ArticleScientific reports2025
The role of gut microbiota at different developmental stages in the adaptation of the Etiella zinckenella to a plant host.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Article
- Dietary effects on the development and population dynamics of the Thelazia callipaeda vector Phortica okadai revealed by age-stage, two-sex life table analysis.Parasites & vectors · 2026Article
- Insect Gut Microbiota as a Reservoir of Industrially Relevant Enzymes: A Comprehensive Review.Microbial ecology · 2026Review
- Evolution, multifunctionality, and agricultural potential of insect microbiomes and the holobiont concept.The ISME journal · 2026Review
- Diet chemistry and cross-kingdom microbiota associate with black soldier fly larvae performance on regional side streams.Animal microbiome · 2026Article
- Shredder identity matters: taxon-specific gut microbiota in aquatic shredders drives bacterial diversity during leaf breakdown in streams.ISME communications · 2026Article
- Influence of Host's Plant Diet on Gut Microbial Communities and Metabolic Potential inInsects · 2025Article
- Changes in the Microbiota of the Scale Insect (Biology · 2025Article
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6 authors.
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Abstract
Insect gut symbiotic microbiota play a crucial role in the nutritional, physiological, and behavioral aspects of their hosts, providing valuable insights for investigating the co-evolution of insects and plants. Sophora alopecuroides L. serves as an important windbreak plant, while Etiella zinckenella is a major pest that infests its seeds. However, the structure of the gut microbiota community in E. zinckenella remains poorly understood. In this study, we analyzed the gut microbiota of E. zinckenella across different developmental stages-larvae (1st-5th instars), pupae, and adults-infesting S. alopecuroides using 16 S rRNA high-throughput sequencing. The results revealed that the dominant phyla throughout the development of E. zinckenella were Proteobacteria and Bacteroidota, although the dominant genera varied significantly across stages. Diversity analysis of gut microbiota at different developmental stages indicated that microbial diversity was significantly higher in the larval stage compared to the pupal and adult stages. Functional predictions further highlighted the richness of metabolic pathways within the gut microbiota of E. zinckenella. Notably, carbohydrate metabolism functions were significantly more abundant during the larval stage, while lipid metabolism functions were substantially lower. Our findings demonstrate dynamic changes in the composition and diversity of the gut microbiota across the developmental stages of E. zinckenella, underscoring the critical roles of these bacteria during specific stages of the insect's life cycle. This study lays the groundwork for future strategies aimed at controlling E. zinckenella through modulation of its gut microbiota, offering significant theoretical implications.
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