Abstract

The Gag polyprotein is implied in the budding as well as the establishment of the supramolecular architecture of infectious retroviral particles. It is also involved in the early phases of the replication of retroviruses by protecting and transporting the viral genome towards the nucleus of the infected cell until its integration in the host genome. Therefore, understanding the structure–function relationships of the Gag subunits is crucial as each of them can represent a therapeutic target. Though the field has been explored for some time in the area of Human Immunodeficiency Virus (HIV), it is only in the last decade that structural data on Feline Immunodeficiency Virus (FIV) Gag subunits have emerged. As FIV is an important veterinary issue, both in domestic cats and endangered feline species, such data are of prime importance for the development of anti-FIV molecules targeting Gag. This review will focus on the recent advances and perspectives on the structure–function relationships of each subunit of the FIV Gag polyprotein.

Highlights

  • Feline Immunodeficiency Virus (FIV) is a retrovirus belonging to the lentivirus genus and infects both domestic and wild feline species

  • The mechanisms of action of Gag have been well defined for Human Immunodeficiency Virus (HIV)-1: the assembly a new viral particle is initiated by the interaction of nucleocapsid domain (NC) with the viral RNA [7] with a role of a new viral particle is initiated by the interaction of NC with the viral RNA [7] with of the “late domain” in selecting the correct genomic RNA [8]

  • This ability to bind nucleic acids is due to the presence of two zinc finger domains (ZF) in NC, containing the seacids is due to the presence of two zinc finger domains (ZF) in NC, containing the sequence quence Cys-X2-Cys-X4-His-X4-Cys, which is conserved between human immunodeficiency virus type 1 (HIV-1) and FIV

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Summary

Introduction

Feline Immunodeficiency Virus (FIV) is a retrovirus belonging to the lentivirus genus and infects both domestic and wild feline species. FIV infects domestic cats, and wild feline species such as lions, hyenas, cheetahs, or pumas, representing an issue both for domestic veterinary practice and wildlife preservation [3]. It is estimated that 4 to 12% of domestic or wild felines are infected, with a disparity depending on the infected species and the countries considered. A vaccine (Fel-o-Vax) has been developed for domestic cats but is only efficient against some of the FIV subtypes. It is only used in a small number of countries where theses subtypes represent the majority of the circulating strains [6].

The Importance of the Gag Polyprotein for the Replication of Lentiviruses
FIV CA
Crystal structure of monomeric the monomeric
FIV p13
Structure–function
Findings
7.7.Conclusions
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