Thanh Lam Tuan, Toffaletti Dena L, Tenor Jennifer L, Giamberardino Charles, Sempowski Gregory D, Asfaw Yohannes, Phan Hai Trieu, Van Duong Anh, Trinh Nguyen Mai, Thwaites Guy E, Ashton Philip M, Chau Nguyen Va Vinh, Baker Stephen G, Perfect John R, Day Jeremy N
Oxford University Clinical Research Unit, Wellcome Trust Asia Africa Programme, Ho Chi Minh City, Vietnam.
Division of Infectious Diseases, Department of Medicine and Department of Molecular Genetics and Microbiology, Duke University, North Carolina, USA.
Med Mycol. 2020 Nov 10;58(8):1149-1161. doi: 10.1093/mmy/myaa013.
We previously observed a substantial burden of cryptococcal meningitis in Vietnam atypically arising in individuals who are uninfected with human immunodeficiency virus (HIV). This disease was associated with a single genotype of Cryptococcus neoformans (sequence type [ST]5), which was significantly less common in HIV-infected individuals. Aiming to compare the phenotypic characteristics of ST5 and non-ST5 C. neoformans, we selected 30 representative Vietnamese isolates and compared their in vitro pathogenic potential and in vivo virulence. ST5 and non-ST5 organisms exhibited comparable characteristics with respect to in vitro virulence markers including melanin production, replication at 37°C, and growth in cerebrospinal fluid. However, the ST5 isolates had significantly increased variability in cellular and capsular sizing compared with non-ST5 organisms (P < .001). Counterintuitively, mice infected with ST5 isolates had significantly longer survival with lower fungal burdens at day 7 than non-ST5 isolates. Notably, ST5 isolates induced significantly greater initial inflammatory responses than non-ST5 strains, measured by TNF-α concentrations (P < .001). Despite being generally less virulent in the mouse model, we hypothesize that the significant within strain variation seen in ST5 isolates in the tested phenotypes may represent an evolutionary advantage enabling adaptation to novel niches including apparently immunocompetent human hosts.
我们之前观察到,越南的新型隐球菌性脑膜炎负担沉重,且非典型地发生在未感染人类免疫缺陷病毒(HIV)的个体中。这种疾病与新型隐球菌的单一基因型(序列型[ST]5)有关,该基因型在HIV感染个体中明显较少见。为了比较ST5和非ST5新型隐球菌的表型特征,我们选择了30株具有代表性的越南分离株,并比较了它们的体外致病潜力和体内毒力。ST5和非ST5菌株在体外毒力标志物方面表现出相当的特征,包括黑色素产生、在37°C下的复制以及在脑脊液中的生长。然而,与非ST5菌株相比,ST5分离株在细胞和荚膜大小方面的变异性显著增加(P <.001)。与直觉相反,感染ST5分离株的小鼠在第7天的存活时间明显更长,真菌负担更低。值得注意的是,通过TNF-α浓度测量,ST5分离株诱导的初始炎症反应明显大于非ST5菌株(P <.001)。尽管在小鼠模型中通常毒力较低,但我们推测,在测试表型中ST5分离株所见的显著菌株内变异可能代表一种进化优势,使其能够适应包括明显免疫功能正常的人类宿主在内的新生态位。