ArticleMicrobiome2025
Gut bacterium Acinetobacter sp. assists Camellia weevil with host plant adaptation by degrading tea saponin via the benzoate pathway.
Article in Microbiome, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Comparative Analysis of Gut Microbiota in Eri Silkworm (Insects · 2026Article
- Multi-omics integration reveals the link between gut microbiota dysbiosis, host metabolic dysregulation, and aortic inflammation in abdominal aortic aneurysm.BMC microbiology · 2026Article
- Aphid adaptation to plant secondary metabolites: adaptive mechanism of resistance evolution and future prospects.Horticulture research · 2026Article
- Correction: Gut bacterium Acinetobacter sp. assists Camellia weevil with host plant adaptation by degrading tea saponin via the benzoate pathway.Microbiome · 2025Article
Corrections and comments
- Erratum issued
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundThe extent to which herbivorous insects depend on gut bacteria and the molecular mechanisms by which these microbes help overcome host plant chemical defenses remain controversial. This study explored how the gut symbiont Acinetobacter sp. AS23 of a Camellia weevil (Curculio chinensis) (CW) enhances the weevil's tolerance to toxic tea saponins in host plants.
methodsWe first conducted toxicity assays in which third-instar CW larvae were exposed to fermentation filtrates containing tea saponin degradation products from the weevil's gut bacterium, the AS23 strain. A combination of metabolomic and transcriptomic analyses was used to investigate the degradation pathway and key genes used by the AS23 strain in tea saponin metabolism. We then re-inoculated axenic larvae with bacterial mutants generated through CRISPR-Cas9 and verified gene functions in tea saponin degradation.
resultsToxicity assays demonstrated that the AS23 strain exhibited time-dependent tea saponin degradation capabilities. The benzoate degradation pathway emerged as a core metabolic pathway enriched during tea saponin degradation, with the involvement of four key enzyme genes confirmed through qPCR and functional studies. Knockout strains exhibited a significantly reduced detoxification capacity and increased larval mortality when reintroduced into CWs' gut.
conclusionOur findings elucidated the key role of the AS23 strain in mediating CW larvae tolerance to tea saponins through the benzoate degradation pathway. This study highlights the potential of leveraging microbial saponin degradation pathways for developing environmentally friendly pest control strategies.
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