Tolevamer, an anionic polymer, neutralizes toxins produced by the BI/027 strains of Clostridium difficile

被引:32
作者
Hinkson, Paul L. [1 ]
Dinardo, Carol [1 ]
DeCiero, Daniel [1 ]
Klinger, Jeffrey D. [1 ]
Barker, Robert H., Jr. [1 ]
机构
[1] Genzyme Drug & Biomat Res & Dev, Waltham, MA 02451 USA
关键词
D O I
10.1128/AAC.00041-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Clostridium difficile-associated diarrhea (CDAD) is caused by the toxins the organism produces when it overgrows in the colon as a consequence of antibiotic depletion of normal flora. Conventional antibiotic treatment of CDAD increases the likelihood of recurrent disease by again suppressing normal bacterial flora. Tolevamer, a novel toxin-binding polymer, was developed to ameliorate the disease without adversely affecting normal flora. In the current study, tolevamer was tested for its ability to neutralize clostridial toxins produced by the epidemic BI/027 strains, thereby preventing toxin-mediated tissue culture cell rounding. The titers of toxin-containing C. difficile culture supernatants were determined using confluent cell monolayers, and then the supernatants were used in assays containing dilutions of tolevamer to determine the lowest concentration of tolevamer that prevented >= 90% cytotoxicity. Tolevamer neutralized toxins in the supernatants of all C. difficile strains tested. Specific antibodies against the large clostridial toxins TcdA and TcdB also neutralized the cytopathic effect, suggesting that tolevamer is specifically neutralizing these toxins and that the binary toxin (whose genes are carried by the BI/027 strains) is not a significant source of cytopathology against tissue culture cells in vitro.
引用
收藏
页码:2190 / 2195
页数:6
相关论文
共 56 条
[1]   Correlation of disease severity with fecal toxin levels in patients with Clostridium difficile-associated diarrhea and distribution of PCR ribotypes and toxin yields in vitro of corresponding isolates [J].
Åkerlund, T ;
Svenungsson, B ;
Lagergren, Å ;
Burman, LG .
JOURNAL OF CLINICAL MICROBIOLOGY, 2006, 44 (02) :353-358
[2]   Secular trends in hospital-acquired Clostridium difficile disease in the United States, 1987-2001 [J].
Archibald, LK ;
Banerjee, SN ;
Jarvis, WR .
JOURNAL OF INFECTIOUS DISEASES, 2004, 189 (09) :1585-1589
[3]   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
[4]   Clinical features of Clostridium difficile-associated infections and molecular characterization of strains:: Results of a retrospective study, 2000-2004 [J].
Barbut, Frederic ;
Gariazzo, Beatrice ;
Bonne, Laetitia ;
Lalande, Valerie ;
Burghoffer, Beatrice ;
Luiuz, Ralucca ;
Petit, Jean-Claude .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2007, 28 (02) :131-139
[5]   Review article: tolevamer, a novel toxin-binding polymer: overview of preclinical pharmacology and physicochemical properties [J].
Barker, R. H., Jr. ;
Dagher, R. ;
Davidson, D. M. ;
Marquis, J. K. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2006, 24 (11-12) :1525-1534
[6]   CLOSTRIDIUM-DIFFICILE - A SPECTRUM OF VIRULENCE AND ANALYSIS OF PUTATIVE VIRULENCE DETERMINANTS IN THE HAMSTER MODEL OF ANTIBIOTIC-ASSOCIATED COLITIS [J].
BORRIELLO, SP ;
KETLEY, JM ;
MITCHELL, TJ ;
BARCLAY, FE ;
WELCH, AR ;
PRICE, AB ;
STEPHEN, J .
JOURNAL OF MEDICAL MICROBIOLOGY, 1987, 24 (01) :53-64
[7]   Detection of the ADP-ribosyltransferase toxin gene (cdtA) and its activity in Clostridium difficile isolates from Equidae [J].
Braun, M ;
Herholz, C ;
Straub, R ;
Choisat, B ;
Frey, J ;
Nicolet, J ;
Kuhnert, P .
FEMS MICROBIOLOGY LETTERS, 2000, 184 (01) :29-33
[8]   Toxin binding of tolevamer, a polyanionic drug that protects against antibiotic-associated diarrhea [J].
Braunlin, W ;
Xu, QW ;
Hook, P ;
Fitzpatrick, R ;
Klinger, JD ;
Burrier, R ;
Kurtz, CB .
BIOPHYSICAL JOURNAL, 2004, 87 (01) :534-539
[9]  
Centers for Disease Control and Prevention (CDC), 2005, MMWR Morb Mortal Wkly Rep, V54, P1201
[10]   Toxins A and B from Clostridium difficile differ with respect to enzymatic potencies, cellular substrate specificities, and surface binding to cultured cells [J].
ChavesOlarte, E ;
Weidmann, M ;
vonEichelStreiber, C ;
Thelestam, M .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (07) :1734-1741