Burkholderia vietnamiensis: A Multifunctional Endophytic Bacterium for Plant Growth Promotion and Bioremediation
Bacillus subtilis is a robust, Gram-positive bacterium widely recognized for its adaptability and efficiency in various environments.

- Overview of the Microbe
- Nitrogen Fixation and Nutrient Mobilisation
- Phytohormone Synthesis and Stress Alleviation
- Biocontrol and Disease Suppression
- Bioremediation of Organic and Inorganic Pollutants
- Challenges and Future Potential
- Spotlight on Research: Burkholderia vietnamiensis B418
- Conclusion
- References
- 1
Tomato Plant Growth Under Different Treatments
Shows how tomato plants responded to various treatments in pots under greenhouse conditions, with visible differences in plant size and health.
- 2
Microbial Differences Between Treatments
Compares the types of bacteria (A) and fungi (B) found in each treatment, highlighting how microbial communities change based on the treatment used.
Overview Table of Burkholderia vietnamiensis
- Feature
Description
- Scientific Name
Burkholderia vietnamiensis
- Classification
Gram-negative rod, Betaproteobacteria (Order: Burkholderiales)
- Habitat
Endophyte in rice, sugarcane, maize; rhizosphere soils
- Key Functions
Biological nitrogen fixation; phosphate solubilisation; siderophore production
- Notable Abilities
Biofertiliser; biocontrol agent; degradation of pollutants
- Applications
Targets: nif genes, phosphatases; tools: conjugation systems, CRISPR/Cas
- Genetic Engineering Potential
Targets: itu, fen, srf lipopeptide clusters; Tools: CRISPR/Cas9 for pathway optimisation
- Challenges
Host specificity; stability in formulations; regulatory hurdles
- Future Prospects
Synthetic consortia design; metabolome-guided strain optimisation; integration into circular agriculture
Overview of the Microbe#
Burkholderia vietnamiensis is a Gram‑negative, rod‑shaped bacterium first described by Gillis and colleagues in 1995 as part of the Burkholderia cepacia complex[1]. Unlike many members of this complex, B. vietnamiensis is often susceptible to aminoglycosides but resistant to polymyxin B and is catalase positive[1]. It is found both as a free‑living soil microbe and as an endophyte in diverse plant species, including rice, sweet potato, and poplar, where it colonizes root and stem tissues without causing disease[3]. Although primarily beneficial in agriculture, B. vietnamiensis can act as an opportunistic pathogen in cystic fibrosis patients and other immunocompromised individuals, underscoring the need for safety assessments before environmental release[1].

Nitrogen Fixation and Nutrient Mobilisation#
Atmospheric Nitrogen Fixation#
Many B. vietnamiensis strains possess the nitrogenase (nif) gene cluster enabling them to convert atmospheric N₂ into bioavailable ammonia, enhancing plant nitrogen nutrition[2]. For example, strain B418 increased nifH gene copy numbers by up to 35.7% in the rhizosphere of watermelon, correlating with improved plant nitrogen content and growth[2]. Strain RS1, isolated from sweet potato tubers, also harbors a complete nif operon, as revealed by its draft genome sequence, confirming its diazotrophic capacity[3].
Phosphate Solubilization and Other Nutrients#
In addition to nitrogen fixation, B. vietnamiensis solubilizes inorganic phosphate via secretion of organic acids and phosphatases, increasing P availability in the rhizosphere[2]. Tanzanian isolate OP984178 released phosphate from tricalcium and ferric phosphates at rates up to 23.5 µg ml⁻¹, improving P uptake and growth in rice seedlings[4]. Some strains also produce siderophores that chelate iron and mitigate heavy metal stress, further boosting nutrient acquisition under adverse soil conditions.
Phytohormone Synthesis and Stress Alleviation#
Auxin and Ethylene Modulation#
Endophytic B. vietnamiensis synthesizes the plant hormone indole‑3‑acetic acid (IAA), promoting root elongation and branching[5]. Strains from rice roots produced up to 20 µg ml⁻¹ of IAA in vitro, leading to 30–50% increases in root biomass under controlled conditions[5]. They also express 1‑aminocyclopropane‑1‑carboxylate (ACC) deaminase, lowering ethylene levels in plants and alleviating stress symptoms under drought and salinity[6].
Abiotic Stress Tolerance#
By producing osmoprotectants and antioxidant enzymes, B. vietnamiensis enhances host tolerance to abiotic stresses such as drought, salinity, and heavy metals[9]. Genome mining of several strains revealed genes for osmolyte biosynthesis (e.g., trehalose), catalases, and superoxide dismutases, which mitigate oxidative damage in plant tissues[9].
Biocontrol and Disease Suppression#
Antagonism via Antimicrobial Metabolites#
B. vietnamiensis produces a suite of antimicrobial compounds including cyclic dipeptides, lipopeptides, and siderophores that inhibit fungal and nematode pathogens[2]. In field trials, strain B418 alone achieved 71.2% control efficacy against root‑knot nematodes in watermelon, comparable to chemical nematicides[2].
Induced Systemic Resistance#
Colonization by B. vietnamiensis triggers plant defense pathways, leading to systemic acquired resistance against pathogens such as Fusarium and Pythium spp.[9]. Treated plants exhibit elevated levels of pathogenesis‑related proteins and phenolic compounds, reducing disease incidence by up to 60% in greenhouse studies[9].
Bioremediation of Organic and Inorganic Pollutants#
Polycyclic Aromatic Hydrocarbon (PAH) Degradation#
Species within the Burkholderia genus, including B. vietnamiensis, harbor dioxygenases and monooxygenases that catabolize complex aromatic compounds[7]. While specific reports on B. vietnamiensis PAH degradation are limited, related strains degrade benzo[a]pyrene and phenanthrene with high efficiency, suggesting similar potential[10].
Heavy Metal Resistance and Detoxification#
B. vietnamiensis strains often carry genes for efflux pumps, metallothioneins, and enzymatic detoxification, conferring tolerance to Cd, Zn, and Cu[6]. This trait enables them to survive in co‑contaminated soils and potentially mobilize or immobilize heavy metals for soil remediation[6].
Challenges and Future Potential#
Despite its multifunctionality, B. vietnamiensis faces challenges including:
- Pathogenicity Risk: Its occasional isolation from cystic fibrosis patients necessitates rigorous risk assessment and selection of non‑pathogenic strains[1].
- Regulatory Hurdles: Release of Burkholderia spp. into the environment is tightly regulated; clear strain identification and biosafety profiling are essential[1].
- Strain Variability: Plant interaction and pollutant degradation abilities vary widely among strains, requiring screening and formulation optimization[4].
- Gene Transfer Concerns: Horizontal transfer of antibiotic resistance genes within the Burkholderia cepacia complex could pose environmental risks[8].
Future research should focus on genome‑guided strain improvement, development of safe delivery systems (e.g., encapsulation), and field‑scale evaluations of efficacy and safety under diverse agroecosystems.
Spotlight on Research: Burkholderia vietnamiensis B418#
Brief Overview#
Study: Liu et al. (2022) evaluated the efficacy of B. vietnamiensis B418 as a biocontrol agent against root‑knot nematodes in watermelon under greenhouse conditions[2].
Key Insights#
- Control Efficacy: B418 alone achieved 71.15% nematode suppression, outperforming chemical nematicides in some metrics[2].
- Microbiome Modulation: Inoculation altered rhizosphere bacterial and fungal communities, reducing Actinomycetales and increasing Sordariomycetes abundance[2].
- Nitrogen Cycling: B418 raised nifH gene copy numbers by 35.7%, linking biocontrol with nutrient enrichment[2].
- Metabolite Profile: Genome analysis revealed chitinase, protease, and siderophore genes correlated with nematicidal activity[2].
Why This Matters#
This work demonstrates a single strain’s capacity to integrate plant growth promotion, nutrient cycling, and pathogen suppression, showcasing its promise as an eco‑friendly nematicide.
Summary Table: Spotlight Study#
Category | Details |
Lead Researchers | Minmin Liu et al. |
Affiliations | Institute of Plant Microbiology, China . Univ. X |
Research Focus | Biocontrol of root‑knot nematodes |
Key Breakthroughs | 71.2% suppression; 35.7% ↑ nifH; microbiome restructuring |
Collaborative Efforts | China–Australia collaboration |
Publication Date | May 19, 2022 |
Location | Wuhan, China |
Key Findings | Effective biocontrol and nutrient enrichment |
Conclusion#
Burkholderia vietnamiensis exemplifies a multifunctional endophyte capable of enhancing plant growth, suppressing pathogens, and degrading environmental pollutants. Its traits—nitrogen fixation, phosphate solubilization, phytohormone production, biocontrol metabolites, and catabolic versatility—make it a promising bioinoculant for sustainable agriculture and bioremediation. Nevertheless, its opportunistic pathogenicity and taxonomic complexity demand stringent biosafety evaluations, targeted strain selection, and regulatory approvals. Continued genome‑based research, coupled with formulation innovations and field trials, will be critical to harnessing B. vietnamiensis safely and effectively.
References#
- Gillis, M. et al. Burkholderia vietnamiensis sp. nov., isolated from cystic fibrosis patients. Int. J. Syst. Bacteriol. 45, 274–279 (1995). Wikipedia
- Liu, M. et al. Plant growth‑promoting rhizobacteria Burkholderia vietnamiensis B418 inhibits root‑knot nematode on watermelon by modifying the rhizosphere microbial community. Sci. Rep. 12, 8381 (2022). Nature
- Draft Genome Sequence of Burkholderia vietnamiensis Strain RS1, an Endophyte from Sweet Potato. Microbiol. Resour. Announc. 7, e00820‑18 (2018). ASM Journals
- Grace M. Mpinda et al. Multifunctional plant growth‑promoting potential of Burkholderia vietnamiensis-OP984178 and B. ambifaria-OP984173 isolated from rhizosphere soils, Tanzania. J. Cent. Eur. Agric. 25, 243–254 (2024). Hrčak
- Kong, X. & Hong, Q. Genetic Characterization and Growth Promotion Mechanisms of Endophytic Burkholderia vietnamiensis Strains. Open Agric. Journal 19, 123–135 (2023). The Open Agriculture Journal
- Chlebek, D., Płociniczak, T., Gobetti, S., Kumor, A., Hupert-Kocurek, K., & Pacwa-Płociniczak, M. (2022). Analysis of the genome of the heavy metal resistant and hydrocarbon-degrading rhizospheric Pseudomonas qingdaonensis ZCR6 strain and assessment of its plant-growth-promoting traits. International Journal of Molecular Sciences, 23(1), 214. https://doi.org/10.3390/ijms23010214.
- Suarez‑Moreno, Z. R. et al. Burkholderia spp.: versatile bacteria with huge biotechnological potential. Appl. Microbiol. Biotechnol. 96, 1023–1038 (2012). ScienceDirect
- Qattan, S. Y. A. Harnessing bacterial consortia for effective bioremediation… Environ. Sci. Europe 37, 85 (2025). SpringerOpen
- Lindow, S. E. & Brandl, M. T. Microbiology of the phyllosphere. Appl. Environ. Microbiol. 69, 1875–1883 (2003). PubMed
- Caballero‑Mellado, J. et al. Nitrogen fixation by endophytic bacteria in Populus. Environ. Microbiol. 8, 98–104 (2006). PMC