Sullivan D, Haynes K, Moran G, Shanley D, Coleman D
School of Dental Science, Department of Oral Medicine and Pathology, Trinity College, University of Dublin, Republic of Ireland.
J Clin Microbiol. 1996 Jul;34(7):1739-44. doi: 10.1128/JCM.34.7.1739-1744.1996.
Six separate human immunodeficiency virus-positive patients with cryptococcal meningitis were each found to have been infected with a unique strain of Cryptococcus neoformans on the basis of genomic DNA finger-printing analysis with the microsatellite sequence-containing oligonucleotide probe (GGAT)4 and by random amplification of polymorphic DNA. Two patients (A and B) experienced a recurrent episode of infection. Between 12 and 16 single-colony isolates recovered from primary isolation media (> 50% of C. neoformans colonies recovered) from cerebrospinal fluid specimens were fingerprinted from both patients during each episode. The fingerprints of both isolate collections from patient B were very similar, although minor polymorphisms were evident in both sets of profiles. The fingerprints of the isolate collection from the initial episode of infection in patient A were also identical to each other, apart from minor polymorphisms, but they were clearly different from the corresponding profiles of the isolate collection from the recurrent episode, the latter of which were completely identical, apart from minor polymorphisms in a single isolate. Furthermore, prolonged storage and in vitro subculture of the isolates did not alter the fingerprint profiles. These results provided convincing evidence that patients A and B were each infected with a single C. neoformans strain during each episode of infection and that in patient B, the same strain persisted and caused both episodes, while in patient A, a different strain was responsible for each episode. The prevalence of polymorphisms in multiple single-colony isolates from both patients also suggested that C. neoformans populations may undergo microevolution.
通过使用含微卫星序列的寡核苷酸探针(GGAT)4进行基因组DNA指纹分析以及随机扩增多态性DNA,在6例分别感染人类免疫缺陷病毒且患有隐球菌性脑膜炎的患者中,每例均发现感染了新型隐球菌的独特菌株。2例患者(A和B)经历了感染复发。在每次发作期间,从2例患者脑脊液标本的初次分离培养基(>50%的新型隐球菌菌落被回收)中回收的12至16个单菌落分离株进行了指纹分析。患者B的两组分离株指纹非常相似,尽管两组图谱中均有明显的微小多态性。患者A初次感染发作期分离株的指纹除微小多态性外彼此也相同,但与复发期分离株的相应图谱明显不同,后者除单个分离株有微小多态性外完全相同。此外,分离株的长期保存和体外传代培养并未改变指纹图谱。这些结果提供了令人信服的证据,表明患者A和B在每次感染发作期间均感染了单一的新型隐球菌菌株,并且在患者B中,同一菌株持续存在并导致了两次发作,而在患者A中,每次发作由不同菌株引起。来自两名患者的多个单菌落分离株中多态性的普遍性也表明新型隐球菌群体可能经历微观进化。