Potential Mechanism of Action of 3′-Demethoxy-6-O-demethyl-isoguaiacin on Methicillin Resistant Staphylococcus aureus

• Main Authors: Juan Manuel J. Favela-Hernández, Aldo F. Clemente-Soto, Isaías Balderas-Rentería, Elvira Garza-González, María del Rayo Camacho-Corona
• Format: Article
• Language: English
• Published: MDPI AG 2015-07-01
• Series: Molecules
• Subjects: Larrea tridentata; 3′-demethoxy-6-O-demethylisoguaiacin; methicillin-resistant Staphylococcus aureus; microarrays; real time PCR; mode of action
• Online Access: http://www.mdpi.com/1420-3049/20/7/12450

Bacterial infections represent one of the main threats to global public health. One of the major causative agents associated with high morbidity and mortality infections in hospitals worldwide is methicillin-resistant Staphylococcus aureus. Therefore, there is a need to develop new antibacterial agents to treat these infections, and natural products are a rich source of them. In previous studies, we reported that lignan 3′-demethoxy-6-O-demethylisoguaiacin, isolated and characterized from Larrea tridentate, showed the best activity towards methicillin-resistant S. aureus. Thus, the aim of this study was to determine the potential molecular mechanism of the antibacterial activity of 3′-demethoxy-6-O-demethylisoguaiacin against methicillin-resistant S. aureus using microarray technology. Results of microarray genome expression were validated by real-time polymerase chain reaction (RT-PCR). The genetic profile expression results showed that lignan 3′-demethoxy-6-O-demethylisoguaiacin had activity on cell membrane affecting proteins of the ATP-binding cassette (ABC) transport system causing bacteria death. This molecular mechanism is not present in any antibacterial commercial drug and could be a new target for the development of novel antibacterial agents.