Turini Gonzales Marioto Denise, Navarro Dos Santos Ferraro Ana Carolina, Goulart de Andrade Fábio, Barros Oliveira Marília, Itano Eiko Nakagawa, Petrofeza Silvana, Venancio Emerson José
Postgraduate Program in Experimental Pathology, Department of Pathological Sciences - State University of Londrina, Londrina, PR, Brazil.
Department of Histology - State University of Londrina, Londrina, PR, Brazil.
Med Mycol. 2017 Oct 1;55(7):774-784. doi: 10.1093/mmy/myw135.
MicroRNAs (miRNAs) are small single stranded RNA sequences involved in post-transcriptional regulation of different biological and physiological processes. Paracoccidioidomycosis (PCM) is an infection caused by Paracoccidioides brasiliensis, and it is a major cause of mortality due to systemic mycoses in Brazil. To date, there have been few reports on the role of miRNAs in the immune response against fungi, especially PCM. The objective of this study was to evaluate the differential expression of miRNAs related to the inflammatory response associated with pulmonary infection by P. brasiliensis. For this purpose, lungs from BALB/c mice, intravenously infected with P. brasiliensis (2.7×107 yeast cells/ml, n = 12) and noninfected BALB/c mice (n = 8), were collected at the 28 and 56 day after infection. The lung parenchyma presented a great number of yeast cells, granulomas, and edema at 28 days and a framework of resolution of the inflammatory process after 56 days. The mRNAs gata-3, ror-γt, foxp3, and IL-6 were positively regulated at the moment at the 56 day, while the TGF-β1 mRNA was positively regulated at both moments. The miRNAs 126a-5p, 340-5p, 30b-5p, 19b-3p, 221-3p, 20a-5p, 130a-3p, and 301a-3p, 466k presented the greatest increase in expression levels 28 days after infection, and the miRNAs let-7f-5p, let-7a-5p, 5p-26b, let-7e-5p and 369-3p, 466k presented a greater increase in levels of expression 56 days after infection. This study shows a set of differentially expressed miRNAs possibly involved in the immune response in mice during pulmonary infection by P. brasiliensis.
微小RNA(miRNA)是参与不同生物和生理过程转录后调控的小单链RNA序列。副球孢子菌病(PCM)是由巴西副球孢子菌引起的一种感染,是巴西系统性真菌病导致死亡的主要原因。迄今为止,关于miRNA在抗真菌免疫反应,尤其是PCM免疫反应中的作用的报道很少。本研究的目的是评估与巴西副球孢子菌肺部感染相关的炎症反应相关的miRNA的差异表达。为此,在感染后第28天和第56天收集静脉注射巴西副球孢子菌(2.7×10⁷酵母细胞/ml,n = 12)的BALB/c小鼠和未感染的BALB/c小鼠(n = 8)的肺组织。肺实质在感染后28天出现大量酵母细胞、肉芽肿和水肿,56天后炎症过程开始消退。gata-3、ror-γt、foxp3和IL-6的mRNA在第56天时呈正调控,而TGF-β1 mRNA在两个时间点均呈正调控。miRNAs 126a-5p、340-5p、30b-5p、19b-3p、221-3p、20a-5p、130a-3p和301a-3p、466k在感染后28天表达水平增加最为显著,而miRNAs let-7f-5p、let-7a-5p、5p-26b、let-7e-5p和369-3p、466k在感染后56天表达水平增加更为显著。本研究显示了一组差异表达的miRNA,它们可能参与了巴西副球孢子菌肺部感染期间小鼠的免疫反应。