Cellular vacuolation and mitochondrial-associated factors induced by Clostridium perfringens epsilon toxin detected using acoustic flow cytometry

被引:13
作者
Ferrarezi, Marina C. [1 ]
Curci, Vera C. L. M. [2 ]
Cardoso, Tereza C. [1 ]
机构
[1] Univ Sao Paulo State, Dept Apoio Prod & Saude Anim, BR-16050680 Sao Paulo, Brazil
[2] APTA, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Mitochondria; Mitochondrion; Clostridium perfringens; Necrosis; In vitro assay; ALPHA;
D O I
10.1016/j.anaerobe.2013.09.009
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Epsilon toxin (ETX) produced by Clostridium perfringens types B and D is a potent toxin that is responsible for fatal enterotoxaemia. In vitro, ETX, which is considered as a pore-forming toxin, forms a heptamer in Madin-Darby canine kidney (MOCK) cell membranes, which is considered to be a pre-pore stage. After binding of the ETX, vacuoles inside cell cytoplasm are produced. ETX causes decreased levels of essential coenzymes required for host cell energy. Here, we optimized and applied acoustic flow cytometry analysis in order to gain further insight into ETX-pathogenesis. Using acoustic flow cytometer analysis, which considered highly sensitive, ETX-exposed MOCK cells revealed mitochondrial membrane decreases followed by 25.48% and 45.45% of the exposed cells expressing the Bax and BCL-2 proteins at a pre-pore stage, respectively. These results together with high cytotoxicity and visualization of cell vacuoles, demonstrates that acoustic flow cytometry analysis potentially represents an effective tool to study ETX pathogenesis. (C) 2013 Published by Elsevier Ltd.
引用
收藏
页码:55 / 59
页数:5
相关论文
共 25 条
[1]   Cytotoxic effects induced by oxidative stress in cultured mammalian cells and protection provided by Hsp27 expression [J].
Arrigo, AP ;
Firdaus, WJJ ;
Mellier, G ;
Moulin, M ;
Paul, C ;
Diaz-latoud, C ;
Kretz-remy, C .
METHODS, 2005, 35 (02) :126-138
[2]  
Borrmann E, 2001, FEMS IMMUNOL MED MIC, V31, P85, DOI 10.1111/j.1574-695X.2001.tb00503.x
[3]   Programmed cell death via mitochondria: Different modes of dying [J].
Bras, M ;
Queenan, B ;
Susin, SA .
BIOCHEMISTRY-MOSCOW, 2005, 70 (02) :231-+
[4]   Pore-forming epsilon toxin causes membrane permeabilization and rapid ATP depletion-mediated cell death in renal collecting duct cells [J].
Chassin, C. ;
Bens, M. ;
de Barry, J. ;
Courjaret, R. ;
Bossu, J. L. ;
Cluzeaud, F. ;
Ben Mkaddem, S. ;
Gibert, M. ;
Poulain, B. ;
Popoff, M. R. ;
Vandewalle, A. .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2007, 293 (03) :F927-F937
[5]   Characterization of the high affinity binding of epsilon toxin from Clostridium perfringens to the renal system [J].
Dorca-Arevalo, Jonatan ;
Martin-Satue, Mireia ;
Blasi, Juan .
VETERINARY MICROBIOLOGY, 2012, 157 (1-2) :179-189
[6]   Coenzyme depletion by members of the aerolysin family of pore-forming toxins leads to diminished ATP levels and cell death [J].
Fennessey, Christine M. ;
Ivie, Susan E. ;
McClain, Mark S. .
MOLECULAR BIOSYSTEMS, 2012, 8 (08) :2097-2105
[7]   Clostridium perfringens epsilon toxin is cytotoxic for human renal tubular epithelial cells [J].
Fernandez Miyakawa, Mariano E. ;
Zabal, Osvaldo ;
Silberstein, Claudia .
HUMAN & EXPERIMENTAL TOXICOLOGY, 2011, 30 (04) :275-282
[8]  
Givan AL, 2011, METHODS MOL BIOL, V699, P1, DOI 10.1007/978-1-61737-950-5_1
[9]  
Goddard G, 2005, CYTOM PART A, V69, P66
[10]   Analytical performance of an ultrasonic particle focusing flow cytometer [J].
Goddard, Gregory R. ;
Sanders, Claire K. ;
Martin, John C. ;
Kaduchak, Gregory ;
Graves, Steven W. .
ANALYTICAL CHEMISTRY, 2007, 79 (22) :8740-8746