Relevant Genes Linked to Virulence Are Required for Salmonella Typhimurium to Survive Intracellularly in the Social Amoeba Dictyostelium discoideum
Author
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Riquelme, Sebastián
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Varas, Macarena
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Valenzuela, Camila
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Velozo Hermosilla, Paula Elizabeth
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Chahin, Nicolás
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Aguilera, Paulina
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Sabag, Andrea
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Labra, Bayron
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Álvarez Armijo, Sergio
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Chávez, Francisco P.
Author
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Santiviago Cid, Carlos
Admission date
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2016-12-27T20:16:22Z
Available date
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2016-12-27T20:16:22Z
Publication date
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2016
Cita de ítem
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Frontiers in Microbiology August 2016 | Volume 7 | Article 1305
es_ES
Identifier
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10.3389/fmicb.2016.01305
Identifier
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https://repositorio.uchile.cl/handle/2250/142145
Abstract
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The social amoeba Dictyostelium discoideum has proven to be a useful model for studying relevant aspects of the host-pathogen interaction. In this work, D. discoideum was used as a model to study the ability of Salmonella Typhimurium to survive in amoebae and to evaluate the contribution of selected genes in this process. To do this, we performed infection assays using axenic cultures of D. discoideum co-cultured with wild-type S. Typhimurium and/or defined mutant strains. Our results confirmed that wild-type S. Typhimurium is able to survive intracellularly in D. discoideum. In contrast, mutants AaroA and A waaL are defective in intracellular survival in this amoeba. Next, we included in our study a group of mutants in genes directly linked to Salmonella virulence. Of note, mutants Delta invA, Delta ssaD, Delta cIpV, and Delta phoPQ also showed an impaired ability to survive intracellularly in D, discoideum. This indicates that S. Typhimurium requires a functional biosynthetic pathway of aromatic compounds, a lipopolysaccharide containing a complete O-antigen, the type III secretion systems (T3SS) encoded in SPI-1 and SPI-2, the type VI secretion system (T6SS) encoded in SPI-6 and PhoP/PhoQ two-component system to survive in D. discoideurn. To our knowledge, this is the first report on the requirement of O-antigen and T6SS in the survival of Salmonella within amoebae. In addition, mutants AinvA and AssaD were internalized in higher numbers than the wild -type strain during competitive infections, suggesting that S. Typhimurium requires the T3SS encoded in SPI-1 and SPI-2 to evade phagocytosis by D. discoideum. Altogether, these results indicate that S. Typhimurium exploits a common set of genes and molecular mechanisms to survive within amoeba and animal host cells. The use of D. discoideum as a model for host pathogen interactions will allow us to discover the gene repertoire used by Salmonella to survive inside the amoeba and to study the cellular processes that are affected during infection.