Springer Deborah J, Billmyre R Blake, Filler Elan E, Voelz Kerstin, Pursall Rhiannon, Mieczkowski Piotr A, Larsen Robert A, Dietrich Fred S, May Robin C, Filler Scott G, Heitman Joseph
Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, United States of America.
David Geffen School of Medicine at UCLA, Division of Infectious Diseases, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Los Angeles, California, United States of America.
PLoS Pathog. 2014 Aug 21;10(8):e1004285. doi: 10.1371/journal.ppat.1004285. eCollection 2014 Aug.
Ongoing Cryptococcus gattii outbreaks in the Western United States and Canada illustrate the impact of environmental reservoirs and both clonal and recombining propagation in driving emergence and expansion of microbial pathogens. C. gattii comprises four distinct molecular types: VGI, VGII, VGIII, and VGIV, with no evidence of nuclear genetic exchange, indicating these represent distinct species. C. gattii VGII isolates are causing the Pacific Northwest outbreak, whereas VGIII isolates frequently infect HIV/AIDS patients in Southern California. VGI, VGII, and VGIII have been isolated from patients and animals in the Western US, suggesting these molecular types occur in the environment. However, only two environmental isolates of C. gattii have ever been reported from California: CBS7750 (VGII) and WM161 (VGIII). The incongruence of frequent clinical presence and uncommon environmental isolation suggests an unknown C. gattii reservoir in California. Here we report frequent isolation of C. gattii VGIII MATα and MATa isolates and infrequent isolation of VGI MATα from environmental sources in Southern California. VGIII isolates were obtained from soil debris associated with tree species not previously reported as hosts from sites near residences of infected patients. These isolates are fertile under laboratory conditions, produce abundant spores, and are part of both locally and more distantly recombining populations. MLST and whole genome sequence analysis provide compelling evidence that these environmental isolates are the source of human infections. Isolates displayed wide-ranging virulence in macrophage and animal models. When clinical and environmental isolates with indistinguishable MLST profiles were compared, environmental isolates were less virulent. Taken together, our studies reveal an environmental source and risk of C. gattii to HIV/AIDS patients with implications for the >1,000,000 cryptococcal infections occurring annually for which the causative isolate is rarely assigned species status. Thus, the C. gattii global health burden could be more substantial than currently appreciated.
美国西部和加拿大持续爆发的加氏隐球菌疫情,说明了环境宿主以及克隆和重组繁殖在推动微生物病原体出现和传播方面的影响。加氏隐球菌包括四种不同的分子类型:VGI、VGII、VGIII和VGIV,没有核基因交换的证据,表明它们代表不同的物种。加氏隐球菌VGII分离株引发了太平洋西北地区的疫情,而VGIII分离株经常感染南加州的艾滋病毒/艾滋病患者。VGI、VGII和VGIII已在美国西部的患者和动物中分离出来,表明这些分子类型存在于环境中。然而,加利福尼亚州仅报告过两例加氏隐球菌环境分离株:CBS7750(VGII)和WM161(VGIII)。临床中频繁出现与环境中罕见分离的不一致表明,加利福尼亚州存在未知的加氏隐球菌宿主。在此,我们报告在南加州的环境来源中频繁分离出加氏隐球菌VGIII MATα和MATa分离株,以及偶尔分离出VGI MATα。VGIII分离株是从与树木物种相关的土壤碎片中获得的,这些树木物种以前未被报告为感染患者住所附近地点的宿主。这些分离株在实验室条件下可育,产生大量孢子,并且是本地和更远处重组群体的一部分。多位点序列分型(MLST)和全基因组序列分析提供了令人信服的证据,表明这些环境分离株是人类感染的来源。分离株在巨噬细胞和动物模型中表现出广泛的毒力。当比较具有难以区分的MLST谱型的临床和环境分离株时,环境分离株的毒力较低。综上所述,我们的研究揭示了加氏隐球菌的环境来源及其对艾滋病毒/艾滋病患者的风险,这对每年发生的超过100万例隐球菌感染具有重要意义,而这些感染的致病分离株很少被确定物种状态。因此,加氏隐球菌对全球健康的负担可能比目前所认识到的更为严重。