Burkholderia pseudomallei as an Enteric Pathogen: Identification of Virulence Factors Mediating Gastrointestinal Infection
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Updated: Dec 3, 2025

Total Protein Extraction and 2-D Gel Electrophoresis Methods for Burkholderia Species
Published on: October 15, 2013
Javier I Sanchez-Villamil1, Daniel Tapia1, Grace I Borlee2
1Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, USA.
Abstract:
Burkholderia pseudomallei is a Gram-negative bacterium and the causative agent of melioidosis. Despite advances in our understanding of the disease, B. pseudomallei poses a significant health risk, especially in regions of endemicity, where treatment requires prolonged antibiotic therapy. Even though the respiratory and percutaneous routes are well documented and considered the main ways to acquire the pathogen, the gastrointestinal tract is believed to be an underreported and underrecognized route of infection. In the present study, we describe the development of in vitro and in vivo models to study B. pseudomallei gastrointestinal infection. Further, we report that the type 6 secretion system (T6SS) and type 1 fimbriae are important virulence factors required for gastrointestinal infection. Using a human intestinal epithelial cell line and mouse primary intestinal epithelial cells (IECs), we demonstrated that B. pseudomallei adheres, invades, and forms multinucleated giant cells, ultimately leading to cell toxicity. We demonstrated that mannose-sensitive type 1 fimbria is involved in the initial adherence of B. pseudomallei to IECs, although the impact on full virulence was limited. Finally, we also showed that B. pseudomallei requires a functional T6SS for full virulence, bacterial dissemination, and lethality in mice infected by the intragastric route. Overall, we showed that B. pseudomallei is an enteric pathogen and that type 1 fimbria is important for B. pseudomallei intestinal adherence, and we identify a new role for T6SS as a key virulence factor in gastrointestinal infection. These studies highlight the importance of gastrointestinal melioidosis as an understudied route of infection and open a new avenue for the pathogenesis of B. pseudomallei.
Insights
Burkholderia pseudomallei causes melioidosis and can infect the gastrointestinal tract. This study shows type 1 fimbriae aid adherence, while the type 6 secretion system (T6SS) is crucial for virulence and lethality in gut infections.
Area of Science:
- Microbiology
- Infectious Diseases
- Pathogenesis
Background:
- Burkholderia pseudomallei is a Gram-negative bacterium causing melioidosis.
- Gastrointestinal infection by B. pseudomallei is underrecognized despite significant health risks.
- Established infection routes include respiratory and percutaneous, necessitating prolonged treatment.
Purpose of the Study:
- To develop in vitro and in vivo models for studying B. pseudomallei gastrointestinal infection.
- To investigate the roles of type 6 secretion system (T6SS) and type 1 fimbriae in gastrointestinal pathogenesis.
- To elucidate the mechanisms of B. pseudomallei interaction with intestinal epithelial cells.
Main Methods:
- Utilized human intestinal epithelial cell lines and primary mouse intestinal epithelial cells (IECs).
- Developed in vitro and in vivo models for intragastric infection.
- Employed genetic manipulation to study the function of T6SS and type 1 fimbriae.
Main Results:
- B. pseudomallei adheres to, invades, and causes toxicity in IECs, forming multinucleated giant cells.
- Mannose-sensitive type 1 fimbriae mediate initial bacterial adherence to IECs.
- A functional T6SS is essential for B. pseudomallei virulence, dissemination, and lethality in a mouse model of gastrointestinal infection.
Conclusions:
- B. pseudomallei acts as an enteric pathogen, with the gastrointestinal tract being a significant infection route.
- Type 1 fimbriae are important for intestinal adherence, and T6SS is a key virulence factor in gastrointestinal infections.
- Highlights the need for further research into gastrointestinal melioidosis and B. pseudomallei pathogenesis.
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