Jain N, Wickes B L, Keller S M, Fu J, Casadevall A, Jain P, Ragan M A, Banerjee U, Fries B C
Department of Microbiology, All India Institute of Medical Sciences, New Delhi, India.
J Clin Microbiol. 2005 Nov;43(11):5733-42. doi: 10.1128/JCM.43.11.5733-5742.2005.
Little is known about the molecular epidemiology of the human pathogenic fungus Cryptococcus neoformans in India, a country now in the midst of an epidemic of AIDS-related cryptococcosis. We studied 57 clinical isolates from several regions in India, of which 51 were C. neoformans var. grubii, 1 was C. neoformans var. neoformans, and 5 were C. neoformans var. gattii. This strain set included 18 additional sequential isolates from 14 patients. Strains were characterized phenotypically by measuring the polysaccharide capsule and by determining the MICs of standard antifungals. Molecular typing was performed by a PCR-based method using the minisatellite-specific core sequence (M13), by electrophoretic karyotyping, by restriction fragment length polymorphisms with the C. neoformans transposon 1 (TCN-1), and by URA5 DNA sequence analysis. Overall, Indian isolates were less heterogeneous than isolates from other regions and included a subset that clustered into one group based on URA5 DNA sequence analysis. In summary, our results demonstrate (i) differences in genetic diversity of C. neoformans isolates from India compared to isolates from other regions in the world; (ii) that DNA typing with the TCN-1 probe can adequately distinguish C. neoformans var. grubii strains; (iii) that TCN-1 sequences are absent in many C. neoformans var. gattii strains, supporting previous studies indicating that these strains have a limited geographical dispersal; and (iv) that human cryptococcal infection can be associated with microevolution of the infecting strain and by simultaneous coinfection with two distinct C. neoformans strains.
在印度这个目前正处于艾滋病相关隐球菌病流行之中的国家,对于人类致病真菌新型隐球菌的分子流行病学了解甚少。我们研究了来自印度多个地区的57株临床分离株,其中51株为新型隐球菌格鲁比变种,1株为新型隐球菌新型变种,5株为新型隐球菌加蒂变种。这个菌株集还包括来自14名患者的另外18株连续分离株。通过测量多糖荚膜和测定标准抗真菌药物的最低抑菌浓度对菌株进行表型特征分析。通过使用小卫星特异性核心序列(M13)的基于聚合酶链反应的方法、电泳核型分析、利用新型隐球菌转座子1(TCN-1)的限制性片段长度多态性分析以及URA5 DNA序列分析进行分子分型。总体而言,印度分离株的异质性低于其他地区的分离株,并且根据URA5 DNA序列分析,其中有一部分聚为一组。总之,我们的结果表明:(i)与世界其他地区的分离株相比,印度新型隐球菌分离株的遗传多样性存在差异;(ii)用TCN-1探针进行DNA分型能够充分区分新型隐球菌格鲁比变种菌株;(iii)许多新型隐球菌加蒂变种菌株中不存在TCN-1序列,这支持了先前的研究,表明这些菌株的地理分布有限;(iv)人类隐球菌感染可能与感染菌株的微进化以及同时感染两种不同的新型隐球菌菌株有关。