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Review of the management of feral animals and their impact on ...

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myxomatosis acquire lifel<strong>on</strong>g immunity. Since myxomatosis established in Australian<br />

rabbit populati<strong>on</strong>s, highly virulent strains, have been introduced many times <strong>on</strong> <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

premise that <str<strong>on</strong>g>the</str<strong>on</strong>g>y would kill a high proporti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> rabbits <str<strong>on</strong>g>and</str<strong>on</strong>g> thus c<strong>on</strong>trol <str<strong>on</strong>g>the</str<strong>on</strong>g>ir<br />

populati<strong>on</strong>s. This has generally proven unsuccessful so far. The European rabbit flea<br />

(Spilopsyllus cuniculi) was introduced into some Australian wild rabbit populati<strong>on</strong>s in<br />

1968 as a vector for <str<strong>on</strong>g>the</str<strong>on</strong>g> myxoma virus (Sobey & C<strong>on</strong>olly 1971). However <str<strong>on</strong>g>the</str<strong>on</strong>g> flea is<br />

unable to cope with arid c<strong>on</strong>diti<strong>on</strong>s <str<strong>on</strong>g>and</str<strong>on</strong>g> does not occur permanently with populati<strong>on</strong>s<br />

in arid regi<strong>on</strong>s (Cooke 1984). To overcome this, <str<strong>on</strong>g>the</str<strong>on</strong>g> Spanish flea was introduced into<br />

Australia as a vector in <str<strong>on</strong>g>the</str<strong>on</strong>g> more arid z<strong>on</strong>es (Williams et al. 1995) <str<strong>on</strong>g>and</str<strong>on</strong>g> its distributi<strong>on</strong><br />

will complement that <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> European rabbit flea. Highest flea infestati<strong>on</strong> levels occur<br />

in summer/autumn (Abreu 1980), <str<strong>on</strong>g>the</str<strong>on</strong>g> time when myxomatosis is most prevalent in<br />

inl<str<strong>on</strong>g>and</str<strong>on</strong>g> Australia (Parer & Korn 1989). Despite a decrease in <str<strong>on</strong>g>the</str<strong>on</strong>g> effectiveness <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

myxoma virus since its initial release in <str<strong>on</strong>g>the</str<strong>on</strong>g> 1950s, it c<strong>on</strong>tinues to have an important<br />

role in rabbit c<strong>on</strong>trol. Like most effective bioc<strong>on</strong>trols, despite initial high research <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

implementati<strong>on</strong> costs, it has remained an extremely cost effective form <str<strong>on</strong>g>of</str<strong>on</strong>g> rabbit<br />

<str<strong>on</strong>g>management</str<strong>on</strong>g> due to little or no <strong>on</strong>-going costs. Parer et al. (1985) dem<strong>on</strong>strated that in<br />

<str<strong>on</strong>g>the</str<strong>on</strong>g> absence <str<strong>on</strong>g>of</str<strong>on</strong>g> myxomatosis, rabbit populati<strong>on</strong>s can again increase rapidly.<br />

Rabbit haemorrhagic disease<br />

Rabbit haemorrhagic disease (RHD, formerly known as Calicivirus) is an acute <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

fatal infectious disease <str<strong>on</strong>g>of</str<strong>on</strong>g> rabbits. The virus escaped <strong>on</strong>to <str<strong>on</strong>g>the</str<strong>on</strong>g> mainl<str<strong>on</strong>g>and</str<strong>on</strong>g> in 1995 during<br />

field investigati<strong>on</strong>s <strong>on</strong> Wardang Isl<str<strong>on</strong>g>and</str<strong>on</strong>g>, South Australia, possibly as a result <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

windborne vectors (Cooke 1996). In September 1996 RHD was accepted as a<br />

biological c<strong>on</strong>trol agent under <str<strong>on</strong>g>the</str<strong>on</strong>g> Comm<strong>on</strong>wealth Biological C<strong>on</strong>trol Act 1984 <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

later also accepted by <str<strong>on</strong>g>the</str<strong>on</strong>g> States <str<strong>on</strong>g>and</str<strong>on</strong>g> Nor<str<strong>on</strong>g>the</str<strong>on</strong>g>rn Territory. The virus is transmitted<br />

through direct c<strong>on</strong>tact between infected <str<strong>on</strong>g>and</str<strong>on</strong>g> susceptible rabbits <str<strong>on</strong>g>and</str<strong>on</strong>g> by c<strong>on</strong>tact with<br />

<str<strong>on</strong>g>the</str<strong>on</strong>g> secreti<strong>on</strong>s or excreti<strong>on</strong>s <str<strong>on</strong>g>of</str<strong>on</strong>g> infective rabbits, or items such as food <str<strong>on</strong>g>and</str<strong>on</strong>g> water that<br />

have been c<strong>on</strong>taminated (Xu & Chen 1989). Rabbits, which survive an RHD<br />

epizootic, may persist as carriers for up to a m<strong>on</strong>th (Gregg et al. 1991). Mortality rates<br />

in excess <str<strong>on</strong>g>of</str<strong>on</strong>g> 90 percent have been observed in some South Australian populati<strong>on</strong>s<br />

(Mutze et al. 1998) where naturally recurring outbreaks have kept <str<strong>on</strong>g>the</str<strong>on</strong>g> populati<strong>on</strong> at an<br />

average populati<strong>on</strong> level <strong>on</strong>ly 17 percent <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> l<strong>on</strong>g-term pre-RHD average (Mutze et<br />

al. 1998b). More humid sites do not always fare as well with some sites observing<br />

little change in rabbit numbers following <str<strong>on</strong>g>the</str<strong>on</strong>g> arrival <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> virus (An<strong>on</strong> 1997).<br />

The <str<strong>on</strong>g>impact</str<strong>on</strong>g> <str<strong>on</strong>g>of</str<strong>on</strong>g> RHD <strong>on</strong> rabbits in <str<strong>on</strong>g>the</str<strong>on</strong>g> higher rainfall areas <str<strong>on</strong>g>of</str<strong>on</strong>g> south-eastern Australia<br />

has been highly variable. The Invasive Animal CRC will investigate methods <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

increasing <str<strong>on</strong>g>the</str<strong>on</strong>g> effectiveness <str<strong>on</strong>g>of</str<strong>on</strong>g> RHD in <str<strong>on</strong>g>the</str<strong>on</strong>g>se areas. One avenue <str<strong>on</strong>g>of</str<strong>on</strong>g> research will focus<br />

<strong>on</strong> <str<strong>on</strong>g>the</str<strong>on</strong>g> development <str<strong>on</strong>g>of</str<strong>on</strong>g> a virus that can be released <strong>on</strong> bait in susceptible populati<strong>on</strong>s<br />

in <str<strong>on</strong>g>the</str<strong>on</strong>g>se areas. This would provide a cheap <str<strong>on</strong>g>and</str<strong>on</strong>g> simple tool to aid rabbit c<strong>on</strong>trol.<br />

Immunoc<strong>on</strong>tracepti<strong>on</strong><br />

Current research in molecular biotechnology aims to insert into <str<strong>on</strong>g>the</str<strong>on</strong>g> myxoma virus<br />

genetic informati<strong>on</strong> coding for specific antigens derived from surface proteins <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

rabbit sperm <str<strong>on</strong>g>and</str<strong>on</strong>g> egg. It is hoped that infecti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> rabbits by this modified virus will<br />

cause an immune resp<strong>on</strong>se, blocking fertilisati<strong>on</strong> or embryo implantati<strong>on</strong> in females<br />

that survive <str<strong>on</strong>g>the</str<strong>on</strong>g> disease (Tyndale-Biscoe 1991, Tyndale-Biscoe & Jacks<strong>on</strong> 1991). The<br />

intended strategy is for such a genetically modified myxoma virus to infect wild rabbit<br />

populati<strong>on</strong>s <str<strong>on</strong>g>and</str<strong>on</strong>g> induce sterility in sufficient proporti<strong>on</strong>s to cause rabbit populati<strong>on</strong>s to<br />

decline. If both sperm <str<strong>on</strong>g>and</str<strong>on</strong>g> egg antigens are inserted into <str<strong>on</strong>g>the</str<strong>on</strong>g> virus <str<strong>on</strong>g>the</str<strong>on</strong>g> proporti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

131

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