Fries B C, Casadevall A
Department of Medicine, Division of Infectious Disease, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
J Infect Dis. 1998 Dec;178(6):1761-6. doi: 10.1086/314521.
Serial isolates of Cryptococcus neoformans from patients with chronic infection can exhibit minor karyotype changes as a result of chromosome length polymorphism (CLP). This study investigated whether serial C. neoformans isolates with CLP from 4 patients with AIDS exhibited biologic and phenotypic differences. CLP permits the identification of serial isolates in murine mixed infection. The parameters studied were virulence in mice, capsule size, colony morphology, melanization, protease production, MICs of antifungal drugs, and growth rates in vitro. Two parameters of virulence in mice were studied: persistence in tissue and survival time after lethal infection. Serial C. neoformans isolates were shown to differ in ability to persist in vivo, virulence in a murine infection model, in vitro growth rates at 37 degreesC, and capsule size. Melanin and protease production and MICs of antifungal drugs were comparable for serial isolates. These observations suggest microevolution of C. neoformans during human infection. This process may allow the fungal population to change, escape eradication by the immune system, and thus cause chronic infections.
慢性感染患者的新型隐球菌系列分离株可能会因染色体长度多态性(CLP)而出现微小的核型变化。本研究调查了来自4名艾滋病患者的具有CLP的新型隐球菌系列分离株是否表现出生物学和表型差异。CLP有助于在小鼠混合感染中鉴定系列分离株。所研究的参数包括对小鼠的毒力、荚膜大小、菌落形态、黑色素生成、蛋白酶产生、抗真菌药物的最低抑菌浓度(MIC)以及体外生长速率。研究了对小鼠毒力的两个参数:在组织中的持久性和致死感染后的存活时间。结果显示,新型隐球菌系列分离株在体内的持久性能力、在小鼠感染模型中的毒力、37℃时的体外生长速率以及荚膜大小方面存在差异。系列分离株的黑色素和蛋白酶产生以及抗真菌药物的MIC相当。这些观察结果表明新型隐球菌在人类感染过程中发生了微进化。这一过程可能使真菌群体发生变化,逃避免疫系统的清除,从而导致慢性感染。