Zheng T, Hamel K L, Buddle B M
AgResearch Grasslands, Hopkirk Research Institute, Private Bag 11008, Palmerston North 4442, New Zealand.
N Z Vet J. 2010 Feb;58(1):23-8. doi: 10.1080/00480169.2010.65057.
To establish an immunoassay to detect antibodies against enteroviruses in brushtail possums (Trichosurus vulpecula), and to determine the prevalence of seropositive samples of antibodies to enteroviruses in wild possums in New Zealand.
A sandwich ELISA was established to detect antibodies to enteroviruses in possums. The IgG fraction of guinea-pig polyclonal antibodies to enteroviruses of possums was used as the capture antibody to bind the enteroviral antigens prior to incubating with test sera from possums. The bound antibodies from the test sera were detected using a conjugate specific to possum immunoglobulins. An archival serum bank was surveyed for the prevalence of seropositive samples, from possums, to the virus. The sera were collected from possums from areas of Northland, Wanganui, Castlepoint, Paraparaumu, Shannon, Orongorongo, Nelson, Hokitika, Banks Peninsula, Riverton, Kawau Island, Chatham Island and Stewart Island, between 1993 and 1996. Possums were captured from farmland, forest margin, scrub, beech, exotic forest or native forest.
Antibodies to the enteroviruses were detected in possums from Shannon (56/270; 21%), Wanganui (4/46; 9%), Kawau Island (3/44; 7%), and Orongorongo (1/43; 2%). The proportion of seropositive possums per area was similar for those found on the forest margin or pasture grazed by sheep and cattle compared with those in the forest. Seropositive possums were significantly older than those that were seronegative (p<0.01).
The distribution of enteroviruses in possums was clustered in the Manawatu-Wanganui regions, where the viruses were originally isolated. The limited distribution was likely due to the lack of contact between possum populations due to natural barriers. If a recombinant enterovirus carrying a biocontrol agent against possums was released it would encounter little interference from field strains in the majority of the country, due to the limited distribution of these viruses in the field.
建立一种免疫测定法,用于检测帚尾袋貂(Trichosurus vulpecula)体内抗肠道病毒的抗体,并确定新西兰野生袋貂中肠道病毒抗体血清阳性样本的流行率。
建立夹心酶联免疫吸附测定法(ELISA)以检测袋貂体内抗肠道病毒的抗体。用豚鼠针对袋貂肠道病毒的多克隆抗体的IgG部分作为捕获抗体,在与袋貂的测试血清孵育之前结合肠道病毒抗原。使用针对袋貂免疫球蛋白的特异性结合物检测测试血清中结合的抗体。对一个存档血清库进行调查,以确定来自袋貂的血清阳性样本对该病毒的流行率。血清采集自1993年至1996年间来自北地、旺阿努伊、卡斯尔波因特、帕拉帕鲁姆、香农、奥龙戈龙戈、尼尔森、霍基蒂卡、班克斯半岛、里弗顿、卡沃岛、查塔姆岛和斯图尔特岛等地的袋貂。袋貂捕获自农田、林缘、灌木丛、山毛榉林、外来林或原生林。
在来自香农(56/270;21%)、旺阿努伊(4/46;9%)、卡沃岛(3/44;7%)和奥龙戈龙戈(1/43;2%)的袋貂中检测到抗肠道病毒的抗体。与森林中的袋貂相比,在林缘或牛羊放牧的牧场中发现的每地区血清阳性袋貂的比例相似。血清阳性的袋貂明显比血清阴性的袋貂年龄大(p<0.01)。
肠道病毒在袋貂中的分布集中在最初分离出这些病毒的马纳瓦图-旺阿努伊地区。分布有限可能是由于自然屏障导致袋貂种群之间缺乏接触。如果释放一种携带针对袋貂的生物防治剂的重组肠道病毒,由于这些病毒在野外分布有限,它在该国大部分地区几乎不会受到野外毒株的干扰。