Rabbit haemorrhagic disease: does a pre-existing RHDV-like virus reduce the effectiveness of RHD as a biological control in Australia?

2002 ◽  
Vol 29 (6) ◽  
pp. 673 ◽  
Author(s):  
B. D. Cooke ◽  
S. McPhee ◽  
A. J. Robinson ◽  
L. Capucci

Serological data from wild rabbits support the hypothesis that a second RHDV-like virus was already present in Australia before rabbit haemorrhagic disease virus (RHDV) was introduced as a biological control agent. This putative virus apparently persists in most wild rabbit populations in the presence of RHDV, and antibodies raised against it appear to protect some rabbits from fatal rabbit haemorrhagic disease (RHD). High titres of these antibodies are most commonly found in rabbits from high rainfall areas; this may explain why the initial mortality from RHD declined as the disease spread from dry areas into wetter regions and why it remains less effective as a biological control in wetter regions today. The implications for further advances in rabbit control are discussed, including the need to isolate this putative RHDV-like virus and develop specific ELISA tests to facilitate its detection in the field.


2004 ◽  
Vol 31 (6) ◽  
pp. 605 ◽  
Author(s):  
John S. Bruce ◽  
Laurie E. Twigg

Although several different cELISAs have been used to assess the exposure of European rabbits to rabbit haemorrhagic disease (RHD), the interpretation of the results of such assays is not always straight-forward. Here we report on such difficulties, and on the likely presence of a non-virulent rabbit haemorrhagic disease virus–like virus (nvRHDV-LV) in south-western Australia. Analysis of sera collected from European rabbits at Kojaneerup (near Albany) in Western Australia provided the first serological evidence of the likely presence of a nvRHDV-LV in wild rabbit populations outside the east coast of Australia and New Zealand, before the deliberate introduction of RHDV as biological control agent in both countries. Six out of 30 rabbits (20%) sampled 1–2 months before the known arrival of RHDV at Kojaneerup were seropositive to RHD on the basis of their IgG isoELISAs. However, none of these positive samples were positive for the RHDV antibody cELISA (1 : 10), indicating likely exposure to nvRHDV-LV. Subsequent serological analysis of 986 rabbits sampled between September 1996 and August 1999 at Kojaneerup indicated that nvRHDV-LV persisted in these rabbits following the natural arrival of RHDV in September 1996. At least 10–34% of rabbits appeared to have been exposed to nvRHDV-LV during the 3-year study. The presence of nvRHDV-LV seemed to offer only limited protection to rabbits from RHDV during the initial epizootic; however, persistence of nvRHDV-LV may have mitigated further RHDV activity after this epizootic. Fewer than 1% of rabbits (9 of 986) showed evidence of RHDV-challenge during the 30 months following the initial RHDV epizootic. Furthermore, except for the epizootic in September 1996, no clinical signs of the disease were apparent in the population until RHDV was deliberately reintroduced in April 1999. Mortality of rabbits exposed to RHDV at this time appeared to be correlated with their IgG isoELISA titre.



2004 ◽  
Vol 31 (4) ◽  
pp. 415 ◽  
Author(s):  
B. D. Cooke ◽  
J.-L. Chapuis ◽  
V. Magnet ◽  
A. Lucas ◽  
J. Kovaliski

Rabbits have caused enormous damage to the vegetation on seven islands in the sub-Antarctic Kerguelen archipelago, including the main island, Grande Terre. Rabbit sera collected during 2001–02 were tested for antibodies against myxoma virus and rabbit haemorrhagic disease virus with a view to considering the wider use of these viruses to control rabbits. The results confirmed work done 15–20 years earlier that suggested that myxoma virus has not spread across all parts of Grande Terre and occurs at low prevalence among rabbits. By contrast, on Ile du Cimetière, where European rabbit fleas were introduced in 1987–88, the prevalence of myxoma antibodies is high and the rabbit population is relatively low, supporting the idea that the fleas are effective vectors of myxoma virus. Consequently, there should be benefits in releasing fleas on Grand Terre to enhance disease transmission. Reactivity of some rabbit sera in RHD-specific ELISAs suggested that a virus similar to RHDV may be present at low prevalence on Grande Terre but most rabbits are likely to be susceptible and this virus could be considered for use as a future biological control agent.



2004 ◽  
Vol 31 (6) ◽  
pp. 651
Author(s):  
G. Story ◽  
J. Scanlan ◽  
R. Palmer ◽  
D. Berman

Rabbit haemorrhagic disease virus (RHDV) escaped from quarantine facilities on Wardang Island in September 1995 and spread through South Australia to Queensland by December 1995. To determine the impact of this biological control agent on wild rabbit populations in Queensland, shot sample and spotlight count data were collected at six sites. RHDV spread across Queensland from the south-west to the east at a rate of at least 91 km month–1 between October 1995 and October 1996. The initial impact on rabbit density appeared highly variable, with an increase of 81% (255 ± 79 (s.e.) to 385 ± 73 rabbits km–2) at one site and a decrease of 83% (129 ± 27 to 22 ± 18 rabbits km–2) at another during the first outbreak. However, after 30 months of RHDV activity, counts were at least 90% below counts conducted before RHDV arrived. Using a population model to account for environmental conditions, the mean suppression of rabbit density caused by rabbit haemorrhagic disease (RHD) was estimated to be 74% (ranging from 43% to 94% between sites). No outbreaks were observed when the density of susceptible rabbits was lower than 12 km–2. Where rabbit density remains low for long periods RHDV may not persist. This is perhaps most likely to occur in the isolated populations towards the northern edge of the range of rabbits in Australia. RHDV may have to be reintroduced into these populations. Further south in areas more suitable for rabbits, RHDV is more likely to persist, resulting in a high density of immune rabbits. In such areas conventional control techniques may be more important to enhance the influence of RHD.



2006 ◽  
Vol 33 (4) ◽  
pp. 305 ◽  
Author(s):  
J. Henning ◽  
P. R. Davies ◽  
J. Meers

As part of a longitudinal study of the epidemiology of rabbit haemorrhagic disease virus (RHDV) in New Zealand, serum samples were obtained from trapped feral animals that may have consumed European rabbit (Oryctolagus cuniculus) carcasses (non-target species). During a 21-month period when RHDV infection was monitored in a defined wild rabbit population, 16 feral house cats (Felis catus), 11 stoats (Mustela erminea), four ferrets (Mustela furo) and 126 hedgehogs (Erinaceus europaeus) were incidentally captured in the rabbit traps. The proportions of samples that were seropositive to RHDV were 38% for cats, 18% for stoats, 25% for ferrets and 4% for hedgehogs. Seropositive non-target species were trapped in April 2000, in the absence of an overt epidemic of rabbit haemorrhagic disease (RHD) in the rabbit population, but evidence of recent infection in rabbits was shown. Seropositive non-target species were found up to 2.5 months before and 1 month after this RHDV activity in wild rabbits was detected. Seropositive predators were also trapped on the site between 1 and 4.5 months after a dramatic RHD epidemic in February 2001. This study has shown that high antibody titres can be found in non-target species when there is no overt evidence of RHDV infection in the rabbit population, although a temporal relationship could not be assessed statistically owning to the small sample sizes. Predators and scavengers might be able to contribute to localised spread of RHDV through their movements.



2014 ◽  
Vol 41 (2) ◽  
pp. 95 ◽  
Author(s):  
Jerry Olsen ◽  
Brian Cooke ◽  
Susan Trost ◽  
David Judge

Context Some ecologists argue that nesting success and abundance of wedge-tailed eagles (Aquila audax) are strongly linked to the abundance of introduced wild rabbits (Oryctolagus cuniculus). Consequently, concerns were expressed about eagle population viability when the biological control agent rabbit haemorrhagic disease virus (RHDV) heavily reduced rabbit numbers. However, observations following the spread of rabbit haemorrhagic disease (RHD) in Australia and Spain (where Aquila adalberti is an equivalent of A. audax) question this assertion. Eagle numbers did not fall even though rabbits declined regionally by up to 90% in both countries. Aims To reconsider the assumption of a strong link between rabbit abundance and wedge-tailed eagle breeding and population maintenance. Dispelling misconceptions, if any, about the eagles’ dependence on rabbits would benefit the future management of both eagles and rabbits. Methods We reviewed the literature associated with claims that eagles were heavily dependent on rabbits and asked whether these views could be substantiated given the lack of changes in eagle abundance following the spread of RHD. Data on eagle egg-clutch size and nesting success were also reviewed. Conclusions There is little evidence that eagles depend heavily on rabbits as prey. Instead, as rabbits decline, more kangaroos, reptiles and birds are eaten, partly because more native prey becomes available. Eagles have a high proportion of rabbits in their diets mainly where degradation of natural ecosystems, including that caused by rabbits, results in native prey being rare or unavailable. There has been minimal variation in average clutch size following major perturbations in rabbit population size. Implications Rather than perpetuating the idea that high populations of rabbits are needed for wedge-tailed eagle conservation, resources would be better re-directed into understanding continental-scale eagle population dynamics. This would provide a more rational framework to assist decisions on future biological control agents for rabbits.



2010 ◽  
Vol 37 (4) ◽  
pp. 311 ◽  
Author(s):  
Greg Mutze ◽  
Ron Sinclair ◽  
David Peacock ◽  
John Kovaliski ◽  
Lorenzo Capucci

Context. European rabbits are serious environmental and agricultural pests throughout their range in Australia. Rabbit haemorrhagic disease virus (RHDV) greatly reduced rabbit numbers in arid central Australia but had less impact in cooler, higher-rainfall areas. RHDV-like benign caliciviruses (bCVs) have been implicated in limiting the impact of RHDV in the higher-rainfall regions of Australia and also in Europe. Aims. Experimental releases of RHDV on bait were tested as a means of initiating disease outbreaks. Serological evidence of antibodies to bCVs was examined to determine whether they reduce mortality rates and/or spread of the released RHDV, and how that might influence the effectiveness of future RHDV releases for rabbit management. Methods. Four experimental releases were conducted in high-rainfall and coastal regions of southern Australia. Virus activity was implied from recapture rates and serological changes in marked rabbits, and genetic sequencing of virus recovered from dead rabbits. Changes in rabbit abundance were estimated from spotlight transect counts. Key results. Release of RHDV on bait produced disease outbreaks that challenged almost all animals within the general release area and spread up to 4 km beyond the release sites. Recapture rates were high in marked rabbits that possessed antibodies from previous exposure to RHDV and extremely low amongst rabbits that lacked any detectable antibodies. Rabbits carrying antibodies classified as being due to previous infection with bCVs had recapture rates that were dependent on circulating antibody titre and were ~55% of recapture rates in rabbits with clear antibodies to RHDV. Conclusions. This is the first quantified evidence that antibodies produced against bCVs provide significant protection against RHD outbreaks in field populations of rabbits. Implications. bCVs can greatly reduce the impact of RHDV on wild-rabbit populations in Australia and presumably elsewhere. RHDV can be effectively released on bait although further releases are likely to be of minor or inconsistent benefit for controlling rabbit numbers where bCVs are common.



2020 ◽  
Vol 8 (1) ◽  
pp. e001002 ◽  
Author(s):  
Carina Luisa Carvalho ◽  
Fábio Alexandre Abade dos Santos ◽  
Teresa Fagulha ◽  
Paulo Carvalho ◽  
Paula Mendonça ◽  
...  

Myxoma virus (MYXV) and rabbit haemorrhagic disease virus 2 (RHDV2) are two major pathogens that affect the European rabbit (Oryctolagus cuniculus). Between August 2017 and August 2019, 1166 wild rabbits (971 legally hunted and 195 found dead) were tested by PCR-based methods for MYXV and RHDV2 within the scope of an ongoing surveillance programme on wild leporids in Portugal. Despite never having been reported before and being considered a rare event, coinfection by RHDV2 and MYXV was detected in one juvenile wild rabbit found dead in the Évora district located in Alentejo. The relative frequency of coinfection in the group of diseased rabbits (found dead in the field) was 0.52 per cent (1/195). The positivity percentage of each single virus was much higher, namely, 14.36 per cent (28/195) for MYXV and 55.38 per cent (108/195) for RHDV2, within the 2 years of sample collection considered.





2004 ◽  
Vol 31 (2) ◽  
pp. 183 ◽  
Author(s):  
G. Story ◽  
D. Berman ◽  
R. Palmer ◽  
J. Scanlan

Rabbit haemorrhagic disease virus (RHDV) escaped from quarantine facilities on Wardang Island in September 1995 and spread through South Australia to Queensland by December 1995. To determine the impact of this biological control agent on wild rabbit populations in Queensland, shot sample and spotlight count data were collected at six sites. RHDV spread across Queensland from the south-west to the east at a rate of at least 91 km month–1 between October 1995 and October 1996. The initial impact on rabbit density appeared highly variable, with an increase of 81% (255 ± 79 (s.e.) to 385 ± 73 rabbits km–2) at one site and a decrease of 83% (129 ± 27 to 22 ± 18 rabbits km–2) at another during the first outbreak. However, after 30 months of RHDV activity, counts were at least 90% below counts conducted before RHDV arrived. Using a population model to account for environmental conditions, the mean suppression of rabbit density caused by rabbit haemorrhagic disease (RHD) was estimated to be 74% (ranging from 43% to 94% between sites). No outbreaks were observed when the density of susceptible rabbits was lower than 12 km–2. Where rabbit density remains low for long periods RHDV may not persist. This is perhaps most likely to occur in the isolated populations towards the northern edge of the range of rabbits in Australia. RHDV may have to be reintroduced into these populations. Further south in areas more suitable for rabbits, RHDV is more likely to persist, resulting in a high density of immune rabbits. In such areas conventional control techniques may be more important to enhance the influence of RHD.



2014 ◽  
Vol 41 (2) ◽  
pp. 136 ◽  
Author(s):  
Carlos Rouco ◽  
Grant Norbury ◽  
Dave Ramsay

Context European rabbits (Oryctolagus cuniculus) are serious economic and environmental pests in Australia and New Zealand. Since the illegal introduction of rabbit haemorrhagic disease virus (RHDV) in New Zealand in 1997, the disease has persisted in most rabbit populations, with major epizootics occurring usually each autumn. Aims We evaluated the efficacy of the virus as a biological control agent in the southern South Island. Methods We used an index of rabbit abundance (kills per hunter) based on a region-wide annual rabbit-hunting competition to evaluate rabbit population trends 7 years before and 16 years after the first outbreak of RHD. We also evaluated the influence of rainfall and temperature in the preceding year on post-RHD trends in the index. Key results Kill rates declined by 60% following the initial epizootic. They remained low for the following 3 years and then increased steadily to intermediate levels punctuated by occasional declines. The instantaneous rate of increase in kill rates during the increase phase was low, but above zero (0.04 per year). No relationship between kill rates and rainfall was apparent, but there was a negative relationship between kill rates and winter temperature in the preceding season. Conclusions The kill-rate data obtained from this hunting competition suggest that RHD still appears to be killing rabbits. Every 2–3 years over the past decade, kill rates have been as low as they were when government rabbit-control programs were in place before RHD arrived, but the efficacy of RHD as a biological control agent is waning compared with the first outbreaks of the disease. This concurs with findings based on spotlight counts. Implications The data collected from this hunting competition are a good example of how ‘citizen science’ can be used to capture large volumes of pest-monitoring data from a wide geographic region for very little cost. The information is a valuable addition to understanding the effects of a major wildlife disease.



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