Listeria monocytogenes encodes a functional ESX-1 secretion system whose expression is detrimental to in vivo infection.
Jorge PinheiroOlga ReisAna VieiraInes M MouraLuisa Zanolli MorenoFilipe CarvalhoM Graciela PucciarelliFrancisco García-Del PortilloSandra SousaDidier CabanesPublished in: Virulence (2016)
Bacterial pathogenicity deeply depends on the ability to secrete virulence factors that bind specific targets on host cells and manipulate host responses. The Gram-positive bacterium Listeria monocytogenes is a human foodborne pathogen that remains a serious public health concern. To transport proteins across its cell envelope, this facultative intracellular pathogen engages a set of specialized secretion systems. Here we show that L. monocytogenes EGDe uses a specialized secretion system, named ESX-1, to secrete EsxA, a homolog of the virulence determinants ESAT-6 and EsxA of Mycobacterium tuberculosis and Staphylococcus aureus, respectively. Our data show that the L. monocytogenes ESX-1 secretion system and its substrates are dispensable for bacterial invasion and intracellular multiplication in eukaryotic cell lines. Surprisingly, we found that the EssC-dependent secretion of EsxA has a detrimental effect on L. monocytogenes in vivo infection.
Keyphrases
- listeria monocytogenes
- staphylococcus aureus
- public health
- biofilm formation
- mycobacterium tuberculosis
- escherichia coli
- pseudomonas aeruginosa
- palliative care
- endothelial cells
- candida albicans
- induced apoptosis
- poor prognosis
- stem cells
- cell death
- single cell
- electronic health record
- reactive oxygen species
- multidrug resistant
- cell cycle arrest
- bone marrow
- machine learning