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Listeria monocytogenes is an ubiquitous bacteria responsible for the human listeriosis which can range from gastroenteritis to fatal meningitis. It is a rare but severe illness for pregnant women, elderly and immuno-compromised subjects with a death rate around 30%. During infection, the bacterium penetrates the cell and secretes multiple virulence factors that modulate the host's gene expression. LntA is one of these virulence factors and it targets Interferons-stimulated genes. While interferons (IFNs) are able to limit viral infections, their role in bacterial infection remains unclear. In the case of Listeria, the expression of interferons-stimulated-genes (ISG) enhances its pathogenicity (2). Lebreton et a.l (1) solved the 3D structure of lntA by x-rays crystallography (PDBID: 2XL4) in order to elucidate the mechanisms of interactions with the transcriptional machinery.

Function

Once the bacteria reaches the host's cytoplasm, the expression of LntA is activated, the protein is excreted and addressed to the nucleus thanks to a peptide signal. Then, LntA interacts with the transcription factor BAHD1 (link to a presentation and the structure of BAHD1). In absence of infection, BAHD1 represses the expression of ISG by promoting the local formation of heterochromatin while the interaction of LntA with BAHD1 has the effect of removing the chromatin repressor from the host’s DNA. Therefore, L. monocytogenes virulence factor induces a strong interferon response which enhances its pathogenicity. The mechanisms by which Listeria benefits from the synthesis of interferons are not fully understood. One hypothesis could be that Listeria monocytogenes takes advantage of the arrest of cellular-cycle induced by interferons (6). Indeed, this mechanism could be similar to those used by other pathogens such as Salmonella (7) or Yersinia (8) which are able to promote an inflammatory response in gut epithelium in order to facilitate their dissemination and colonization. In addition, Lebreton et al showed that when listeria grows outside the cell, the transcription rate of lntA is almost null and that a constitutive expression of LntA has an antibacterial effect. Thus, the efficiency of LntA requires a precise temporal and quantitative regulation.

Structure

LntA is a small basic protein of 9.7 kDa. This protein is highly conserved in L. monocytogenes and is absent in almost all non-pathogenic Listeria strains (1). This characteristic suggests that lntA plays a key role in Listeria’s virulence. The acidic part of LntA is composed of aspartic acid (17,8%) and the basic part is composed of lysine and arginine (18,6%).(Green Links) LntA is composed of 5 alpha-helix, three of them are long antiparallel helix and can be seen as the core of the protein. The two remaining helix stick out the core. The 3 first helix are named , and . The 2 others are and H5. These two helix are less rigid than the three first, probably because they are bonded to the BAHD1. Furthermore, the Lysine 180 and 181 are placed on this H5 helix, and they are responsible for the ligation to BAHD1 so it can cause a conformational change. Many amino acids may be involved in the interaction of LntA with its ligand, such as BAHD1. A has proven to be essential for the interaction with the transcription factor BAHD1 (1). Indeed, when this motif is substituted by two aspartic acid amino acids (K180D/K181D by mutation of LntA), a local redistribution of the charges is observed and lntA is not able anymore to interact with BAHD1 (green link). ^[1]