Green tea and epigallocatechin-3-gallate are bactericidal against Bacillus anthracis

被引:9
作者
Falcinelli, Shane D. [1 ,3 ]
Shi, Maggie C. [1 ]
Friedlander, Arthur M. [1 ,2 ]
Chua, Jennifer [1 ]
机构
[1] US Army, Med Res Inst Infect Dis, Bacteriol Div, 1425 Porter St, Ft Detrick, MD 21702 USA
[2] Uniformed Serv Univ Hlth Sci, Dept Med, Bethesda, MD 20814 USA
[3] Univ N Carolina, Chapel Hill, NC USA
关键词
Bacillus anthracis; epigallocatechin-3-gallate; green tea; EGCG; RESISTANT STAPHYLOCOCCUS-AUREUS; HUMAN SERUM-ALBUMIN; CATECHINS; GALLATE; MACROPHAGES; BINDING; EGCG; PHARMACOKINETICS; POLYPHENOLS; METABOLISM;
D O I
10.1093/femsle/fnx127
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bacillus anthracis, the etiological agent of anthrax, is listed as a category A biothreat agent by the United States Centers for Disease Control and Prevention. The virulence of the organism is due to expression of two exotoxins and capsule, which interfere with host cellular signaling, alter host water homeostasis and inhibit phagocytosis of the pathogen, respectively. Concerns regarding the past and possible future use of B. anthracis as a bioterrorism agent have resulted in an impetus to develop more effective protective measures and therapeutics. In this study, green tea was found to inhibit the in vitro growth of B. anthracis. Epigallocatechin-3-gallate (EGCG), a compound found abundantly in green tea, was shown to be responsible for this activity. EGCG was bactericidal against both the attenuated B. anthracis ANR and the virulent encapsulated B. anthracis Ames strain. This study highlights the antimicrobial activity of green tea and EGCG against anthrax and suggests the need for further investigation of EGCG as a therapeutic candidate against B. anthracis.
引用
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页数:8
相关论文
共 37 条
[1]   Green tea polyphenol inhibits Mycobacterium tuberculosis survival within human macrophages [J].
Anand, PK ;
Kaul, D ;
Sharma, M .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2006, 38 (04) :600-609
[2]   Albumin stabilizes (-)-epigallocatechin gallate in human serum: Binding capacity and antioxidant property [J].
Bae, Min-Jung ;
Ishii, Takeshi ;
Minoda, Kanako ;
Kawada, Yukiko ;
Ichikawa, Tatsuya ;
Mori, Taiki ;
Kamihira, Miya ;
Nakayama, Tsutomu .
MOLECULAR NUTRITION & FOOD RESEARCH, 2009, 53 (06) :709-715
[3]  
Baillie L, 2008, MICROBIOLOGIST MAGAZ, V9, P34
[4]  
Bhagwat S., 2014, USDA DATABASE FLAVON
[5]   Epigallocatechin 3-Gallate and Green Tea Catechins: United They Work, Divided They Fail [J].
Bode, Ann M. ;
Dong, Zigang .
CANCER PREVENTION RESEARCH, 2009, 2 (06) :514-517
[6]   Beneficial effects of green tea -: A review [J].
Cabrera, C ;
Artacho, R ;
Giménez, R .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 2006, 25 (02) :79-99
[7]   Efficacy of a capsule conjugate vaccine against inhalational anthrax in rabbits and monkeys [J].
Chabot, Donald J. ;
Joyce, Joseph ;
Caulfield, Michael ;
Cook, James ;
Hepler, Robert ;
Wang, Su ;
Vietri, Nicholas J. ;
Ruthel, Gordon ;
Shoop, Wesley ;
Pitt, Louise ;
Leffel, Elizabeth ;
Ribot, Wilson ;
Friedlander, Arthur M. .
VACCINE, 2012, 30 (05) :846-852
[8]  
Chow HHS, 2003, CLIN CANCER RES, V9, P3312
[9]   Potent inhibitors of anthrax lethal factor from green tea [J].
Dell'Aica, I ;
Donà, M ;
Tonello, F ;
Piris, A ;
Mock, M ;
Montecucco, C ;
Garbisa, S .
EMBO REPORTS, 2004, 5 (04) :418-422
[10]   Biopharmaceutical evaluation of epigallocatechin gallate-loaded cationic lipid nanoparticles (EGCG-LNs): In vivo,in vitro and ex vivo studies [J].
Fangueiro, Joana F. ;
Calpena, Ana C. ;
Clares, Beatriz ;
Andreani, Tatiana ;
Egea, Maria A. ;
Veiga, Francisco J. ;
Garcia, Maria L. ;
Silva, Amelia M. ;
Souto, Eliana B. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2016, 502 (1-2) :161-169