Journal article
The Impact of ExoS on Pseudomonas aeruginosa Internalization by Epithelial Cells Is Independent of fleQ and Correlates with Bistability of Type Three Secretion System Gene Expression
mBio, Vol.9(3), p.e00668-18
05/01/2018
DOI: 10.1128/mBio.00668-18
PMCID: PMC5930308
PMID: 29717012
Abstract
is internalized into multiple types of epithelial cell
and
and yet is often regarded as an exclusively extracellular pathogen. Paradoxically, ExoS, a type three secretion system (T3SS) effector, has antiphagocytic activities but is required for intracellular survival of
and its occupation of bleb niches in epithelial cells. Here, we addressed mechanisms for this dichotomy using invasive (ExoS-expressing)
and corresponding effector-null isogenic T3SS mutants, effector-null mutants of cytotoxic
with and without ExoS transformation, antibiotic exclusion assays, and imaging using a T3SS-GFP reporter. Except for effector-null PA103, all strains were internalized while encoding ExoS. Intracellular bacteria showed T3SS activation that continued in replicating daughter cells. Correcting the
mutation in effector-null PA103 promoted internalization by >10-fold with or without ExoS. Conversely, mutating
in PAO1 reduced internalization by >10-fold, also with or without ExoS. Effector-null PA103 remained less well internalized than PAO1 matched for
status, but only with ExoS expression, suggesting additional differences between these strains. Quantifying T3SS activation using GFP fluorescence and quantitative reverse transcription-PCR (qRT-PCR) showed that T3SS expression was hyperinducible for strain PA103Δ
versus other isolates and was unrelated to
status. These findings support the principle that
is not exclusively an extracellular pathogen, with internalization influenced by the relative proportions of T3SS-positive and T3SS-negative bacteria in the population during host cell interaction. These data also challenge current thinking about T3SS effector delivery into host cells and suggest that T3SS bistability is an important consideration in studying
pathogenesis.
is often referred to as an extracellular pathogen, despite its demonstrated capacity to invade and survive within host cells. Fueling the confusion,
encodes T3SS effectors with anti-internalization activity that, paradoxically, play critical roles in intracellular survival. Here, we sought to address why ExoS does not prevent internalization of the
strains that natively encode it. Results showed that ExoS exerted unusually strong anti-internalization activity under conditions of expression in the effector-null background of strain PA103, often used to study T3SS effector activity. Inhibition of internalization was associated with T3SS hyperinducibility and ExoS delivery. PA103
mutation, preventing flagellar assembly, further reduced internalization but did so independently of ExoS. The results revealed intracellular T3SS expression by all strains and suggested that T3SS bistability influences
internalization. These findings reconcile controversies in the literature surrounding
internalization and support the principle that
is not exclusively an extracellular pathogen.
Details
- Title: Subtitle
- The Impact of ExoS on Pseudomonas aeruginosa Internalization by Epithelial Cells Is Independent of fleQ and Correlates with Bistability of Type Three Secretion System Gene Expression
- Creators
- Abby R Kroken - School of Optometry, University of California, Berkeley, Berkeley, California, USACamille K Chen - School of Optometry, University of California, Berkeley, Berkeley, California, USADavid J Evans - College of Pharmacy, Touro University California, Vallejo, California, USATimothy L Yahr - Department of Microbiology and Immunology, University of Iowa, Iowa City, Iowa, USASuzanne M J Fleiszig - Graduate Groups in Vision Science, Microbiology, and Infectious Diseases & Immunity, University of California, Berkeley, Berkeley, California, USA
- Resource Type
- Journal article
- Publication Details
- mBio, Vol.9(3), p.e00668-18
- DOI
- 10.1128/mBio.00668-18
- PMID
- 29717012
- PMCID
- PMC5930308
- NLM abbreviation
- mBio
- ISSN
- 2161-2129
- eISSN
- 2150-7511
- Publisher
- United States
- Grant note
- F32 EY025969 / NEI NIH HHS R01 EY011221 / NEI NIH HHS P30 DK089507 / NIDDK NIH HHS P30 DK054759 / NIDDK NIH HHS
- Language
- English
- Date published
- 05/01/2018
- Academic Unit
- Microbiology and Immunology
- Record Identifier
- 9984001204902771
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