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The herbal-derived honokiol and magnolol enhances immune response to infection with methicillin-sensitive Staphylococcus aureus (MSSA) and methicillin-resistant S. aureus (MRSA)

  • Applied microbial and cell physiology
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Abstract

The emergence of antibiotic resistant strains such as methicillin-resistant Staphylococcus aureus (MRSA) reminds us an urgent need to develop a new immune-modulating agent for preventing S. aureus infection. In this study, we found that herbal medicines, honokiol and magnolol, caused a significant cellular immune modulatory effect during S. aureus infection. In mouse macrophages, these compounds drove upregulation of an antioxidant effect in response to S. aureus, resulting in a dampened total cellular reactive oxygen species (ROS) production and decreased production of inflammatory cytokines/chemokines, whereas honokiol induced increased types I and III interferon messenger RNA (mRNA) expression levels in response to MSSA infection. Moreover, the internalization of S. aureus by human alveolar epithelial cells was inhibited by these compounds. Furthermore, honokiol and magnolol treatment promoted a delay in killing during MSSA infection in Caenorhabditis elegans, suggesting antimicrobial function in vivo. In conclusion, honokiol and magnolol may be considered as attractive immune-modulating treatment for S. aureus infection.

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Acknowledgments

This work was supported by grants from by the Korean Health Technology R&D Projects (R1306922), Ministry for Health & Welfare, Republic of Korea (O.S.S), and by the Cooperative Research Program for Agriculture Science & Technology Development (Project No. PJ009769 to Y.K.), Rural Development Administration, Republic of Korea.

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Correspondence to Younghoon Kim.

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Younghoon Kim and Ok Sarah Shin contributed equally to this study.

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Choi, EJ., Kim, HI., Kim, JA. et al. The herbal-derived honokiol and magnolol enhances immune response to infection with methicillin-sensitive Staphylococcus aureus (MSSA) and methicillin-resistant S. aureus (MRSA). Appl Microbiol Biotechnol 99, 4387–4396 (2015). https://doi.org/10.1007/s00253-015-6382-y

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