The fungal diversity in the lungs of children with cystic fibrosis captured by sputum-induction and bronchoalveolar lavage

被引:0
|
作者
Weiser, Rebecca [1 ]
Ronchetti, Katherine [2 ,3 ]
Tame, Jo-Dee [2 ,3 ,4 ]
Hoehn, Sven [5 ]
Jurkowski, Tomasz P. [5 ]
Mahenthiralingam, Eshwar [1 ]
Forton, Julian T. [2 ,6 ]
机构
[1] Cardiff Univ, Sch Biosci, Organisms & Environm Div, Microbiomes Microbes & Informat Grp, Sir Martin Evans Bldg,Pk Pl, Cardiff, Wales
[2] Noahs Ark Childrens Hosp Wales, Dept Paediat Resp Med, Cardiff, Wales
[3] Noahs Ark Childrens Hosp Wales, Dept Paediat Physiotherapy, Cardiff, Wales
[4] Cardiff Univ, Sch Healthcare Sci, Cardiff, Wales
[5] Cardiff Univ, Cardiff Sch Biosci, Mol Biosci Div, Sir Martin Evans Bldg,Pk Pl, Cardiff, Wales
[6] Cardiff Univ, Sch Med, Cardiff, Wales
基金
英国惠康基金;
关键词
Cystic fibrosis; Lung infection; Respiratory sampling; Fungal pathogens; Mycobiota diversity; INFECTIONS; MYCOBIOME;
D O I
10.1016/j.jcf.2024.07.011
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: The prevalence of fungi in cystic fibrosis (CF) lung infections is poorly understood and studies have focused on adult patients. We investigated the fungal diversity in children with CF using bronchoalveolar lavage (BAL) and induced sputum (IS) samples to capture multiple lung niches. Methods: Sequencing of the fungal ITS2 region and molecular mycobiota diversity analysis was performed on 25 matched sets of BAL-IS samples from 23 children collected as part of the CF-SpIT study (UKCRN14615; ISRCTNR12473810). Results: Aspergillus and Candida were detected in all samples and were the most abundant and prevalent genera, followed by Dipodascus, Lecanicillium and Simplicillium. The presumptive CF pathogens Exophiala, Lomentospora and Scedosporium were identified at variable abundances in 100 %, 64 %, and 24 % of sample sets, respectively. Fungal pathogens observed at high relative abundance (>= 40 %) were not accurately diagnosed by routine culture microbiology in over 50% of the cohort. The fungal communities captured by BAL and IS samples were similar in diversity and composition, with exception to C. albicans being significantly increased in IS samples. The respiratory mycobiota varied greatly between individuals, with only 13 of 25 sample sets containing a dominant fungal taxon. In 11/25 BAL sample sets, airway compartmentalisation was observed with diverse mycobiota detected from different lobes of the lung. Conclusions: The paediatric mycobiota is diverse, complex and inadequately diagnosed by conventional microbiology. Overlapping fungal communities were identified in BAL and IS samples, showing that IS can capture fungal genera associated with the lower airway. Compartmentalisation of the lower airway presents difficulties for consistent mycobiota sampling.
引用
收藏
页码:382 / 389
页数:8
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