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

3'-去甲氧基-6-O-去甲基异愈创木酚素对耐甲氧西林金黄色葡萄球菌的潜在作用机制

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作者:Juan Manuel J Favela-Hernández ,Aldo F Clemente-Soto ,Isaías Balderas-Rentería ,Elvira Garza-González ,María del Rayo Camacho-Corona

Abstract

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. Keywords: 3′-demethoxy-6-O-demethylisoguaiacin; Larrea tridentata; methicillin-resistant Staphylococcus aureus; microarrays; mode of action; real time PCR.

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