Light regulation in critical human pathogens of clinical relevance such as Acinetobacter baumannii, Staphylococcus aureus and Pseudomonas aeruginosa
- PMID: 37269546
- DOI: 10.1007/s43630-023-00437-x
Light regulation in critical human pathogens of clinical relevance such as Acinetobacter baumannii, Staphylococcus aureus and Pseudomonas aeruginosa
Abstract
It is now clearly recognized that light modulates the physiology of many bacterial chemotrophs, either directly or indirectly. An interesting case are bacterial pathogens of clinical relevance. This work summarizes, discusses, and provides novel complementary information to what is currently known about light sensing and responses in critical human pathogens such as Acinetobacter baumannii, Pseudomonas aeruginosa and Staphylococcus aureus. These pathogens are associated with severe hospital and community infections difficult to treat due to resistance to multiple drugs. Moreover, light responses in Brucella abortus, an important animal and human pathogen, are also compiled. Evidence recovered so far indicates that light modulates aspects related to pathogenesis, persistence, and antibiotic susceptibility in these pathogens; such as motility, biofilm formation, iron uptake, tolerance to antibiotics, hemolysis and virulence. The pathogens elicit differential responses to light depending likely on their pathophysiology, ability to cause disease and characteristics of the host. The response to light is not restricted to discrete physiological traits but is global. In higher organisms, light provides spatial and temporal information. Then, it is crucial to understand what information light is providing in these bacterial pathogens. Our current hypothesis postulates that light serves as a signal that allows these pathogens to synchronize their behavior to the circadian rhythm of the host, to optimize infection. Advances on the molecular mechanism of light signal transduction and physiological responses to light, as well as in the relation between light and bacterial infection, would not only enlarge our understanding of bacterial pathogenesis but also could potentially provide alternative treatment options for infectious illnesses.
© 2023. The Author(s), under exclusive licence to European Photochemistry Association, European Society for Photobiology.
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References
-
- Tuttobene, M. R., Perez, J. F., Pavesi, E. S., Perez Mora, B., Biancotti, D., Cribb, P., et al. (2021). Light modulates important pathogenic determinants and virulence in ESKAPE pathogens Acinetobacter baumannii, Pseudomonas aeruginosa, and Staphylococcus aureus. Journal of Bacteriology., 203, 5. https://doi.org/10.1128/JB.00566-20 - DOI
-
- Mussi, M. A., Gaddy, J. A., Cabruja, M., Arivett, B. A., Viale, A. M., Rasia, R., et al. (2010). The opportunistic human pathogen Acinetobacter baumannii senses and responds to light. Journal of Bacteriology., 192(24), 6336–6345. https://doi.org/10.1128/JB.00917-10 - DOI - PubMed - PMC
-
- Mukherjee, S., Jemielita, M., Stergioula, V., Tikhonov, M., & Bassler, B. L. (2019). Photosensing and quorum sensing are integrated to control Pseudomonas aeruginosa collective behaviors. PLoS Biology., 17(12), e3000579. https://doi.org/10.1371/journal.pbio.3000579 - DOI - PubMed - PMC
-
- van der Horst, M. A., Key, J., & Hellingwerf, K. J. (2007). Photosensing in chemotrophic, non-phototrophic bacteria: Let there be light sensing too. Trends in Microbiology., 15(12), 554–562. https://doi.org/10.1016/j.tim.2007.09.009 - DOI - PubMed
-
- Swartz, T. E., Tseng, T. S., Frederickson, M. A., Paris, G., Comerci, D. J., Rajashekara, G., et al. (2007). Blue-light-activated histidine kinases: Two-component sensors in bacteria. Science, 317(5841), 1090–1093. https://doi.org/10.1126/science.1144306 - DOI - PubMed
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