Comparative Identification of MicroRNAs in Apis cerana cerana Workers' Midguts in Response to Nosema ceranae Invasion
文献类型: 外文期刊
第一作者: Chen, Dafu
作者: Chen, Dafu;Du, Yu;Chen, Huazhi;Fan, Yuanchan;Fan, Xiaoxue;Zhu, Zhiwei;Wang, Jie;Xiong, Cuiling;Zheng, Yanzhen;Guo, Rui;Hou, Chunsheng;Diao, Qingyun
作者机构:
关键词: Apis cerana cerana; midgut; immune defense; Nosema ceranae; microRNA; target mRNA; regulatory network
期刊名称:INSECTS ( 影响因子:2.769; 五年影响因子:3.046 )
ISSN:
年卷期: 2019 年 10 卷 9 期
页码:
收录情况: SCI
摘要: Here, the expression profiles and differentially expressed miRNAs (DEmiRNAs) in the midguts of Apis cerana cerana workers at 7 d and 10 d post-inoculation (dpi) with N. ceranae were investigated via small RNA sequencing and bioinformatics. Five hundred and twenty nine (529) known miRNAs and 25 novel miRNAs were identified in this study, and the expression of 16 predicted miRNAs was confirmed by Stem-loop RT-PCR. A total of 14 DEmiRNAs were detected in the midgut at 7 dpi, including eight up-regulated and six down-regulated miRNAs, while 12 DEmiRNAs were observed in the midgut at 10 dpi, including nine up-regulated and three down-regulated ones. Additionally, five DEmiRNAs were shared, while nine and seven DEmiRNAs were specifically expressed in midguts at 7 dpi and 10 dpi. Gene ontology analysis suggested some DEmiRNAs and corresponding target mRNAs were involved in various functions including immune system processes and response to stimulus. KEGG pathway analysis shed light on the potential functions of some DEmiRNAs in regulating target mRNAs engaged in material and energy metabolisms, cellular immunity and the humoral immune system. Further investigation demonstrated a complex regulation network between DEmiRNAs and their target mRNAs, with miR-598-y, miR-252-y, miR-92-x and miR-3654-y at the center. Our results can facilitate future exploration of the regulatory roles of miRNAs in host responses to N. ceranae, and provide potential candidates for further investigation of the molecular mechanisms underlying eastern honeybee-microsporidian interactions.
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