TY - JOUR
T1 - Molecular analysis of fungal populations in patients with oral candidiasis using next-generation sequencing
AU - Imabayashi, Yumi
AU - Moriyama, Masafumi
AU - Takeshita, Toru
AU - Ieda, Shinsuke
AU - Hayashida, Jun Nosuke
AU - Tanaka, Akihiko
AU - Maehara, Takashi
AU - Furukawa, Sachiko
AU - Ohta, Miho
AU - Kubota, Keigo
AU - Yamauchi, Masaki
AU - Ishiguro, Noriko
AU - Yamashita, Yoshihisa
AU - Nakamura, Seiji
N1 - Funding Information:
We appreciate the technical support from the Research Support Center, Research Center for Human Disease Modeling, Kyushu University Graduate School of Medical Sciences. This work was supported in part by grants from the Ministry of Education, Culture, Sports, Science, and Technology of Japan (26670868, 15K20542).
PY - 2016/6/16
Y1 - 2016/6/16
N2 - Oral candidiasis is closely associated with changes in oral fungal biodiversity and is caused primarily by Candida albicans. However, the widespread use of empiric and prophylactic antifungal drugs has caused a shift in fungal biodiversity towards other Candida or yeast species. Recently, next-generation sequencing (NGS) has provided an improvement over conventional culture techniques, allowing rapid comprehensive analysis of oral fungal biodiversity. In this study, we used NGS to examine the oral fungal biodiversity of 27 patients with pseudomembranous oral candidiasis (POC) and 66 healthy controls. The total number of fungal species in patients with POC and healthy controls was 67 and 86, respectively. The copy number of total PCR products and the proportion of non-C. albicans, especially C. dubliniensis, in patients with POC, were higher than those in healthy controls. The detection patterns in patients with POC were similar to those in controls after antifungal treatment. Interestingly, the number of fungal species and the copy number of total PCR products in healthy controls increased with aging. These results suggest that high fungal biodiversity and aging might be involved in the pathogenesis of oral candidiasis. We therefore conclude that NGS is a useful technique for investigating oral candida infections.
AB - Oral candidiasis is closely associated with changes in oral fungal biodiversity and is caused primarily by Candida albicans. However, the widespread use of empiric and prophylactic antifungal drugs has caused a shift in fungal biodiversity towards other Candida or yeast species. Recently, next-generation sequencing (NGS) has provided an improvement over conventional culture techniques, allowing rapid comprehensive analysis of oral fungal biodiversity. In this study, we used NGS to examine the oral fungal biodiversity of 27 patients with pseudomembranous oral candidiasis (POC) and 66 healthy controls. The total number of fungal species in patients with POC and healthy controls was 67 and 86, respectively. The copy number of total PCR products and the proportion of non-C. albicans, especially C. dubliniensis, in patients with POC, were higher than those in healthy controls. The detection patterns in patients with POC were similar to those in controls after antifungal treatment. Interestingly, the number of fungal species and the copy number of total PCR products in healthy controls increased with aging. These results suggest that high fungal biodiversity and aging might be involved in the pathogenesis of oral candidiasis. We therefore conclude that NGS is a useful technique for investigating oral candida infections.
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U2 - 10.1038/srep28110
DO - 10.1038/srep28110
M3 - Article
C2 - 27305838
AN - SCOPUS:84975464245
SN - 2045-2322
VL - 6
JO - Scientific Reports
JF - Scientific Reports
M1 - 28110
ER -