Pimarane-type Diterpenes Obtained by Biotransformation: Antimicrobial Properties Against Clinically Isolated Gram-positive Multidrug-resistant Bacteria

作者: Thiago S. Porto , Marília R. Simão , Lucas Z. Carlos , Carlos H. G. Martins , Niege A. J. C. Furtado

DOI: 10.1002/PTR.4887

关键词:

摘要: The present study describes the antimicrobial activity of five pimarane-type diterpenes obtained by fungal biotransformation against several nosocomial multidrug-resistant bacteria. Among investigated metabolites, ent-8(14),15-pimaradien-3β-ol was most active compound, with very promising minimal inhibitory concentration values (between 8.0 and 25.0 µg mL−1). Time-kill assays using this metabolite Staphylococcus aureus (HCRP180) revealed that compound exerted its bactericidal effect within 24 h at all evaluated concentrations (8.0, 16.0, 24.0 When associated vancomycin their values, resulting combination able to drastically reduce number viable strains S. first 6 h, compared these chemicals alone. checkerboard conducted microorganism did not evidence any synergistic effects when same employed. In conclusion, our results point out is an important in search for new effective agents. Copyright © 2012 John Wiley & Sons, Ltd.

参考文章(37)
R L White, D S Burgess, M Manduru, J A Bosso, Comparison of three different in vitro methods of detecting synergy: time-kill, checkerboard, and E test. Antimicrobial Agents and Chemotherapy. ,vol. 40, pp. 1914- 1918 ,(1996) , 10.1128/AAC.40.8.1914
Akihiko Matsuo, Seiryû Uto, Mitsuru Nakayama, Shûichi Hayashi, Kazuo Yamasaki, Ryoji Kasai, Osamu Tanaka, (−)-thermarol, a new ent-pimarane-class diterpene diol from Jungermannia thermarum (liverwort) Tetrahedron Letters. ,vol. 17, pp. 2451- 2454 ,(1976) , 10.1016/0040-4039(76)90017-4
Thiago S Porto, Rander Rangel, Niege AJC Furtado, Tatiane C De Carvalho, Carlos HG Martins, Rodrigo CS Veneziani, Fernando B Da Costa, Adriana HC Vinholis, Wilson R Cunha, Vladimir CG Heleno, Sergio R Ambrosio, None, Pimarane-type diterpenes: antimicrobial activity against oral pathogens. Molecules. ,vol. 14, pp. 191- 199 ,(2009) , 10.3390/MOLECULES14010191
Ariana B Souza, Carlos HG Martins, Maria GM Souza, Niege AJC Furtado, Vladimir CG Heleno, João PB de Sousa, Erilda MP Rocha, Jairo K Bastos, Wilson R Cunha, Rodrigo CS Veneziani, Sérgio R Ambrósio, None, Antimicrobial activity of terpenoids from Copaifera langsdorffii Desf. against cariogenic bacteria. Phytotherapy Research. ,vol. 25, pp. 215- 220 ,(2011) , 10.1002/PTR.3244
Maria Cícera Silva‐Carvalho, Lenise Arneiro Teixeira, Fabienne Antunes Ferreira, Apoena Ribeiro, Bernadete Teixeira Ferreira‐Carvalho, Agnes Marie Sá Figueiredo, None, Comparison of different methods for detecting methicillin resistance in MRSA isolates belonging to international lineages commonly isolated in the American continent Microbiology and Immunology. ,vol. 53, pp. 117- 122 ,(2009) , 10.1111/J.1348-0421.2008.00096.X
Michael Greenberg, Michael Dodds, Minmin Tian, Naturally occurring phenolic antibacterial compounds show effectiveness against oral bacteria by a quantitative structure-activity relationship study. Journal of Agricultural and Food Chemistry. ,vol. 56, pp. 11151- 11156 ,(2008) , 10.1021/JF8020859
Silvia Marquina, José Luis Parra, Manasés González, Alejandro Zamilpa, Jaime Escalante, María R. Trejo-Hernández, Laura Álvarez, Hydroxylation of the diterpenes ent-kaur-16-en-19-oic and ent-beyer-15-en-19-oic acids by the fungus Aspergillus niger Phytochemistry. ,vol. 70, pp. 2017- 2022 ,(2009) , 10.1016/J.PHYTOCHEM.2009.09.005
Rong-Dih Lin, Yi-Ping Chin, Wen-Chi Hou, Mei-Hsien Lee, The effects of antibiotics combined with natural polyphenols against clinical methicillin-resistant Staphylococcus aureus (MRSA). Planta Medica. ,vol. 74, pp. 840- 846 ,(2008) , 10.1055/S-2008-1074559
David J. Newman, Gordon M. Cragg, Natural Products As Sources of New Drugs over the 30 Years from 1981 to 2010 Journal of Natural Products. ,vol. 75, pp. 311- 335 ,(2012) , 10.1021/NP200906S
Steven M. Ansell, Karl H. Pegel, David A.H. Taylor, Diterpenes from the timber of 20 Erythroxylum species Phytochemistry. ,vol. 32, pp. 953- 959 ,(1993) , 10.1016/0031-9422(93)85235-J