Genetic Evidence for Inhibition of Bacterial Division Protein FtsZ by Berberine

被引:150
作者
Boberek, Jaroslaw M. [1 ]
Stach, Jem [2 ]
Good, Liam [1 ]
机构
[1] Univ London Royal Vet Coll, Dept Pathol & Infect Dis, London, England
[2] Newcastle Univ, Sch Biol, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
来源
PLOS ONE | 2010年 / 5卷 / 10期
关键词
ESCHERICHIA-COLI; CELL-DIVISION; HYDRASTIS-CANADENSIS; ANTIMICROBIAL ACTIVITY; SMALL-MOLECULE; CANCER-CELLS; IN-VITRO; RING; APOPTOSIS; BINDING;
D O I
10.1371/journal.pone.0013745
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Berberine is a plant alkaloid that is widely used as an anti-infective in traditional medicine. Escherichia coli exposed to berberine form filaments, suggesting an antibacterial mechanism that involves inhibition of cell division. Berberine is a DNA ligand and may induce filamentation through induction of the SOS response. Also, there is biochemical evidence for berberine inhibition of the cell division protein FtsZ. Here we aimed to assess possible berberine mechanism(s) of action in growing bacteria using genetics tools. Methodology/Principal Findings: First, we tested whether berberine inhibits bacterial growth through DNA damage and induction of the SOS response. The SOS response induced by berberine was much lower compared to that induced by mitomycin C in an SOS response reporter strain. Also, cell filamentation was observed in an SOS-negative E. coli strain. To test whether berberine inhibits FtsZ, we assessed its effects on formation of the cell division Z-rings, and observed a dramatic reduction in Z-rings in the presence of berberine. We next used two different strategies for RNA silencing of ftsZ and both resulted in sensitisation of bacteria to berberine, visible as a drop in the Minimum Inhibitory Concentration (MIC). Furthermore, Fractional Inhibitory Concentration Indices (FICIs) showed a high level of synergy between ftsZ silencing and berberine treatment (FICI values of 0.23 and 0.25 for peptide nucleic acid-and expressed antisense RNA-based silencing of ftsZ, respectively). Finally, over-expression of ftsZ led to a mild rescue effect in berberine-treated cells. Conclusions: The results argue against DNA binding as the primary mechanism of action of berberine and support the hypothesis that its antibacterial properties are due to inhibition of the cell division protein FtsZ. In addition, the genetic approach used here provides a means to rapidly test the activity of other putative FtsZ inhibitors.
引用
收藏
页数:9
相关论文
共 51 条
[1]   BERBERINE SULFATE - ANTIMICROBIAL ACTIVITY, BIOASSAY, AND MODE OF ACTION [J].
AMIN, AH ;
SUBBAIAH, TV ;
ABBASI, KM .
CANADIAN JOURNAL OF MICROBIOLOGY, 1969, 15 (09) :1067-&
[2]   Sanguinarine blocks cytokinesis in bacteria by inhibiting FtsZ assembly and bundling [J].
Beuria, TK ;
Santra, MK ;
Panda, D .
BIOCHEMISTRY, 2005, 44 (50) :16584-16593
[3]   Berberine-DNA complexation: New insights into the cooperative binding and energetic aspects [J].
Bhadra, Kakali ;
Maiti, Motilal ;
Kumar, Gopinatha Suresh .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2008, 1780 (09) :1054-1061
[4]   CELL-DIVISION INHIBITORS SULA AND MINCD PREVENT FORMATION OF THE FTSZ RING [J].
BI, E ;
LUTKENHAUS, J .
JOURNAL OF BACTERIOLOGY, 1993, 175 (04) :1118-1125
[5]   FTSZ RING STRUCTURE ASSOCIATED WITH DIVISION IN ESCHERICHIA-COLI [J].
BI, E ;
LUTKENHAUS, J .
NATURE, 1991, 354 (6349) :161-164
[6]  
Choi MS, 2008, ANTICANCER RES, V28, P3777
[7]   Spectroscopic and thermodynamic studies on the binding of sanguinarine and berberine to triple and double helical DNA and RNA structures [J].
Das, S ;
Kumar, GS ;
Ray, A ;
Maiti, M .
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2003, 20 (05) :703-713
[8]   Inhibition of bacterial cell division protein FtsZ by cinnamaldehyde [J].
Domadia, Prerna ;
Swarup, Sanjay ;
Bhunia, Anirban ;
Sivaraman, J. ;
Dasgupta, Debjani .
BIOCHEMICAL PHARMACOLOGY, 2007, 74 (06) :831-840
[9]   Berberine targets assembly of Escherichia coli cell division protein FtsZ [J].
Domadia, Prerna N. ;
Bhunia, Anirban ;
Sivaraman, J. ;
Swarup, Sanjay ;
Dasgupta, Debjani .
BIOCHEMISTRY, 2008, 47 (10) :3225-3234
[10]   Antimicrobial synergy between mRNA- and protein-level inhibitors [J].
Dryselius, R ;
Nekhotiaeva, N ;
Good, L .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 56 (01) :97-103