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  3. Missing elimination via membrane vesicle shedding contributes to the diminished calcium sensitivity of listeriolysin O.
 

Missing elimination via membrane vesicle shedding contributes to the diminished calcium sensitivity of listeriolysin O.

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BORIS DOI
10.7892/boris.120795
Publisher DOI
10.1038/s41598-018-34031-4
PubMed ID
30367146
Description
The lytic capacity of cholesterol-dependent cytolysins is enhanced in the extracellular calcium-free environment through a combination of limited membrane repair and diminished membrane toxin removal. For a typical neurotoxin of the group, pneumolysin, this effect has already been observed at reduced (1 mM) calcium conditions, which are pathophysiologically relevant. Here, we tested another neurotoxin of the group, listeriolysin O from L. monocytogenes, active in the primary vacuole after bacterium phagocytosis in host cells. Reduced calcium did not increase the lytic capacity of listeriolysin (in contrast to pneumolysin), while calcium-free conditions elevated it 2.5 times compared to 10 times for pneumolysin (at equivalent hemolytic capacities). To clarify these differences, we analyzed membrane vesicle shedding, known to be a calcium-dependent process for toxin removal from eukaryotic cell membranes. Both pneumolysin and listeriolysin initiated vesicle shedding, which was completely blocked by the lack of extracellular calcium. Lack of calcium, however, elevated the toxin load per a cell only for pneumolysin and not for listeriolysin. This result indicates that vesicle shedding does not play a role in the membrane removal of listeriolysin and outlines a major difference between it and other members of the CDC group. Furthermore, it provides new tools for studying membrane vesicle shedding.
Date of Publication
2018-10-26
Publication Type
Article
Subject(s)
600 - Technology::610 - Medicine & health
500 - Science::570 - Life sciences; biology
Language(s)
en
Contributor(s)
Maurer, Jana
Hupp, Sabrina
Institut für Anatomie
Pillich, Helena
Mitchell, Timothy J
Chakraborty, Trinad
Iliev, Asparouh I
Additional Credits
Institut für Anatomie
Series
Scientific Reports
Publisher
Nature Publishing Group
ISSN
2045-2322
Access(Rights)
open.access
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