Comparative Transcriptome Investigation of Nosema ceranae Infecting Eastern Honey Bee Workers

is the original host for , a widespread fungal parasite resulting in honey bee nosemosis, which leads to severe losses to the apiculture industry throughout the world. However, knowledge of infecting eastern honey bees is extremely limited. Currently, the mechanism underlying infection is still larg...

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Veröffentlicht in:Insects (Basel, Switzerland) Switzerland), 2022-02, Vol.13 (3), p.241
Hauptverfasser: Fan, Yuanchan, Wang, Jie, Yu, Kejun, Zhang, Wende, Cai, Zongbing, Sun, Minghui, Hu, Ying, Zhao, Xiao, Xiong, Cuiling, Niu, Qingsheng, Chen, Dafu, Guo, Rui
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Sprache:eng
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Zusammenfassung:is the original host for , a widespread fungal parasite resulting in honey bee nosemosis, which leads to severe losses to the apiculture industry throughout the world. However, knowledge of infecting eastern honey bees is extremely limited. Currently, the mechanism underlying infection is still largely unknown. Based on our previously gained high-quality transcriptome datasets derived from spores (NcCK group), infecting workers at seven days post inoculation (dpi) and 10 dpi (NcT1 and NcT2 groups), comparative transcriptomic investigation was conducted in this work, with a focus on virulence factor-associated differentially expressed genes (DEGs). Microscopic observation showed that the midguts of workers were effectively infected after inoculation with clean spores of . In total, 1411, 604, and 38 DEGs were identified from NcCK vs. NcT1, NcCK vs. NcT2, and NcT1 vs. NcT2 comparison groups. Venn analysis showed that 10 upregulated genes and nine downregulated ones were shared by the aforementioned comparison groups. The GO category indicated that these DEGs were involved in a series of functional terms relevant to biological process, cellular component, and molecular function such as metabolic process, cell part, and catalytic activity. Additionally, KEGG pathway analysis suggested that the DEGs were engaged in an array of pathways of great importance such as metabolic pathway, glycolysis, and the biosynthesis of secondary metabolites. Furthermore, expression clustering analysis demonstrated that the majority of genes encoding virulence factors such as ricin B lectins and polar tube proteins displayed apparent upregulation, whereas a few virulence factor-associated genes such as hexokinase gene and 6-phosphofructokinase gene presented downregulation during the fungal infection. Finally, the expression trend of 14 DEGs was confirmed by RT-qPCR, validating the reliability of our transcriptome datasets. These results together demonstrated that an overall alteration of the transcriptome of occurred during the infection of workers, and most of the virulence factor-related genes were induced to activation to promote the fungal invasion. Our findings not only lay a foundation for clarifying the molecular mechanism underlying infection of eastern honey bee workers and microsporidian-host interaction.
ISSN:2075-4450
2075-4450
DOI:10.3390/insects13030241