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Development of reverse genetics systems and investigation of host response antagonism and reassortment potential for Cache Valley and Kairi viruses, two emerging orthobunyaviruses of the Americas.

Authors :
Dunlop JI
Szemiel AM
Navarro A
Wilkie GS
Tong L
Modha S
Mair D
Sreenu VB
Da Silva Filipe A
Li P
Huang YS
Brennan B
Hughes J
Vanlandingham DL
Higgs S
Elliott RM
Kohl A
Source :
PLoS neglected tropical diseases [PLoS Negl Trop Dis] 2018 Oct 29; Vol. 12 (10), pp. e0006884. Date of Electronic Publication: 2018 Oct 29 (Print Publication: 2018).
Publication Year :
2018

Abstract

Orthobunyaviruses such as Cache Valley virus (CVV) and Kairi virus (KRIV) are important animal pathogens. Periodic outbreaks of CVV have resulted in the significant loss of lambs on North American farms, whilst KRIV has mainly been detected in South and Central America with little overlap in geographical range. Vaccines or treatments for these viruses are unavailable. One approach to develop novel vaccine candidates is based on the use of reverse genetics to produce attenuated viruses that elicit immune responses but cannot revert to full virulence. The full genomes of both viruses were sequenced to obtain up to date genome sequence information. Following sequencing, minigenome systems and reverse genetics systems for both CVV and KRIV were developed. Both CVV and KRIV showed a wide in vitro cell host range, with BHK-21 cells a suitable host cell line for virus propagation and titration. To develop attenuated viruses, the open reading frames of the NSs proteins were disrupted. The recombinant viruses with no NSs protein expression induced the production of type I interferon (IFN), indicating that for both viruses NSs functions as an IFN antagonist and that such attenuated viruses could form the basis for attenuated viral vaccines. To assess the potential for reassortment between CVV and KRIV, which could be relevant during vaccination campaigns in areas of overlap, we attempted to produce M segment reassortants by reverse genetics. We were unable to obtain such viruses, suggesting that it is an unlikely event.<br />Competing Interests: I have read the journal’s policy and the authors of this manuscript have the following competing interests: Anti CVV and KRIV N antibodies described in this study were produced by the MRC-University of Glasgow Centre for Virus Research in collaboration with Cambridge Research Biochemicals (CRB). Antibodies are distributed by CRB under license from the University of Glasgow.

Details

Language :
English
ISSN :
1935-2735
Volume :
12
Issue :
10
Database :
MEDLINE
Journal :
PLoS neglected tropical diseases
Publication Type :
Academic Journal
Accession number :
30372452
Full Text :
https://doi.org/10.1371/journal.pntd.0006884