It is well known that high doses of ultraviolet rays are associated with acute and chronic impacts on skin health, including inflammation and photoaging. However, many vacationers expose themselves to high doses of UV rays in pursuit of the sun. Human skin is home to a vast array of bacteria, fungi, and viruses that make up the skin microbiome. These microbes play essential roles in skin homeostasis. Therefore, it is worth questioning whether sunlight can impact this microbiome.
A study conducted by Nabiha YUSUF and her colleagues aimed to test the effect of UVA and UVB rays on the human skin microbiome. To do this, participants were exposed to doses of UVA (22 - 47 J/cm2) or UVB (100 - 350 mJ/cm2), and samples were collected. The DNA was isolated and sequenced to identify the microbial composition of each sample. The results are reported in the following table.
Overall, the composition of the microbiota was altered after UV exposure. Disruption of the skin's microbial components can impact the host's health. Proteobacteria, which include cyanobacteria and bacteria of the genus Pseudomonas, constitute a vast phylum of Gram-negative bacteria in healthy human skin. However, a disturbed microbiota of Proteobacteria has been associated with psoriasis, eczema, and diabetic foot ulcers, with a greater diversity of Proteobacteria being correlated with protective anti-inflammatory immune responses. Thus, an imbalance in proteobacteria, and consequently of the skin microbiota, may suggest a deterioration of skin health in individuals who seek the sun.
The way microorganisms respond and cope with UV rays can vary significantly. It has been suggested that Gram-positive bacteria are better adapted to the oxidative stress associated with UV rays than Gram-negative bacteria, because their cell walls filter out a significant portion of UV rays. The results of the previously mentioned study may be attributed to various unique adaptation mechanisms inherent to these bacteria.
Although the precise mechanisms by which the sun alters the skin microbiome are not well understood, assumptions have been made. It has been demonstrated that UV exposure has altered the skin metabolome in mice, leading to an increase in amino acid metabolism and a decrease in fatty acid, sphingolipid, and histidine metabolism. These results indicate that UV exposure results in changes in the metabolites present on the skin, on which microbes depend.
Furthermore, UV rays also suppress adaptive immunity and activate innate immunity. The immunosuppression caused by UV rays is primarily due to their impact on the persistence, phenotype, and specificity of resident memory T lymphocytes. In vivo, it has been demonstrated that an exposure of 50 mJ/cm2 of UVB to psoriatic skin lesions causes the death of T cells. Changes in the skin immune system following UV exposure can potentially alter the immune selective pressures to which the microbiome is exposed, and thus affect the skin microbiota.
These results should be approached with caution, as the number of participants is small (n = 6), which can impact statistical significance. Additionally, they may be influenced by other factors, such as temperature and lifestyle, making it challenging to determine if the microbial variation is directly associated with UV exposure.