Li Yi-Hsuan, Chang Zih-Ting, Yen Ming-Ren, Huang Yu-Feng, Chen Tzu-Han, Chang Ju-Chun, Wu Ming-Cheng, Yang Yu-Liang, Chen Yue-Wen, Nai Yu-Shin
Department of Entomology, National Chung Hsing University, Taichung City 40227, Taiwan.
Department of Biotechnology and Animal Science, National Ilan University, Yi-Lan City 26047, Taiwan.
Insects. 2022 Aug 9;13(8):716. doi: 10.3390/insects13080716.
is one of the fungal parasites of . It causes physical and behavioral effects in honey bees. However, only a few studies have reported on gene expression profiling during infection. In this study, the transcriptome profile of mature spores at each time point of infection (5, 10, and 20 days post-infection, d.p.i.) were investigated. Based on the transcriptome and expression profile analysis, a total of 878, 952, and 981 differentially expressed genes (DEGs) (fold change ≥ 2 or ≤ -2) were identified in spores (NcSp) at 5 d.p.i., 10 d.p.i., and 20 d.p.i., respectively. Moreover, 70 upregulated genes and 340 downregulated genes among common DEGs (so-called common DEGs) and 166 stage-specific genes at each stage of infection were identified. The Gene Ontology (GO) analysis indicated that the DEGs and corresponding common DEGs are involved in the functions of cytosol (GO:0005829), cytoplasm (GO:0005737), and ATP binding (GO:0005524). Furthermore, the pathway analysis found that the DEGs and common DEGs are involved in metabolism, environmental information processing, and organismal systems. Four upregulated common DEGs with higher fold-change values, highly associated with spore proteins and transcription factors, were selected for validation. In addition, the stage-specific genes are highly involved in the mechanism of pre-mRNA splicing according to GO enrichment analysis; thus, three of them showed high expression at each d.p.i. and were also subjected to validation. The relative gene expression levels showed a similar tendency as the transcriptome predictions at different d.p.i., revealing that the gene expression of during infection may be related to the mechanism of gene transcription, protein synthesis, and structural proteins. Our data suggest that the gene expression profiling of at the transcriptomic level could be a reference for the monitoring of nosemosis at the genetic level.
是……的真菌寄生虫之一。它会对蜜蜂产生生理和行为影响。然而,仅有少数研究报道了感染期间的基因表达谱。在本研究中,对感染后每个时间点(感染后5、10和20天,d.p.i.)成熟孢子的转录组谱进行了研究。基于转录组和表达谱分析,分别在感染后5天、10天和20天的孢子(NcSp)中鉴定出总共878、952和981个差异表达基因(DEGs)(变化倍数≥2或≤ -2)。此外,在共同DEGs(所谓的共同DEGs)中鉴定出70个上调基因和340个下调基因,以及在感染各阶段的166个阶段特异性基因。基因本体论(GO)分析表明,DEGs和相应的共同DEGs参与了胞质溶胶(GO:0005829)、细胞质(GO:0005737)和ATP结合(GO:0005524)的功能。此外,通路分析发现DEGs和共同DEGs参与了代谢、环境信息处理和生物体系统。选择了四个上调倍数较高且与孢子蛋白和转录因子高度相关的共同DEGs进行验证。另外,根据GO富集分析,阶段特异性基因高度参与前体mRNA剪接机制;因此,其中三个在每个d.p.i.时均表现出高表达,也进行了验证。相对基因表达水平在不同d.p.i.时显示出与转录组预测相似的趋势,表明感染期间的基因表达可能与基因转录、蛋白质合成和结构蛋白的机制有关。我们的数据表明,在转录组水平上的基因表达谱可为在遗传水平上监测微孢子虫病提供参考。