Intracellular lipid droplets are exploited by Junın virus in a nucleoprotein-dependent process

被引:1
|
作者
Vazquez, Cecilia Alejandra [1 ,2 ]
Escudero-Perez, Beatriz [3 ,4 ]
Hayashi, Jennifer M. [5 ]
Leon, Kristoffer E. [5 ]
Moreira, Joao Paulo [5 ]
Catana, Mayra Alejandra Castaneda [2 ]
Groseth, Allison [6 ]
Ott, Melanie [5 ]
Oestereich, Lisa [3 ,4 ]
Munoz-Fontela, Cesar [3 ,4 ]
Garcia, Cybele Carina [2 ]
Cordo, Sandra Myriam [1 ]
机构
[1] Univ Buenos Aires UBA, CONICET, Inst Quim Biol Fac Ciencias Exactas & Nat IQUIBICE, Fac Ciencias Exactas & Nat FCEyN,Dept Quim Biol QB, RA-C1428EHA Buenos Aires, Argentina
[2] Univ Buenos Aires UBA, Fac Ciencias Exactas & Nat FCEyN, Inst Quim Biol Fac Ciencias Exactas & Nat IQUIBICE, CONICET,Dept Quim Biol QB,Lab Estrategias Antivira, RA-C1428EHA Buenos Aires, Argentina
[3] Bernhard Nocht Inst Trop Med, D-20359 Hamburg, Germany
[4] German Ctr Infect Res DZIF, Partner Site Hamburg Lubeck Borstel Riems, D-20359 Hamburg, Germany
[5] David Gladstone Inst, San Francisco, CA 94158 USA
[6] Friedrich Loeffler Inst, Inst Mol Virol & Cell Biol, Lab Arenavirus Biol, D-17493 Greifswald Insel Riems, Germany
关键词
Jun & imath; n & imath; n virus; Lassa virus; Lipid droplets; Nucleoprotein; INHIBITION; FLAVIVIRUSES; HEPATOCYTES; MECHANISM;
D O I
10.1242/jcs.261745
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lipid droplets (LDs) are organelles involved in lipid storage, maintenance of energy homeostasis, protein sequestration, signaling events and inter-organelle interactions. Recently, LDs have been shown to favor the replication of members from different viral families, such as the Flaviviridae and Coronaviridae. . In this work, we show that LDs are essential organelles for members of the Arenaviridae family. A virus-driven reduction of LD number was observed in cultures infected with Jun & imath;n mammarenavirus (JUNV), caused in part by action of the viral nucleoprotein. Notably, we identified a new pool of nucleoprotein and viral RNA that localizes in the vicinity of LDs, suggesting that LDs play a role during the viral replication cycle. Regarding the mechanism behind LD exhaustion, we found evidence that lipophagy is involved in LD degradation with the resulting fatty acids being substrates of fatty acid beta-oxidation, which fuels viral multiplication. This work highlights the importance of LDs during the replication cycle of JUNV, contributing to the knowledge of the metabolic changes these mammarenaviruses cause in their hosts.
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页数:12
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