Nugent G, Whitford E J, Yockney I, Perry M, Tompkins D M, Holtslag N, Cross M L
Landcare Research, PO Box 40, Lincoln 7640, New Zealand.
J Comp Pathol. 2013 Jan;148(1):33-42. doi: 10.1016/j.jcpa.2012.05.006. Epub 2012 Jun 30.
Brushtail possums (Trichosurus vulpecula) are the major wildlife reservoir of Mycobacterium bovis, the causative agent of bovine tuberculosis (BTB), in New Zealand. Primary diagnosis of BTB in wild possums is by palpation to detect peripheral lymphadenomegaly followed by necropsy examination, which frequently identifies gross tuberculous lesions in the peripheral lymph nodes and lungs. Experimental infection studies were conducted with wild possums in an attempt to emulate field BTB, focussing on percutaneous administration of virulent M. bovis in the paws. In a preliminary study, viable M. bovis bacilli were recovered from lymph nodes draining fore- or hindlimbs 12 days after percutaneous injection. Subsequently, 21 wild possums were injected interdigitally with 500 colony forming units (cfu) of M. bovis, radio-collared and released; 17/18 possums recaptured 8 weeks later had an established M. bovis lymphatic infection, with 16 having culture-positive gross lesions in the superficial and/or deep axillary lymph nodes. A dual-site infection model was established, involving simultaneous interdigital injection of 100 cfu of M. bovis into front and rear paws of 19 wild possums; this identified that the average degree of lymphadenitis involved 30-fold enlargement of the draining lymph node by 7-8 weeks post injection (wpi). A time-course study demonstrated establishment of M. bovis infection in peripheral lymph nodes of 9/11 possums at 3-5 wpi of doses ranging from 60 to 190 cfu, but with no development of gross lesions; by 7 weeks, 8/8 animals injected similarly had both an established infection and gross lesions of peripheral lymph nodes. The incidence and progression of peripheral lesion development, together with indications of sequential infection of the lungs, liver and mesenteric lymph nodes(MLNs), indicates that a low-dose percutaneous M. bovis infection model is likely to emulate natural disease in possums.
帚尾袋貂(Trichosurus vulpecula)是新西兰牛结核分枝杆菌(牛结核病的病原体)的主要野生动物宿主。野生袋貂牛结核病的初步诊断方法是触诊以检测外周淋巴结肿大,随后进行尸检,尸检常常能在周围淋巴结和肺部发现明显的结核病变。为了模拟野外牛结核病情况,对野生袋貂进行了实验性感染研究,重点是经皮将有毒力的牛分枝杆菌注射到爪子中。在一项初步研究中,经皮注射12天后,从引流前肢或后肢的淋巴结中回收了活的牛分枝杆菌杆菌。随后,给21只野生袋貂趾间注射500个牛分枝杆菌菌落形成单位(cfu),戴上无线电项圈后放生;8周后重新捕获的17/18只袋貂已确诊感染牛分枝杆菌,其中16只在浅表和/或深部腋窝淋巴结有培养阳性的明显病变。建立了双部位感染模型:将100 cfu的牛分枝杆菌同时注射到19只野生袋貂的前爪和后爪趾间;这表明到注射后7 - 8周(wpi),平均淋巴结炎程度使引流淋巴结肿大了30倍。一项时间进程研究表明,在3 - 5 wpi时,9/11只袋貂外周淋巴结感染了牛分枝杆菌,剂量范围为60至190 cfu,但未出现明显病变;到7周时,同样注射的8/8只动物既确诊感染,外周淋巴结也出现了明显病变。外周病变发展的发生率和进程,以及肺部、肝脏和肠系膜淋巴结(MLN)相继感染的迹象表明,低剂量经皮牛分枝杆菌感染模型可能模拟袋貂的自然疾病。