# Enhanced Biocontrol of Root-Knot Nematodes Through Co-Cultivation of Clonostachys rosea and Bacillus velezensis: Proline-Driven Bacterial Fitness and Synergistic Metabolite Production

**Authors:** Jie Zhang, Yajing Song, Manhong Sun, Jiangkuan Cui, Yuankai Chi, Mingcong Xia, Runhong Sun, Chao Wu, Qianqian Dong, Lirong Yang

PMC · DOI: 10.3390/jof12020158 · 2026-02-22

## TL;DR

Combining two microbes boosts control of root-knot nematodes by enhancing bacterial fitness and producing more effective compounds.

## Contribution

A co-culture of Clonostachys rosea and Bacillus velezensis is engineered to improve biocontrol through synergistic metabolite production and proline utilization.

## Key findings

- Co-culture achieved 95.3% nematode mortality and 78.0% increase in plant biomass.
- L-proline modulates bacterial fitness and biofilm formation in the co-culture.
- Synergistic accumulation of nematicidal and plant-growth-promoting metabolites enhances biocontrol efficacy.

## Abstract

The ascomycete fungus Clonostachys rosea is a promising biocontrol agent against root-knot nematodes. To develop a more effective and stable biocontrol strategy, we rationally constructed a co-culture system by partnering C. rosea with the plant growth-promoting bacterium Bacillus velezensis. Through systematic optimization of the medium and inoculation protocol, the co-culture demonstrated significantly enhanced performance, achieving 95.3% mortality of Meloidogyne incognita juveniles, a 78.0% increase in tomato shoot dry weight, and 69.2% disease control efficacy in pot trials. Metabolomic profiling indicated that the co-culture triggered a distinct metabolic profile compared to the respective monocultures. The enhanced efficacy was associated with the accumulation of two functional metabolite groups. First, the co-culture synergistically accumulated direct-effect compounds with reported nematicidal (e.g., daidzin, L-tryptophan) and plant-growth-promoting (e.g., isopentenyladenine, melatonin, and indole-3-propionic acid) activities. In parallel, L-proline emerged as a critical microbial interaction modulator. Targeted quantification showed a clear proline abundance gradient: highest in the C. rosea monoculture, intermediate in co-culture, and lowest in the B. velezensis monoculture. This gradient suggests that proline produced by C. rosea is likely utilized by B. velezensis, a finding further supported by the observation that proline enhanced bacterial biofilm formation and upregulated the matrix genes epsC and tasA. Accordingly, the co-culture itself formed significantly more robust biofilms. Thus, the enhanced biocontrol can be attributed to synergistic metabolite accumulation together with proline-mediated fitness gains in the bacterial partner, establishing a metabolic basis for rationally engineering microbial consortia.

## Linked entities

- **Chemicals:** L-proline (PubChem CID 145742), daidzin (PubChem CID 107971), L-tryptophan (PubChem CID 6305), isopentenyladenine (PubChem CID 92180), melatonin (PubChem CID 896), indole-3-propionic acid (PubChem CID 3744)
- **Species:** Clonostachys rosea (taxon 29856), Bacillus velezensis (taxon 492670), Meloidogyne incognita (taxon 6306)

## Full-text entities

- **Diseases:** M. incognita (MESH:C566367), fungal (MESH:D009181), cyst (MESH:D003560), Root-Knot Nematodes (MESH:D009349), injury to (MESH:D014947), Meloidogyne incognita (MESH:C000656845), root (MESH:D011843)
- **Chemicals:** cytokinin (MESH:D003583), lipopeptides (MESH:D055666), Daidzin (MESH:C013908), lipid (MESH:D008055), indole-3-acetic acid (MESH:C030737), L-tryptophan (MESH:D014364), peptaibols (MESH:D054848), short-chain fatty acids (MESH:D005232), auxin (MESH:D007210), glucose (MESH:D005947), Melatonin (MESH:D008550), crystal violet (MESH:D005840), ornithine (MESH:D009952), H2O2 (MESH:D006861), Medium 2 (-), verticillin (MESH:C009654), amino acid (MESH:D000596), MgSO4 (MESH:D008278), aspartate (MESH:D001224), arginine (MESH:D001120), pestalone (MESH:C442628), phenylalanine (MESH:D010649), alpha-linolenic acid (MESH:D017962), abamectin (MESH:C048324), LA (MESH:D007811), water (MESH:D014867), arachidonic acid (MESH:D016718), glutamate (MESH:D018698), acetic acid (MESH:D019342), isopentenyladenine (MESH:C001478), NaOH (MESH:D012972), ethanol (MESH:D000431), NaCl (MESH:D012965), gold (MESH:D006046), L-Proline (MESH:D011392), methanol (MESH:D000432), linoleic acid (MESH:D019787), fengycin (MESH:C049972), osmium tetroxide (MESH:D009993), fusaristatin A. (MESH:C522435), phosphate (MESH:D010710), glycerophospholipid (MESH:D020404), 3-indolepropionic acid (MESH:C095446), formic acid (MESH:C030544), wheat bran (MESH:D004043), nitrogen (MESH:D009584), alanine (MESH:D000409), agar (MESH:D000362), acetonitrile (MESH:C032159)
- **Species:** Solanum lycopersicum (tomato, species) [taxon 4081], Lacticaseibacillus casei (species) [taxon 1582], Homo sapiens (human, species) [taxon 9606], Streptomyces rapamycinicus (species) [taxon 1226757], Pestalotia sp. (species) [taxon 2026558], Arachis hypogaea (goober, species) [taxon 3818], Trichoderma asperellum (species) [taxon 101201], Aspergillus nidulans (species) [taxon 162425], Chiropterotriton sp. L (species) [taxon 269210], Clonostachys rosea (species) [taxon 29856], Meloidogyne incognita (southern root-knot nematode, species) [taxon 6306], Fusarium tricinctum (species) [taxon 61284], Glycine max (soybean, species) [taxon 3847], Bacillus subtilis (species) [taxon 1423], Bacillus amyloliquefaciens (species) [taxon 1390], Nematodes (genus) [taxon 333870]
- **Cell lines:** S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232)

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941432/full.md

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Source: https://tomesphere.com/paper/PMC12941432