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Final Risk Analysis - Biosecurity New Zealand

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5. Akabane and other Simbu Group Viruses<br />

5.1. HAZARD IDENTIFICATION<br />

5.1.1. Aetiological agent<br />

Family: Bunyaviridae; Genus: Bunyavirus, Serogroup Simbu. Akabane disease virus and<br />

related viruses belong to a group known collectively as Simbu viruses (St George and<br />

Kirkland 2004). The group includes viruses such as Aino, Tinaroo, Peaton and Cache Valley<br />

viruses that cause similar syndromes.<br />

5.1.2. OIE list<br />

Not listed.<br />

5.1.3. <strong>New</strong> <strong>Zealand</strong> status<br />

Listed on the unwanted organisms register as an exotic unwanted organism.<br />

5.1.4. Epidemiology<br />

Akabane and related viruses have been isolated from Culicoides spp. (midges) and<br />

mosquitoes. Culicoides spp. are assumed to be the vectors of these viruses (St George and<br />

Kirkland 2004). Cattle and other ruminants including sheep (Charles 1994; Haughey et al<br />

1988; St George and Kirkland 2004) and goats (Han and Du 2003) are susceptible.<br />

Viruses in the Simbu-group occur endemically in large areas of Africa, Asia, the Middle East<br />

and Australia (Charles 1994; Haughey et al 1988; St George and Kirkland 2004) and the<br />

related Cache Valley virus occurs in Texas (Edwards 1994; Edwards et al 1989). No reference<br />

was found to the occurrence of the virus group in Canada or the European Union.<br />

The incubation period (infection to start of viraemia) for Akabane virus is from 1-6 days (St<br />

George 1998) and the viraemic period lasts for 3-4 days (St George and Kirkland 2004). In<br />

non-pregnant animals infection does not lead to the development of any signs (Gard et al<br />

1989). Akabane virus crosses from maternal to foetal circulation in infected pregnant females<br />

and causes the development of malformed calves, particularly cases of arthrogryposis and<br />

hydroencephaly (Charles 1994; Parsonson et al 1977; Parsonson et al 1988; St George and<br />

Kirkland 2004). In cattle maximal damage occurs when infection takes place at about the 12th<br />

to 16th week of gestation (St George and Kirkland 2004). Once a foetus has become immunocompetent<br />

it can mount an immune reaction and damage is less apparent or does not occur.<br />

Infected calves are usually non viable (Charles 1994). Calves born alive are not contagious<br />

and will not infect vectors.<br />

Major epidemics of foetal malformations due to Akabane virus have been reported in Japan<br />

and Australia (St George and Kirkland 2004). However, animals that have been exposed to<br />

the infection become immune and this leads to the establishment of a mainly immune<br />

population of cattle in endemic areas. For this reason foetal abnormalities usually occur<br />

sporadically in endemically infected areas but seroconversion in animals is common<br />

MAF <strong>Biosecurity</strong> <strong>New</strong> <strong>Zealand</strong> Import <strong>Risk</strong> <strong>Analysis</strong>: Cattle from Australia, Canada, the EU & the USA ● 15

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