Non-lipophilic mycobiota of human skin 1 of 5Published by Polish Botanical Society Acta Mycologica ORIGINAL RESEARCH PAPER Non-lipophilic mycobiota of human skin Katarzyna Talaga, Paweł Krzyściak* Department of Mycology, Chair of Microbiology, Jagiellonian University Medical College, Czysta 18, 31-121 Cracow, Poland * Corresponding author. Email: pawel.krzysciak@uj.edu.pl Abstract The human skin is inhabited by many species of bacteria and fungi, which are its natural microbiota. Fungi colonizing the skin, including those causing disease, characterized by great variety and variability, can be influenced by various fac- tors. The purpose of this study was to investigate the composition of the non-lipid- dependent fungal microbiota of skin, including the presence of species potentially pathogenic for humans. Fifty-six volunteers of both sexes aged 22–78 were sub- jected to the study. Swabs were taken from the face, chest, back and interdigital spaces of hands. Mycobiota isolated proved to vary both in terms of the location of occurrence and gender of patients. Interdigital spaces of hands, dominated by yeasts, constitute a location on human skin most contaminated with fungi. Molds were more often isolated from the face and chest. The back was the least contami- nated location. There was no difference in fungal incidence in relation to sex. Keywords mycobiota; yeasts; microbial diversity; molds Introduction The human skin is inhabited by many species of bacteria and fungi, which are its natu- ral microbiota. These organisms perform many beneficial functions. Among others, through competition, they do not allow pathogenic species to colonize the skin [1,2]. Mycobiota of skin is dominated mainly by lipophilic fungi of the genus Malassezia. Additionally, other species of yeast, mainly of the genus Candida and Cryptococcus, may exist on the skin. Species composition of skin mycobiota is characterized by great diversity and variability, which can be influenced by various factors such as age, oc- cupation, and the climate of the place of residence [3–5]. Monitoring of currently dominant fungal species belonging to the natural micro- biota as well as the frequency and location of infection caused by these fungi is im- portant for epidemiological studies. Collecting these data allows drawing conclusions about ongoing changes and forecasting changes to mycobiota in the near future. The aim of this study was to determine settlement of human’s skin by non-lipo- philic fungi. Material and methods The study involved 56 generally healthy (no responding symptoms of fungal infection of skin and antifungal therapy) volunteers (41 women and 15 men) aged over 18 years. The mean age was 43.7 for women ±13.5 years (range 22–78 years, median = 42 years), and for men 48.9 ±15.7 years (range 17–75, median = 50). DOI: 10.5586/am.1068 Publication history Received: 2015-09-22 Accepted: 2016-01-08 Published: 2016-01-29 Handling editor Tomasz Leski, Institute of Dendrology of the Polish Academy of Sciences, Poland Authors’ contributions PK contributed to the idea of research and collected the samples; both authors reviewed other studies and analyzed the data; both authors were involved in drafting and revising the manuscript; both authors approved the final version of the manuscript Funding This study was founded from subsidies for the development of young scientist awarded by the Polish Ministry of Science and Higher Education for Jagiellonian University Medical College (internal designation K/ DSC/001394). Competing interests No competing interests have been declared. Copyright notice © The Author(s) 2016. This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits redistribution, commercial and non- commercial, provided that the article is properly cited. Citation Talaga K, Krzyściak P. Non- lipophilic mycobiota of human skin. Acta Mycol. 2015;50(2):1068. http://dx.doi. org/10.5586/am.1068 Digital signature This PDF has been certified using digital signature with a trusted timestamp to assure its origin and integrity. A verification trust dialog appears on the PDF document when it is opened in a compatible PDF reader. Certificate properties provide further details such as certification time and a signing reason in case any alterations made to the final content. If the certificate is missing or invalid it is recommended to verify the article on the journal website. mailto:pawel.krzysciak%40uj.edu.pl?subject=Non-lipophilic%20mycobiota%20of%20human%20skin http://dx.doi.org/10.5586/am.1068 http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/ http://dx.doi.org/10.5586/am.1068 http://dx.doi.org/10.5586/am.1068 2 of 5© The Author(s) 2016 Published by Polish Botanical Society Acta Mycol 50(2):1068 Talaga and Krzyściak / Non-lipophilic mycobiota of skin The study was conducted in 2012–2014. Swabs were taken from nasolabial folds, the area of the breastbone, the back and interdigital spaces of hands for every study participant. Then the swabs were immediately cultured on Sabouraud glucose agar (SGA) with chloramphenicol and incubated at 27°C for 2–3 weeks and periodically checked. The growing colonies were subcultured on appropriate media (rice agar for yeasts and sporulation enhancement medium for molds, i.e., Czapek–Dox agar). The fungal identification to the genus level was based on identification keys according to Atlas of clinical fungi (2nd ed.) [6]. For yeasts, in some cases, species identification was con- firmed by API 20C AUX strips (bioMérieux) according to manufacturer’s procedure. For the mold colony, we performed adhesive tape slides in lactophenol cotton blue. In cases in which this method was not enough to ID genera, we performed slide cultures. For molds colony we perform scotch type slides in lactophenol cotton blue in cases that this method was not enough to ID genera we perform slide culture. The study was approved by the Bioethical Committee of Jagiellonian University (No. KBET/164/B/2012). Statistical analysis was performed using R Language and Environment for Statisti- cal Computing software [7]. The significance level for all statistical tests was set at alpha (p) ≤ 0.05. Results A positive culture from at least one location was obtained from 38 participants (n = 27; 65.8% of women and n = 11; 73.3% of men). There were no differences in the overall incidence of colonization between the sexes (Fisher’s exact test, p = 0.7508). Altogether, 72 (22.6%) positive cultures were obtained from 223 swabs (36 strains of yeast-like fungi and 30 of molds; 10 cultures showed mixed mycobiota – yeasts and molds). No fungi were iso- lated from any location in 18 participants. In 19 patients, a few species of fungi were isolated simultaneously from a single location. Further re- sults are given in Tab. 1. The most frequently cul- tured yeasts in all locations were representatives of the genus Candida. Among the molds, the most popular kinds were Aspergillus, which was isolated from swabs from the face and back, and Penicillium isolated from the chest and smears from interdigital spaces of hands. One participant was found to be colonized by one species (Candida lusitaniae) at all test sites on the skin. Fungi were usually iso- lated from the interdigital spaces of fingers (n = 26, 43%), and least often from the back (n = 12, 18% of par- ticipants; Fig. 1). There were no differences in the frequency of isolation of fungi on the grounds of sex Tab. 1 Frequency of isolation of fungi from different locations on the skin depending on the gender of the test participants. Gender Group of fungi Face Chest Back Hands n % n % n % n % F Lack of fungi 25 62.50 26 63.41 31 75.61 23 63.41 Yeasts 6 15.00 6 14.63 5 12.20 13 14.63 Molds 9 22.50 7 17.07 3 7.32 1 2.44 Mixed 0 0.00 2 4.88 2 4.88 4 9.76 M Lack of fungi 11 73.33 11 73.33 13 86.67 7 46.67 Yeasts 3 20.00 0 0.00 1 6.67 2 13.33 Molds 1 6.67 4 26.67 1 6.67 4 26.67 Mixed 0 0.00 0 0.00 0 0.00 2 13.33 F+M Lack of fungi 36 65.45 37 66.07 44 78.57 30 53.57 Yeasts 9 16.36 6 10.71 6 10.71 15 26.79 Molds 10 18.18 11 19.64 4 7.14 5 8.93 Mixed 0 0.00 2 3.57 2 3.57 6 10.71 F – female; M – male; n – number of samples. One participant refused to take a swab from her face because of her makeup. 3 of 5© The Author(s) 2016 Published by Polish Botanical Society Acta Mycol 50(2):1068 Talaga and Krzyściak / Non-lipophilic mycobiota of skin in relation to isolation location (Cochran–Mantel–Haenszel test, p = 0.8371). How- ever, after grouping the results for both sexes, it was found that the incidence of fungi depending on location is significantly different (chi-square test, p = 0.01191). In order to find a relationship between the location and the isolated fungi, correspondence analysis was carried out, the results of which are shown in Fig. 2. Therefore, it can be concluded that the occurrence of yeasts is associated with interdigital spaces, while the face and chest are associated with a higher incidence of molds. The back turned out to be the location from which fungi were isolated least frequently. Face Chest Back Interdigital spaces 0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 100% 36 37 44 30 9 6 6 15 10 11 4 5 2 2 6 Prevalence of fungal colonization on the skin surface Mixed Molds Yeasts Absence Body sites P e rc e n ta g e Fig. 1 The incidence of fungal colonization depending on the skin location. molds mixed yeasts absence face chest back interdigital Fig. 2 Correspondence analysis: the presence of fungi and location. The blue indicates the location; the red indicates fungal group. 4 of 5© The Author(s) 2016 Published by Polish Botanical Society Acta Mycol 50(2):1068 Talaga and Krzyściak / Non-lipophilic mycobiota of skin Discussion There are no effective methods to assess the actual presence of fungi on the skin. Culture methods have their limitations associated with the lack of providing all es- sential conditions for growth for each species of mycobiota in vitro. It appears that the solution to this problem could be the application of molecular techniques. However, interpretation of the occurrence of species based on the isolation and sequencing of DNA in projects investigating the human microbiota is also problematic. The mere discovery of fungal DNA does not mean that an entire cell is present. And even if a fungal cell is present, it is not possible to assume that it is alive. Another very impor- tant problem is widespread contamination of laboratory equipment such as reagents, test tubes, swabs, etc. with microbial DNA [8]. Furthermore, interpretation of the results of cultures and the results of molecular studies causes a number of problems mainly due to the fact that occasional isolation or finding the presence of fungal DNA do not mean that a particular species colonizes the skin, it could be transient. Fungi on the skin may occur accidentally as a result of contamination with soil, plant remnants, or after exposure to water or air. Many fungi, including molds, are anemochorous; therefore, their spores are commonly airborne and may passively fall on the skin. This is confirmed by our findings indicating a lower incidence of fungi on the covered skin of the back and the highest prevalence in interdigital spaces which are exposed not only to the atmosphere but also to tap water and all kinds of contamination being the origin or the breeding ground for fungi. Re- search of the mycobiome, independent of culture, showed that, apart from the DNA of Malassezia, the most common was the DNA of Penicillium and Aspergillus molds [3]. Also in the present study, based on culturing methods, these two kinds of fungi were predominant. Most fungi were isolated from interdigital swabs. In the report entitled Environ- mental and hand hygiene of the Polish people, published by Dettol and Children’s Me- morial Health Institute [2], fungi were isolated in women from 17 (15 yeasts and 2 molds) out of 636 samples and in men from 10 (9 yeasts and 1 mold) out of 550 samples. The study suggests that there are no differences in the incidence of yeasts between the sexes (chi-squared test with Yates’ correction for continuity, p = 0.5004, own calculations). Our study also failed to demonstrate a more frequent colonization of interdigital spaces by yeasts in women than in men; it was approximately 14% for each group (Fisher’s exact test, p = 0.3064). In this respect, it is curious that there is a higher incidence of candidiasis of in- terdigital spaces of hands and candidiasis of fingernails in women [9]. Saprotrophic yeasts have similar life requirements to the requirements of the pathogen called Can- dida albicans. It is known that Candida albicans is usually found on the skin. Other Candida species that are predominant there are C. tropicalis, C. parapsilosis and C. orthopsilosis [3]. Following deliberate inoculation of hands, after 45 minutes, Candida parapsilosis showed greater survivability (C. albicans was also cultured in an amount of around 2.5–5% initial inoculum) [10]. The question arises of whether an earlier colonization by other species of yeasts is a safeguard against or predisposes people to infections with C. albicans. The presence of C. albicans on the skin of hands is usually associated with poor hygiene. These fungi live in the gastrointestinal tract and mucous membranes of the reproductive organs, from where they can be easily transferred to one’s hands, par- ticularly when using the restroom. As reported in studies of the American Society for Microbiology, women wash their hands more often (75–93%) than men (58–77%) after using the restroom. In Great Britain, this is only 32% of men and 64% of women. These figures are somehow contrary to a higher incidence of mycosis in women. It is possible that mere washing without the use of disinfectants could also give rise to colonization. As was shown by Biedunkiewicz and Schulz’s research, 66% of tap water samples contained fungi, of which the most numerous were yeasts (81.3% of the isolated fungi) [1]. Moreover, it is known that detergents damage the protective lipid layer of the skin [11], which, together with maintaining skin’s moisture (also through creams and emollients), may favor colonization and, consequently, infection. The problem of the presence of fungi on healthy skin and associating coloniza- tion with potential development of infection needs further investigation. One must 5 of 5© The Author(s) 2016 Published by Polish Botanical Society Acta Mycol 50(2):1068 Talaga and Krzyściak / Non-lipophilic mycobiota of skin remember that the promoted molecular testing techniques do not allow us to assess the presence and viability of cells and merely finding the presence of a particular spe- cies, whether with the use of molecular methods or culturing, does not mean that the given species is a permanent component of skin mycobiota. Conclusions ■ Human skin locations most contaminated with fungi are interdigital spaces of hands. ■ Interdigital spaces of hands are dominated by yeasts, whereas molds are prevalent on the face and chest. However, there were usually no fungi isolations from the back. ■ There is no difference in the incidence of fungi depending on gender. References 1. Biedunkiewicz A, Schulz Ł. Fungi of the genus Exophiala in tap water. Mikologia Lekarska. 2012;19:23–26. 2. Raport marki Dettol i Centrum Zdrowia Dziecka. Higiena rąk i otoczenia Polaków [Inter- net]. 2007 [cited 2016 Jan 21]. Available from: http://pis.lodz.pl/data/other/hr_polacy.pdf 3. Findley K, Oh J, Yang J, Conlan S, Deming C, Meyer JA, et al., Topographic diversity of fungal and bacterial communities in human skin. Nature. 2013;498(7454):367–370. http:// dx.doi.org/10.1038/nature12171 4. Hannigan GD, Grice EA. Microbial ecology of the skin in the era of metagenomics and molecular microbiology. Cold Spring Harb Perspect Med. 2013;3(12):a015362. http:// dx.doi.org/10.1101/cshperspect.a015362 5. Pawłowicz A, Adamski Z. Flora dermatofitowa i oportunistyczna w zmianach grzybiczych dłoni, stóp oraz paznokci u pacjentów Kliniki Dermatologii AM w Poznaniu w latach 1984-1994. Mikologia Lekarska. 1994;2:95–100. 6. de Hoog GS, Guarrao J, Gene J, Figueras MJ. Atlas of clinical fungi. 2nd ed. Centraalbu- reau voor Schimmelcultures Utreht. Reus: Universitat Rovira i Virgili; 2000. 7. R Core Team. A language and environment for statistical computing [Internet]. Vienna: R Foundation for Statistical Computing; 2013 [cited 2016 Jan 21]. Available from: http:// www.r-project.org 8. Salter S, Cox MJ, Turek EM, Calus ST, Cookson WS, Moffatt MF, et al. Reagent and labora- tory contamination can critically impact sequence-based microbiome analyses. BMC Biol. 2014;12:87 http://dx.doi.org/10.1186/s12915-014-0087-z 9. Kwaśniewska J, Szefer E, Jaskółowska A. Niektóre aspekty grzybic skóry i paznokci na pod- stawie danych pacjentów zakładu diagnostyki i leczenia chorób pasożytniczych i grzybic uniwersytetu medycznego w Łodzi. Mikologia Lekarska. 2012;19(1):17–22. 10. Rangel-Frausto MS, Houston AK, Bale MJ, Fu C. Wenzel RP. An experimental model for study of Candida survival and transmission in human volunteers. Eur J Clin Microbiol Infect Dis. 1994;13(7):590–595. http://dx.doi.org/10.1007/BF01971311 11. Okuda M, Yoshiike T, Ogawa H. Detergent-induced epidermal barrier dysfunction and its prevention. J Dermatol Sci. 2002;30(3):173–179. http://dx.doi.org/10.1016/ S0923-1811(02)00106-8 http://pis.lodz.pl/data/other/hr_polacy.pdf http://dx.doi.org/10.1038/nature12171 http://dx.doi.org/10.1038/nature12171 http://dx.doi.org/10.1101/cshperspect.a015362 http://dx.doi.org/10.1101/cshperspect.a015362 http://www.r-project.org http://www.r-project.org http://dx.doi.org/10.1186/s12915-014-0087-z http://dx.doi.org/10.1007/BF01971311 http://dx.doi.org/10.1016/S0923-1811(02)00106-8 http://dx.doi.org/10.1016/S0923-1811(02)00106-8 Abstract Introduction Material and methods Results Discussion Conclusions References 2016-01-26T13:40:10+0000 Piotr Otręba