i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
IPATIMUP - Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.
Helicobacter. 2024 Jan-Feb;29(1):e13031. doi: 10.1111/hel.13031. Epub 2023 Nov 23.
Outer membrane vesicles (OMVs) are spontaneously released by Gram-negative bacteria and influence bacteria-host interactions by acting as a delivery system for bacterial components and by interacting directly with host cells. Helicobacter pylori, a pathogenic bacterium that chronically colonizes the human stomach, also sheds OMVs, and their impact on bacterial-mediated diseases is still being elucidated.
Transcriptomic profiling of the human gastric cell line MKN74 upon challenge with H. pylori OMVs compared to control and infected cells was performed using the Ion AmpliSeq™ Transcriptome Human Gene Expression Panel to understand the gene expression changes that human gastric epithelial cells might undergo when exposed to H. pylori OMVs.
H. pylori OMVs per se modify the gene expression profile of gastric epithelial cells, adding another layer of (gene) regulation to the already complex host-bacteria interaction. The most enriched pathways include those related to amino acid metabolism, mitogen-activated protein kinase signaling, autophagy, and ferroptosis, whereas the cell cycle, DNA replication, and DNA repair were the most downregulated. The transcriptomic changes induced by OMVs were mostly similar to those induced by the parental bacteria, likely amplifying the effects of the bacterium itself.
Our data provide a valuable portrayal of the transcriptomic remodeling of gastric cells induced by H. pylori OMVs. It demonstrates the breadth of cellular pathways and genes affected by OMVs, most previously unreported, which can be further dissected for the underlying molecular mediators and explored to understand the pathobiology of the full spectrum of H. pylori-mediated diseases.
外膜囊泡(OMVs)是革兰氏阴性菌自发释放的,通过作为细菌成分的传递系统以及直接与宿主细胞相互作用来影响细菌-宿主相互作用。定植于人类胃部的致病性细菌幽门螺杆菌(H. pylori)也会脱落 OMVs,但其对细菌介导疾病的影响仍在研究中。
使用 Ion AmpliSeq™ Transcriptome Human Gene Expression Panel 对与 H. pylori OMVs 相比对照和感染细胞的人胃细胞系 MKN74 进行转录组谱分析,以了解人胃上皮细胞在暴露于 H. pylori OMVs 时可能经历的基因表达变化。
H. pylori OMVs 本身会改变胃上皮细胞的基因表达谱,为已经复杂的宿主-细菌相互作用增加了另一层(基因)调控。最富集的途径包括与氨基酸代谢、丝裂原激活蛋白激酶信号转导、自噬和铁死亡相关的途径,而细胞周期、DNA 复制和 DNA 修复则被下调最多。OMVs 诱导的转录组变化与亲本细菌诱导的变化大多相似,可能放大了细菌本身的作用。
我们的数据提供了 H. pylori OMVs 诱导胃细胞转录组重排的有价值描述。它展示了受 OMVs 影响的细胞途径和基因的广泛程度,其中大多数以前未报道过,可以进一步剖析潜在的分子介质,并进行探索以了解 H. pylori 介导的各种疾病的病理生物学。