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一步软琼脂富集和分离抑制分生孢子萌发的人肺细菌

One-Step Soft Agar Enrichment and Isolation of Human Lung Bacteria Inhibiting the Germination of Conidia.

作者信息

Palmieri Fabio, Diserens Jérémy, Gresse Manon, Magnin Margo, Helle Julina, Salamin Benoît, Bisanti Lorenzo, Bernasconi Eric, Pernot Julie, Shanmuganathan Apiha, Trompette Aurélien, von Garnier Christophe, Junier Thomas, Neuenschwander Samuel, Bindschedler Saskia, Pagni Marco, Koutsokera Angela, Ubags Niki, Junier Pilar

机构信息

Laboratory of Microbiology, Institute of Biology, Faculty of Science, University of Neuchâtel, 2000 Neuchâtel, Switzerland.

Division of Pulmonary Medicine, Department of Medicine, Lausanne University Hospital (CHUV), University of Lausanne (UNIL), 1066 Epalinges, Switzerland.

出版信息

Microorganisms. 2024 Oct 7;12(10):2025. doi: 10.3390/microorganisms12102025.

Abstract

Fungi of the genus are widespread in the environment, where they produce large quantities of airborne conidia. Inhalation of spp. conidia in immunocompromised individuals can cause a wide spectrum of diseases, ranging from hypersensitivity responses to lethal invasive infections. Upon deposition in the lung epithelial surface, conidia encounter and interact with complex microbial communities that constitute the lung microbiota. The lung microbiota has been suggested to influence the establishment and growth of spp. in the human airways. However, the mechanisms underlying this interaction have not yet been sufficiently investigated. In this study, we aimed to enrich and isolate bacterial strains capable of inhibiting the germination and growth of conidia from bronchoalveolar lavage fluid (BALF) samples of lung transplant recipients using a novel enrichment method. This method is based on a soft agar overlay plate assay in which bacteria are directly in contact with conidia, allowing inhibition to be readily observed during enrichment. We isolated a total of five clonal bacterial strains with identical genotypic fingerprints, as shown by random amplified polymorphic DNA PCR (RAPD-PCR). All strains were identified as (strains b1-b5). The strains were able to inhibit the germination and growth of in a soft agar confrontation assay, as well as in a germination multiplate assay. Moreover, when compared with ten strains isolated from expectoration through standard methods, no significant differences in inhibitory potential were observed. Additionally, we showed inhibition of growth on Calu-3 cell culture monolayers. However, the isolated strains were shown to cause significant damage to the cell monolayers. Overall, although is a known opportunistic lung pathogen and antagonist of , we validated this novel one-step enrichment approach for the isolation of bacterial strains antagonistic to from BALF samples as a proof-of-concept. This opens up a new venue for the targeted enrichment of antagonistic bacterial strains against specific fungal pathogens.

摘要

属真菌在环境中广泛分布,在那里它们产生大量的空气传播分生孢子。免疫功能低下的个体吸入属分生孢子可引发多种疾病,从超敏反应到致命的侵袭性感染。分生孢子沉积在肺上皮表面后,会与构成肺部微生物群的复杂微生物群落相遇并相互作用。有人提出肺部微生物群会影响属真菌在人类气道中的定植和生长。然而,这种相互作用的潜在机制尚未得到充分研究。在本研究中,我们旨在使用一种新的富集方法,从肺移植受者的支气管肺泡灌洗(BALF)样本中富集并分离能够抑制分生孢子萌发和生长的细菌菌株。该方法基于软琼脂覆盖平板试验,其中细菌直接与分生孢子接触,便于在富集过程中观察到抑制作用。通过随机扩增多态性DNA聚合酶链反应(RAPD-PCR),我们共分离出五株具有相同基因型指纹的克隆细菌菌株。所有菌株均被鉴定为(菌株b1 - b5)。在软琼脂对峙试验以及萌发多平板试验中,这些菌株均能够抑制的萌发和生长。此外,与通过标准方法从痰液中分离出的十株菌株相比,未观察到抑制潜力的显著差异。另外,我们还证明了对Calu - 3细胞培养单层上生长的抑制作用。然而,所分离的菌株对细胞单层造成了显著损伤。总体而言,尽管是一种已知的机会性肺部病原体且是的拮抗剂,但我们验证了这种从BALF样本中分离拮抗细菌菌株的新型一步富集方法,作为概念验证。这为针对特定真菌病原体的拮抗细菌菌株的靶向富集开辟了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f5e/11509576/198fad3c0ee7/microorganisms-12-02025-g001.jpg

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