Inhibition of platelet aggregation by anthrax edema toxin

被引:13
作者
Alam, S [1 ]
Gupta, M [1 ]
Bhatnagar, R [1 ]
机构
[1] Jawaharlal Nehru Univ, Ctr Biotechnol, New Delhi 110067, India
关键词
edema toxin; platelet aggregation; hemorrhage; bleeding time;
D O I
10.1016/j.bbrc.2005.11.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Edema toxin is a key virulence determinant in anthrax pathogenesis that causes augmentation of cAMP inside host cells. This exotoxin has been implicated in facilitating bacterial invasion by impairing host defenses. Here, we report for the first time that edema toxin plays an important role in suppression of platelet aggregation; an effect that could be of vital significance in anthrax afflicted subjects. It was found that edema toxin induces a dose dependent and time dependent increase in cAMP inside rabbit platelets. Elevation of cAMP led to suppression of platelet aggregation as demonstrated by in vitro aggregation assays. A 95% Suppression of platelet aggregation in response to thrombin and a complete Suppression in response to ADP, at toxin concentrations of 7 and 2.2 nM, respectively, were observed. Antibody neutralized wild type edema factor and non-toxic mutants of this binary toxin failed to show any alteration in the normal aggregation pattern. Edema toxin caused the activation of cAMP dependent protein kinase A inside platelets, a phenomenon that could be speculated to initiate the cascade of events responsible for Suppressing platelet aggregation. Furthermore. in vivo bleeding time registered a sharp increase in response to edema toxin. These findings can explicate the systemic occurrence of hemorrhage, which is a prominent symptom of anthrax. ThiS Study exemplifies how Bacillus anthracis has evolved the ability to use host's physiological processes by mimicking the eukaryotic signal transduction machinery, thus inflicting persistent infection. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:107 / 114
页数:8
相关论文
共 40 条
[1]   PATHOLOGY OF INHALATIONAL ANTHRAX IN 42 CASES FROM THE SVERDLOVSK OUTBREAK OF 1979 [J].
ABRAMOVA, FA ;
GRINBERG, LM ;
YAMPOLSKAYA, OV ;
WALKER, DH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (06) :2291-2294
[2]   The adenylate cyclase toxins [J].
Ahuja, N ;
Kumar, P ;
Bhatnagar, R .
CRITICAL REVIEWS IN MICROBIOLOGY, 2004, 30 (03) :187-196
[3]   Deletion mutants of protective antigen that inhibit anthrax toxin both in vitro and in vivo [J].
Ahuja, N ;
Kumar, P ;
Alam, S ;
Gupta, M ;
Bhatnagar, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 307 (03) :446-450
[4]   Rapid purification of recombinant anthrax-protective antigen under nondenaturing conditions [J].
Ahuja, N ;
Kumar, P ;
Bhatnagar, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 286 (01) :6-11
[5]   Anthrax toxin [J].
Bhatnagar, R ;
Batra, S .
CRITICAL REVIEWS IN MICROBIOLOGY, 2001, 27 (03) :167-200
[6]   Regulation of glycoprotein Ib-IX-von Willebrand factor interaction by cAMP-dependent protein kinase-mediated phosphorylation at Ser166 of glycoprotein Ibβ [J].
Bodnar, RJ ;
Xi, XD ;
Li, ZY ;
Berndt, MC ;
Du, XP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (49) :47080-47087
[7]   Death due to bioterrorism-related inhalational anthrax - Report of 2 patients [J].
Borio, L ;
Frank, D ;
Mani, V ;
Chiriboga, C ;
Pollanen, M ;
Ripple, M ;
Ali, S ;
DiAngelo, C ;
Lee, J ;
Arden, J ;
Titus, J ;
Fowler, D ;
O'Toole, T ;
Masur, H ;
Bartlett, J ;
Inglesby, T .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (20) :2554-2559
[8]   AGGREGATION OF BLOOD PLATELETS BY ADENOSINE DIPHOSPHATE AND ITS REVERSAL [J].
BORN, GVR .
NATURE, 1962, 194 (4832) :927-&
[9]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[10]   Exposing a killer: Pathologists angle for anthrax [J].
Chensue, SW .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 163 (05) :1699-1702