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Following in Real Time the Impact of Pneumococcal Virulence Factors in an Acute Mouse Pneumonia Model Using Bioluminescent Bacteria
Published on: February 23, 2014
Virulence factors and mechanisms of paediatric pneumonia caused by Enterococcus faecalis
Zhiying Tian1, Asif Iqbal Khan1, Ata Ur Rehman1
1Laboratory of Biochemistry and Molecular Biology, Department of Biotechnology, College of Basic Medicine, Dalian Medical University, Dalian, China.
Insights
Pathogenic Enterococcus faecalis in the gut releases lipoteichoic acid (LTA), which triggers immune responses leading to paediatric pneumonia. This study identifies LTA as a key virulence factor in intestinal bacteria causing lung inflammation.
Area of Science:
- Microbiology
- Immunology
- Paediatric Medicine
Background:
- Paediatric pneumonia is a major cause of mortality in developing nations, often due to delayed pathogen identification.
- Understanding the causative agents and mechanisms of paediatric pneumonia is crucial for effective treatment.
Purpose of the Study:
- To investigate the in vivo mechanisms by which pathogenic Enterococcus faecalis induces pneumonia.
- To identify potential virulence factors of E. faecalis isolated from paediatric pneumonia patients.
Main Methods:
- Determined bacterial virulence factors from E. faecalis strains isolated from paediatric pneumonia patients.
- Investigated the role of lipoteichoic acid (LTA) in disrupting intestinal barrier function and activating immune cells in vivo.
Main Results:
- Lipoteichoic acid (LTA) from pathogenic E. faecalis reduces platelet-activating factor receptor (PAFR) expression, disrupting intestinal tight junctions and allowing LTA entry into circulation.
- LTA does not directly infiltrate the lungs but activates immune cells (CD8+ T cells, type 2 innate lymphocytes), leading to inflammation via Interleukin-6 and Interleukin-17.
Conclusions:
- Lipoteichoic acid (LTA) from intestinal pathogenic E. faecalis is a virulence factor that causes paediatric pneumonia.
- Intestinal bacterial virulence factors can induce systemic immune responses, contributing to lung inflammation and infectious diseases.
Abstract:
Paediatric pneumonia is a respiratory infection that affects infants and young children under the age of 3. This disease is the leading cause of infant and child mortality in developing countries because of the weak immune system of young children. The difficulty and length of time required to identify the pathogen and causative agent are the main reasons for this high mortality rate. In addition, the identification of certain causative agents is particularly important for the treatment of paediatric pneumonia. In this study, we explored the possible mechanisms by which pathogenic Enterococcus faecalis induced pneumonia in vivo. The potential virulence factors of bacteria isolated from the intestines of paediatric pneumonia patients were determined. Taken together, the results suggested that lysophosphatidic acid (LTA) from pathogenic E. faecalis decreases the expression of platelet-activating factor receptor (PAFR), which in turn disrupts the function of intestinal tight junctions (Occ and Ccldn1), leading to the entry of LE-LTA into the bloodstream because of the disruption of the intestinal barrier. Although LTA can enter circulation, it cannot directly infiltrate the lungs, which indicates that lung inflammation in mice is not caused by the direct entry of LE-LTA into the lungs. We further found that LTA activates immune cells, such as CD8 + T cells and type 2 innate lymphocytes, in vivo. Interleukin-6 and interleukin-17 can produce large amounts of inflammatory factors and thus promote the development of pneumonia. In conclusion, our findings demonstrate that the LTA of pathogenic E. faecalis in the intestine is a virulence factor that can cause paediatric pneumonia. This study found that intestinal bacterial virulence factors can induce immune responses in the lungs and blood. These findings could provide further insight into the mechanism of infectious diseases in the lung that are caused by bacteria in the intestine.
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