Apoptosis induced by Pseudomonas aeruginosa: a lonely killer?

Abstract

Apoptosis is a fundamental biological process allowing tissue homeostasis through the regulation of cell populations by eliminating unnecessary elements. During infection, pathogens have evolved to take advantage of this process for their own and are able to induce the apoptosis of cells, i.e. immune cells by the host itself. Pseudomonas aeruginosa is one of the most studied opportunistic bacteria due to its significant involvement worldwide in pneumonia, corneal infections and wound burns. Several research groups have pointed out the ability of these bacteria to interfere and/or evade host immune system by inducing apoptosis of the targeted cells. In May 2014, looking up ‘Pseudomonas aeruginosa’ and ‘apoptosis’ keywords in PubMed search engine retrieve more than 300 hits. Pseudomonas aeruginosa seems to induce apoptosis through direct interaction with the host cells (the most studied system being the type-III secretion system: T3SS) or through secreting factors such as pyocyanin. T3SS, the most well-studied virulence apparatus of P. aeruginosa is composed of a needle complex through which exoenzymes are injected into the host cells (Galle et al., 2012,2012). Recently, Beyaert's laboratory described an exotoxin-independent function of the T3SS in the killing of macrophages in an acute lung infection model (Galle et al., 2012,2012). Although, T3SS is a major virulence system, it is not fully required for the bacteria to display virulence as T3SS negative strains are shown to exihibit signficant virulence (example of Elsen's paper). In short, a wide variety of P. aeruginosa virulence factors are involved in inducing apoptosis by several distinct mechanisms, from the activation of the mitochondrial pathway, the generation of reactive oxygen species to the activation of the caspase pathways (Table 1). The ability of P. aeruginosa to induce apoptosis in various in vitro model of infection (macrophages, neutrophils, epithelial cells …) or in vivo models such as lungs, cornea and burn wounds infections is not mediated by a single bacterial cell but rather by a multicellular population of P. aeruginosa. Members of such population interact with each other through a number of chemical signals known globally on for quorum sensing (QS). Quoting Rutherford and Bassler (2012), ‘Quorum sensing is a bacterial cell-cell communication process that involves the production, detection, and response to extracellular signaling molecules called autoinducers’. QS molecules were shown to regulate virulence factors such as toxins, exotoxin A, pyocyanin, … and so in fine apoptosis (Rutherford and Bassler, 2012). The best described QS signalling systems in P. aeruginosa are the N-acyl homoserine lactones systems Las and Rhl. The Las system produces and responds to N-oxododecanoyl homoserine lactone and the Rhl system to N-butanoyl homoserine lactone respectively. Las system is known to control the production of various virulence factors involved in host cell damages such as exotoxin A (Jones et al., 1993). On the other hand, Rhl system was described to repress the expression of genes responsible for the assembly and function of the T3SS (Bleves et al., 2005). Last but not least, QS molecule such as 3-oxododecanoyl-L-homoserine lactone (3-oxo-C12-HSL) itself has been shown to induce apoptosis. Several studies have demonstrated that incubation of different cell lines with 3-oxo-C12-HSL molecule resulted in the induction of apoptosis involving calcium signalling, the mitochondrial pathway and caspase activations (Table 2). Interestingly, N-butanoyl-L-homoserine lactone (known as C4-HSL, the second major QS molecule in P. aeruginosa) harbouring a shorter fatty acid chain has not been shown to induce apoptosis compared with 3-oxo-C12-HSL (Tateda et al., 2003; Holban et al., 2014). Knowing that P. aeruginosa is able to induce apoptosis through its QS systems molecule, studies focusing on apoptosis induction should be considered with the context of QS signalling. Particularly, QS considerations should be taken into account when comparing studies using different multiplicity of infection or bacteria preparation protocols, processes that influence QS molecules concentration and/or bacteria population numbers. None declared.