Fungal Dysbiosis in Children with Celiac Disease

被引:14
作者
El Mouzan, Mohammad [1 ]
Al-Hussaini, Abdulrahman [2 ]
Fanelli, Brian [3 ]
Assiri, Asaad [4 ]
AlSaleem, Badr [5 ]
Al Mofarreh, Mohammad [6 ]
Al Sarkhy, Ahmed [1 ]
Alasmi, Mona [1 ]
机构
[1] King Saud Univ, Dept Pediat Gastroenterol, POB 2925, Riyadh 11461, Saudi Arabia
[2] Univ King Saud Bin Abdulaziz Hlth Sci, King Fahad Med City, Childrens Hosp, Gastroenterol Div, POB 59046, Riyadh 11525, Saudi Arabia
[3] CosmosID, 1600 E Gude Dr,Suite 210, Rockville, MD 20850 USA
[4] King Saud Univ, Dept Pediat Gastroenterol & Supervisor, Prince Abdullah Bin Khalid Celiac Dis Res Chair, POB 2925, Riyadh 11461, Saudi Arabia
[5] King Fahad Med City, Children Hosp, Div Gastroenterol, Pediat Intestinal Failure & Parenteral Nutr Progr, POB 59046, Riyadh 11525, Saudi Arabia
[6] Al Mofarreh PolyClin, Takhassosi St,POB 9789, Riyadh 11423, Saudi Arabia
关键词
Microbiota; Fungi; Dysbiosis; Celiac disease; Saudi children; DUODENAL MICROBIOTA COMPOSITION; ANTI-SACCHAROMYCES-CEREVISIAE; CANDIDA-ALBICANS; ANTIBIOTIC USE; RISK; ASSOCIATION; ANTIBODIES; GUT;
D O I
10.1007/s10620-021-06823-8
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Although intestinal fungi are known to interact with the immune system, the relationship between intestinal fungi and childhood celiac disease (CeD), an immune-mediated condition, has rarely been reported. Aims The aim of this study was to describe gut fungal profiles in a cohort of children with new-onset CeD. Methods Mucosal and fecal samples were collected from children with CeD and controls and subjected to metagenomics analysis of fungal microbiota communities. DNA libraries were sequenced using Illumina HiSeq platform 2 x 150 bp. Bioinformatic analysis was performed to quantify the relative abundance of fungi. Shannon alpha diversity metrics and beta diversity principal coordinate (PCo) analyses were calculated, and DESeq tests were performed between celiac and non-celiac groups. Results Overall more abundant taxa in samples of children with CeD included Tricholomataceae, Saccharomycetaceae, Saccharomycetes Saccharomyces cerevisiae, and Candida, whereas less abundant taxa included Pichiaceae, Pichia kudriavzevii, Pneumocystis, and Pneumocystis jirovecii. Alpha diversity between CeD and control individuals did not differ significantly, and beta diversity PCo analysis showed overlap of samples from CeD and controls for both fecal or mucosal samples; however, there was a clear separation between mucosal and fecal overall samples Conclusions We report fungal dysbiosis in children with CeD, suggesting a possible role in the pathogenesis of CeD. Further larger, controlled, prospective and longitudinal studies are needed to verify the results of this study and clarify the functional role of fungi in CeD.
引用
收藏
页码:216 / 223
页数:8
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