Animal Health Department, Faculty of Veterinary Sciences, SALUVET, Complutense University of Madrid, Ciudad Universitaria s/n, Madrid, Spain.
Animal Medicine and Surgery Department, Faculty of Veterinary Sciences, Complutense University of Madrid, Ciudad Universitaria s/n, Madrid, Spain.
Transbound Emerg Dis. 2020 Jan;67(1):234-249. doi: 10.1111/tbed.13345. Epub 2019 Sep 18.
In this work, an experimental model for chronic besnoitiosis in bovine was developed and characterized. Using a previously established calf model, two new variables (parasite stage and inoculation route) were combined and used. Twelve Holstein Friesian 3-month-old male calves were randomly divided into four groups of three animals each. Bradyzoites were obtained from a chronically infected bull and used for inoculation via three different inoculation routes. Three groups were inoculated with 10 bradyzoites by intravenous (G1), subcutaneous (G2) and intradermal (G3) routes, and a non-infected control group (G4) was inoculated with PBS. The trial lasted for 90 days and included daily clinical monitoring as well as weekly skin biopsies and blood sampling. Sera were obtained to analyse both cellular and humoral responses. Once the calves were euthanized, tissues from the skin, eyes, respiratory and reproductive tracts, among others, were collected to study presence of the parasite. Clinically, the infection was classified as mild to moderate for the acute stage since all infected calves showed lymphadenopathy from four days post-infection (pi) and fever from one week pi until 24 days pi. However, the most relevant results were achieved during the chronic stage that was classified as moderate to severe. In fact, pathognomonic conjunctival cysts were observed in all infected calves from 40 days pi onwards and were more abundant in G3. Moreover, one calf from this group developed skin lesions (49 days pi). The microscopic tissue cysts and Besnoitia DNA were detected primarily in skin, reproductive tract and respiratory tissue samples, and parasite load was higher in G3. In conclusion, the parasite stage (bradyzoite) and the inoculation route are key factors that influence the outcome of an infection. In particular, the intradermal route led to more severe clinical signs of the chronic phase in the inoculated calves.
本研究建立并描述了一种慢性贝氏巴贝斯虫病的牛实验模型。使用先前建立的小牛模型,结合了两个新变量(寄生虫阶段和接种途径)。将 12 头 3 月龄荷斯坦弗里森雄性小牛随机分为 4 组,每组 3 头。缓殖子从慢性感染公牛中获得,通过三种不同的接种途径进行接种。三组小牛分别通过静脉(G1)、皮下(G2)和皮内(G3)途径接种 10 个缓殖子,非感染对照组(G4)接种 PBS。试验持续 90 天,包括每天临床监测以及每周皮肤活检和采血。采集血清以分析细胞和体液反应。小牛安乐死后,收集皮肤、眼睛、呼吸道和生殖器官等组织,研究寄生虫的存在。临床感染在急性阶段被分类为轻度至中度,因为所有感染的小牛在感染后 4 天(pi)出现淋巴结病,从 1 周 pi 开始发热,直到 24 天 pi。然而,在慢性阶段的结果更为显著,该阶段被分类为中度至重度。事实上,从 40 天 pi 开始,所有感染的小牛都出现了特征性的结膜囊肿,而在 G3 中更为丰富。此外,该组的一头小牛出现了皮肤损伤(49 天 pi)。在组织学上,主要在皮肤、生殖道和呼吸道组织样本中检测到微小的组织囊肿和贝氏巴贝斯虫 DNA,并且 G3 中的寄生虫载量更高。总之,寄生虫阶段(缓殖子)和接种途径是影响感染结果的关键因素。特别是,皮内途径导致接种小牛慢性期更严重的临床症状。