Centro de Diagnóstico e Pesquisa em Biologia Molecular Dr Ivo Ricci, São Carlos, SP, Brazil.
Departamento de Patologia, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Mycopathologia. 2022 Jun;187(2-3):157-168. doi: 10.1007/s11046-021-00608-3. Epub 2021 Dec 6.
Paracoccidioidomycosis (PCM) is a systemic mycosis caused by a group of cryptic species embedded in the Paracoccidioides brasiliensis complex and Paracoccidioides lutzii. Four species were recently inferred to belong to the P. brasiliensis complex, but the high genetic diversity found in both human and environmental samples have suggested that the number of lineages may be higher. This study aimed to assess the 43-kilodalton glycoprotein genotypes (PbGP43) in paraffin-embedded samples from PCM patients to infer the phylogenetic lineages of the P. brasiliensis complex responsible for causing the infection. Formalin-fixed, paraffin-embedded (FFPE) tissue samples from patients with histopathological diagnosis of PCM were analyzed. DNAs were extracted and amplified for a region of the second exon of the PbGP43 gene. Products were sequenced and aligned with other PbGP43 sequences available. A haplotype network and the phylogenetic relationships among sequences were inferred. Amino acid substitutions were investigated regarding the potential to modify physicochemical properties in the proteins. Six phylogenetic lineages were identified as belonging to the P. brasiliensis complex. Two lineages did not group with any of the four recognized species of the complex, and, interestingly, one of them comprised only FFPE samples. A coinfection involving two lineages was found. Five parsimony-informative sites were identified and three of them showed radical non-synonymous substitutions with the potential to promote changes in the protein. This study expands the knowledge regarding the genetic diversity existing in the P. brasiliensis complex and shows the potential of FFPE samples in species identification and in detecting coinfections.
球孢子菌病(PCM)是一种系统性真菌病,由一组隐型种引起,这些种嵌入到巴西副球孢子菌复合体和路氏副球孢子菌中。最近推断出有四个种属于巴西副球孢子菌复合体,但在人和环境样本中发现的高度遗传多样性表明,谱系的数量可能更高。本研究旨在评估石蜡包埋 PCM 患者样本中的 43 千道尔顿糖蛋白基因型(PbGP43),以推断引起感染的巴西副球孢子菌复合体的系统发育谱系。对具有 PCM 组织病理学诊断的患者的福尔马林固定、石蜡包埋(FFPE)组织样本进行了分析。提取和扩增 PbGP43 基因第二外显子的一个区域的 DNA。对产物进行测序,并与其他可用的 PbGP43 序列进行比对。推断了单倍型网络和序列之间的系统发育关系。研究了氨基酸取代与蛋白质理化性质改变的潜在关系。确定了六个属于巴西副球孢子菌复合体的系统发育谱系。有两个谱系与该复合体的四个公认种都没有分组,而且有趣的是,其中一个仅由 FFPE 样本组成。发现了涉及两个谱系的合并感染。确定了五个简约信息位点,其中三个具有潜在的激进非同义取代,可能导致蛋白质发生变化。本研究扩展了关于巴西副球孢子菌复合体中存在遗传多样性的知识,并显示了 FFPE 样本在物种鉴定和检测合并感染方面的潜力。