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Journal articles on the topic 'Ross River Virus'

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Published: 4 June 2021
Last updated: 20 February 2023

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1

Wolstenholme, John. "Ross River virus: an Australian export?" Medical Journal of Australia 156, no. 8 (April 1992): 515–16. http://dx.doi.org/10.5694/j.1326-5377.1992.tb121407.x.

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2

Russell, Richard C. "Ross River Virus: Ecology and Distribution." Annual Review of Entomology 47, no. 1 (January 2002): 1–31. http://dx.doi.org/10.1146/annurev.ento.47.091201.145100.

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3

Vale, TG, DM Spratt, and MJ Cloonan. "Serological Evidence of Arbovirus Infection in Native and Domesticated Mammals on the South Coast of New-South-Wales." Australian Journal of Zoology 39, no. 1 (1991): 1. http://dx.doi.org/10.1071/zo9910001.

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Sera from twelve species of native and five species of introduced mammals collected on the south coast of New South Wales between 1982 and 1988 were tested for antibodies to the following arboviruses: Ross River virus (621 animals tested); Barmah Forest virus (371); Gan Gan virus (337); Trubanaman virus (378). Serum neutralising antibodies to Ross River virus were found in bandicoots, wallabies, kangaroos, cattle, goat and horses; to Barmah Forest virus in kangaroo, cattle and horses; to Gan Gan virus in kangaroos, wallabies, rat, cows, horses and sheep; and to Trubanaman virus in kangaroos, wallabies, cows and horses. Titres to Ross River virus in seropositive native animal sera ranged from 32 to 1024 and those in seropositive domesticated animal sera ranged from 8 to 32 768. Prevalence of serum antibodies in macropodids, cattle and horses was: Ross River virus, 68, 19, 62%; Barmah Forest virus, 4, 26, 9%; Gan Gan virus, 44, 13, 13%; Trubanaman virus, 60, 3, 10% respectively. Evidence suggests that: (1) kangaroos and wallabies are major vertebrate hosts for Ross River virus; (2) the role of bandicoots warrants further investigation; (3) horses may be important amplifying hosts of the virus, which causes epidemic polyarthritis in man in Australia.
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4

Douglas, William A. C. "Ross River virus disease and rheumatoid arthritis." Medical Journal of Australia 167, no. 4 (August 1997): 229–30. http://dx.doi.org/10.5694/j.1326-5377.1997.tb138860.x.

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5

Fraser, J. R. E. "Epidemic Polyarthritis and Ross River Virus Disease." Clinics in Rheumatic Diseases 12, no. 2 (August 1986): 369–88. http://dx.doi.org/10.1016/s0307-742x(21)00556-7.

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6

Woodruff, Rosalie E., Charles S. Guest, Michael G. Garner, Niels Becker, and Michael Lindsay. "Early Warning of Ross River Virus Epidemics." Epidemiology 17, no. 5 (September 2006): 569–75. http://dx.doi.org/10.1097/01.ede.0000229467.92742.7b.

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7

Tong, S. "Climate variability and Ross River virus transmission." Journal of Epidemiology & Community Health 56, no. 8 (August 1, 2002): 617–21. http://dx.doi.org/10.1136/jech.56.8.617.

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8

Yao, Jiansheng, Ellen G. Strauss, and James H. Strauss. "Molecular Genetic Study of the Interaction of Sindbis Virus E2 with Ross River Virus E1 for Virus Budding." Journal of Virology 72, no. 2 (February 1, 1998): 1418–23. http://dx.doi.org/10.1128/jvi.72.2.1418-1423.1998.

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ABSTRACT Glycoprotein PE2 of Sindbis virus will form a heterodimer with glycoprotein E1 of Ross River virus that is cleaved to an E2/E1 heterodimer and transported to the cell plasma membrane, but this chimeric heterodimer fails to interact with Sindbis virus nucleocapsids, and very little budding to produce mature virus occurs upon infection with chimeric viruses. We have isolated in both Sindbis virus E2 and in Ross River virus E1 a series of suppressing mutations that adapt these two proteins to one another and allow increased levels of chimeric virus production. Two adaptive E1 changes in an ectodomain immediately adjacent to the membrane anchor and five adaptive E2 changes in a 12-residue ectodomain centered on Asp-242 have been identified. One change in Ross River virus E1 (Gln-411→Leu) and one change in Sindbis virus E2 (Asp-248→Tyr) were investigated in detail. Each change individually leads to about a 10-fold increase in virus production, and combined the two changes lead to a 100-fold increase in virus. During passage of a chimeric virus containing Ross River virus E1 and Sindbis virus E2, the E2 change was first selected, followed by the E1 change. Heterodimers containing these two adaptive mutations have a demonstrably increased degree of interaction with Sindbis virus nucleocapsids. In the parental chimera, no interaction between heterodimers and capsids was visible at the plasma membrane in electron microscopic studies, whereas alignment of nucleocapsids along the plasma membrane, indicating interaction of heterodimers with nucleocapsids, was readily seen in the adapted chimera. The significance of these findings in light of our current understanding of alphavirus budding is discussed.
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9

Aaskov, John, Andrei Fokine, and Wenjun Liu. "Ross River virus evolution: implications for vaccine development." Future Virology 7, no. 2 (February 2012): 173–78. http://dx.doi.org/10.2217/fvl.11.139.

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10

Dugdale, Alan E. "Itching bites may limit Ross River virus infection." Medical Journal of Australia 177, no. 7 (October 2002): 399–400. http://dx.doi.org/10.5694/j.1326-5377.2002.tb04859.x.

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11

Sorokin, Michael. "Itching bites may limit Ross River virus infection." Medical Journal of Australia 178, no. 3 (February 2003): 143–44. http://dx.doi.org/10.5694/j.1326-5377.2003.tb05119.x.

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12

Ryan, Peter A., Jillann F. Farmer, Brian H. Kay, and Andreas Suhrbier. "Itching bites may limit Ross River virus infection." Medical Journal of Australia 178, no. 3 (February 2003): 143–44. http://dx.doi.org/10.5694/j.1326-5377.2003.tb05120.x.

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13

Aubry, Maite, Anita Teissier, Michael Huart, Sébastien Merceron, Jessica Vanhomwegen, Claudine Roche, Anne-Laure Vial, et al. "Ross River Virus Seroprevalence, French Polynesia, 2014–2015." Emerging Infectious Diseases 23, no. 10 (October 2017): 1751–53. http://dx.doi.org/10.3201/eid2310.170583.

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14

Campbell, J., J. Aldred, and G. Davis. "Isolation of Ross River virus from Aedes camptorhynchus." Medical Journal of Australia 150, no. 10 (May 1989): 602–3. http://dx.doi.org/10.5694/j.1326-5377.1989.tb136702.x.

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15

Allanson, Benjamin, Nathan Tobias Harvey, Peter John Beaton, and Benjamin Andrew Wood. "Purpuric exanthem caused by Ross River virus infection." Pathology 47, no. 2 (February 2015): 171–73. http://dx.doi.org/10.1097/pat.0000000000000222.

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16

Penna, John E., and Louise G. Irving. "Evidence for meningitis in Ross River virus infection." Medical Journal of Australia 159, no. 7 (October 1993): 492–93. http://dx.doi.org/10.5694/j.1326-5377.1993.tb137987.x.

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17

Bourée, Patrice, Sophie Delaigue, and Francine Bisaro. "Séjour en Australie : attention au Ross River Virus." Option/Bio 27, no. 545-546 (June 2016): 26–27. http://dx.doi.org/10.1016/s0992-5945(16)30176-3.

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18

Aaskov, John, Linda Williams, and Sylvia Yu. "A candidate Ross River virus vaccine: preclinical evaluation." Vaccine 15, no. 12-13 (August 1997): 1396–404. http://dx.doi.org/10.1016/s0264-410x(97)00051-0.

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19

Scrimgeour, Euan M., John G. Aaskov, and Leonard R. Matz. "Ross River virus arthritis in Papua New Guinea." Transactions of the Royal Society of Tropical Medicine and Hygiene 81, no. 5 (September 1987): 833–34. http://dx.doi.org/10.1016/0035-9203(87)90045-9.

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20

Seay, A. R., E. R. Kern, and R. S. Murray. "Interferon treatment of experimental Ross River virus polymyositis." Neurology 37, no. 7 (July 1, 1987): 1189. http://dx.doi.org/10.1212/wnl.37.7.1189.

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21

Klapsing, Philipp, J. Dick MacLean, Sarah Glaze, Karen L. McClean, Michael A. Drebot, Robert S. Lanciotti, and Grant L. Campbell. "Ross River Virus Disease Reemergence, Fiji, 2003–2004." Emerging Infectious Diseases 11, no. 4 (April 2005): 613–15. http://dx.doi.org/10.3201/eid1104.041070.

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22

WOLSTENHOLME, J. "Ross River virus disease - the first recorded outbreak?" Australian and New Zealand Journal of Medicine 23, no. 4 (August 1993): 417–18. http://dx.doi.org/10.1111/j.1445-5994.1993.tb01455.x.

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23

Srivastava, Umang, Michelle Nelson, Yung-Chang Su, and Suresh Mahalingam. "Mechanisms of Chikungunya virus disease informed by Ross River virus research." Future Virology 3, no. 6 (November 2008): 509–11. http://dx.doi.org/10.2217/17460794.3.6.509.

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24

Zhang, Wei, Bonnie R. Fisher, Norman H. Olson, James H. Strauss, Richard J. Kuhn, and Timothy S. Baker. "Aura Virus Structure Suggests that the T=4 Organization Is a Fundamental Property of Viral Structural Proteins." Journal of Virology 76, no. 14 (July 15, 2002): 7239–46. http://dx.doi.org/10.1128/jvi.76.14.7239-7246.2002.

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ABSTRACT Aura and Sindbis viruses are closely related alphaviruses. Unlike other alphaviruses, Aura virus efficiently encapsidates both genomic RNA (11.8 kb) and subgenomic RNA (4.2 kb) to form virus particles. Previous studies on negatively stained Aura virus particles predicted that there were two major size classes with potential T=3 and T=4 capsid structures. We have used cryoelectron microscopy and three-dimensional image reconstruction techniques to examine the native morphology of different classes of Aura virus particles produced in BHK cells. Purified particles separated into two components in a sucrose gradient. Reconstructions of particles in the top and bottom components were computed to resolutions of 17 and 21 Å, respectively, and compared with reconstructions of Sindbis virus and Ross River virus particles. Aura virus particles of both top and bottom components have similar, T=4 structures that resemble those of other alphaviruses. The morphology of Aura virus glycoprotein spikes closely resembles that of Sindbis virus spikes and is detectably different from that of Ross River virus spikes. Thus, some aspects of the surface structure of members of the Sindbis virus lineage have been conserved, but other aspects have diverged from the Semliki Forest/Ross River virus lineage.
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25

Harley, David O., and Philip Weinstein. "The Southern Oscillation Index and Ross River virus outbreaks." Medical Journal of Australia 165, no. 9 (November 1996): 531–32. http://dx.doi.org/10.5694/j.1326-5377.1996.tb138630.x.

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26

Watson, D. Ashley R., and Stephen A. Ross. "Corticosteroids for the complications of Ross River virus infection." Medical Journal of Australia 168, no. 2 (January 1998): 92. http://dx.doi.org/10.5694/j.1326-5377.1998.tb126727.x.

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27

Mylonas, Andrea D., Allison M. Brown, Tracy L. Carthew, David M. Purdie, Nirmala Pandeya, Louisa G. Collins, Andreas Suhrbier, et al. "Natural history of Ross River virus‐induced epidemic polyarthritis." Medical Journal of Australia 177, no. 7 (October 2002): 356–60. http://dx.doi.org/10.5694/j.1326-5377.2002.tb04837.x.

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28

Cheong, Ian R. "Ross River virus — are we wasting money doing tests?" Medical Journal of Australia 178, no. 3 (February 2003): 143. http://dx.doi.org/10.5694/j.1326-5377.2003.tb05118.x.

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29

Aubry, Maite, Mike Kama, Jessica Vanhomwegen, Anita Teissier, Teheipuaura Mariteragi-Helle, Stephane Hue, Martin L. Hibberd, et al. "Ross River Virus Antibody Prevalence, Fiji Islands, 2013–2015." Emerging Infectious Diseases 25, no. 4 (April 2019): 827–30. http://dx.doi.org/10.3201/eid2504.180694.

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30

Aaskov, J. G., J. Y. Chen, N. T. Hanh, and P. M. Dennington. "Surveillance for Ross River virus infection using blood donors." American Journal of Tropical Medicine and Hygiene 58, no. 6 (June 1, 1998): 726–30. http://dx.doi.org/10.4269/ajtmh.1998.58.726.

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31

Carter, IWJ, JRE Fraser, and MJ Cloonan. "Specific IgA antibody response in Ross River virus infection." Immunology and Cell Biology 65, no. 6 (December 1987): 511–13. http://dx.doi.org/10.1038/icb.1987.60.

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32

Woodruff, Rosalie E., Charles S. Guest, Michael G. Garner, Niels Becker, Janette Lindesay, Terence Carvan, and Kristie Ebi. "Predicting Ross River Virus Epidemics from Regional Weather Data." Epidemiology 13, no. 4 (July 2002): 384–93. http://dx.doi.org/10.1097/00001648-200207000-00005.

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33

Allchin, Lisa, Helen Ptolemy, George Truman, and Krishna Hort. "Ross River virus in Western Sydney: A serological survey." New South Wales Public Health Bulletin 14, no. 12 (2003): 224. http://dx.doi.org/10.1071/nb03061.

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34

Fraser, J. R. E., M. J. Rowley, and B. Tait. "Collagen antibodies in Ross River virus disease (epidemic polyarthritis)." Rheumatology International 7, no. 6 (December 1987): 267–69. http://dx.doi.org/10.1007/bf00270527.

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35

Fraser, J. R. E., A. L. Cunningham, J. D. Mathews, and A. Riglar. "Immune complexes and ross river virus disease (epidemic polyarthritis)." Rheumatology International 8, no. 3 (June 1988): 113–17. http://dx.doi.org/10.1007/bf00272432.

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36

Aaskov, J. G., U. Hadding, and D. Bitter-Suermann. "Interaction of Ross River Virus with the Complement System." Journal of General Virology 66, no. 1 (January 1, 1985): 121–29. http://dx.doi.org/10.1099/0022-1317-66-1-121.

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37

Harley, David, Scott Ritchie, Chris Bain, and Adrian C. Sleigh. "Risks for Ross River virus disease in tropical Australia." International Journal of Epidemiology 34, no. 3 (January 19, 2005): 548–55. http://dx.doi.org/10.1093/ije/dyh411.

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38

Hossain, Iqbal, Paul Anantharajah Tambyah, and Annelies Wilder‐Smith. "Ross River Virus Disease in a Traveler to Australia." Journal of Travel Medicine 16, no. 6 (November 1, 2009): 420–23. http://dx.doi.org/10.1111/j.1708-8305.2009.00345.x.

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39

SCRIMGEOUR, E. M. "Suspected Ross River virus encephalitis in Papua New Guinea." Australian and New Zealand Journal of Medicine 29, no. 4 (August 1999): 559. http://dx.doi.org/10.1111/j.1445-5994.1999.tb00759.x.

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40

Aubry, Maite, Jérôme Finke, Anita Teissier, Claudine Roche, Julien Broult, Sylvie Paulous, Philippe Desprès, Van-Mai Cao-Lormeau, and Didier Musso. "Silent Circulation of Ross River Virus in French Polynesia." International Journal of Infectious Diseases 37 (August 2015): 19–24. http://dx.doi.org/10.1016/j.ijid.2015.06.005.

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41

Heil, Marintha L., Alison Albee, James H. Strauss, and Richard J. Kuhn. "An Amino Acid Substitution in the Coding Region of the E2 Glycoprotein Adapts Ross River Virus To Utilize Heparan Sulfate as an Attachment Moiety." Journal of Virology 75, no. 14 (July 15, 2001): 6303–9. http://dx.doi.org/10.1128/jvi.75.14.6303-6309.2001.

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ABSTRACT Passage of Ross River virus strain NB5092 in avian cells has been previously shown to select for virus variants that have enhanced replication in these cells. Sequencing of these variants identified two independent sites that might be responsible for the phenotype. We now demonstrate, using a molecular cDNA clone of the wild-type T48 strain, that an amino acid substitution at residue 218 in the E2 glycoprotein can account for the phenotype. Substitutions that replaced the wild-type asparagine with basic residues had enhanced replication in avian cells while acidic or neutral residues had little or no observable effect. Ross River virus mutants that had increased replication in avian cells also grew better in BHK cells than the wild-type virus, whereas the remaining mutants were unaffected in growth. Replication in both BHK and avian cells of Ross River virus mutants N218K and N218R was inhibited by the presence of heparin or by the pretreatment of the cells with heparinase. Binding of the mutants, but not of the wild type, to a heparin-Sepharose column produced binding comparable to that of Sindbis virus, which has previously been shown to bind heparin. Replication of these mutants was also adversely affected when they were grown in a CHO cell line that was deficient in heparan sulfate production. These results demonstrate that amino acid 218 of the E2 glycoprotein can be modified to create an heparan sulfate binding site and this modification expands the host range of Ross River virus in cultured cells to cells of avian origin.
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42

Russell, Tanya L., Paul F. Horwood, Humpress Harrington, Allan Apairamo, Nathan J. Kama, Albino Bobogare, David MacLaren, and Thomas R. Burkot. "Seroprevalence of dengue, Zika, chikungunya and Ross River viruses across the Solomon Islands." PLOS Neglected Tropical Diseases 16, no. 2 (February 10, 2022): e0009848. http://dx.doi.org/10.1371/journal.pntd.0009848.

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Across the Pacific, and including in the Solomon Islands, outbreaks of arboviruses such as dengue, chikungunya, and Zika are increasing in frequency, scale and impact. Outbreaks of mosquito-borne disease have the potential to overwhelm the health systems of small island nations. This study mapped the seroprevalence of dengue, Zika, chikungunya and Ross River viruses in 5 study sites in the Solomon Islands. Serum samples from 1,021 participants were analysed by ELISA. Overall, 56% of participants were flavivirus-seropositive for dengue (28%), Zika (1%) or both flaviviruses (27%); and 53% of participants were alphavirus-seropositive for chikungunya (3%), Ross River virus (31%) or both alphaviruses (18%). Seroprevalence for both flaviviruses and alphaviruses varied by village and age of the participant. The most prevalent arboviruses in the Solomon Islands were dengue and Ross River virus. The high seroprevalence of dengue suggests that herd immunity may be a driver of dengue outbreak dynamics in the Solomon Islands. Despite being undetected prior to this survey, serology results suggest that Ross River virus transmission is endemic. There is a real need to increase the diagnostic capacities for each of the arboviruses to support effective case management and to provide timely information to inform vector control efforts and other outbreak mitigation interventions.
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43

Farmer, Jillann, and Andreas Suhrbier. "Interpreting paired serology for Ross River virus and Barmah Forest virus diseases." Australian Journal of General Practice 48, no. 9 (September 1, 2019): 645–49. http://dx.doi.org/10.31128/ajgp-02-19-4845.

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44

Koolhof, Iain S., Simon M. Firestone, Silvana Bettiol, Michael Charleston, Katherine B. Gibney, Peter J. Neville, Andrew Jardine, and Scott Carver. "Optimising predictive modelling of Ross River virus using meteorological variables." PLOS Neglected Tropical Diseases 15, no. 3 (March 9, 2021): e0009252. http://dx.doi.org/10.1371/journal.pntd.0009252.

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Background Statistical models are regularly used in the forecasting and surveillance of infectious diseases to guide public health. Variable selection assists in determining factors associated with disease transmission, however, often overlooked in this process is the evaluation and suitability of the statistical model used in forecasting disease transmission and outbreaks. Here we aim to evaluate several modelling methods to optimise predictive modelling of Ross River virus (RRV) disease notifications and outbreaks in epidemiological important regions of Victoria and Western Australia. Methodology/Principal findings We developed several statistical methods using meteorological and RRV surveillance data from July 2000 until June 2018 in Victoria and from July 1991 until June 2018 in Western Australia. Models were developed for 11 Local Government Areas (LGAs) in Victoria and seven LGAs in Western Australia. We found generalised additive models and generalised boosted regression models, and generalised additive models and negative binomial models to be the best fit models when predicting RRV outbreaks and notifications, respectively. No association was found with a model’s ability to predict RRV notifications in LGAs with greater RRV activity, or for outbreak predictions to have a higher accuracy in LGAs with greater RRV notifications. Moreover, we assessed the use of factor analysis to generate independent variables used in predictive modelling. In the majority of LGAs, this method did not result in better model predictive performance. Conclusions/Significance We demonstrate that models which are developed and used for predicting disease notifications may not be suitable for predicting disease outbreaks, or vice versa. Furthermore, poor predictive performance in modelling disease transmissions may be the result of inappropriate model selection methods. Our findings provide approaches and methods to facilitate the selection of the best fit statistical model for predicting mosquito-borne disease notifications and outbreaks used for disease surveillance.
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45

Selden, Suzanne M., and Scott Cameron. "Changing epidemiology of Ross River virus disease in South Australia." Medical Journal of Australia 165, no. 6 (September 1996): 313–17. http://dx.doi.org/10.5694/j.1326-5377.1996.tb124989.x.

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46

Harley, D., S. Ritchie, D. Phillips, and A. van den Hurk. "Mosquito isolates of Ross River virus from Cairns, Queensland, Australia." American Journal of Tropical Medicine and Hygiene 62, no. 5 (May 1, 2000): 561–65. http://dx.doi.org/10.4269/ajtmh.2000.62.561.

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47

Hoad, Veronica C., David J. Speers, Anthony J. Keller, Gary K. Dowse, Clive R. Seed, Michael D. A. Lindsay, Helen M. Faddy, and Joanne Pink. "First reported case of transfusion‐transmitted Ross River virus infection." Medical Journal of Australia 202, no. 5 (March 2015): 267–69. http://dx.doi.org/10.5694/mja14.01522.

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48

Ryan, P. A., K. A. Do, and B. H. Kay. "Definition of Ross River Virus Vectors at Maroochy Shire, Australia." Journal of Medical Entomology 37, no. 1 (January 1, 2000): 146–52. http://dx.doi.org/10.1603/0022-2585-37.1.146.

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49

Cunningham, Anthony L., and JRE Fraser. "ROSS RIVER VIRUS INFECTION OF HUMAN SYNOVIAL CELLS IN VITRO." Australian Journal of Experimental Biology and Medical Science 63, no. 2 (April 1985): 197–204. http://dx.doi.org/10.1038/icb.1985.22.

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50

Pröll, S., G. Dobler, M. Pfeffer, T. Jelinek, H. D. Nothdurft, and T. Löscher. "Persistierende Arthralgien bei Ross-River-Virus-Erkrankung nach Ozeanien-Reise." DMW - Deutsche Medizinische Wochenschrift 124, no. 24 (June 1999): 759–62. http://dx.doi.org/10.1055/s-2007-1024409.

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