Mode-of-Action Studies of the Novel Bisquaternary Bisnaphthalimide MT02 againstStaphylococcus aureus
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Published:2010-10-11
Issue:1
Volume:55
Page:311-320
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ISSN:0066-4804
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Container-title:Antimicrobial Agents and Chemotherapy
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language:en
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Short-container-title:Antimicrob. Agents Chemother.
Author:
Menzel Thomas M.,Tischer Maximilian,François Patrice,Nickel Joachim,Schrenzel Jacques,Bruhn Heike,Albrecht Annette,Lehmann Leane,Holzgrabe Ulrike,Ohlsen Knut
Abstract
ABSTRACTScreening of various bisquaternary bisnaphthalimides against a variety of human pathogens revealed one compound, designated MT02, with strong inhibitory effects against Gram-positive bacteria. The MICs ranged from 0.31 μg/ml against community-acquired methicillin-resistantStaphylococcus aureus(MRSA) lineage USA300 to 20 μg/ml againstStreptococcus pneumoniae. Radioactive whole-cell labeling experiments indicated a strong impact of MT02 on bacterial DNA replication. DNA microarray studies generated a transcriptional signature characterized by stronger expression of genes involved in DNA metabolism, DNA replication, SOS response, and transport of positively charged compounds. Furthermore, surface plasmon resonance and gel retardation experiments demonstrated direct binding of MT02 to DNA in a concentration-dependent, reversible, and non-sequence-specific manner. The data presented suggest that the bisquaternary bisnaphthalimide MT02 exerts anti-Gram-positive activity by binding to DNA and thereby preventing appropriate DNA replication.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Reference39 articles.
1. Baba, T., F. Takeuchi, M. Kuroda, H. Yuzawa, K. Aoki, A. Oguchi, Y. Nagai, N. Iwama, K. Asano, T. Naimi, H. Kuroda, L. Cui, K. Yamamoto, and K. Hiramatsu. 2002. Genome and virulence determinants of high virulence community-acquired MRSA. Lancet 359:1819-1827. 2. Bender, W., M. Staudt, C. Trankle, K. Mohr, and U. Holzgrabe. 2000. Probing the size of a hydrophobic binding pocket within the allosteric site of muscarinic acetylcholine M2-receptors. Life Sci. 66:1675-1682. 3. Braña, M. F., M. Cacho, M. A. Garcia, B. de Pascual-Teresa, A. Ramos, M. T. Dominguez, J. M. Pozuelo, C. Abradelo, M. F. Rey-Stolle, M. Yuste, M. Banez-Coronel, and J. C. Lacal. 2004. New analogues of amonafide and elinafide, containing aromatic heterocycles: synthesis, antitumor activity, molecular modeling, and DNA binding properties. J. Med. Chem. 47:1391-1399. 4. Braña, M. F., J. M. Castellano, M. Moran, M. J. Perez de Vega, C. R. Romerdahl, X. D. Qian, P. Bousquet, F. Emling, E. Schlick, and G. Keilhauer. 1993. Bis-naphthalimides: a new class of antitumor agents. Anticancer Drug Des. 8:257-268. 5. Braña, M. F., and A. Ramos. 2001. Naphthalimides as anti-cancer agents: synthesis and biological activity. Curr. Med. Chem. Anticancer Agents 1:237-255.
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