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• W2107985229 abstract "ABSTRACT The multifunctional-autoprocessing repeats-in-toxin (MARTX Vv ) toxin of Vibrio vulnificus plays a significant role in the pathogenesis of this bacterium through delivery of up to five effector domains to the host cells. Previous studies have established that the MARTX Vv toxin is linked to V. vulnificus dependent induction of apoptosis, but the region of the large multifunction protein essential for this activity was not previously identified. Recently, we showed that the Makes Caterpillar Floppy-like MARTX effector domain (MCF Vv ) is an autoproteolytic cysteine protease that induces rounding of various cell types. In this study, we demonstrate that cell rounding induced by MCF Vv is coupled to reduced metabolic rate and inhibition of cellular proliferation. Moreover, delivery of MCF Vv into host cells either as a fusion to the N-terminal fragment of anthrax toxin lethal factor or when naturally delivered as a V. vulnificus MARTX toxin led to loss of mitochondrial membrane potential, release of cytochrome c , activation of Bax and Bak, and processing of caspases and poly-(ADP-ribose) polymerase (PARP-γ). These studies specifically link the MCF Vv effector domain to induction of the intrinsic apoptosis pathway by V. vulnificus ." @default.
• W2107985229 created "2016-06-24" @default.
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• W2107985229 date "2015-11-01" @default.
• W2107985229 modified "2023-09-25" @default.
• W2107985229 title "The Makes Caterpillars Floppy (MCF)-Like Domain of Vibrio vulnificus Induces Mitochondrion-Mediated Apoptosis" @default.
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• W2107985229 doi "https://doi.org/10.1128/iai.00570-15" @default.
• W2107985229 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4598404" @default.
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• W2107985229 hasPublicationYear "2015" @default.
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