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Biomedical subjects

H A Standfast

Publications and source records attributed to H A Standfast.

At least 19 recordsLinked to original sources
PubMed1997

Ross River virus in mosquitoes (Diptera:Culicidae) during the 1994 epidemic around Brisbane, Australia.

During the summer 1994 outbreak of epidemic polyarthritis in suburban Brisbane, 29,931 adult female mosquitoes were collected by octenol-CO2 light traps and tested for virus by species in pools of approximately 20 using an in situ enzyme-linked immunoassay. Overall, 63 isolations of Ross River (RR) virus were made from 7 different mosquito species, including 23 from freshwater-breeding Culex annulirostris Skuse, 13 from peridomestic Aedes notoscriptus (Skuse), 4 from Aedes procax (Skuse), 12 from the brackish water-breeding Aedes funereus (Theobald), 9 from saltmarsh Aedes vigilax (Skuse), and 1 each from Culex sitiens Wiedemann and Aedes alternans (Westwood). The RR virus minimum infection rate in mosquitoes ranged from 1.6 to 2.5/1,000 from March to June 1994. This study implicates freshwater and brackish water mosquitoes as important suburban vectors of RR virus and indicates the need for refocusing mosquito control priorities.

Aedes↗
PubMed1985

Vectors of bluetongue virus in Australia.

Two of the 5 serotypes of bluetongue virus (BTV) known from Australia have been isolated from field collected insects. Serotype 20 was isolated in 1975 from a mixed pool of 214 insects containing several Culicoides species. Serotype 1 has been isolated from C. (Avaritia) fulvus Sen & Das Gupta collected at Beatrice Hill in the Northern Territory and from C. (Avaritia) brevitarsis Kieffer collected at Peachester in southeast Queensland. All other isolates of bluetongue (BT) group viruses have been made from sentinel cattle. An additional 2 species of the subgenus Avaritia, C. wadai Kitaoka and C. actoni Smith, 1 species of the subgenus Culicoides, C. peregrinus Kieffer and 1 species of the Schultzei group, C. oxystoma Kieffer have been infected in the laboratory. Serotype 20 was transmitted from sheep to sheep by C. fulvus and serotype 1 by C. fulvus and C. actoni. The infection rates established for Culicoides fed on sheep infected with serotype 20 were C. fulvus 62%; C. wadai 11%; C. actoni 2% and C. brevitarsis 0.3%. All species of insects successfully infected are widely distributed in the Oriental region. Attempts to infect species that are restricted in range to the Australasian region have been unsuccessful. The 3 species with highest experimental infection rates: C. fulvus, C. wadai and C. actoni, are confined in Australia to areas with an annual summer rainfall in excess of 800 mm, and do not penetrate to the drier areas where sheep are commercially husbanded. C. brevitarsis is the vector responsible for transmission in the coastal dairying areas, and although it does occur where sheep are reared, it is an inefficient vector. It breeds in discrete cow dung pats on pasture and is more closely associated with cattle than with sheep when the 2 hosts occur together. More than 1 species of Culicoides is responsible for the transmission of BT group viruses in Australia and no BT disease of sheep has been recorded because the more efficient vector species are not present in sheep rearing areas.

Animals↗
PubMed1985

Mortality of Culicoides brevitarsis fed on cattle treated with ivermectin.

Adult female Culicoides brevitarsis Kieffer, important vectors of arboviruses affecting livestock in Australia, were fed on penned Hereford yearling cattle which had been given a single subcutaneous injection of ivermectin at a dose of 200 mcg/kg. The mean mortality of engorged females 48 hr after feeding on the treated cattle was 99% for 10 days posttreatment and in excess of 40% for 18 days posttreatment. Based on these results, it appears that ivermectin administered subcutaneously could be a useful tool for the control of Culicoides-transmitted diseases and would provide an attractive alternative to "slaughter out" programs in the case of a major exotic disease threat.

Animals↗
PubMed1984

Isolation of arboviruses from insects collected at Beatrice Hill, Northern Territory of Australia, 1974-1976.

Between October 1974 and May 1976, 57 596 mosquitoes, 169 957 Culicoides, 5923 Lasiohelea and 1043 phlebotomines were collected for virus isolation at Beatrice Hill (lat. 12 degrees 39'S.,long. 131 degrees 20'E.) in the Northern Territory of Australia. A total of 94 viruses belonging to 22 different serological groupings was isolated. The following species of insect yielded viruses which were identified and those viruses marked with an asterisk represent a new record of insect host: Culex annulirostris: Ross River, Kokobera, Barmah Forest, Corriparta, Eubenangee*, Wongorr; Anopheles amictus: Mapputta*; An bancroftii: bovine ephemeral fever*; An farauti: Eubenangee*; An annulipes: Mapputta; Culicoides marksi: Barmah Forest*, Belmont, Eubenangee*, Wallal, Warrego, Leanyer*, Parker's Farm*, Humpty Doo*; C. peregrinus: Beatrice Hill*; C. oxystoma: Bunyip Creek*, Marrakai*; C. pallidothorax: Wongorr*; C. histrio: Thimiri*; Lasiohelea spp.: Humpty Doo*. Pools of mixed species of Culicoides yielded bluetongue, Belmont, CSIRO Village, Warrego and Facey's Paddock viruses. Filter-passing agents not yet identified, were isolated from Cx annulirostris and An bancroftii. As well as providing new locality records for all but one of the 22 viruses isolated, the study yielded five new viruses (bluetongue serotype 20, CSIRO Village, Marrakai, Beatrice Hill and Humpty Doo viruses) and a new record for Thimiri virus which had not been recorded previously in Australia nor had it been isolated from an arthropod. Nine of the viruses isolated occur in more than one family of Diptera.

Animals↗
PubMed1980

Peaton virus: a new Simbu group arbovirus isolated from cattle and Culicoides brevitarsis in Australia.

A new member of the Simbu group of arboviruses, for which the name Peaton virus is proposed, has been isolated from midges and cattle in Australia. Nine isolates were obtained from 101 pools of the biting midge Culicoides brevitarsis collected at Peachester, Qld, (26.51 degrees S., 152.53 degrees E.) between 30 November and 8 December 1976. Three isolations of the same virus were made from the blood of sentinel cattle collected at Grafton and Tamworth, N.S.W., on 20 January and 13 April 1977, respectively. Peaton virus was shown to be a member of the Simbu group of arboviruses by complement-fixation tests using antisera prepared against Australian strains of Akabane and Aino viruses. It was readily distinguishable from these viruses in cross-neutralization tests in tissue cultures and mice. A serological survey of sentinel cattle showed that neutralizing antibody was detectable only in cattle within the recorded limits of the suspected vector C. brevitarsis. Neutralizing antibody in blood serum was detected in 22 of 157 sheep, 21 of 137 horses, 7 of 18 buffaloes, 7 of 20 goats and 3 of 62 pigs, but not in 22 camels, 34 dogs, 3 cats, 76 human beings, 240 marsupials, 19 reptiles or 31 wild birds. The pathogenecity of Peaton virus has yet to be determined. The Yale Arbovirus Research Unit and the Center for Disease Control, Fort Collins, U.S.A., found that Peaton virus was distinguishable from all other Simbu group viruses and thus is a new virus.

Animals↗
PubMed1978

Onchocerca sweetae (Nematoda: Filarioidea): notes on the intermediate host.

Microfilariae of Onchocerca sweetae are broadly distributed in the superficial layers of the dermis of the water buffalo (Bubalus bubalis). A total of 2855 insects representing 20 species were collected from O. sweetae-infected bait buffaloes. Only one species, Culicoides sp. "M", ingested microfilariae from buffalo skin. Larval development of O. sweetae was observed in the thorax of this species. Atotal of 829 insects, representing 7 species and including 749 parous Culicoides spp. were collected from light and Manitoba traps. Developing filarioid larvae were observed only in Culicoides sp. "M". It is concluded that Culicoides sp. "M" is a natural intermediate host of O. sweetae in the Northern Territory of Australia.

Animals↗
PubMed1978

Isolations of akabane virus from sentinel cattle and Culicoides brevitarsis.

A total of 14 isolations of Akabane virus were made from the blood of five cattle during sub-clinical infection. The serial isolation of this virus from four of these animals suggests a viraemia of at least 3 or 4 days. Neutralising antibody to Akabane virus in the serum of infected calves reached an initial peak titre of 32 to 256 four to five days after the viraemia but later uose further to a range of 64 to 512. Three isolations of Akabane virus were made from Culicoides brevitarsis collected nearby in the same period. C. brevitarsis was the dominant haematophagous midge present during that time. These findings strengthen the case for C. brevitarsis to be considered as a vector of Akabane virus.

Animals↗
PubMed1977

The isolation of Saumarez Reef virus, a new flavivirus, from bird ticks Ornithodoros capensis and Ixodes eudyptidis in Australia.

Strains of a new flavivirus, for which the name Saumarez Reef Virus is proposed, were isolated from seabird ticks collected from four localities. Two strains were isolated from ticks of the species Ornithodoros capensis Neumann 1901 collected from the nests of Sooty Terns, Sterna fuscata Linnaeus 1766 on coral cays off the east coast of Queensland, Australia. The other three strains were isolated from ticks of the species Ixodes eudyptidis Maskell 1885 taken from two dead Silver Gulls Larus novaehollandiae Stephens 1826 in northern Tasmania. The new virus was compared serologically with 50 other flaviviruses at the Yale Arbovirus Research Unit and was found to be most closely related to Tyuleniy virus.

Animals↗