Research Article Volume 8 Issue 2
1Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Iran
2Department of Epidemiology and Biostatistics, School of Public Health, Tehran University of Medical Sciences, Iran
Correspondence: Seyed Jamal Hashemi, Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran , Tel +98- 21 4293 3150, Fax +98 21 88951392
Received: September 20, 2018 | Published: March 22, 2019
Citation: Rafat Z, Hashemi SJ, Ghazvini RD, et al. Study of skin and nail Trichosporon species as a normal flora based on age groups in healthy persons in TehranIran. Biom Biostat Int J. 2019;8(2):44-46. DOI: 10.15406/bbij.2019.08.00269
The skin is the body's largest organ that hosts heterogeneous inhabitants. Until now, the diversity of the cutaneous microbiome was mainly investigated for bacteria and there is a little information about the skin fungal flora and Trichosporon is occasionally found as normal flora of skin. In this study, differences in Trichosporon community structure associated with 9 different skin sites of 238 healthy people during 10 months from July to March 2016, are described. These subjects were divided by age into 4 groups: infants, children, adults and geriatrics. The collected samples were examined by culture on Sabouraud Chloramphenicol Agar and Sabouraud Cycloheximide Chloramphenicol Agar. For precise identification of isolates in the species level, ITS1-5. 8S-ITS2 r DNA regions were sequenced. The frequency of Trichosporon species was not significantly different between age groups. The most Trichosporon isolations were related to the adult age group and the fewest in the infants. T.asahii was the predominant isolated species in all age groups. This study showed statistically significant effect of the subjects’ sex on Trichosporon population resident on human skin surface.
Keywords: skin residents, cutaneous Trichosporon composition, different age groups, DNA-sequencing, culture, Microbial epidemiology, Iran
Ethics statement
This study was approved by ethical committee of Tehran University of medical science (the number of Ethics Committee protocol: IR.TUMS.SPH.REC.1395.1339). A written informed consent was obtained from all subjects or their guardians prior to sample collection. All data were de-identified.
Sampling
A total of 238 healthy people, in four age groups, were studied. These subjects were including 119 males and 119 females, with equal gender distribution in all age groups. All samples were selected from 5 areas of Tehran (North, South, East, West and Center of this city). The distribution of subjects in each group was as follows:
At the time of sampling, the age and gender of each subject were recorded. The subjects haven’t washed their hands, feet, or other areas just before sampling and the sampling was made after the activities of the day. The following areas were sampled by means of a cotton-tipped swab moisted with sterile serum physiology: the forehead, dorsum of hands, dorsum of feet, finger nails, toenails, the axilla, the groin, the interdigital spaces of hand and foot and the sub mammary space in women. All swabs were cultured on Sabouraud Chloramphenicol Agar (SC, Merck, Germany). All cultures were incubated in 25°C for 4 days. Isolated colonies then were cultured on Sabouraud Dextrose Agar with chloramphenicol and cycloheximide (Micro media, Hungary) in 25°C after 4 days. This medium is a selective solid medium for differentiation Trichosporon spp from Geothricum candidum. Unlike Geothricum candidum, Trichosporon isolates grow on this medium. In this study for a correct determination of isolates in the species level, DNA sequencing was performed.
Molecular technique
DNA Extraction: An aliquot of 100 μL of cell suspension was transferred to micro tubes and incubated at 100°C in a boiling water-bath for 10 min, then centrifuged at 5,000 x g for 5 minutes. The upper aqueous layer (containing the DNA) was carefully transferred to a clean tube and was used for PCR.
PCR conditions and sequencing: PCR amplification of ITS1-5. 8S-ITS2 rDNA regions were performed.15 Positive PCR products were sent for sequencing at Bioneer Advanced Nucleic Acids core facility. The ITS sequences were then parsed from the coating and separately used to perform individual nucleotide–nucleotide searches using the BLASTn algorithm at the NCBI website (http://www/ncbi.nlm.nih.gov/BLAST/). Fungal identifications were made based on maximum identities ≥ 99% and query coverage ≥ 98% with this method.
Statistical tests: In this study, one tail chi-square test was performed for each analysis.
In this study, on each medium that the growth of Trichosporon was positive, one isolate was identified and for precise identification of isolates in the species level, DNA sequencing was performed. Among the studied population, divided into 4 groups by age including infants, children, adults and the elderly, 12 persons were positive for Trichosporon isolation. The highest prevalence of Trichosporon isolation was related to the adults age group (n=7, 58.33%) and the lowest prevalence was related to the infants (n=1, 8.33 %) and showed the age of subjects was not significantly effective on cutaneous Trichosporon community (p > 0.01). Also in this study T asahii (n=11, 91.66%) among all species was predominant in all age groups follow by T.coremiiforme (n=1, 9.09). It should be noted there was not a significant difference between isolated species according the age (Table 1). In this study 238 healthy people including 119 males and 119 females were examined. From 12 persons who were positive for Trichosporon isolation, the isolation of Trichosporon was significantly different between males (n=4, 33.33%) and females (n= 8, 66.66%) and there was significant difference in cutaneous Trichosporon population between the genders. (p = 0.01) (Table 2).
Age group |
Infants |
Children |
Adults |
Elderly |
Total |
|||||
Trichosporon species |
Number |
% |
Number |
% |
Number |
% |
Number |
% |
Number |
% |
T. asahii |
0 |
0 |
1 |
100 |
7 |
100 |
3 |
100 |
11 |
91.66 |
T.coremiiforme |
1 |
100 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
8.33 |
Total |
1 |
100 |
1 |
100 |
7 |
100 |
3 |
100 |
12 |
100 |
Table 1 The frequency of Trichosporon species in different age groups
Gender |
Men |
Women |
Total |
|||
Trichosporon species |
Number |
% |
Number |
% |
Number |
% |
T.asahii |
4 |
100 |
7 |
87.5 |
11 |
91.66 |
T.coremiiforme |
0 |
0 |
1 |
12.5 |
1 |
8.33 |
Total |
4 |
100 |
8 |
100 |
12 |
100 |
Table 2 The frequency of Trichosporon species in regard to gender
Considering Trichosporon isolation in regard to anatomic sites, from 19 positive sites for Trichosporon isolation, the highest prevalence of Trichosporon isolation was related to the axilla (n=4, 21.5%) and the groin (n=4, 21.5%) and the lowest prevalence was related to the sub mammary space in women (n= 0, 0.%) and dorsum of hands (n= 0, 0.%). Also in this study, T.asahii (n= 15, 78.94%) showed the highest prevalence of Trichosporon isolations in all studied anatomical sites (Table 3).
Trichosporon species |
T.asahii |
T.coremiiforme |
Total |
|||
Anatomic site of body |
Number |
% |
Number |
% |
Number |
% |
Forehead |
1 |
6.66 |
1 |
25 |
2 |
10.52 |
Dorsum of hands |
0 |
0 |
0 |
0 |
0 |
0 |
Dorsum of feet |
1 |
6.66 |
0 |
0 |
1 |
5.26 |
Finger nail |
3 |
20 |
0 |
0 |
3 |
15.78 |
Toe nail |
3 |
20 |
0 |
0 |
3 |
15.78 |
Axilla |
3 |
20 |
1 |
25 |
4 |
21.05 |
Groin |
3 |
20 |
1 |
25 |
4 |
21.05 |
Inter digital space of feet |
1 |
6.66 |
1 |
25 |
2 |
10.52 |
Sub mammary space |
0 |
0 |
0 |
0 |
0 |
0 |
total |
15 |
100 |
4 |
100 |
19 |
100 |
Table 3 The frequency of Trichosporon species in regard to anatomic site of the body
The authors appreciate the support of Tehran University of Medical Sciences, Tehran, Iran.
Authors declare that there is no conflict of interest.
©2019 Rafat, et al. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.
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