Positive Linkage in Bacterial Microbiota at the Plant-Insect Interface Benefits an Invasive Bark Beetle

IF 6.3 1区 生物学 Q1 PLANT SCIENCES Plant, Cell & Environment Pub Date : 2025-03-17 DOI:10.1111/pce.15470
Chihang Cheng, Fanghua Liu, Yi Wu, Peng Li, Wei Chen, Chenhao Wu, Jianghua Sun
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Abstract

Symbiotic microbes facilitate rapid adaptation of invasive insects on novel plants via multifaceted function provisions, but little was known on the importance of cross linkages in symbiotic microbiota to insect invasiveness. Novel host pine Pinus tabuliformis is inherently unsuitable for invasive red turpentine beetle (RTB) in China; however, Novosphingobium and Erwinia/Serratia in gallery microbiota (at the interface between RTB larvae and pine phloem) have been discovered to help beetles via biodegrading pine detrimental compounds naringenin and pinitol, respectively. Here, we further revealed significant positive linkage of the two functions, with higher activity level conferring more growth benefit to RTB larvae. Abundance of Erwinia/Serratia was remarkably increased in response to pinitol, while naringenin-biodegrading Novosphingobium was unable to utilize this main phloem carbohydrate directly. High-activity bacterial microbiota produced nutritive metabolites (sucrose and hexadecanoic acid) from pinitol consumption that facilitated growth of both Novosphingobium and beetle larvae. Functional proteins of several bacterial taxa were enriched in high-activity microbiota that appeared to form a metabolic network collectively to regulate the nutrient production. Our results indicate that positive interaction between Erwinia/Serratia and Novosphingobium is critical for RTB invasion success, while Bacilli bacteria might restrict this linkage, providing new insights into symbiotic microbial interactions for insect herbivores.

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植物-昆虫界面细菌微生物群的正连锁有利于入侵树皮甲虫。
共生微生物通过多方面的功能提供促进入侵昆虫对新型植物的快速适应,但对共生微生物群中交叉联系对昆虫入侵的重要性知之甚少。新寄主油松不适宜红松节油甲虫(RTB)入侵然而,在廊道微生物群(RTB幼虫和松树韧皮部之间的界面)中发现Novosphingobium和Erwinia/Serratia分别通过生物降解松树有害化合物柚皮素和pinitol来帮助甲虫。本研究进一步揭示了这两种功能之间存在显著的正相关关系,活性水平越高,RTB幼虫的生长效益越大。Erwinia/Serratia对pinitol的反应显著增加,而降解柚皮素的Novosphingobium不能直接利用这种主要的韧皮部碳水化合物。高活性细菌微生物群通过消耗松糖醇产生营养代谢物(蔗糖和棕榈酸),促进了新鞘藻和甲虫幼虫的生长。多种细菌分类群的功能蛋白富集于高活性微生物群中,这些微生物群似乎共同形成一个代谢网络来调节营养物质的产生。研究结果表明,Erwinia/Serratia和Novosphingobium之间的正相互作用是RTB入侵成功的关键,而芽孢杆菌可能限制这种联系,为昆虫食草动物的共生微生物相互作用提供了新的见解。
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来源期刊
Plant, Cell & Environment
Plant, Cell & Environment 生物-植物科学
CiteScore
13.30
自引率
4.10%
发文量
253
审稿时长
1.8 months
期刊介绍: Plant, Cell & Environment is a premier plant science journal, offering valuable insights into plant responses to their environment. Committed to publishing high-quality theoretical and experimental research, the journal covers a broad spectrum of factors, spanning from molecular to community levels. Researchers exploring various aspects of plant biology, physiology, and ecology contribute to the journal's comprehensive understanding of plant-environment interactions.
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