Porin loss impacts the host inflammatory response to outer membrane vesicles of Klebsiella pneumoniae
Document Type
Article
Publication Date
3-1-2016
Abstract
Antibiotic-resistant strains of Klebsiella pneumoniae often exhibit porin loss. In this study, we investigated how porin loss impacted the composition of secreted outer membrane vesicles as well as their ability to trigger proinflammatory cytokine secretion by macrophages. We hypothesize that porin loss associated with antibiotic resistance will directly impact both the composition of outer membrane vesicles and their interactions with phagocytic cells. Using clonally related clinical isolates of extended-spectrum beta-lactamase (ESBL)-positive Klebsiella pneumoniae with different patterns of porin expression, we demonstrated that altered expression of OmpK35 and OmpK36 results in broad alterations to the protein profile of secreted vesicles. Additionally, the level of OmpA incorporation was elevated in strains lacking a single porin. Porin loss significantly impacted macrophage inflammatory responses to purified vesicles. Outer membrane vesicles lacking both OmpK35 and OmpK36 elicited significantly lower levels of proinflammatory cytokine secretion than vesicles from strains expressing one or both porins. These data demonstrate that antibiotic resistance-associated porin loss has a broad and significant effect on both the composition of outer membrane vesicles and their interactions with phagocytic cells, which may impact bacterial survival and inflammatory reactions in the host.
Publication Title
Antimicrobial Agents and Chemotherapy
Volume
60
Issue
3
First Page
1360
Last Page
1369
Digital Object Identifier (DOI)
10.1128/AAC.01627-15
PubMed ID
26666932
ISSN
00664804
E-ISSN
10986596
Citation Information
Turner, Cahill, B. K., Dilello, S. K., Gutel, D., Brunson, D. N., Albertí, S., & Ellis, T. N. (2015). Porin Loss Impacts the Host Inflammatory Response to Outer Membrane Vesicles of Klebsiella pneumoniae. Antimicrobial Agents and Chemotherapy, 60(3), 1360–1369. https://doi.org/10.1128/AAC.01627-15