Since the establishment of West Nile virus (WNV) in North America, concern has arisen that this virus may also pose a biosecurity threat to Australia. West Nile virus is maintained in an enzootic transmission cycle between birds and ornithophilic Culex spp. mosquitoes. Since its introduction into the United States in 1999, it has been responsible for over 11,000 human cases of neurological disease and over 1,000 human deaths. In addition, WNV has caused extensive equine and avian mortality. Should an exotic, virulent strain of WNV be introduced into Australia, it may have significant impact on human and animal health. This thesis examines entomological factors which may influence the potential for an exotic, pathogenic strain of WNV to become established in eastern Australia and be maintained in urban transmission cycles. Further, it aims to elucidate the most likely candidate vectors for the maintenance of WNV in natural transmission cycles. Components include: a) laboratory-based vector competence experiments to assess the ability of Australian mosquito species to become infected with and transmit a North American strain of WNV; b) identification of the vertebrate origin of mosquito bloodmeals using serological and molecular assays; c) an evaluation of the efficacy of bird-baited traps for collecting ornithophilic mosquitoes at ground level and in the tree canopy; and d) examination of the prevalence of endemic arboviruses, including Kunjin virus (KUNV; an Australian subtype of WNV) in mosquitoes collected from urban centres of eastern Australia. Vector competence experiments were conducted with field-collected Australian mosquito species. Nineteen species were were exposed to a 1999 New York strain of WNV using an artificial membrane feeding apparatus and transmission was attempted using an in vitro modified capillary tube method. A number of Culex species, including Culex quinquefasciatus and Culex gelidus, demonstrated high vector competence for WNV. Culex annulirostris, the primary KUNV vector, was the most competent vector, displaying transmission rates of 84%. Other common species, including Aedes vigilax, Aedes procax and Verrallina spp. were less susceptible to infection. Approximately 1,200 blood engorged mosquitoes were analysed using an enzyme-linked immunosorbent assay to determine host species. Overall, 90% of bloodmeals from Cx. quinquefasciatus were avian in origin, while 22% of bloodmeals from Cx. annulirostris were from birds. Molecular assays were further used to determine which bird species were commonly targeted by a selection of ornithophilic mosquito species. Mitochondrial DNA sequence data indicated that most (93%) avian bloodmeals from Cx. quinquefasciatus were obtained from passerine birds (order Passeriformes). Avian species commonly targeted by Cx. quinquefasciatus included Sphecotheres vieilloti (Australasian figbird; 39% of total identified), Sturnus tristis (common myna; 19%) and Philemon buceroides (helmeted friarbird; 17%). Alternatively, the majority (87%) of avian bloodmeals identified from Cx. annulirostris were from non-passerine birds, with most bloodmeals obtained from ducks (72%; family Anatidae). Seven field-based Latin Square trials conducted in Brisbane and Cairns showed that conventional CO2-baited CDC traps yielded higher numbers of Culex spp. than novel bird-baited traps, both at ground level and in the tree canopy. In Brisbane, CO2-baited CDC traps placed at ground level (approximately 1 m from ground) collected significantly more Cx. annulirostris than those at canopy height (5-10 m) during two trials, and more Ae. vigilax and Aedes procax during one trial each. Conversely, in Cairns, CO2-baited CDC traps placed in the tree canopy collected significantly more Culex squamosus during two trials, and significantly more Aedeomyia catasticta and Culex cubiculi during one trial each. Consistently low yields of ornithophilic species including Culex australicus and Cx. quinquefasciatus in all traps tested suggests the need to employ alternative trapping measures to target these species in urban areas. Over 1,800 mosquito pools (comprising over 65,000 individual mosquitoes collected from urban environments) were tested for evidence of arboviral infection. None of the pools showed evidence of flavivirus infection, but two alphaviruses were isolated from mosquito pools from Cairns. One isolate of Barmah Forest virus was obtained from a pool of 100 Ae. vigilax, and a pool of 89 Verrallina carmenti yielded an isolate of Ross River virus. In addition, an isolate most similar to a newly described bunyavirus, Stretch Lagoon orbivirus, was obtained from a single Aedes alternans collected from Sydney. The outcomes of this thesis demonstrate that a number of Australian mosquito species can become infected with and transmit a virulent strain of WNV, should it be introduced into Australia. Analysis of the host feeding patterns of these potential vectors in urban environments demonstrates that a number of candidate vectors, including Cx. quinquefasciatus and Cx. annulirostris, readily feed on common bird species. Further, the absence of detectable flavivirus infection in urban mosquito populations shown here suggests that endemic urban flaviviruses would have minimal influence on potential WNV transmission. Notwithstanding other ecological factors that may influence the likelihood of enzootic or epizootic transmission including susceptibility of vertebrate hosts and mechanisms of introduction, the potential establishment of an exotic, virulent strain of WNV in urban areas of Australia is certainly possible given the evidence provided in this thesis.
| Identifer | oai:union.ndltd.org:ADTP/254174 |
| Creators | Cassie Jansen |
| Source Sets | Australiasian Digital Theses Program |
| Detected Language | English |
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