Lashnits Erin, Robveille Cynthia, Neupane Pradeep, Richardson Toni, Linder Keith, McKeon Gabriel, Maggi Ricardo, Breitschwerdt Edward B
School of Veterinary Medicine, University of Wisconsin-Madison, 2015 Linden Dr., Madison, WI 53706, USA.
Intracellular Pathogens Research Laboratory, Comparative Medicine Institute, College of Veterinary Medicine, North Carolina State University, 1051 William Moore Dr., Raleigh, NC 27607, USA.
Pathogens. 2025 Apr 26;14(5):421. doi: 10.3390/pathogens14050421.
is an important zoonotic pathogen with a wide range of clinical manifestations in humans. Despite advances in understanding its pathogenesis, there is no broadly applicable laboratory animal model for bartonellosis. This study aimed to assess the potential utility of an experimental model of chronic infection using ferrets, a species previously utilized in various human pathogen studies. Six ferrets (n = 6) were divided into three groups: a control group (n = 2), a low-dose infection group (n = 2), and a high-dose infection group (n = 2). The two infection groups were inoculated intradermally with 10 (low dose) and 10 (high dose) CFU/mL , respectively. Clinical signs, serological responses, and bacteriological findings were monitored over seven weeks; ferrets were then euthanized and tissues were examined histologically. Only minimal or transient systemic clinical signs and laboratory abnormalities developed in inoculated ferrets. The high-dose group seroconverted to antigen within two weeks, maintaining elevated titers throughout the study. Histopathological examination revealed that four -infected ferrets had notable microscopic inflammatory lesions in the liver parenchyma (3/4), heart (1/4), and brain (1/4); similar lesions were not observed in the tissues of the two control ferrets. Despite the presence of microscopic lesions and seroconversion in the high-dose group, bacteremia was not documented and DNA was not successfully amplified by quantitative PCR from lesional organs. This pilot study demonstrated that ferrets may serve as a promising model for investigating pathogenesis, diagnosis, treatment, and prevention.
是一种重要的人畜共患病原体,可在人类中引起广泛的临床表现。尽管在理解其发病机制方面取得了进展,但目前尚无广泛适用的巴尔通体病实验动物模型。本研究旨在评估使用雪貂建立慢性感染实验模型的潜在效用,雪貂是一种先前已用于各种人类病原体研究的物种。将六只雪貂(n = 6)分为三组:对照组(n = 2)、低剂量感染组(n = 2)和高剂量感染组(n = 2)。两个感染组分别皮内接种10(低剂量)和10(高剂量)CFU/mL。在七周内监测临床症状、血清学反应和细菌学结果;然后对雪貂实施安乐死并对组织进行组织学检查。接种的雪貂仅出现轻微或短暂的全身临床症状和实验室异常。高剂量组在两周内血清转化为抗原,在整个研究过程中滴度持续升高。组织病理学检查显示,四只感染雪貂的肝实质(3/4)、心脏(1/4)和脑(1/4)有明显的微观炎症病变;两只对照雪貂的组织中未观察到类似病变。尽管高剂量组存在微观病变和血清转化,但未记录到菌血症,且定量PCR未从病变器官成功扩增出巴尔通体DNA。这项初步研究表明,雪貂可能是研究巴尔通体病发病机制、诊断、治疗和预防的有前景的模型。