International Journal of Molecular Sciences (Jan 2023)

ame-miR-34 Modulates the Larval Body Weight and Immune Response of <i>Apis mellifera</i> Workers to <i>Ascosphara apis</i> Invasion

  • Ying Wu,
  • Yilong Guo,
  • Xiaoxue Fan,
  • Haodong Zhao,
  • Yiqiong Zhang,
  • Sijia Guo,
  • Xin Jing,
  • Zhitan Liu,
  • Peilin Feng,
  • Xiaoyu Liu,
  • Peiyuan Zou,
  • Qiming Li,
  • Zhihao Na,
  • Kuihao Zhang,
  • Dafu Chen,
  • Rui Guo

DOI
https://doi.org/10.3390/ijms24021214
Journal volume & issue
Vol. 24, no. 2
p. 1214

Abstract

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MiRNAs are critical regulators of numerous physiological and pathological processes. Ascosphaera apis exclusively infects bee larvae and causes chalkbrood disease. However, the function and mechanism of miRNAs in the bee larval response to A. apis infection is poorly understood. Here, ame-miR-34, a previously predicted miRNA involved in the response of Apis mellifera larvae to A. apis invasion, was subjected to molecular validation, and overexpression and knockdown were then conducted to explore the regulatory functions of ame-miR-34 in larval body weight and immune response. Stem-loop RT-PCR and Sanger sequencing confirmed the authenticity of ame-miR-34 in the larval gut of A. mellifera. RT-qPCR results demonstrated that compared with that in the uninfected larval guts, the expression level of ame-miR-34 was significantly downregulated (p A. apis-infected 4-, 5-, and 6-day-old larvae, indicative of the remarkable suppression of host ame-miR-34 due to A. apis infection. In comparison with the corresponding negative control (NC) groups, the expression level of ame-miR-34 in the larval guts in the mimic-miR-34 group was significantly upregulated (p p hsp and abct in the guts of A. apis-infected 4-, 5-, and 6-day-old larvae were significantly upregulated after ame-miR-34 overexpression. In contrast, after ame-miR-34 knockdown, the expression levels of the aforementioned two key genes in the A. apis-infected 4-, 5-, and 6-day-old larval guts were significantly downregulated. Together, the results demonstrated that effective overexpression and knockdown of ame-miR-34 in both noninfected and A. apis-infected A. mellifera larval guts could be achieved by the feeding method, and ame-miR-34 exerted a regulatory function in the host immune response to A. apis invasion through positive regulation of the expression of hsp and abct. Our findings not only provide a valuable reference for the functional investigation of bee larval miRNAs but also reveal the regulatory role of ame-miR-34 in A. mellifera larval weight and immune response. Additionally, the results of this study may provide a promising molecular target for the treatment of chalkbrood disease.

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