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Bat B, CHU Purpan, Toulouse, France \n French National Institute for Agricultural and Environmental Research, France \n Cited By :1 \n Export Date: 11 April 2023 \n Correspondence Address: Korcsmaros, T.; Earlham Institute, Norwich Research Park, United Kingdom; email: Tamas.Korcsmaros@earlham.ac.uk", "unhandledTickets" : 0, "deleted" : false, "lastRefresh" : "2024-03-07T19:49:02.773+0000", "lastModified" : "2024-03-07T19:41:46.225+0000", "created" : "2022-08-25T19:33:12.996+0000", "creator" : { "otype" : "Author", "mtid" : 10020542, "link" : "/api/author/10020542", "label" : "Ari Eszter (Bioinformatika, evolúció)", "familyName" : "Ari", "givenName" : "Eszter", "published" : true, "oldId" : 10020542, "snippet" : true }, "lastDuplumOK" : "2024-03-07T19:41:46.498+0000", "lastDuplumSearch" : "2024-03-07T19:41:46.498+0000", "core" : true, "citation" : true, "publicationPending" : false, "type" : { "otype" : "PublicationType", "mtid" : 24, "link" : "/api/publicationtype/24", "label" : 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Some intracellular pathogens such as Salmonella enterica serovar Typhimurium hijack this process during pathogenesis. Here we investigate potential protein-protein interactions between host transcription factors and secreted effector proteins of Salmonella and their effect on host gene transcription. A systems-level analysis identified Salmonella effector proteins that had the potential to affect core autophagy gene regulation. The effect of a SPI-1 effector protein, SopE, that was predicted to interact with regulatory proteins of the autophagy process, was investigated to validate our approach. We then confirmed experimentally that SopE can directly bind to SP1, a host transcription factor, which modulates the expression of the autophagy gene MAP1LC3B . We also revealed that SopE might have a double role in the modulation of autophagy: Following initial increase of MAP1LC3B transcription triggered by Salmonella infection, subsequent decrease in MAP1LC3B transcription at 6h post-infection was SopE-dependent. SopE also played a role in modulation of the autophagy flux machinery, in particular MAP1LC3B and p62 autophagy proteins, depending on the level of autophagy already taking place. Upon typical infection of epithelial cells, the autophagic flux is increased. However, when autophagy was chemically induced prior to infection, SopE dampened the autophagic flux. The same was also observed when most of the intracellular Salmonella cells were not associated with the SCV (strain lacking sifA ) regardless of the autophagy induction status before infection. We demonstrated how regulatory network analysis can be used to better characterise the impact of pathogenic effector proteins, in this case, Salmonella . This study complements previous work in which we had demonstrated that specific pathogen effectors can affect the autophagy process through direct interaction with autophagy proteins. Here we show that effector proteins can also influence the upstream regulation of the process. 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