Growth phase-dependent invasion of Pseudomonas aeruginosa and its survival within HeLa cells
1Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, Florida 32610, USA.
Abstract:
Clinical isolates of Pseudomonas aeruginosa are classified into invasive and noninvasive (cytolytic) strains. In a noninvasive PA103 background, ExoS and ExoT have recently been shown to function as anti-internalization factors. However, these two factors seemed not to have such a function in an invasive strain PAK background. In this study, using HeLa tissue culture cells, we observed that the internalization of invasive strain PAK is dependent on its growth phases, with the stationary-phase cells internalized about 100-fold more efficiently than the exponential-phase cells. This growth phase-dependent internalization was not observed in the noninvasive PA103 strain. Further analysis of various mutant derivatives of the invasive PAK and the noninvasive PA103 strains demonstrated that ExoS or ExoT that is injected into host cells by a type III secretion machinery functions as an anti-internalization factor in both types of strains. In correlation with the growth phase-dependent internalization, the invasive strain PAK translocates much higher amount of ExoS and ExoT into HeLa cells when it is in an exponential-growth phase than when it is in a stationary-growth phase, whereas the translocation of ExoT by the noninvasive strain PA103 is consistently high regardless of the growth phases, suggesting a difference in the regulatory mechanism of type III secretion between the two types of strains. Consistent with the invasive phenotype of the parent strain, an internalized PAK derivative survived well within the HeLa cells, whereas the viability of internalized PA103 derivative was dramatically decreased and completely cleared within 48 h. These results indicate that the invasive strains of P. aeruginosa have evolved the mechanism of intracellular survival, whereas the noninvasive P. aeruginosa strains have lost or not acquired the ability to survive within the epithelial cells.
Insights
Invasive Pseudomonas aeruginosa strains internalize into host cells more efficiently during stationary phase, with toxins ExoS and ExoT acting as anti-internalization factors. Invasive strains also exhibit enhanced intracellular survival compared to noninvasive strains.
Area of Science:
- Microbiology
- Cell Biology
- Bacterial Pathogenesis
Background:
- Pseudomonas aeruginosa strains are categorized as invasive or noninvasive.
- ExoS and ExoT are toxins previously identified as anti-internalization factors in noninvasive strains.
- Their role in invasive strains was unclear, prompting further investigation.
Purpose of the Study:
- To investigate the differential internalization of invasive (PAK) and noninvasive (PA103) Pseudomonas aeruginosa strains in HeLa cells.
- To determine the role of ExoS and ExoT in strain-specific internalization and intracellular survival.
- To explore the regulation of type III secretion in relation to bacterial growth phase.
Main Methods:
- Utilized HeLa tissue culture cells to study bacterial internalization.
- Generated and analyzed mutant derivatives of PAK and PA103 strains.
- Quantified bacterial translocation of ExoS and ExoT using type III secretion machinery.
- Assessed the intracellular viability of internalized bacteria.
Main Results:
- Invasive PAK strain internalization is growth phase-dependent, with higher efficiency in stationary phase.
- ExoS or ExoT function as anti-internalization factors in both invasive and noninvasive strains.
- PAK translocates more ExoS/ExoT in exponential phase, while PA103 translocation is consistent.
- Internalized PAK survives intracellularly, whereas PA103 is cleared within 48 hours.
Conclusions:
- Invasive P. aeruginosa strains possess mechanisms for intracellular survival.
- Noninvasive strains lack or have lost the ability to survive within epithelial cells.
- Differential regulation of type III secretion and growth phase impact bacterial invasion and survival.
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