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持续的军团病及相关抗生素治疗导致肺部微生物组严重紊乱,富含机会性病原体。

Persistent Legionnaires' Disease and Associated Antibiotic Treatment Engender a Highly Disturbed Pulmonary Microbiome Enriched in Opportunistic Microorganisms.

机构信息

Institut Pasteur, Biologie des Bactéries Intracellulaires, Paris, France.

CNRS UMR 3525, Paris, France.

出版信息

mBio. 2020 May 19;11(3):e00889-20. doi: 10.1128/mBio.00889-20.

DOI:10.1128/mBio.00889-20
PMID:32430469
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7240155/
Abstract

Despite the importance of pneumonia to public health, little is known about the composition of the lung microbiome during infectious diseases, such as pneumonia, and how it evolves during antibiotic therapy. To study the possible relation of the pulmonary microbiome to the severity and outcome of this respiratory disease, we analyzed the dynamics of the pathogen and the human lung microbiome during persistent infections caused by the bacterium and their evolution during antimicrobial treatment. We collected 10 bronchoalveolar lavage fluid samples from three patients during long-term hospitalization due to pneumonia and performed a unique longitudinal study of the interkingdom microbiome, analyzing the samples for presence of bacteria, archaea, fungi, and protozoa by high-throughput Illumina sequencing of marker genes. The lung microbiome of the patients was characterized by a strong predominance of the pathogen, a low diversity of the bacterial fraction, and an increased presence of opportunistic microorganisms. The fungal fraction was more stable than the bacterial fraction. During long-term treatment, no genomic changes or antibiotic resistance-associated mutations that could explain the persistent infection occurred, according to whole-genome sequencing analyses of the pathogen. After antibiotic treatment, the microbiome did not recover rapidly but was mainly constituted of antibiotic-resistant species and enriched in bacteria, archaea, fungi, or protozoa associated with pathogenicity. The lung microbiome seems to contribute to nonresolving pneumonia, as it is strongly disturbed during infection and enriched in opportunistic and/or antibiotic-resistant bacteria and microorganisms, including fungi, archaea, and protozoa that are often associated with infections. The composition and dynamics of the lung microbiome during pneumonia are not known, although the lung microbiome might influence the severity and outcome of this infectious disease, similar to what was shown for the microbiome at other body sites. Here we report the findings of a comprehensive analysis of the lung microbiome composition of three patients with long-term pneumonia due to and its evolution during antibiotic treatment. This work adds to our understanding of how the microbiome changes during disease and antibiotic treatment and points to microorganisms and their interactions that might be beneficial. In addition to bacteria and fungi, our analyses included archaea and eukaryotes (protozoa), showing that both are present in the pulmonary microbiota and that they might also play a role in the response to the microbiome disturbance.

摘要

尽管肺炎对公共卫生至关重要,但人们对感染性疾病(如肺炎)期间肺部微生物组的组成以及抗生素治疗期间的演变过程知之甚少。为了研究肺部微生物组与这种呼吸道疾病的严重程度和结果之间可能存在的关系,我们分析了细菌引起的持续性感染期间病原体和人类肺部微生物组的动态及其在抗菌治疗期间的演变。我们从三名因肺炎长期住院的患者中收集了 10 份支气管肺泡灌洗液样本,并对它们进行了独特的跨域微生物组纵向研究,通过高通量 Illumina 标记基因测序分析样本中细菌、古菌、真菌和原生动物的存在。患者的肺部微生物组以病原体的强烈优势为特征,细菌部分的多样性较低,机会性微生物的存在增加。真菌部分比细菌部分更稳定。根据对病原体的全基因组测序分析,在长期治疗过程中,没有发生可以解释持续性感染的基因组变化或与抗生素耐药性相关的突变。抗生素治疗后,微生物组并未迅速恢复,而是主要由抗生素耐药物种组成,并富含与致病性相关的细菌、古菌、真菌或原生动物。肺部微生物组似乎有助于非解决性肺炎,因为它在感染过程中受到强烈干扰,并富含机会性和/或抗生素耐药细菌和微生物,包括与感染相关的真菌、古菌和原生动物。尽管肺部微生物组可能与其他部位的微生物组一样,影响这种传染病的严重程度和结果,但肺炎期间肺部微生物组的组成和动态尚不清楚。在这里,我们报告了对三例因肺炎导致的长期肺炎患者肺部微生物组组成及其在抗生素治疗过程中的演变进行全面分析的结果。这项工作增加了我们对疾病和抗生素治疗过程中微生物组变化的理解,并指出了可能有益的微生物及其相互作用。除了细菌和真菌,我们的分析还包括古菌和真核生物(原生动物),表明两者都存在于肺部微生物群中,并且它们也可能在对微生物组干扰的反应中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/7240155/25c0af764140/mBio.00889-20-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/7240155/f6278529b331/mBio.00889-20-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/7240155/8d4ebc6713a4/mBio.00889-20-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/7240155/607737f5ef3b/mBio.00889-20-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/7240155/25c0af764140/mBio.00889-20-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/7240155/f6278529b331/mBio.00889-20-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/7240155/8d4ebc6713a4/mBio.00889-20-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/7240155/607737f5ef3b/mBio.00889-20-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/7240155/25c0af764140/mBio.00889-20-f0004.jpg

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