites to productively infect, and the mechanisms by which viruses usurp these molecules is diverse. One group of cellular metabolites important in virus infection is the polyamines, small positively-charged molecules involved in cell cycle, translation, and nucleic acid synthesis, among other cellular functions. Polyamines also support replication of diverse viruses, and they are important for processes such as transcription, translation, and viral protein enzymatic activity. Rift Valley fever virus (RVFV) is a negative-sense RNA virus that requires polyamines to produce infectious particles. In polyamine depleted conditions, noninfectious particles are produced that interfere with virus replication and stimulate immune signaling. Here, we find that RVFV relies on virion-associated polyamines to maintain infectivity. We show that RVFV replication is facilitated by any of the three biogenic polyamines; however, we specifically find spermidine associated with purified virions. Using a panel of polyamine homologs, we observe that virions can also associate with (R)-3-methylspermidine and norspermidine, though not with other less homologous molecules. Using polyamine reporter cells, we demonstrate that virion-associated polyamines transmit from one infected cell to another. Finally, we find that virions devoid of polyamines are unstable and cannot be supplemented with exogenous polyamines to regain stability or infectivity. These data highlight a unique role for polyamines, and spermidine in particular, in maintaining virus infectivity, a function not previously appreciated. Further, these studies are the first to identify polyamines associated with RVFV virions. Targeting polyamines represents a promising antiviral strategy, and this work highlights a new mechanism by which we can inhibit virus replication through FDA-approved polyamine depleting pharmaceuticals.


2016 ◽  
Vol 7 ◽  
Author(s):  
Noor A. Ahsan ◽  
Gavin C. Sampey ◽  
Ben Lepene ◽  
Yao Akpamagbo ◽  
Robert A. Barclay ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document