TY - JOUR
T1 - Molecular biology and genetic diversity of Rift Valley fever virus
AU - Ikegami, Tetsuro
N1 - Funding Information:
I thank Mike Bray at NIH for his critical review and communications with author to improve the manuscript; Brian Bird, Serena Carroll and Stuart Nichol at the Centers for Disease Control and Prevention, Atlanta, GA for their permission to generate Figs. 5, 7 and 8 as well as a critical review and comments by Brian Bird; Bob Swanepoel at the National Institute for Communicable Diseases, Sandringham, South Africa, for permission to use Fig. 6 ; Alex Freiberg at The University of Texas Medical Branch (UTMB) for providing Fig. 3 , and Scott Weaver at UTMB for providing Fig. 1 and for critical review of the manuscript. This study has been performed as a part of the SRI project #P19177 (DHS contract#HSHQDC-09-C-00120). T.I. is supported by 5 U54 AI057156 through the Western Regional Center of Excellence , by NIH Grant R01 AI08764301 , and by the Sealy Center for Vaccine Development at UTMB . The Virus Pathogen Database and Analysis Resource (ViPR) introduced in the text is wholly funded with federal funds from NIH/NIAID and Department of Health and Human Services under Contract #HHSN272200900041C .
PY - 2012/9
Y1 - 2012/9
N2 - Rift Valley fever virus (RVFV), a member of the family Bunyaviridae, genus Phlebovirus, is the causative agent of Rift Valley fever (RVF), a mosquito-borne disease of ruminant animals and humans. The generation of a large sequence database has facilitated studies of the evolution and spread of the virus. Bayesian analyses indicate that currently circulating strains of RVFV are descended from an ancestral species that emerged from a natural reservoir in Africa when large-scale cattle and sheep farming were introduced during the 19th century. Viruses descended from multiple lineages persist in that region, through infection of reservoir animals and vertical transmission in mosquitoes, emerging in years of heavy rainfall to cause epizootics and epidemics. On a number of occasions, viruses from these lineages have been transported outside the enzootic region through the movement of infected animals or mosquitoes, triggering outbreaks in countries such as Egypt, Saudi Arabia, Mauritania and Madagascar, where RVF had not previously been seen. Such viruses could potentially become established in their new environments through infection of wild and domestic ruminants and other animals and vertical transmission in local mosquito species. Despite their extensive geographic dispersion, all strains of RVFV remain closely related at the nucleotide and amino acid level. The high degree of conservation of genes encoding the virion surface glycoproteins suggests that a single vaccine should protect against all currently circulating RVFV strains. Similarly, preservation of the sequence of the RNA-dependent RNA polymerase across viral lineages implies that antiviral drugs targeting the enzyme should be effective against all strains. Researchers should be encouraged to collect additional RVFV isolates and perform whole-genome sequencing and phylogenetic analysis, so as to enhance our understanding of the continuing evolution of this important virus. This review forms part of a series of invited papers in Antiviral Research on the genetic diversity of emerging viruses.
AB - Rift Valley fever virus (RVFV), a member of the family Bunyaviridae, genus Phlebovirus, is the causative agent of Rift Valley fever (RVF), a mosquito-borne disease of ruminant animals and humans. The generation of a large sequence database has facilitated studies of the evolution and spread of the virus. Bayesian analyses indicate that currently circulating strains of RVFV are descended from an ancestral species that emerged from a natural reservoir in Africa when large-scale cattle and sheep farming were introduced during the 19th century. Viruses descended from multiple lineages persist in that region, through infection of reservoir animals and vertical transmission in mosquitoes, emerging in years of heavy rainfall to cause epizootics and epidemics. On a number of occasions, viruses from these lineages have been transported outside the enzootic region through the movement of infected animals or mosquitoes, triggering outbreaks in countries such as Egypt, Saudi Arabia, Mauritania and Madagascar, where RVF had not previously been seen. Such viruses could potentially become established in their new environments through infection of wild and domestic ruminants and other animals and vertical transmission in local mosquito species. Despite their extensive geographic dispersion, all strains of RVFV remain closely related at the nucleotide and amino acid level. The high degree of conservation of genes encoding the virion surface glycoproteins suggests that a single vaccine should protect against all currently circulating RVFV strains. Similarly, preservation of the sequence of the RNA-dependent RNA polymerase across viral lineages implies that antiviral drugs targeting the enzyme should be effective against all strains. Researchers should be encouraged to collect additional RVFV isolates and perform whole-genome sequencing and phylogenetic analysis, so as to enhance our understanding of the continuing evolution of this important virus. This review forms part of a series of invited papers in Antiviral Research on the genetic diversity of emerging viruses.
KW - Bunyavirus
KW - Genetic diversity
KW - Phlebovirus
KW - Phylogenetics
KW - Rift Valley fever virus
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U2 - 10.1016/j.antiviral.2012.06.001
DO - 10.1016/j.antiviral.2012.06.001
M3 - Review article
C2 - 22710362
AN - SCOPUS:84865282834
SN - 0166-3542
VL - 95
SP - 293
EP - 310
JO - Antiviral research
JF - Antiviral research
IS - 3
ER -