Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Wildlife Research Wildlife Research Society
Ecology, management and conservation in natural and modified habitats
RESEARCH ARTICLE (Open Access)

A review of viral and parasitic infections in wild deer in Australia with relevance to livestock and human health

Jose L. Huaman A , Karla J. Helbig A , Teresa G. Carvalho A , Mark Doyle B , Jordan Hampton https://orcid.org/0000-0003-0472-3241 C , David M. Forsyth https://orcid.org/0000-0001-5356-9573 D , Anthony R. Pople https://orcid.org/0000-0002-5172-3407 E and Carlo Pacioni https://orcid.org/0000-0001-5115-4120 F G *
+ Author Affiliations
- Author Affiliations

A Department of Microbiology, Anatomy, Physiology and Pharmacology, School of Agriculture, Biomedicine and Environment, La Trobe University, Melbourne, Vic., Australia.

B South East Local Land Services, Bega, NSW, Australia.

C Faculty of Science, University of Melbourne, Parkville, Vic., Australia.

D Vertebrate Pest Research Unit, New South Wales Department of Primary Industries, Orange Agricultural Institute, Orange, NSW, Australia.

E Department of Agriculture and Fisheries, Invasive Plants and Animals Research, Biosecurity Queensland, Ecosciences Precinct, Brisbane, Qld, Australia.

F Department of Environment, Land, Water and Planning, Arthur Rylah Institute for Environmental Research, Melbourne, Vic., Australia.

G Environmental and Conservation Sciences, Murdoch University, Perth, WA, Australia.

* Correspondence to: carlo.pacioni@gmail.com

Handling Editor: Graham Nugent

Wildlife Research 50(9) 593-602 https://doi.org/10.1071/WR22118
Submitted: 30 June 2022  Accepted: 28 April 2023   Published: 11 July 2023

© 2023 The Author(s) (or their employer(s)). Published by CSIRO Publishing. This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND)

Abstract

Wild animals harbour a diverse range of pathogens. In Europe and North America, cervids (Family Cervidae) can act as reservoirs for viral, prion, bacterial, and parasitic infections. Wild deer often inhabit agricultural land, therefore representing a biosecurity risk due to their potential ability to transmit diseases to livestock. Multiple studies have investigated the infection status of wild deer in Australia, mostly during the 1970s and 1980s, and deer populations have increased greatly in abundance and distribution since then. Those studies provide an important baseline for the pathogens carried by wild deer in Australia but are limited by small sample size, the small number of deer species studied, and the disease detection methods used. Recent investigations using ELISA (Enzyme-Linked Immunosorbent Assay), PCR-based assays, and next-generation sequencing have substantially increased our understanding of viral and parasitic infections in Australian deer. These studies indicate that deer may act as reservoirs for pathogens such as Pestivirus, Neospora caninum and Entamoeba bovis. The use of next-generation sequencing has led to the discovery of novel viruses such as Picobirnavirus and a novel species of the genus Bopivirus, both of which pose transmission risks for domestic animals. Recent research confirms that wild deer could be a future source of viral and parasitic infections for domestic livestock and other wildlife species.

Keywords: chital deer, fallow deer, genetics, infectious disease, invasive species, pest control, rusa deer, sambar deer, wildlife diseases.


References

Al-Habsi, K, Yang, R, Ryan, U, Jacobson, C, and Miller, DW (2017). Morphological and molecular characterization of an uninucleated cyst-producing Entamoeba spp. in captured Rangeland goats in Western Australia. Veterinary Parasitology 235, 41–46.
Morphological and molecular characterization of an uninucleated cyst-producing Entamoeba spp. in captured Rangeland goats in Western Australia.Crossref | GoogleScholarGoogle Scholar |

Barroso, P, Acevedo, P, and Vicente, J (2021). The importance of long-term studies on wildlife diseases and their interfaces with humans and domestic animals: a review. Transboundary and Emerging Diseases 68, 1895–1909.
The importance of long-term studies on wildlife diseases and their interfaces with humans and domestic animals: a review.Crossref | GoogleScholarGoogle Scholar |

Bengsen, AJ, Forsyth, DM, Pople, A, Brennan, M, Amos, M, Leeson, M, Cox, TE, Gray, B, Orgill, O, Hampton, JO, Crittle, T, and Haebich, K (2022). Effectiveness and costs of helicopter-based shooting of deer. Wildlife Research , .
Effectiveness and costs of helicopter-based shooting of deer.Crossref | GoogleScholarGoogle Scholar |

Bentley A (1998) ‘An introduction to the deer of Australia with special reference to Victoria.’ 3rd edn. (Australian Deer Research Foundation: Melbourne, VIC, Australia)

Bryan, JH, Foley, DH, and Sutherst, RW (1996). Malaria transmission and climate change in Australia. Medical Journal of Australia 164, 345–347.
Malaria transmission and climate change in Australia.Crossref | GoogleScholarGoogle Scholar |

Böhm, M, White, PCL, Chambers, J, Smith, L, and Hutchings, MR (2007). Wild deer as a source of infection for livestock and humans in the UK. The Veterinary Journal 174, 260–276.
Wild deer as a source of infection for livestock and humans in the UK.Crossref | GoogleScholarGoogle Scholar |

Chow, TL, and Davis, RW (1964). The susceptibility of mule deer to infectious bovine rhinotracheitis. American Journal of Veterinary Research 25, 518–519.

Cinque, K, Stevens, MA, Haydon, SR, Jex, AR, Gasser, RB, and Campbell, BE (2008). Investigating public health impacts of deer in a protected drinking water supply watershed. Water Science and Technology 58, 127–132.
Investigating public health impacts of deer in a protected drinking water supply watershed.Crossref | GoogleScholarGoogle Scholar |

Conner, MM, Ebinger, MR, Blanchong, JA, and Cross, PC (2008). Infectious disease in cervids of North America: data, models, and management challenges. Annals of the New York Academy of Sciences 1134, 146–172.
Infectious disease in cervids of North America: data, models, and management challenges.Crossref | GoogleScholarGoogle Scholar |

Cripps, JK, Pacioni, C, Scroggie, MP, Woolnough, AP, and Ramsey, DS (2019). Introduced deer and their potential role in disease transmission to livestock in Australia. Mammal Review 49, 60–77.
Introduced deer and their potential role in disease transmission to livestock in Australia.Crossref | GoogleScholarGoogle Scholar |

Crittle T, Millynn B (2020) Pest animal mapping 2020 final report. NSW Department of Primary Industries, Orange, NSW, Australia.

Cunningham, AA, Daszak, P, and Wood, JLN (2017). One Health, emerging infectious diseases and wildlife: two decades of progress? Philosophical Transactions of the Royal Society B: Biological Sciences 372, 20160167.
One Health, emerging infectious diseases and wildlife: two decades of progress?Crossref | GoogleScholarGoogle Scholar |

Cunningham, CX, Perry, GLW, Bowman, DMJS, Forsyth, DM, Driessen, MM, Appleby, M, Brook, BW, Hocking, G, Buettel, JC, French, BJ, Hamer, R, Bryant, SL, Taylor, M, Gardiner, R, Proft, K, Scoleri, VP, Chiu-Werner, A, Travers, T, Thompson, L, Guy, T, and Johnson, CN (2022). Dynamics and predicted distribution of an irrupting ‘sleeper’ population: fallow deer in Tasmania. Biological Invasions 24, 1131–1147.
Dynamics and predicted distribution of an irrupting ‘sleeper’ population: fallow deer in Tasmania.Crossref | GoogleScholarGoogle Scholar |

Davidson, MJ, Huaman, JL, Pacioni, C, Stephens, D, Hitchen, Y, and Carvalho, TG (2022). Active shedding of Neospora caninum detected in Australian wild canids in a nonexperimental context. Transboundary and Emerging Diseases 69, 1862–1871.
Active shedding of Neospora caninum detected in Australian wild canids in a nonexperimental context.Crossref | GoogleScholarGoogle Scholar |

Davies C (2014) Investigating the parasite fauna of Victorian deer, using scat morphometrics, DNA, and faecal egg counts. Honours thesis, Monash University, VIC, Australia.

Davis, NE, Bennett, A, Forsyth, DM, Bowman, DMJS, Lefroy, EC, Wood, SW, Woolnough, AP, West, P, Hampton, JO, and Johnson, CN (2016). A systematic review of the impacts and management of introduced deer (family Cervidae) in Australia. Wildlife Research 43, 515–532.
A systematic review of the impacts and management of introduced deer (family Cervidae) in Australia.Crossref | GoogleScholarGoogle Scholar |

Endalew, AD, Faburay, B, Wilson, WC, and Richt, JA (2019). Schmallenberg disease – a newly emerged culicoides-borne viral disease of ruminants. Viruses 11, 1065.
Schmallenberg disease – a newly emerged culicoides-borne viral disease of ruminants.Crossref | GoogleScholarGoogle Scholar |

English, A (1982). Serological survey of wild fallow deer (Dama dama) in New South Wales, Australia. Veterinary Record 110, 153–154.

Fabisiak, M, Sałamaszyńska, A, and Stadejek, T (2018). Detection of seroconversion to bovine herpesvirus 1 related alphaherpesvirus and bovine viral diarrhea virus in polish free-living deer. Polish Journal of Veterinary Sciences 21, 437–440.
Detection of seroconversion to bovine herpesvirus 1 related alphaherpesvirus and bovine viral diarrhea virus in polish free-living deer.Crossref | GoogleScholarGoogle Scholar |

Forsyth DM, Stamation K, Woodford L (2015) Distributions of sambar deer, rusa deer and sika deer in Victoria. Arthur Rylah Institute for Environmental Research Unpublished Client Report. Arthur Rylah Institute for Environmental Research, Heidelberg, Victoria.

Forsyth DM, Stamation K, Woodford L (2016) Distributions of fallow deer, red deer, hog deer and chital deer in Victoria. Arthur Rylah Institute for Environmental Research Unpublished Client Report. Arthur Rylah Institute for Environmental Research, Heidelberg, Victoria.

Fouque, F, and Reeder, JC (2019). Impact of past and on-going changes on climate and weather on vector-borne diseases transmission: a look at the evidence. Infectious Diseases of Poverty 8, 51.
Impact of past and on-going changes on climate and weather on vector-borne diseases transmission: a look at the evidence.Crossref | GoogleScholarGoogle Scholar |

Game Management Authority (2006) Wilsons promontory national park hog deer control program. Game Management Authority, Melbourne, VIC, Australia.

Garcia-Bocanegra, I, Cano-Terriza, D, Vidal, G, Rosell, R, Paniagua, J, Jimenez-Ruiz, S, Exposito, C, Rivero-Juarez, A, Arenas, A, and Pujols, J (2017). Monitoring of schmallenberg virus in spanish wild artiodactyls, 2006-2015. PLoS ONE 12, e0182212.
Monitoring of schmallenberg virus in spanish wild artiodactyls, 2006-2015.Crossref | GoogleScholarGoogle Scholar |

Geoghegan, JL, Walker, PJ, Duchemin, J-B, Jeanne, I, and Holmes, EC (2014). Seasonal drivers of the epidemiology of arthropod-borne viruses in Australia. PLoS Neglected Tropical Diseases 8, e3325.
Seasonal drivers of the epidemiology of arthropod-borne viruses in Australia.Crossref | GoogleScholarGoogle Scholar |

Gu X, Kirkland PD (2008) Infectious bovine rhinotracheitis. The Department of Agriculture and Water, Canberra, ACT, Australia.

Hale, VL, Dennis, PM, McBride, DS, Nolting, JM, Madden, C, Huey, D, Ehrlich, M, Grieser, J, Winston, J, Lombardi, D, Gibson, S, Saif, L, Killian, ML, Lantz, K, Tell, RM, Torchetti, M, Robbe-Austerman, S, Nelson, MI, Faith, SA, and Bowman, AS (2022). SARS-CoV-2 infection in free-ranging white-tailed deer. Nature 602, 481–486.
SARS-CoV-2 infection in free-ranging white-tailed deer.Crossref | GoogleScholarGoogle Scholar |

Hall, GP, and Gill, KP (2005). Management of wild deer in Australia. Journal of Wildlife Management 69, 837–844.
Management of wild deer in Australia.Crossref | GoogleScholarGoogle Scholar |

Hoffmann, B, Scheuch, M, Hoper, D, Jungblut, R, Holsteg, M, Schirrmeier, H, Eschbaumer, M, Goller, KV, Wernike, K, Fischer, M, Breithaupt, A, Mettenleiter, TC, and Beer, M (2012). Novel orthobunyavirus in cattle, Europe, 2011. Emerging Infectious Diseases 18, 469–472.
Novel orthobunyavirus in cattle, Europe, 2011.Crossref | GoogleScholarGoogle Scholar |

Holding, M, Otter, AD, Dowall, S, Takumi, K, Hicks, B, Coleman, T, Hemingway, G, Royds, M, Findlay-Wilson, S, Curran-French, M, Vipond, R, Sprong, H, and Hewson, R (2022). Screening of wild deer populations for exposure to SARS-CoV-2 in the United Kingdom, 2020–2021. Transboundary and Emerging Diseases 69, e3244–e3249.
Screening of wild deer populations for exposure to SARS-CoV-2 in the United Kingdom, 2020–2021.Crossref | GoogleScholarGoogle Scholar |

Huaman, JL, Pacioni, C, Forsyth, DM, Pople, A, Hampton, JO, Carvalho, TG, and Helbig, KJ (2020). Serosurveillance and molecular investigation of wild deer in Australia reveals seroprevalence of pestivirus infection. Viruses 12, 752.
Serosurveillance and molecular investigation of wild deer in Australia reveals seroprevalence of pestivirus infection.Crossref | GoogleScholarGoogle Scholar |

Huaman, JL, Pacioni, C, Forsyth, DM, Pople, A, Hampton, JO, Helbig, KJ, and Carvalho, TG (2021a). Evaluation of haemoparasite and Sarcocystis infections in Australian wild deer. International Journal for Parasitology: Parasites and Wildlife 15, 262–269.
Evaluation of haemoparasite and Sarcocystis infections in Australian wild deer.Crossref | GoogleScholarGoogle Scholar |

Huaman, JL, Pacioni, C, Sarker, S, Doyle, M, Forsyth, DM, Pople, A, Carvalho, TG, and Helbig, KJ (2021b). Novel picornavirus detected in wild deer: identification, genomic characterisation, and prevalence in Australia. Viruses 13, 2412.
Novel picornavirus detected in wild deer: identification, genomic characterisation, and prevalence in Australia.Crossref | GoogleScholarGoogle Scholar |

Huaman, JL, Pacioni, C, Sarker, S, Doyle, M, Forsyth, DM, Pople, A, Hampton, JO, Carvalho, TG, and Helbig, KJ (2021c). Molecular epidemiology and characterization of picobirnavirus in wild deer and cattle from Australia: evidence of genogroup I and II in the upper respiratory tract. Viruses 13, 1492.
Molecular epidemiology and characterization of picobirnavirus in wild deer and cattle from Australia: evidence of genogroup I and II in the upper respiratory tract.Crossref | GoogleScholarGoogle Scholar |

Huaman, JL, Pacioni, C, Forsyth, DM, Pople, A, Hampton, JO, Carvalho, TG, and Helbig, KJ (2022a). Detection and characterisation of an endogenous betaretrovirus in Australian wild deer. Viruses 14, 252.
Detection and characterisation of an endogenous betaretrovirus in Australian wild deer.Crossref | GoogleScholarGoogle Scholar |

Huaman, JL, Pacioni, C, Kenchington-Evans, L, Doyle, M, Helbig, KJ, and Carvalho, TG (2022b). First evidence of Entamoeba parasites in Australian wild deer and assessment of transmission to cattle. Frontiers in Cellular and Infection Microbiology 12, 883031.
First evidence of Entamoeba parasites in Australian wild deer and assessment of transmission to cattle.Crossref | GoogleScholarGoogle Scholar |

Jenkins, DJ, Baker, A, Porter, M, Shamsi, S, and Barton, DP (2020). Wild fallow deer (Dama dama) as definitive hosts of Fasciola hepatica (liver fluke) in alpine New South Wales. Australian Veterinary Journal 98, 546–549.
Wild fallow deer (Dama dama) as definitive hosts of Fasciola hepatica (liver fluke) in alpine New South Wales.Crossref | GoogleScholarGoogle Scholar |

Jimenez-Ruiz, S, Risalde, MA, Acevedo, P, Arnal, MC, Gomez-Guillamon, F, Prieto, P, Gens, MJ, Cano-Terriza, D, Fernandez de Luco, D, Vicente, J, and Garcia-Bocanegra, I (2021). Serosurveillance of Schmallenberg virus in wild ruminants in Spain. Transboundary and Emerging Diseases 68, 347–354.
Serosurveillance of Schmallenberg virus in wild ruminants in Spain.Crossref | GoogleScholarGoogle Scholar |

Kalman, D, and Egyed, L (2005). PCR detection of bovine herpesviruses from nonbovine ruminants in hungary. Journal of Wildlife Diseases 41, 482–488.
PCR detection of bovine herpesviruses from nonbovine ruminants in hungary.Crossref | GoogleScholarGoogle Scholar |

Koehler, AV, Haydon, SR, Jex, AR, and Gasser, RB (2016). Cryptosporidium and Giardia taxa in faecal samples from animals in catchments supplying the city of Melbourne with drinking water (2011 to 2015). Parasites & Vectors 9, 315.
Cryptosporidium and Giardia taxa in faecal samples from animals in catchments supplying the city of Melbourne with drinking water (2011 to 2015).Crossref | GoogleScholarGoogle Scholar |

Lamb, J, Doyle, E, Barwick, J, Chambers, M, and Kahn, L (2021). Prevalence and pathology of liver fluke (Fasciola hepatica) in fallow deer (Dama dama). Veterinary Parasitology 293, 109427.
Prevalence and pathology of liver fluke (Fasciola hepatica) in fallow deer (Dama dama).Crossref | GoogleScholarGoogle Scholar |

Malik, YS, Kumar, N, Sharma, K, Dhama, K, Shabbir, MZ, Ganesh, B, Kobayashi, N, and Banyai, K (2014). Epidemiology, phylogeny, and evolution of emerging enteric Picobirnaviruses of animal origin and their relationship to human strains. BioMed Research International 2014, 780752.
Epidemiology, phylogeny, and evolution of emerging enteric Picobirnaviruses of animal origin and their relationship to human strains.Crossref | GoogleScholarGoogle Scholar |

Martin, C, Pastoret, P-P, Brochier, B, Humblet, M-F, and Saegerman, C (2011). A survey of the transmission of infectious diseases/infections between wild and domestic ungulates in Europe. Veterinary Research 42, 70.
A survey of the transmission of infectious diseases/infections between wild and domestic ungulates in Europe.Crossref | GoogleScholarGoogle Scholar |

Mazeri, S, Rydevik, G, Handel, I, Bronsvoort, BMd, and Sargison, N (2017). Estimation of the impact of Fasciola hepatica infection on time taken for UK beef cattle to reach slaughter weight. Scientific Reports 7, 7319.
Estimation of the impact of Fasciola hepatica infection on time taken for UK beef cattle to reach slaughter weight.Crossref | GoogleScholarGoogle Scholar |

McClymont, H, Bambrick, H, Si, X, Vardoulakis, S, and Hu, W (2022). Future perspectives of emerging infectious diseases control: a One Health approach. One Health 14, 100371.
Future perspectives of emerging infectious diseases control: a One Health approach.Crossref | GoogleScholarGoogle Scholar |

McKenzie, RA, Green, PE, Thornton, AM, Chung, YS, MacKenzie, AR, Cybinski, DH, and George, TDS (1985). Diseases of deer in south eastern Queensland. Australian Veterinary Journal 62, 424–424.
Diseases of deer in south eastern Queensland.Crossref | GoogleScholarGoogle Scholar |

Miller, RS, Farnsworth, ML, and Malmberg, JL (2013). Diseases at the livestock-wildlife interface: status, challenges, and opportunities in the United States. Preventive Veterinary Medicine 110, 119–132.
Diseases at the livestock-wildlife interface: status, challenges, and opportunities in the United States.Crossref | GoogleScholarGoogle Scholar |

Mollema, L, Rijsewijk, FAM, Nodelijk, G, and de Jong, MCM (2005). Quantification of the transmission of bovine herpesvirus 1 among red deer (Cervus elaphus) under experimental conditions. Veterinary Microbiology 111, 25–34.
Quantification of the transmission of bovine herpesvirus 1 among red deer (Cervus elaphus) under experimental conditions.Crossref | GoogleScholarGoogle Scholar |

Moloney, PD, Gormley, AM, Toop, SD, Flesch, JS, Forsyth, DM, Ramsey, DSL, and Hampton, JO (2022). Bayesian modelling reveals differences in long-term trends in the harvest of native and introduced species by recreational hunters in Australia. Wildlife Research 49, 673–685.
Bayesian modelling reveals differences in long-term trends in the harvest of native and introduced species by recreational hunters in Australia.Crossref | GoogleScholarGoogle Scholar |

Moreira-Soto, A, Walzer, C, Czirják, GÁ, Richter, MH, Marino, SF, Posautz, A, De Yebra Rodo, P, McEwen, GK, Drexler, JF, and Greenwood, AD (2022). Serological evidence that SARS-CoV-2 has not emerged in deer in Germany or Austria during the COVID-19 pandemic. Microorganisms 10, 748.
Serological evidence that SARS-CoV-2 has not emerged in deer in Germany or Austria during the COVID-19 pandemic.Crossref | GoogleScholarGoogle Scholar |

Morgan, ER, Lundervold, M, Medley, GF, Shaikenov, BS, Torgerson, PR, and Milner-Gulland, EJ (2006). Assessing risks of disease transmission between wildlife and livestock: the Saiga antelope as a case study. Biological Conservation 131, 244–254.
Assessing risks of disease transmission between wildlife and livestock: the Saiga antelope as a case study.Crossref | GoogleScholarGoogle Scholar |

Moriarty, A (2004a). The liberation, distribution, abundance and management of wild deer in Australia. Wildlife Research 31, 291–299.
The liberation, distribution, abundance and management of wild deer in Australia.Crossref | GoogleScholarGoogle Scholar |

Moriarty AJ (2004b) Ecology and environmental impact of Javan rusa deer (Cervus timorensis russa) in the Royal National Park. PhD thesis, Western Sydney University, NSW, Australia.

Morner, T, Obendorf, DL, Artois, M, and Woodford, MH (2002). Surveillance and monitoring of wildlife diseases. Revue Scientifique et Technique 21, 67–76.
Surveillance and monitoring of wildlife diseases.Crossref | GoogleScholarGoogle Scholar |

Mouchantat, S, Wernike, K, Lutz, W, Hoffmann, B, Ulrich, RG, Borner, K, Wittstatt, U, and Beer, M (2015). A broad spectrum screening of Schmallenberg virus antibodies in wildlife animals in Germany. Veterinary Research 46, 99.
A broad spectrum screening of Schmallenberg virus antibodies in wildlife animals in Germany.Crossref | GoogleScholarGoogle Scholar |

Munday BL (1966) Diseases of Tasmania’s free-living animals. Tasmanian Department of Agriculture, Hobart, TAS, Australia.

Munday, BL (1972). A serological study of some infectious diseases of Tasmanian wildlife. Journal of Wildlife Diseases 8, 169–175.
A serological study of some infectious diseases of Tasmanian wildlife.Crossref | GoogleScholarGoogle Scholar |

Murphy, HL, and Ly, H (2021). Understanding the prevalence of SARS-CoV-2 (COVID-19) exposure in companion, captive, wild, and farmed animals. Virulence 12, 2777–2786.
Understanding the prevalence of SARS-CoV-2 (COVID-19) exposure in companion, captive, wild, and farmed animals.Crossref | GoogleScholarGoogle Scholar |

Mylrea, GE, Mulley, RC, and English, AW (1991). Gastrointestinal helminthosis in fallow deer (Dama dama) and their response to treatment with anthelmintics. Australian Veterinary Journal 68, 74–75.
Gastrointestinal helminthosis in fallow deer (Dama dama) and their response to treatment with anthelmintics.Crossref | GoogleScholarGoogle Scholar |

Ng, J, Yang, R, Whiffin, V, Cox, P, and Ryan, U (2011). Identification of zoonotic Cryptosporidium and Giardia genotypes infecting animals in Sydney’s water catchments. Experimental Parasitology 128, 138–144.
Identification of zoonotic Cryptosporidium and Giardia genotypes infecting animals in Sydney’s water catchments.Crossref | GoogleScholarGoogle Scholar |

Nolan, MJ, Jex, AR, Koehler, AV, Haydon, SR, Stevens, MA, and Gasser, RB (2013). Molecular-based investigation of Cryptosporidium and Giardia from animals in water catchments in southeastern Australia. Water Research 47, 1726–1740.
Molecular-based investigation of Cryptosporidium and Giardia from animals in water catchments in southeastern Australia.Crossref | GoogleScholarGoogle Scholar |

Palmer, MV, Martins, M, Falkenberg, S, Buckley, A, Caserta, LC, Mitchell, PK, Cassmann, ED, Rollins, A, Zylich, NC, Renshaw, RW, Guarino, C, Wagner, B, Lager, K, and Diel, DG (2021). Susceptibility of white-tailed deer (Odocoileus virginianus) to SARS-CoV-2. Journal of Virology 95, e00083–00021.
Susceptibility of white-tailed deer (Odocoileus virginianus) to SARS-CoV-2.Crossref | GoogleScholarGoogle Scholar |

Panozzo J (2018) Wild deer as potential reservoirs of economically important gastrointestinal parasites in South Eastern Australia. PhD thesis, Federation University, VIC, Australia.

Passler, T, Ditchkoff, SS, and Walz, PH (2016). Bovine viral diarrhea virus (BVDV) in white-tailed deer (Odocoileus virginianus). Frontiers in Microbiology 7, 945.
Bovine viral diarrhea virus (BVDV) in white-tailed deer (Odocoileus virginianus).Crossref | GoogleScholarGoogle Scholar |

Presidente PJA, Westbury HA (1979) A serological survey of Australian deer. In ‘Deer refresher course. Proceedings post-graduate committee in veterinary science’. (The University of Sydney)

Reichel, MP (2000). Neospora caninum infections in Australia and New Zealand. Australian Veterinary Journal 78, 258–261.
Neospora caninum infections in Australia and New Zealand.Crossref | GoogleScholarGoogle Scholar |

Rhyan, JC, and Spraker, TR (2010). Emergence of diseases from wildlife reservoirs. Veterinary Pathology 47, 34–39.
Emergence of diseases from wildlife reservoirs.Crossref | GoogleScholarGoogle Scholar |

Rocklov, J, and Dubrow, R (2020). Climate change: an enduring challenge for vector-borne disease prevention and control. Nature Immunology 21, 479–483.
Climate change: an enduring challenge for vector-borne disease prevention and control.Crossref | GoogleScholarGoogle Scholar |

Roeber, F, Jex, AR, and Gasser, RB (2013). Impact of gastrointestinal parasitic nematodes of sheep, and the role of advanced molecular tools for exploring epidemiology and drug resistance – an Australian perspective. Parasites & Vectors 6, 153.
Impact of gastrointestinal parasitic nematodes of sheep, and the role of advanced molecular tools for exploring epidemiology and drug resistance – an Australian perspective.Crossref | GoogleScholarGoogle Scholar |

Ruiz-Fons, F, Sanchez-Matamoros, A, Gortazar, C, and Sanchez-Vizcaino, JM (2014). The role of wildlife in bluetongue virus maintenance in Europe: lessons learned after the natural infection in Spain. Virus Research 182, 50–58.
The role of wildlife in bluetongue virus maintenance in Europe: lessons learned after the natural infection in Spain.Crossref | GoogleScholarGoogle Scholar |

Scharnbock, B, Roch, F-F, Richter, V, Funke, C, Firth, CL, Obritzhauser, W, Baumgartner, W, Kasbohrer, A, and Pinior, B (2018). A meta-analysis of bovine viral diarrhoea virus (BVDV) prevalences in the global cattle population. Scientific Reports 8, 14420.
A meta-analysis of bovine viral diarrhoea virus (BVDV) prevalences in the global cattle population.Crossref | GoogleScholarGoogle Scholar |

Slee, KJ, and Presidente, PJA (1981). Biological and pathological features of sambar in Victoria. Part 1. Haematology, Biochemistry and Serology Australian Deer 6, 7–14.

Smits, SL, Poon, LLM, van Leeuwen, M, Lau, P-N, Perera, HKK, Peiris, JSM, Simon, JH, and Osterhaus, ADME (2011). Genogroup I and II picobirnaviruses in respiratory tracts of pigs. Emerging Infectious Diseases 17, 2328–2330.
Genogroup I and II picobirnaviruses in respiratory tracts of pigs.Crossref | GoogleScholarGoogle Scholar |

Stensvold, CR, Lebbad, M, and Clark, CG (2010). Genetic characterisation of uninucleated cyst-producing Entamoeba spp. from ruminants. International Journal for Parasitology 40, 775–778.
Genetic characterisation of uninucleated cyst-producing Entamoeba spp. from ruminants.Crossref | GoogleScholarGoogle Scholar |

Walker, JG, Plein, M, Morgan, ER, and Vesk, PA (2017). Uncertain links in host–parasite networks: lessons for parasite transmission in a multi-host system. Philosophical Transactions of the Royal Society B: Biological Sciences 372, 20160095.
Uncertain links in host–parasite networks: lessons for parasite transmission in a multi-host system.Crossref | GoogleScholarGoogle Scholar |

Woolhouse, MEJ, Dye, C, Cleaveland, S, Laurenson, MK, and Taylor, LH (2001). Diseases of humans and their domestic mammals: pathogen characteristics, host range and the risk of emergence. Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 356, 991–999.
Diseases of humans and their domestic mammals: pathogen characteristics, host range and the risk of emergence.Crossref | GoogleScholarGoogle Scholar |