Higgitt Roxanne L, Schalkwyk O Louis van, deKlerk-Lorist Lin-Mari, Buss Peter E, Caldwell Peter, Rossouw Leana, Manamela Tebogo, Hausler Guy A, Helden Paul D van, Parsons Sven D C, Miller Michele A
1 Department of Science and Technology-National Research Foundation Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, PO Box 241, Cape Town, 8000, South Africa.
2 Office of the State Veterinarian, Kruger National Park, Department of Agriculture, Forestry and Fisheries, PO Box 12, Skukuza, 1350, South Africa.
J Wildl Dis. 2019 Jul;55(3):529-536. doi: 10.7589/2018-03-089. Epub 2018 Dec 17.
In South Africa, the largest proportion of the African wild dog () population resides in regions where buffaloes have a high prevalence of , the causative agent of bovine tuberculosis (bTB). Recent reports of deaths of wild dogs associated with bTB have raised concerns regarding the threat this disease might pose for this species. In order to understand the potential impact of the disease in wild dogs, diagnostic tools are required to identify infected individuals. The interferon gamma (IFN-γ) release assay (IGRA) is commonly used for tuberculosis (TB) screening of humans, cattle, and other species, and the aim of this study was to develop an IGRA for wild dogs to detect immune sensitization. Blood was collected from immobilized wild dogs from the Ann van Dyk Cheetah Centre (AvDCC; =9) and Kruger National Park (KNP; =31). Heparinized whole blood was incubated overnight in QuantiFERON-TB Gold (QFT) blood collection tubes and with selected mitogens, after which the plasma fraction was harvested. Three canine IFN-γ enzymelinked immunosorbent assays (ELISAs) were compared for detection of wild dog IFN-γ in plasma and the R&D Quantikine canine IFN-γ ELISA was selected for measurement of -specific IFN-γ release in plasma samples. An IGRA result was calculated as the concentration in plasma derived from the QFT TB Antigen tubes minus that in the QFT Nil tube. An IGRA cut-off value was calculated using the IGRA results of unexposed individuals from AvDCC. Using this cut-off value, 74% (23/31) of -exposed KNP wild dogs were IGRA positive, indicating immune sensitization to TB antigens in these animals. Three culture-positive wild dogs from KNP had IFN-γ concentrations between 758 and 1,445 pg/mL, supporting this interpretation. This warrants further investigation into the prevalence of infection in the KNP population.
在南非,非洲野犬种群中最大比例的个体栖息于水牛群中牛结核病(bTB)致病原 流行率较高的地区。最近有报道称野犬因感染bTB而死亡,这引发了人们对该疾病可能对这一物种构成威胁的担忧。为了了解该疾病对野犬的潜在影响,需要诊断工具来识别受感染的个体。干扰素γ(IFN-γ)释放试验(IGRA)通常用于人类、牛和其他物种的结核病(TB)筛查,本研究的目的是开发一种用于野犬的IGRA以检测免疫致敏情况。从安·范·戴克猎豹中心(AvDCC;n = 9)和克鲁格国家公园(KNP;n = 31)的麻醉野犬身上采集血液。将肝素化全血在QuantiFERON-TB Gold(QFT)采血试管中与选定的促有丝分裂原一起孵育过夜,之后收集血浆部分。比较了三种犬IFN-γ酶联免疫吸附测定(ELISA)用于检测血浆中的野犬IFN-γ,选择了R&D Quantikine犬IFN-γ ELISA来测量血浆样本中结核分枝杆菌特异性IFN-γ的释放。IGRA结果计算为QFT结核抗原管中血浆的浓度减去QFT空白管中的浓度。使用来自AvDCC未接触过结核分枝杆菌个体的IGRA结果计算出一个IGRA临界值。使用这个临界值,74%(23/31)接触过结核分枝杆菌的KNP野犬IGRA呈阳性,表明这些动物对结核抗原产生了免疫致敏。来自KNP的三只结核培养阳性的野犬IFN-γ浓度在758至1445 pg/mL之间,支持了这一解释。这值得进一步调查KNP种群中结核分枝杆菌感染的流行情况。