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将新凶手弗朗西斯菌FTN_0096鉴定为参与细胞内复制和宿主反应的一个因子。

Identification of the Francisella novicida FTN_0096 as a factor involved in intracellular replication and host response.

作者信息

Wardhana Dhandy Koesoemo, Shimizu Takashi, Watanabe Kenta, Uda Akihiko, Watarai Masahisa

机构信息

Laboratory of Veterinary Public Health, Joint Graduate School of Veterinary Medicine, Yamaguchi University, Yamaguchi, Japan.

Division of Veterinary Public Health, Department of Veterinary Science, Faculty of Veterinary Medicine, Universitas Airlangga, Surabaya, Indonesia.

出版信息

PLoS One. 2025 Aug 1;20(8):e0329626. doi: 10.1371/journal.pone.0329626. eCollection 2025.

Abstract

Francisella tularensis is the causative agent of the zoonotic disease tularemia. We investigated a pathogenic factor of F. tularensis subsp. novicida (F. novicida). Accordingly, we established a novel infection model using HeLa cells. F. novicida usually infects macrophage lineage cells and less frequently epithelial cells. We successfully infected HeLa cells expressing the Fc receptor (HeLa-FcγRII cells) using F. novicida supplemented with mouse serum containing F. novicida antibodies. A total of 2,232 transposon mutants of F. novicida were screened to determine the relatively fewer cytotoxic strains of the HeLa-FcγRII cells, and 13 strains were thus isolated. Sequencing analysis of transposon insertion sites identified 13 genes, including FTN_0096. We focused on FTN_0096. Although the F. novicida wild-type strain proliferated in HeLa-FcγRII and THP-1 cells, the number of intracellular FTN_0096 mutant decreased. FTN_0096 mutant cannot escape from phagolysosomes in the initial phases of infection. Moreover, FTN_0096 mutant was detected in the mitochondria and Golgi complex. These findings indicate the importance of FTN_0096 of F. novicida for intracellular replication in the cells.

摘要

土拉弗朗西斯菌是人畜共患病兔热病的病原体。我们研究了土拉弗朗西斯菌新凶手亚种(F. novicida)的一种致病因子。据此,我们利用HeLa细胞建立了一种新型感染模型。F. novicida通常感染巨噬细胞系细胞,较少感染上皮细胞。我们使用添加了含有F. novicida抗体的小鼠血清的F. novicida成功感染了表达Fc受体的HeLa细胞(HeLa-FcγRII细胞)。总共筛选了2232个F. novicida转座子突变体,以确定对HeLa-FcγRII细胞细胞毒性相对较小的菌株,从而分离出13株菌株。对转座子插入位点的测序分析确定了13个基因,包括FTN_0096。我们聚焦于FTN_0096。虽然F. novicida野生型菌株在HeLa-FcγRII和THP-1细胞中增殖,但细胞内FTN_0096突变体的数量减少。FTN_0096突变体在感染初期无法从吞噬溶酶体中逃逸。此外,在 mitochondria 和高尔基体复合体中检测到了FTN_0096突变体。这些发现表明F. novicida的FTN_0096对细胞内复制的重要性。 (注:原文中“mitochondria”有误,推测应为“mitochondria”,已按正确的“线粒体”翻译)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f5/12316277/c15e0566fd20/pone.0329626.g001.jpg

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