Baddley John W, Mostert Lizel, Summerbell Richard C, Moser Stephen A
Department of Medicine, Division of Infectious Disease, University of Alabama at Birmingham, Birmingham, AL 34294, USA.
J Clin Microbiol. 2006 Jun;44(6):2207-11. doi: 10.1128/JCM.00205-06.
Phaeoacremonium parasiticum is an agent of opportunistic phaeohyphomycosis belonging to a genus encompassing numerous recently described and soon-to-be-described, difficult-to-identify human pathogens. It appears in the literature to be an uncommon etiologic agent, yet we encountered several cases in a single year. Each presented problems in laboratory identification and case management. We present two cases of invasive disease with definite identification and susceptibility results. These cases are analyzed in relation to a brief review of previous cases known to have been caused by this species. Our first case involved a 40-year-old male cardiac transplant recipient with multiple localized skin lesions. The second featured a 31-year-old female with aplastic anemia and prolonged neutropenia who developed disseminated disease, with multiple positive blood cultures and skin lesions. Both patients died despite aggressive surgical and antifungal therapy. Fungal susceptibility testing showed that our isolates appeared to be susceptible to amphotericin B, itraconazole, voriconazole, ravuconazole, and posaconazole. Because phenotypic identification of Phaeoacremonium is notably problematic, sequence-based confirmation was performed using a recently proposed standard based on use of a segment of the 5' end of the beta-tubulin gene. Sequences from both isolates involved in the cases were over 99% similar to the corresponding sequence of the ex-type isolate of P. parasiticum. The close DNA similarity, corroborated by relevant morphological similarities (e.g., long, thin phialides and tuberculate hyphae bearing warts up to 3 mum high), confirms these two isolates as P. parasiticum.
寄生拟青霉是一种机会性暗色丝孢霉病的病原体,属于一个包含众多最近描述和即将描述的、难以鉴定的人类病原体的属。在文献中它似乎是一种不常见的病原体,但我们在一年内遇到了几例。每例在实验室鉴定和病例管理方面都存在问题。我们报告两例侵袭性疾病病例,有明确的鉴定结果和药敏结果。结合对先前已知由该物种引起的病例的简要回顾对这些病例进行分析。我们的首例病例是一名40岁男性心脏移植受者,有多处局部皮肤病变。第二例是一名31岁女性再生障碍性贫血患者,长期中性粒细胞减少,发生播散性疾病,多次血培养阳性并有皮肤病变。尽管进行了积极的手术和抗真菌治疗,两名患者均死亡。真菌药敏试验表明,我们分离的菌株似乎对两性霉素B、伊曲康唑、伏立康唑、雷夫康唑和泊沙康唑敏感。由于拟青霉的表型鉴定明显存在问题,因此使用最近提出的基于β-微管蛋白基因5'端片段的标准进行了基于序列的确认。病例中涉及的两个分离株的序列与寄生拟青霉模式菌株的相应序列相似度超过99%。密切的DNA相似性,再加上相关的形态学相似性(例如,长而细的瓶梗和有高达3μm高疣的瘤状菌丝)证实这两个分离株为寄生拟青霉。