1. Listeria monocytogenes utilizes glutathione and limited inorganic sulfur compounds as sources of essential cysteine
- Author
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Berude, John C, Kennouche, Paul, Reniere, Michelle L, and Portnoy, Daniel A
- Subjects
Microbiology ,Biological Sciences ,Biodefense ,Infectious Diseases ,Foodborne Illness ,Emerging Infectious Diseases ,Digestive Diseases ,Animals ,Listeria monocytogenes ,Cysteine ,Glutathione Disulfide ,Sulfur Compounds ,Glutathione ,Sulfur ,Bacterial Proteins ,Gene Expression Regulation ,Bacterial ,Mammals ,GSH ,GSSG ,Ctp ,CtaP ,Opp ,OppABCDF ,CysK ,thiosulfate ,auxotrophy ,pathoadaptation ,Agricultural and Veterinary Sciences ,Medical and Health Sciences ,Immunology ,Medical microbiology - Abstract
Listeria monocytogenes (Lm) is a Gram-positive facultative intracellular pathogen that leads a biphasic lifecycle, transitioning its metabolism and selectively inducing virulence genes when it encounters mammalian hosts. Virulence gene expression is controlled by the master virulence regulator PrfA, which is allosterically activated by the host- and bacterially derived glutathione (GSH). The amino acid cysteine is the rate-limiting substrate for GSH synthesis in bacteria and is essential for bacterial growth. Unlike many bacteria, Lm is auxotrophic for cysteine and must import exogenous cysteine for growth and virulence. GSH is enriched in the host cytoplasm, and previous work suggests that Lm utilizes exogenous GSH for PrfA activation. Despite these observations, the import mechanism(s) for GSH remains elusive. Analysis of known GSH importers predicted a homologous importer in Lm comprised of the Ctp ABC transporter and the OppDF ATPases of the Opp oligopeptide importer. Here, we demonstrated that the Ctp complex is a high-affinity GSH/GSSG importer that is required for Lm growth at physiologically relevant concentrations. Furthermore, we demonstrated that OppDF is required for GSH/GSSG import in an Opp-independent manner. These data support a model where Ctp and OppDF form a unique complex for GSH/GSSG import that supports growth and pathogenesis. In addition, we show that Lm utilizes the inorganic sulfur sources thiosulfate and H2S for growth in a CysK-dependent manner in the absence of other cysteine sources. These findings suggest a pathoadaptive role for partial cysteine auxotrophy in Lm, where locally high GSH/GSSG or inorganic sulfur concentrations may signal arrival to distinct host niches.
- Published
- 2024