Weiser Rebecca, Ronchetti Katherine, Tame Jo-Dee, Hoehn Sven, Jurkowski Tomasz P, Mahenthiralingam Eshwar, Forton Julian T
Microbiomes, Microbes and Informatics Group, Organisms and Environment Division, School of Biosciences, Cardiff University, Sir Martin Evans Building, Park Place, Cardiff, UK.
Department of Paediatric Respiratory Medicine, Noah's Ark Children's Hospital for Wales, Cardiff, UK; Department of Paediatric Physiotherapy, Noah's Ark Children's Hospital for Wales, Cardiff, UK.
J Cyst Fibros. 2025 Mar;24(2):382-389. doi: 10.1016/j.jcf.2024.07.011. Epub 2024 Aug 1.
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.
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).
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.
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.
囊性纤维化(CF)肺部感染中真菌的患病率尚不清楚,且研究主要集中在成年患者。我们使用支气管肺泡灌洗(BAL)和诱导痰(IS)样本,对CF患儿的真菌多样性进行了调查,以获取多个肺部微生态位的信息。
对作为CF-SpIT研究(UKCRN14615;ISRCTNR12473810)一部分收集的23名儿童的25组匹配的BAL-IS样本进行真菌ITS2区域测序和分子真菌群落多样性分析。
在所有样本中均检测到曲霉属和念珠菌属,它们是最丰富和最常见的属,其次是双足囊菌属、轮枝顶孢属和单顶孢属。在100%、64%和24%的样本组中分别鉴定出推定的CF病原体外瓶霉属、罗门孢属和赛多孢属,其丰度各不相同。在超过50%的队列中,常规培养微生物学未能准确诊断出相对丰度较高(≥40%)的真菌病原体。BAL和IS样本捕获的真菌群落的多样性和组成相似,但白色念珠菌在IS样本中的含量显著增加。个体之间的呼吸道真菌群落差异很大,25个样本组中只有13个包含优势真菌分类群。在11/25的BAL样本组中,观察到气道分区,从肺的不同叶检测到不同的真菌群落。
儿科真菌群落多样、复杂,传统微生物学诊断不足。在BAL和IS样本中鉴定出重叠的真菌群落,表明IS可以捕获与下呼吸道相关的真菌属。下呼吸道的分区给一致的真菌群落采样带来了困难。