# A Biofilm-State Bacillus thuringiensis Formulation Drives Midgut Structural Disruption and Transcriptomic Reprogramming in Ectropis grisescens

**Authors:** Yimeng Zhang, Hongzheng Hu, Wenhui Pan, Zixuan Wang, Yanqin Chen, Mengqi Qiu, Xueqin Luo, Qiuting Xu, Hongxin Su, Fuyong Lin, Tianpei Huang

PMC · DOI: 10.3390/microorganisms14020366 · Microorganisms · 2026-02-04

## TL;DR

A biofilm-state formulation of Bacillus thuringiensis increases insecticide effectiveness by causing gut damage and altering gene activity in a tea pest.

## Contribution

Demonstrates that biofilm-state Bt, combined with specific inducers, significantly enhances insecticidal efficacy and alters host gut responses.

## Key findings

- Biofilm-state Bt with composite inducers achieved 2.88-fold higher insecticidal efficacy than planktonic Bt.
- Biofilm-state Bt caused severe midgut damage and triggered detoxification and stress-response pathways in Ectropis grisescens.
- Findings suggest Bt physiological state is a key factor in formulation effectiveness.

## Abstract

Bacillus thuringiensis (Bt) is one of the most extensively used microbial insecticides, attributed to the action of insecticidal crystal proteins (ICPs), primarily Cry toxins, which mediate damage to the insect midgut epithelium. Recent evidence suggests that Bt toxicity is also strongly influenced by its physiological state and interactions with the host gut environment. Biofilm formation represents an important adaptive strategy that enhances bacterial stress tolerance and may modulate insecticidal performance, although the underlying mechanisms remain unclear. However, it is still unclear how Bt in the biofilm state alters host responses at the structural and transcriptomic levels. Using the tea plantation pest Ectropis grisescens as a model, we systematically evaluated the insecticidal efficacy of biofilm-state Bt formulations and their synergistic effects with a biofilm inducer system composed of Tween-80, tea saponin, matrine, and tea polyphenols. Bioassays showed that the biofilm-state Bt supplemented with composite inducers achieved the highest corrected mortality and reduced the LC50 against neonate larvae by 2.88-fold compared with conventional planktonic Bt. Histopathological, biochemical, and transcriptomic analyses further revealed that biofilm-state Bt caused more severe midgut damage and induced extensive remodeling of detoxification- and stress-response-related pathways. These findings highlight Bt physiological state as a critical determinant of formulation efficacy and provide a novel framework for Bt optimization through microbial physiological regulation.

## Linked entities

- **Chemicals:** Tween-80 (PubChem CID 443315), tea saponin (PubChem CID 163408272), matrine (PubChem CID 91466)
- **Species:** Ectropis grisescens (taxon 1530245), Bacillus thuringiensis (taxon 1428)

## Full-text entities

- **Diseases:** injury to (MESH:D014947), insulin resistance (MESH:D007333), cytotoxicity (MESH:D064420), infection (MESH:D007239), midgut damage (MESH:C562456), membrane damage (MESH:D015433)
- **Chemicals:** wax (MESH:D014885), nitrogen (MESH:D009584), polysaccharide (MESH:D011134), glycerophospholipid (MESH:D020404), cutin (MESH:C000521), Paraffin (MESH:D010232), metal (MESH:D008670), ethanol (MESH:D000431), isoamyl alcohol (MESH:C029683), TRIzol (MESH:C411644), iron (MESH:D007501), H2O. (MESH:D014867), peroxide (MESH:D010545), matrine (MESH:D000093842), hematoxylin (MESH:D006416), H&amp;E (MESH:D006371), sulfur (MESH:D013455), amino sugar (MESH:D000606), PBS (-), Poly(A) (MESH:D011061), ROS (MESH:D017382), beta-glucan (MESH:D047071), Tween-80 (MESH:D011136), eosin (MESH:D004801), agarose (MESH:D012685), Lipid (MESH:D008055), paraformaldehyde (MESH:C003043), chloroform (MESH:D002725), suberin (MESH:C065875), polyphenols (MESH:D059808)
- **Species:** Ectropis grisescens (species) [taxon 1530245], Bacillus sp. T (species) [taxon 1071724], Homo sapiens (human, species) [taxon 9606], Bacillus thuringiensis (species) [taxon 1428]
- **Mutations:** G033A
- **Cell lines:** BC — Homo sapiens (Human), Primary effusion lymphoma, Cancer cell line (CVCL_1079)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942972/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942972/full.md

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Source: https://tomesphere.com/paper/PMC12942972