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. 2017 Aug;23(8):1289-1299.
doi: 10.3201/eid2308.161440.

Characterization of Fitzroy River Virus and Serologic Evidence of Human and Animal Infection

Characterization of Fitzroy River Virus and Serologic Evidence of Human and Animal Infection

Cheryl A Johansen et al. Emerg Infect Dis. 2017 Aug.

Abstract

In northern Western Australia in 2011 and 2012, surveillance detected a novel arbovirus in mosquitoes. Genetic and phenotypic analyses confirmed that the new flavivirus, named Fitzroy River virus, is related to Sepik virus and Wesselsbron virus, in the yellow fever virus group. Most (81%) isolates came from Aedes normanensis mosquitoes, providing circumstantial evidence of the probable vector. In cell culture, Fitzroy River virus replicated in mosquito (C6/36), mammalian (Vero, PSEK, and BSR), and avian (DF-1) cells. It also infected intraperitoneally inoculated weanling mice and caused mild clinical disease in 3 intracranially inoculated mice. Specific neutralizing antibodies were detected in sentinel horses (12.6%), cattle (6.6%), and chickens (0.5%) in the Northern Territory of Australia and in a subset of humans (0.8%) from northern Western Australia.

Keywords: Aedes normanensis; Australia; Fitzroy River virus; United States; arbovirus; novel flavivirus; viruses; whole-genome sequencing; yellow fever virus group.

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Figures

Figure 1
Figure 1
Locations where Fitzroy River virus–positive mosquitoes were collected (black dots), Western Australia, Australia, 2011 and 2012. Perth (asterisk), the capital city and most densely populated area of Western Australia, is shown to indicate its distance from the Kimberley region.
Figure 2
Figure 2
Phylogenetic tree of the genus Flavivirus, based on full polyprotein nucleotide sequences. Asterisk (*) indicates Fitzroy River virus. Scale bar indicates nucleotide substitutions per site. YFV, yellow fever virus.
Figure 3
Figure 3
Photomicrographs of Fitzroy River virus (FRV)–induced meningoencephalitis in weanling mice inoculated with 1,000 infectious units of FRV. Panels show multifocal mild to severe perivascular and neuropil infiltration of lymphocytes and monocytes (blue arrows in A–C); meningitis in a sulcus (black arrow in A); glial cell activation with notable astrocytosis, neuron degeneration, and neuronophagia (arrowhead in B); occasional hemorrhage (blue arrow in D); mild periventricular spongiosis (blue arrows in C); and meningitis (black arrow in C). Hematoxylin and eosin staining. Original magnifications: A) ×40, B) ×400, C) ×100, D) ×400.

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