Brownlee Rachel D, Imai Denise M, Coleman Denver J, Ardeshir Amir, Abdelrazek Samah M R, Soto Esteban
Comp Med. 2019 Aug 1;69(4):270-275. doi: 10.30802/AALAS-CM-18-000151. Epub 2019 Aug 6.
is a ubiquitous, dematiaceous mold capable of causing cutaneous and subcutaneous lesions in humans. In the last decade, has been associated with emergent systemic fungal infections in aquatic animals, including cultured sturgeon ( spp.), captive amphibians, and wild reptiles. Recently, repetitive extragenic palindromic PCR (rep-PCR) fingerprinting has demonstrated intraspecific variability among isolates from different clinically affected hosts and geographic regions. However, little is known regarding the pathogenic potential of the different genetic clades, and no mammalian model currently exists to investigate phaeohyphomycosis. In this study, we inoculated immunocompetent heterozygotic () and immunodeficient homozygotic () Hsd:Athymic Nude-Fox1 mice subcutaneously or through orogastric gavage with 1 of 3 representative strains that had been recovered from white sturgeon (), green sea turtle (), and human hosts and typed by using rep-PCR analysis. Daily mortality and morbidity were recorded, and dissemination of the fungus was investigated through culture of splenic samples and histologic analysis of the injection site, regional lymph nodes, salivary gland, spleen, liver, mesenteric lymph node, and gastrointestinal tract. No differences in survival, fungal burden, or dissemination were observed between fungal strains, routes of inoculation, or host immune status. Fungal infection was observed after subcutaneous inoculation only, was localized to the inoculation site, and was identified in both and mice. Fungal strain variability was not associated with virulence in a murine model of infection, and this novel mouse model of phaeohyphomycosis recapitulates the human clinical condition.
是一种普遍存在的暗色霉菌,能够在人类中引起皮肤和皮下病变。在过去十年中,已与水生动物中出现的系统性真菌感染有关,包括养殖的鲟鱼( 属)、圈养的两栖动物和野生爬行动物。最近,重复基因外回文PCR(rep-PCR)指纹图谱显示,来自不同临床感染宿主和地理区域的 分离株存在种内变异性。然而,关于不同遗传分支的致病潜力知之甚少,目前尚无哺乳动物模型来研究 暗色丝孢霉病。在本研究中,我们将具有免疫能力的杂合子( )和免疫缺陷的纯合子( )Hsd:Athymic Nude-Fox1小鼠通过皮下注射或经口灌胃接种从白鲟( )、绿海龟( )和人类宿主中分离出的3种代表性 菌株之一,并通过rep-PCR分析进行分型。记录每日死亡率和发病率,并通过脾样本培养以及对注射部位、区域淋巴结、唾液腺、脾脏、肝脏、肠系膜淋巴结和胃肠道进行组织学分析来研究真菌的传播情况。在真菌菌株、接种途径或宿主免疫状态之间未观察到生存、真菌负荷或传播方面的差异。仅在皮下接种后观察到真菌感染,局限于接种部位,并且在 和 小鼠中均被识别。在小鼠感染模型中,真菌菌株变异性与毒力无关,并且这种新型的 暗色丝孢霉病小鼠模型概括了人类临床情况。