Laboratório de Imunopatologia Keizo Asami (LIKA), Universidade Federal de Pernambuco, Av. Moraes Rego, 1235 - Cidade Universitária, Recife, Pernambuco, 50670-901, Brazil.
Diretoria de Metrologia Aplicada às Ciências da Vida - DIMAV, Instituto Nacional de Metrologia, Qualidade e Tecnologia - INMETRO, Duque de Caxias, RJ, Brazil.
Parasitol Res. 2020 May;119(5):1607-1617. doi: 10.1007/s00436-020-06643-1. Epub 2020 Mar 4.
Milk from schistosomotic mothers can modulate the immune response of their offspring. However, its characterization and potential of modulating immunity has not yet been fully elucidated. Thus, the aim of this study was to evaluate whey proteins from the milk of Schistosoma mansoni-infected mice in order to identify the fractions which can act as potential immunomodulatory tools. For this, we did a mass spectrometry (nanoUPLC-MSE) analysis to characterize the proteomic profile of milk from infected (MIM) and non-infected mice (MNIM). It was possible to identify 29 differentially expressed proteins: 15 were only found in MIM, 10 only found in MNIM, and 4 were downregulated in MIM group. Gene Ontology (GO), pathway enrichment analysis, and protein-protein interaction (PPI) analyses indicated differentially expressed proteins linked to biological processes and pathways in MIM group such as the following: fructose 1,6-biphosphate metabolic and glycolytic processes, glucose metabolism, and neutrophil degranulation pathways. The downregulated and unique proteins identified in MNIM group were involved in the positive regulation of B cell activation and receptor signaling pathway, in the innate immune response, complement activation, and phagocytosis. The present findings revealed a protein profile that may be involved in the activation and deactivation of the offspring's immune system in the long term, conferring a protective character due to the previous contact with milk from infected mothers.
感染曼氏血吸虫的母亲的乳汁可以调节其后代的免疫反应。然而,其特征和潜在的免疫调节作用尚未完全阐明。因此,本研究旨在评估曼氏血吸虫感染小鼠乳汁中的乳清蛋白,以鉴定可作为潜在免疫调节工具的乳清蛋白。为此,我们进行了质谱(nanoUPLC-MSE)分析,以表征感染(MIM)和非感染(MNIM)小鼠乳汁的蛋白质组图谱。共鉴定出 29 种差异表达蛋白:15 种仅在 MIM 中发现,10 种仅在 MNIM 中发现,4 种在 MIM 组中下调。基因本体论(GO)、通路富集分析和蛋白质-蛋白质相互作用(PPI)分析表明,MIM 组中差异表达蛋白与以下生物学过程和途径相关:果糖 1,6-二磷酸代谢和糖酵解过程、葡萄糖代谢和嗜中性粒细胞脱颗粒途径。MNIM 组中下调和独特的蛋白参与 B 细胞激活和受体信号通路、固有免疫反应、补体激活和吞噬作用的正向调节。本研究结果揭示了一种蛋白质谱,可能参与长期以来后代免疫系统的激活和失活,由于与感染母亲的乳汁的早期接触而具有保护作用。