Moran Losada Patricia, Chouvarine Philippe, Dorda Marie, Hedtfeld Silke, Mielke Samira, Schulz Angela, Wiehlmann Lutz, Tümmler Burkhard
Clinic for Paediatric Pneumology, Allergology and Neonatology, OE 6710, Hannover Medical School, Hannover, Germany.
Clinic for Paediatric Pneumology, Allergology and Neonatology, OE 6710, Hannover Medical School, Hannover, Germany; Biomedical Research in Endstage and Obstructive Lung Disease (BREATH), Member of the German Center for Lung Research, Hannover, Germany.
ERJ Open Res. 2016 May 9;2(2). doi: 10.1183/23120541.00096-2015. eCollection 2016 Apr.
Chronic airway infections determine most morbidity in people with cystic fibrosis (CF). Herein, we present unbiased quantitative data about the frequency and abundance of DNA viruses, archaea, bacteria, moulds and fungi in CF lower airways. Induced sputa were collected on several occasions from children, adolescents and adults with CF. Deep sputum metagenome sequencing identified, on average, approximately 10 DNA viruses or fungi and several hundred bacterial taxa. The metagenome of a CF patient was typically found to be made up of an individual signature of multiple, lowly abundant species superimposed by few disease-associated pathogens, such as and , as major components. The host-associated signatures ranged from inconspicuous polymicrobial communities in healthy subjects to low-complexity microbiomes dominated by the typical CF pathogens in patients with advanced lung disease. The DNA virus community in CF lungs mainly consisted of phages and occasionally of human pathogens, such as adeno- and herpesviruses. The and populations were composed of one major and numerous minor clone types. The rare clones constitute a low copy genetic resource that could rapidly expand as a response to habitat alterations, such as antimicrobial chemotherapy or invasion of novel microbes.
慢性气道感染决定了囊性纤维化(CF)患者的大部分发病率。在此,我们提供了关于CF下呼吸道中DNA病毒、古菌、细菌、霉菌和真菌的频率和丰度的无偏定量数据。从患有CF的儿童、青少年和成人中多次采集诱导痰。深度痰宏基因组测序平均鉴定出约10种DNA病毒或真菌以及数百种细菌分类群。CF患者的宏基因组通常由多种低丰度物种的个体特征组成,叠加有少数与疾病相关的病原体,如[具体病原体1]和[具体病原体2]作为主要成分。宿主相关特征范围从健康受试者中不明显的多微生物群落到晚期肺病患者中以典型CF病原体为主的低复杂性微生物群。CF肺中的DNA病毒群落主要由噬菌体组成,偶尔也有人类病原体,如腺病毒和疱疹病毒。[具体细菌1]和[具体细菌2]群体由一种主要克隆类型和许多次要克隆类型组成。罕见克隆构成了一种低拷贝遗传资源,可作为对栖息地改变(如抗菌化疗或新微生物入侵)的反应而迅速扩展。