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亨氏巴尔通体细胞内和细胞外转录组图谱的比较。

Comparison of transcriptomic profiles between intracellular and extracellular Bartonella henselae.

作者信息

Gadila Shiva Kumar Goud, Caskey John R, Breitschwerdt Edward B, Maggi Ricardo G, Embers Monica E

机构信息

Division of Immunology, Tulane National Primate Research Center, Tulane University, Covington, LA, USA.

Department of Medicine, Clinical Science Center, University of Wisconsin School of Medicine and Public Health, Madison, MI, USA.

出版信息

Commun Biol. 2025 Jan 29;8(1):143. doi: 10.1038/s42003-025-07535-9.

Abstract

The Bartonella genus of bacteria encompasses ubiquitous species, some of which are pathogenic in humans and animals. Bartonella henselae, the causative agent of Cat Scratch disease, is responsible for a large portion of human Bartonella infections. These bacteria can grow outside of cells, replicate in erythrocytes and invade endothelial and monocytic cells. We have previously reported reduced antibiotic susceptibility of intracellular Bartonella. In this study we performed comparative transcriptomic analyses between the extracellular and intracellular B. henselae phenotypes. Overall, specific genes involved in invasion, virulence, extracellular adhesion of type 4 secretion system were downregulated following intracellular invasion of B. henselae. Downregulation included BadA, a well-characterized adhesin molecule, of critical importance for cell invasion. These studies demonstrate the ability to purify Bartonella RNA from infected cells and offer a repository of gene expression data for future research. The development of novel therapeutics will benefit from the ability to determine target expression by Bartonella in relevant microenvironments.

摘要

巴尔通体属细菌包含广泛存在的物种,其中一些对人类和动物具有致病性。猫抓病的病原体汉赛巴尔通体导致了很大一部分人类巴尔通体感染。这些细菌能够在细胞外生长,在红细胞中复制,并侵入内皮细胞和单核细胞。我们之前曾报道过细胞内巴尔通体对抗生素的敏感性降低。在本研究中,我们对细胞外和细胞内汉赛巴尔通体表型进行了比较转录组分析。总体而言,汉赛巴尔通体细胞内入侵后,参与4型分泌系统的侵袭、毒力、细胞外黏附的特定基因表达下调。下调的基因包括BadA,这是一种特征明确的黏附分子,对细胞侵袭至关重要。这些研究证明了从感染细胞中纯化巴尔通体RNA的能力,并为未来研究提供了基因表达数据库。新型治疗方法的开发将受益于确定巴尔通体在相关微环境中的靶标表达的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b52/11779821/82e2a1889f15/42003_2025_7535_Fig1_HTML.jpg

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