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伯克霍尔德菌在与源自活支气管上皮细胞的巨大质膜囊泡早期接触时的转录组。

Burkholderia cenocepacia transcriptome during the early contacts with giant plasma membrane vesicles derived from live bronchial epithelial cells.

机构信息

iBB-Institute for Bioengineering and Biosciences, Biological Sciences Research Group, Av. Rovisco Pais 1, 1049-001, Lisbon, Portugal.

CQE Instituto Superior Técnico, Departamento de Engenharia Química, Universidade de Lisboa, Av. Rovisco Pais, 1049-001, Lisbon, Portugal.

出版信息

Sci Rep. 2021 Mar 11;11(1):5624. doi: 10.1038/s41598-021-85222-5.

Abstract

Burkholderia cenocepacia is known for its capacity of adherence and interaction with the host, causing severe opportunistic lung infections in cystic fibrosis patients. In this work we produced Giant Plasma Membrane Vesicles (GPMVs) from a bronchial epithelial cell line and validated their use as a cell-like alternative to investigate the steps involved in the adhesion process of B. cenocepacia. RNA-sequencing was performed and the analysis of the B. cenocepacia K56-2 transcriptome after the first contacts with the surface of host cells allowed the recognition of genes implicated in bacterial adaptation and virulence-associated functions. The sensing of host membranes led to a transcriptional shift that caused a cascade of metabolic and physiological adaptations to the host specific environment. Many of the differentially expressed genes encode proteins related with central metabolic pathways, transport systems, cellular processes, and virulence traits. The understanding of the changes in gene expression that occur in the early steps of infection can uncover new proteins implicated in B. cenocepacia-host cell adhesion, against which new blocking agents could be designed to control the progression of the infectious process.

摘要

洋葱伯克霍尔德菌以其与宿主的黏附与相互作用能力而闻名,可导致囊性纤维化患者发生严重的机会性肺部感染。在这项工作中,我们从支气管上皮细胞系中产生了巨大质膜囊泡(GPMVs),并验证了其作为细胞样替代物用于研究洋葱伯克霍尔德菌黏附过程中涉及的步骤的用途。进行了 RNA 测序,并且对与宿主细胞表面的最初接触后 B. cenocepacia K56-2 转录组的分析,识别出了与细菌适应和与毒力相关功能相关的基因。宿主膜的感应导致了转录转移,从而引发了一系列代谢和生理适应宿主特定环境的过程。许多差异表达的基因编码与中心代谢途径、运输系统、细胞过程和毒力特征相关的蛋白质。了解感染早期发生的基因表达变化,可以揭示新的与 B. cenocepacia-宿主细胞黏附相关的蛋白,针对这些蛋白可以设计新的阻断剂来控制感染过程的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cfd/7970998/49221b561ce3/41598_2021_85222_Fig1_HTML.jpg

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