Stenotrophomonas maltophilia virulence and specific variations in trace elements during acute lung infection: implications in cystic fibrosis
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Long Term Chronic Pseudomonas aeruginosa Airway Infection in Mice
Published on: March 17, 2014
Arianna Pompilio1, Domenico Ciavardelli2, Valentina Crocetta1
1Clinical Microbiology Unit, Center of Excellence on Aging, "G. d'Annunzio" University Foundation, Chieti, Italy ; Department of Experimental and Clinical Sciences, School of Medicine, "G. d'Annunzio" University, Chieti, Italy.
Abstract:
Metal ions are necessary for the proper functioning of the immune system, and, therefore, they might have a significant influence on the interaction between bacteria and host. Ionic dyshomeostasis has been recently observed also in cystic fibrosis (CF) patients, whose respiratory tract is frequently colonized by Stenotrophomonas maltophilia. For the first time, here we used an inductively mass spectrometry method to perform a spatial and temporal analysis of the pattern of changes in a broad range of major trace elements in response to pulmonary infection by S. maltophilia. To this, DBA/2 mouse lungs were comparatively infected by a CF strain and by an environmental one. Our results showed that pulmonary ionomic profile was significantly affected during infection. Infected mice showed increased lung levels of Mg, P, S, K, Zn, Se, and Rb. To the contrary, Mn, Fe, Co, and Cu levels resulted significantly decreased. Changes of element concentrations were correlated with pulmonary bacterial load and markers of inflammation, and occurred mostly on day 3 post-exposure, when severity of infection culminated. Interestingly, CF strain - significantly more virulent than the environmental one in our murine model - provoked a more significant impact in perturbing pulmonary metal homeostasis. Particularly, exposure to CF strain exclusively increased P and K levels, while decreased Fe and Mn ones. Overall, our data clearly indicate that S. maltophilia modulates pulmonary metal balance in a concerted and virulence-dependent manner highlighting the potential role of the element dyshomeostasis during the progression of S. maltophilia infection, probably exacerbating the harmful effects of the loss of CF transmembrane conductance regulator function. Further investigations are required to understand the biological significance of these alterations and to confirm they are specifically caused by S. maltophilia.
Insights
Stenotrophomonas maltophilia infection alters lung metal ion balance, with increased Mg, P, K, Zn, Se, Rb and decreased Mn, Fe, Co, Cu. A virulent cystic fibrosis strain caused more significant ion changes.
Area of Science:
- Immunology
- Microbiology
- Trace Element Research
Background:
- Metal ions are crucial for immune function and host-bacterial interactions.
- Ionic dyshomeostasis is observed in cystic fibrosis (CF) patients, often colonized by Stenotrophomonas maltophilia.
- Pulmonary infections can disrupt the delicate balance of essential trace elements.
Purpose of the Study:
- To analyze spatial and temporal changes in lung trace elements during S. maltophilia infection.
- To compare the impact of a CF strain versus an environmental strain on pulmonary ionomics.
- To investigate the relationship between element changes, bacterial load, and inflammation.
Main Methods:
- Inductively coupled plasma mass spectrometry (ICP-MS) for trace element analysis.
- Infection of DBA/2 mouse lungs with S. maltophilia (CF and environmental strains).
- Comparative analysis of ionomic profiles at different time points post-infection.
Main Results:
- S. maltophilia infection significantly altered lung ionomic profiles.
- Increased levels of Mg, P, S, K, Zn, Se, Rb and decreased levels of Mn, Fe, Co, Cu were observed.
- A more virulent CF strain induced greater perturbations in metal homeostasis, including exclusive increases in P and K, and decreases in Fe and Mn.
Conclusions:
- S. maltophilia modulates pulmonary metal balance in a virulence-dependent manner.
- Element dyshomeostasis may play a role in exacerbating CF lung disease.
- Further research is needed to elucidate the biological significance of these ion alterations.
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