Laboratório de Imunopatologia Keizo Asami, LIKA, Universidade Federal de Pernambuco, UFPE, Av. Morais Rêgo s/n, Campus Universitário, Recife, PE 50670-910, Brazil.
Mycopathologia. 2011 Jun;171(6):403-9. doi: 10.1007/s11046-011-9399-5. Epub 2011 Mar 2.
This work was based on the analysis of digital images of histochemical profile from subcutaneous lesions in sporotrichosis (ST) and chromoblastomycosis (CM) patients. An additional aim was the detection of carbohydrate expression using lectin histochemical analysis of the different carbohydrates in the fungal cell wall from four different species (Sporothrix schenckii, Fonsecaea pedrosoi, Phialophora verrucosa, and Cladophialophora carrionii) associated with diseases mentioned earlier. Slides from tissue biopsies from ST and CM positive patients (n=10, each) were stained according to routine techniques. Slides were incubated with 25 μg/ml of Con A lectins and WGA conjugated to peroxidase. Digital image analysis was carried out in a workstation using OPTIMAS™ software system. Routine histochemistry results indicated that there is significantly higher collagen deposition and elastic fibers in ST characteristic lesions compared with that found in CM cases. The ST interstitial fibrosis area was larger than in CM lesions. Comparative lectin binding showed a positive and intense lectin staining pattern in the cell wall of S. schenckii, suggesting a higher expression of glucose/mannose and N-acetyl glucosamine in their cell surface as evidenced by Con A and WGA, respectively. However, these lectins were not effective to recognize some carbohydrates moieties in the F. pedrosoi, P. verrucosa, and C. carrionii. Such findings contribute to additional information about specific recognition processes between fungal parasites and their host cell targets may be mediated by the interaction of carbohydrate-binding proteins, such as lectins, on the surface of one type of cell that combine with complementary sugars on the surface of another cells into fibro-connective tissues associated with lesions.
这项工作基于对孢子丝菌病 (ST) 和暗色丝孢霉病 (CM) 患者皮下病变的组织化学图像的分析。另一个目的是使用凝集素组织化学分析检测不同真菌细胞壁中的不同碳水化合物,以检测与上述疾病相关的四种不同物种(申克孢子丝菌、裴氏着色霉、疣状瓶霉和荚膜组织胞浆菌)中的碳水化合物表达。按照常规技术对来自 ST 和 CM 阳性患者(各 10 例)的组织活检切片进行染色。将切片与 25μg/ml 的 ConA 凝集素和与过氧化物酶偶联的 WGA 孵育。使用 OPTIMAS™软件系统在工作站上进行数字图像分析。常规组织化学结果表明,与 CM 病例相比,ST 特征性病变中的胶原蛋白沉积和弹性纤维明显更高。ST 间质纤维化面积大于 CM 病变。比较凝集素结合显示,S. schenckii 细胞壁中的凝集素染色呈阳性且强烈,表明其细胞表面的葡萄糖/甘露糖和 N-乙酰葡萄糖胺表达更高,分别由 ConA 和 WGA 证实。然而,这些凝集素不能有效识别 F. pedrosoi、P. verrucosa 和 C. carrionii 细胞壁中的一些碳水化合物部分。这些发现为真菌寄生虫与其宿主细胞靶标之间的特定识别过程提供了更多信息,这些识别过程可能是由细胞表面的碳水化合物结合蛋白(如凝集素)与另一种细胞表面的互补糖相互作用介导的,这些蛋白结合到与病变相关的纤维连接组织中。