Department of Oral Biology, University of Florida College of Dentistry, Gainesville, Florida, United States of America.
Department of Pathology, Faculty of Veterinary Medicine, Mansoura University, Mansoura, Egypt.
PLoS Negl Trop Dis. 2023 Jan 19;17(1):e0011068. doi: 10.1371/journal.pntd.0011068. eCollection 2023 Jan.
Infection of the Central Nervous System (CNS) by the encapsulated fungus Cryptococcus neoformans can lead to high mortality meningitis, most commonly in immunocompromised patients. While the mechanisms by which the fungus crosses the blood-brain barrier to initiate infection in the CNS are well recognized, there are still substantial unanswered questions about the disease progression once the fungus is established in the brain. C. neoformans is characterized by a glucuronoxylomannan (GXM)-rich polysaccharide capsule which has been implicated in immune evasion, but its role during the host CNS infection needs further elucidation. Therefore, the present study aims to examine these key questions about the mechanisms underlying cryptococcal meningitis progression and the impact of fungal GXM release by using an intracerebral rodent infection model via stereotaxic surgery. After developing brain infection, we analyzed distinct brain regions and found that while fungal load and brain weight were comparable one-week post-infection, there were region-specific histopathological (with and without brain parenchyma involvement) and disease manifestations. Moreover, we also observed a region-specific correlation between GXM accumulation and glial cell recruitment. Furthermore, mortality was associated with the presence of subarachnoid hemorrhaging and GXM deposition in the meningeal blood vessels and meninges in all regions infected. Our results show that using the present infection model can facilitate clinical and neuropathological observations during the progression of neurocryptococcosis. Importantly, this mouse model can be used to further investigate disease progression as it develops in humans.
中枢神经系统(CNS)被包裹真菌新型隐球菌感染可导致高死亡率脑膜炎,最常见于免疫功能低下的患者。虽然真菌穿过血脑屏障在 CNS 中引发感染的机制已得到充分认识,但对于真菌在大脑中定植后疾病的进展仍存在大量未解决的问题。新型隐球菌的特征是富含葡聚糖(GXM)的多糖荚膜,该荚膜已被牵连到免疫逃避中,但它在宿主 CNS 感染中的作用需要进一步阐明。因此,本研究旨在通过立体定向手术的脑内啮齿动物感染模型来研究隐球菌性脑膜炎进展的这些关键问题以及真菌 GXM 释放的影响。在发展为脑部感染后,我们分析了不同的脑区,发现感染后一周时真菌负荷和脑重虽然相当,但存在特定区域的组织病理学(有无脑实质受累)和疾病表现。此外,我们还观察到 GXM 积累与神经胶质细胞募集之间存在特定区域的相关性。此外,死亡率与所有感染区域蛛网膜下腔出血和脑膜血管中 GXM 沉积有关。我们的研究结果表明,使用本感染模型可以促进神经隐球菌病进展期间的临床和神经病理学观察。重要的是,这种小鼠模型可用于进一步研究疾病的进展,因为它在人类中发展。