文献类型： 外文期刊

作者： Sun, Dage ¹ ; Gou, Hongchao ² ; Zhang, Yu ³ ; Li, Jiayi ¹ ; Dai, Changzhi ¹ ; Shen, Haiyan ² ; Chen, Kaifeng ¹ ; Wang, Yu ¹ ; Pan, Peng ¹ ; Zhu, Ting ¹ ; Xu, Chenggang ¹ ; Shan, Tongling ⁴ ; Liao, Ming ¹ ; Zhang, Jianmin ¹ ;

作者机构： 1.South China Agr Univ, Coll Vet Med, Natl & Reg Joint Engn Lab Medicament Zoonoses Prev, Minist Agr,Key Lab Zoonoses,Key Lab Zoonoses Preve, 483 Wushan Rd, Guangzhou 510642, Peoples R China

2.Guangdong Acad Agr Sci, Inst Anim Hlth, Guangdong Prov Key Lab Livestock Dis Prevent, Sci Observat & Expt Stn Vet Drugs & Diagnost Tech, Guangzhou, Peoples R China

3.Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Coll Stomatol, Sch Med,Dept Prevent Dent, Shanghai, Peoples R China

4.Chinese Acad Agr Sci, Shanghai Vet Res Inst, 518 Ziyue Rd, Shanghai 201100, Peoples R China

5.Zhongkai Univ Agr Engn, Coll Anim Sci & Technol, Dept Prevent Vet Med, 24 Dongsha St, Guangzhou 510642, Peoples R China

关键词： Mitophagy; PHB2; PINK1; PRKN; Salmonella Typhimurium; SseJ

期刊名称：AUTOPHAGY （ 影响因子：14.3； 五年影响因子：17.1 ）

ISSN： 1554-8627

年卷期： 2025 年 21 卷 6 期

页码：

收录情况： SCI

摘要： Despite decades of research on effective methods to resist Salmonella enterica serovar Typhimurium (S. Typhimurium) pathogenicity, the mechanisms of S. Typhimurium-host interactions have not been fully determined. S. Typhimurium is characterized as an important zoonosis in public health worldwide because of its endemicity, high morbidity, and difficulty in applying control and prevention measures. Herein, we introduce a novel bacterial factor, secretion system effector J (SseJ), and its interactive host protein, PHB2 (prohibitin 2). We explored whether SseJ affected S. Typhimurium replication and survival in the host. S. Typhimurium infection caused severe mitochondrial damage and mitophagy, which facilitated S. Typhimurium proliferation in cells. S. Typhimurium SseJ activated the PINK1 (PTEN induced kinase 1)-PRKN (parkin RBR E3 ubiquitin protein ligase)-autophagosome-dependent mitophagy pathway, aided by the mitophagy receptor PHB2, for bacterial survival and persistent infection. Moreover, suppression of mitophagy alleviated the pathogenicity of S. Typhimurium. In conclusion, S. Typhimurium infection could be antagonized by targeting the SseJ-PHB2-mediated host mitochondrial autophagy pathway.Abbreviation: ACTB: actin beta; BafA1: bafilomycin A1; CCCP: carbonyl cyanide m-chlorophenyl hydrazone; co-IP: co-immunoprecipitation; CFU: colony-forming units; COX4/COXIV: cytochrome c oxidase subunit 4; CQ: chloroquine; hpi: h post-bacterial infection; MAP1LC3B/LC3B: microtubule associated protein 1 light chain 3 beta; Mdivi-1:mitophagy inhibitor mitochondrial division inhibitor 1; MFN2: mitofusin 2; MG132: z-leu-leu-leucinal; MOI: multiplicity of infection; mtDNA: mitochondrial DNA; PBS: phosphate-buffered saline; PGAM5: PGAM family member 5, mitochondrial serine/threonine protein phosphatase; PHB2: prohibitin 2; PINK1: PTEN induced kinase 1; qPCR: quantitative real-time reverse transcription PCR; Roc-A: Rocaglamide A; PRKN/Parkin: parkin RBR E3 ubiquitin protein ligase; SCVs: Salmonella-containing vacuoles; siRNA: small interfering RNA; SPI-2: Salmonella pathogenicity island 2; SseJ: secretion system effector J; S. Typhimurium: Salmonella enterica serovar Typhimurium; S.T-Delta SseJ: SseJ gene-deleted Salmonella Typhimurium strains; S.T-C Delta SseJ: SseJ-complemented Salmonella Typhimurium strains; WT: wild-type.