4.6 Article

Comprehensive investigation and regulatory function of lncRNAs engaged in western honey bee larval immune response to Ascosphaera apis invasion

期刊

FRONTIERS IN PHYSIOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphys.2022.1082522

关键词

honey bee; Apis mellifera ligustica; chalkbrood; Ascosphaera apis; ncRNA; lncRNA; ceRNA

资金

  1. The National Natural Science Foundation of China
  2. Earmarked Fund for China Agriculture Research System [31702190]
  3. Master Supervisor Team Fund of Fujian Agriculture and Forestry University [CARS-44-KXJ7]
  4. Natural Science Foundation of Fujian Province
  5. Scientific Research Project of College of Animal Sciences (College of Bee Science) of Fujian Agriculture and Forestry University [2022J01131334]
  6. Undergraduate Innovation and Entrepreneurship Training Program of Fujian province
  7. [202210389114]
  8. [202210389131]

向作者/读者索取更多资源

In this study, lncRNAs associated with the immune response of bee hosts to A. apis invasion were identified and analyzed. A complex regulatory network involving lncRNAs, miRNAs, and mRNAs was constructed. The findings provide candidate DElncRNAs for further functional studies and lay a foundation for understanding the mechanism underlying the immune response to A. apis invasion.
Ascosphaera apis is a fungal pathogen that exclusively infects bee larvae, causing chalkbrood disease, which results in severe damage for beekeeping industry. Long non-coding RNAs (lncRNAs) are versatile regulators in various biological processes such as immune defense and host-pathogen interaction. However, expression pattern and regulatory role of lncRNAs involved in immune response of bee host to A. apis invasion is still very limited. Here, the gut tissues of Apis mellifera ligustica 4-, 5-, and 6-day-old larvae inoculated by A. apis spores (AmT1, AmT2, and AmT3 groups) and corresponding un-inoculated larval guts (AmCK1, AmCK2, and AmCK3 groups) were prepared and subjected to deep sequencing, followed by identification of lncRNAs, analysis of differentially expressed lncRNAs (DElncRNAs), and investigation of competing endogenous RNA (ceRNA) network. In total, 3,746 A. m. ligustica lncRNAs were identified, including 78 sense lncRNAs, 891 antisense lncRNAs, 1,893 intergenic lncRNAs, 346 bidirectional lncRNAs, and 210 intronic lncRNAs. In the 4-, 5-, and 6- comparison groups, 357, 236, and 505 DElncRNAs were discovered. Additionally, 217, 129, and 272 DElncRNAs were respectively predicted to regulate neighboring genes via cis-acting manner, and these targets were associated with a series of GO terms and KEGG pathways of great importance, such as response to stimulus and Jak-STAT signaling pathway. Moreover, 197, 95, and 356 DElncRNAs were observed to target 10, eight, and 21 DEmiRNAs and further target 147, 79, and 315 DEmRNAs, forming complex regulatory networks. Further investigation suggested that these targets were engaged in several key cellular and humoral immune pathways, such as phagosome and MAPK signaling pathway. Ultimately, the expression trends of nine randomly selected DElncRNAs were verified by RT-qPCR, confirming the authenticity and reliability of our transcriptome data. Findings in this current work not only provide candidate DElncRNAs for functional study, but also lay a foundation for unclosing the mechanism underlying DElncRNA-regulated larval immune responses to A. apis invasion.

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