Abstract
Intracellular pathogens such as Listeria monocytogenes subvert cellular functions through the interaction of bacterial effectors with host components. Here we found that a secreted listerial virulence factor, LntA, could target the chromatin repressor BAHD1 in the host cell nucleus to activate interferon (IFN)-stimulated genes (ISGs). IFN-λ expression was induced in response to infection of epithelial cells with bacteria lacking LntA; however, the BAHD1-chromatin associated complex repressed downstream ISGs. In contrast, in cells infected with lntA-expressing bacteria, LntA prevented BAHD1 recruitment to ISGs and stimulated their expression. Murine listeriosis decreased in BAHD1(+/-) mice or when lntA was constitutively expressed. Thus, the LntA-BAHD1 interplay may modulate IFN-λ-mediated immune response to control bacterial colonization of the host.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Cell Line
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Cell Line, Tumor
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Cell Nucleus / metabolism
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Chromatin / metabolism*
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Chromosomal Proteins, Non-Histone / metabolism*
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Down-Regulation
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Gene Expression Profiling
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Gene Expression Regulation
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Host-Pathogen Interactions
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Humans
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Interferons / genetics
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Interferons / immunology
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Interferons / metabolism*
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Interleukins / genetics
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Interleukins / immunology
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Interleukins / metabolism*
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Listeria monocytogenes / genetics
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Listeria monocytogenes / metabolism
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Listeria monocytogenes / pathogenicity*
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Listeriosis / immunology*
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Listeriosis / microbiology
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Mice
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Mice, Inbred BALB C
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Mice, Inbred C57BL
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Molecular Sequence Data
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Signal Transduction
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Virulence Factors / chemistry
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Virulence Factors / genetics
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Virulence Factors / metabolism*
Substances
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BAHD1 protein, human
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BAHD1 protein, mouse
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Chromatin
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Chromosomal Proteins, Non-Histone
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Interleukins
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Virulence Factors
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Interferons