Toward a structural understanding of Clostridium difficile toxins A and B

被引:135
作者
Pruitt, Rory N. [1 ]
Lacy, D. Borden [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Pathol Microbiol & Immunol, Nashville, TN 37232 USA
关键词
C; difficile; bacterial toxin; receptor-binding; pore formation; autoprocessing; glucosyltransferase; RHO-PROTEINS; ADP-RIBOSYLTRANSFERASE; CONFORMATIONAL-CHANGES; HEMORRHAGIC TOXIN; ANTIBODY-RESPONSE; INDUCED APOPTOSIS; SURFACE BINDING; VARIANT STRAIN; PORE FORMATION; LETHAL TOXIN;
D O I
10.3389/fcimb.2012.00028
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Clostridium difficile is a toxin producing bacterium that is a frequent cause of hospital-acquired and antibiotic-associated diarrhea. The incidence, severity, and costs associated with C. difficile associated disease are substantial and increasing, making C. difficile a significant public health concern. The two primary toxins, TcdA and TcdB, disrupt host cell function by inactivating small GTPases that regulate the actin cytoskeleton. This review will discuss the role of these two toxins in pathogenesis and the structural and molecular mechanisms by which they intoxicate cells. A focus will be placed on recent publications highlighting mechanistic similarities and differences between TcdA, TcdB, and different TcdB variants.
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页数:14
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共 125 条
[1]   Increased sporulation rate of epidemic clostridium difficile type 027/NAP1 [J].
Akerlund, Thomas ;
Persson, Ingela ;
Unemo, Magnus ;
Noren, Torbjoern ;
Svenungsson, Bo ;
Wullt, Marlene ;
Burman, Lars G. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2008, 46 (04) :1530-1533
[2]   MONOGLUCOSYLATION OF LOW-MOLECULAR-MASS GTP-BINDING RHO PROTEINS BY CLOSTRIDIAL CYTOTOXINS [J].
AKTORIES, K ;
JUST, I .
TRENDS IN CELL BIOLOGY, 1995, 5 (12) :441-443
[3]   Bacterial toxins that target Rho proteins [J].
Aktories, K .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (05) :827-829
[4]   Bacterial cytotoxins: Targeting eukaryotic switches [J].
Aktories, K ;
Barbieri, JT .
NATURE REVIEWS MICROBIOLOGY, 2005, 3 (05) :397-410
[5]   Four Distinct Structural Domains in Clostridium difficile Toxin B Visualized Using SAXS [J].
Albesa-Jove, David ;
Bertrand, Thomas ;
Carpenter, Elisabeth P. ;
Swain, Gemma V. ;
Lim, Jenson ;
Zhang, Jiancheng ;
Haire, Lesley F. ;
Vasisht, Nish ;
Braun, Veit ;
Lange, Anton ;
von Eichel-Strelber, Christoph ;
Svergun, Dmitri I. ;
Fairweather, Neil F. ;
Brown, Katherine A. .
JOURNAL OF MOLECULAR BIOLOGY, 2010, 396 (05) :1260-1270
[6]   A novel toxin homologous to large clostridial cytotoxins found in culture supernatant of Clostridium perfringens type C [J].
Amimoto, Katsuhiko ;
Noro, Taichi ;
Oishi, Eiji ;
Shimizu, Mitsugu .
MICROBIOLOGY-SGM, 2007, 153 :1198-1206
[7]  
[Anonymous], B J HOPKINS HOSP
[8]   Human monoclonal antibodies directed against toxins A and B prevent Clostridium difficile-induced mortality in hamsters [J].
Babcock, Gregory J. ;
Broering, Teresa J. ;
Hernandez, Hector J. ;
Mandell, Robert B. ;
Donahue, Katherine ;
Boatright, Naomi ;
Stack, Anne M. ;
Lowy, Israel ;
Graziano, Robert ;
Molrine, Deborah ;
Ambrosino, Donna M. ;
Thomas, William D., Jr. .
INFECTION AND IMMUNITY, 2006, 74 (11) :6339-6347
[9]   PURIFICATION AND CHARACTERIZATION OF ALPHA-TOXIN PRODUCED BY CLOSTRIDIUM-NOVYI TYPE-A [J].
BALL, DW ;
VANTASSELL, RL ;
ROBERTS, MD ;
HAHN, PE ;
LYERLY, DM ;
WILKINS, TD .
INFECTION AND IMMUNITY, 1993, 61 (07) :2912-2918
[10]   Clinical features of Clostridium difficile-associated diarrhoea due to binary toxin (actin-specific ADP-ribosyltransferase)-producing strains [J].
Barbut, F ;
Decré, D ;
Lalande, V ;
Burghoffer, A ;
Noussair, L ;
Gigandon, A ;
Espinasse, F ;
Raskine, L ;
Robert, J ;
Mangeol, A ;
Branger, C ;
Petit, JC .
JOURNAL OF MEDICAL MICROBIOLOGY, 2005, 54 (02) :181-185