Laboratory of Immunopathology and Infectious Agents - LIAI, UNIPEX - Experimental Research Unity, Sector 5, Medical School of Botucatu, São Paulo State University (UNESP), Botucatu, Brazil.
Confocal Microscopy Laboratory, UNIPEX - Experimental Research Unity, Medical School of Botucatu, São Paulo State University (UNESP), Botucatu, Brazil.
Front Cell Infect Microbiol. 2021 Feb 10;10:592022. doi: 10.3389/fcimb.2020.592022. eCollection 2020.
Paracoccidioidomycosis is a systemic fungal disease, considered endemic in Latin America. Its etiological agents, fungi of the complex, have restricted geographic habitat, conidia as infecting form, and thermo-dimorphic characteristics. Polymorphonuclear neutrophils (PMNs) are responsible for an important defense response against fungus, releasing Neutrophil Extracellular Traps (NETs), which can wrap and destroy the yeasts. However, it has been described that some pathogens are able to evade from these DNA structures by releasing DNase as an escape mechanism. As different NETs patterns have been identified in PMNs cultures challenged with different isolates of , the general objective of this study was to identify if different patterns of NETs released by human PMNs challenged with Pb18 (virulent) and Pb265 (avirulent) isolates would be correlated with fungal ability to produce a DNase-like protein. To this end, PMNs from healthy subjects were isolated and challenged with both fungal isolates. The production, release, and conformation of NETs in response to the fungi were evaluated by Confocal Microscopy, Scanning Microscopy, and NETs Quantification. The identification of fungal DNase production was assessed by DNase TEST Agar, and the relative gene expression for hypothetical proteins was investigated by RT-qPCR, whose genes had been identified in the fungal genome in the GenBank (PADG_11161 and PADG_08285). It was possible to verify the NETs release by PMNs, showing different NETs formation when in contact with different isolates of the fungus. The Pb18 isolate induced the release of looser, larger, and more looking like degraded NETs compared to the Pb265 isolate, which induced the release of denser and more compact NETs. DNase TEST Agar identified the production of a DNase-like protein, showing that only Pb18 showed the capacity to degrade DNA in these plates. Besides that, we were able to identify that both PADG_08528 and PADG_11161 genes were more expressed during interaction with neutrophil by the virulent isolate, being PADG_08528 highly expressed in these cultures, demonstrating that this gene could have a greater contribution to the production of the protein. Thus, we identified that the virulent isolate is inducing more scattered and loose NETs, probably by releasing a DNase-like protein. This factor could be an important escape mechanism used by the fungus to escape the NETs action.
球孢子菌病是一种系统性真菌病,被认为在拉丁美洲流行。其病原体是复合体中的真菌,具有有限的地理栖息地、分生孢子作为感染形式和热二态特征。多形核中性粒细胞(PMN)是对抗真菌的重要防御反应的责任人,释放中性粒细胞细胞外陷阱(NETs),可以包裹并破坏酵母。然而,已经描述了一些病原体能够通过释放 DNA 酶作为逃避机制来逃避这些 DNA 结构。由于在受到不同分离株挑战的 PMN 培养物中已经鉴定出不同的 NETs 模式,因此本研究的总体目标是确定受到 Pb18(毒力)和 Pb265(无毒性)分离株挑战的人 PMN 释放的不同 NETs 模式是否与真菌产生类似 DNA 酶的蛋白的能力相关。为此,从健康受试者中分离出 PMN 并与两种真菌分离株进行挑战。通过共聚焦显微镜、扫描显微镜和 NETs 定量评估真菌对 NETs 的产生、释放和构象。通过 DNase TEST 琼脂评估真菌 DNA 酶产生的鉴定,通过 RT-qPCR 研究假设蛋白的相对基因表达,其基因已在 GenBank 中鉴定为真菌基因组中的基因(PADG_11161 和 PADG_08285)。可以验证 PMN 释放的 NETs,显示出与不同真菌分离株接触时不同的 NETs 形成。与 Pb265 分离株相比,Pb18 分离株诱导释放更松散、更大且更像降解的 NETs,而 Pb265 分离株诱导释放更密集和更紧凑的 NETs。DNase TEST 琼脂鉴定出类似 DNA 酶的蛋白的产生,表明仅 Pb18 显示出在这些平板中降解 DNA 的能力。除此之外,我们能够确定,毒力分离株在与中性粒细胞相互作用时,PADG_08528 和 PADG_11161 基因均表达更高,在这些培养物中 PADG_08528 高度表达,表明该基因对蛋白的产生可能有更大的贡献。因此,我们确定毒力分离株诱导更分散和松散的 NETs,可能是通过释放类似 DNA 酶的蛋白。该因子可能是真菌逃避 NETs 作用的重要逃避机制。