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Host Entry Factors of Rift Valley Fever Virus Infection

Overview
Journal Adv Virus Res
Specialty Microbiology
Date 2023 Oct 13
PMID 37832991
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Abstract

Rift Valley Fever Virus (RVFV) is a negative sense segmented RNA virus that can cause severe hemorrhagic fever. The tri-segmented virus genome encodes for six (6) multifunctional proteins that engage host factors at a variety of different stages in the replication cycle. The S segment encodes nucleoprotein (N) and nonstructural protein S (NSs), the M segment encodes viral glycoproteins Gn and Gc as well as nonstructural protein M (NSm) and the L segment encodes the viral polymerase (L). Viral glycoproteins Gn and Gc are responsible for entry by binding to a number of host factors. Our recent studies identified a scavenger receptor, LDL receptor related protein 1 (Lrp1), as a potential pro-viral host factor for RVFV and related viruses, including Oropouche virus (OROV) infection. Coincidentally, several recent studies identified other LDL family proteins as viral entry factors and receptors for other viral families. Collectively, these observations suggest that highly conserved LDL family proteins may play a significant role in facilitating entry of viruses from several distinct families. Given the significant roles of viral and host factors during infection, characterization of these interactions is critical for therapeutic targeting with neutralizing antibodies and vaccines.

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References
1.
Lopez N, Muller R, Prehaud C, Bouloy M . The L protein of Rift Valley fever virus can rescue viral ribonucleoproteins and transcribe synthetic genome-like RNA molecules. J Virol. 1995; 69(7):3972-9. PMC: 189128. DOI: 10.1128/JVI.69.7.3972-3979.1995. View

2.
Caminade C, Ndione J, Diallo M, MacLeod D, Faye O, Ba Y . Rift Valley Fever outbreaks in Mauritania and related environmental conditions. Int J Environ Res Public Health. 2014; 11(1):903-18. PMC: 3924481. DOI: 10.3390/ijerph110100903. View

3.
Kalveram B, Lihoradova O, Ikegami T . NSs protein of rift valley fever virus promotes posttranslational downregulation of the TFIIH subunit p62. J Virol. 2011; 85(13):6234-43. PMC: 3126510. DOI: 10.1128/JVI.02255-10. View

4.
Le May N, Dubaele S, Proietti De Santis L, Billecocq A, Bouloy M, Egly J . TFIIH transcription factor, a target for the Rift Valley hemorrhagic fever virus. Cell. 2004; 116(4):541-50. DOI: 10.1016/s0092-8674(04)00132-1. View

5.
ELLIS D, Simpson D, Stamford S, Abdel Wahab K . Rift Valley fever virus: some ultrastructural observations on material from the outbreak in Egypt 1977. J Gen Virol. 1979; 42(2):329-37. DOI: 10.1099/0022-1317-42-2-329. View