Multi-Omics Analysis Reveals Anti-<i>Staphylococcus aureus</i> Activity of Actinomycin D Originating from <i>Streptomyces parvulus</i>

<i>Staphylococcus aureus</i> (<i>S. aureus</i>) is a common pathogen that causes various serious diseases, including chronic infections. Discovering new antibacterial agents is an important aspect of the pharmaceutical field because of the lack of effective antibacterial drug...

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Autores principales: Yuqi Lin, Li Huang, Xiaoyong Zhang, Jiajia Yang, Xiaodan Chen, Fengming Li, Jun Liu, Riming Huang
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:157df331543e4d0fba439efa1cb4055e2021-11-25T17:54:33ZMulti-Omics Analysis Reveals Anti-<i>Staphylococcus aureus</i> Activity of Actinomycin D Originating from <i>Streptomyces parvulus</i>10.3390/ijms2222122311422-00671661-6596https://doaj.org/article/157df331543e4d0fba439efa1cb4055e2021-11-01T00:00:00Zhttps://www.mdpi.com/1422-0067/22/22/12231https://doaj.org/toc/1661-6596https://doaj.org/toc/1422-0067<i>Staphylococcus aureus</i> (<i>S. aureus</i>) is a common pathogen that causes various serious diseases, including chronic infections. Discovering new antibacterial agents is an important aspect of the pharmaceutical field because of the lack of effective antibacterial drugs. In our research, we found that one anti-<i>S. aureus</i> substance is actinomycin D, originating from <i>Streptomyces parvulus</i> (<i>S. parvulus</i>); then, we further focused on the anti-<i>S. aureus</i> ability and the omics profile of <i>S. aureus</i> in response to actinomycin D. The results revealed that actinomycin D had a significant inhibitory activity on <i>S. aureus</i> with a minimum inhibitory concentration (MIC) of 2 μg/mL and a minimum bactericidal concentration (MBC) of 64 μg/mL. Bacterial reactive oxygen species (ROS) increased 3.5-fold upon treatment with actinomycin D, as was measured with the oxidation-sensitive fluorescent probe DCFH-DA, and H<sub>2</sub>O<sub>2</sub> increased 3.5 times with treatment by actinomycin D. Proteomics and metabolomics, respectively, identified differentially expressed proteins in control and treatment groups, and the co-mapped correlation network of proteomics and metabolomics annotated five major pathways that were potentially related to disrupting the energy metabolism and oxidative stress of <i>S. aureus</i>. All findings contributed to providing new insight into the mechanisms of the anti-<i>S. aureus</i> effects of actinomycin D originating from <i>S. parvulus.</i>Yuqi LinLi HuangXiaoyong ZhangJiajia YangXiaodan ChenFengming LiJun LiuRiming HuangMDPI AGarticle<i>Staphylococcus aureus</i><i>Streptomyces parvulus</i>actinomycin Dproteomic and metabolomic profilesBiology (General)QH301-705.5ChemistryQD1-999ENInternational Journal of Molecular Sciences, Vol 22, Iss 12231, p 12231 (2021)
institution DOAJ
collection DOAJ
language EN
topic <i>Staphylococcus aureus</i>
<i>Streptomyces parvulus</i>
actinomycin D
proteomic and metabolomic profiles
Biology (General)
QH301-705.5
Chemistry
QD1-999
spellingShingle <i>Staphylococcus aureus</i>
<i>Streptomyces parvulus</i>
actinomycin D
proteomic and metabolomic profiles
Biology (General)
QH301-705.5
Chemistry
QD1-999
Yuqi Lin
Li Huang
Xiaoyong Zhang
Jiajia Yang
Xiaodan Chen
Fengming Li
Jun Liu
Riming Huang
Multi-Omics Analysis Reveals Anti-<i>Staphylococcus aureus</i> Activity of Actinomycin D Originating from <i>Streptomyces parvulus</i>
description <i>Staphylococcus aureus</i> (<i>S. aureus</i>) is a common pathogen that causes various serious diseases, including chronic infections. Discovering new antibacterial agents is an important aspect of the pharmaceutical field because of the lack of effective antibacterial drugs. In our research, we found that one anti-<i>S. aureus</i> substance is actinomycin D, originating from <i>Streptomyces parvulus</i> (<i>S. parvulus</i>); then, we further focused on the anti-<i>S. aureus</i> ability and the omics profile of <i>S. aureus</i> in response to actinomycin D. The results revealed that actinomycin D had a significant inhibitory activity on <i>S. aureus</i> with a minimum inhibitory concentration (MIC) of 2 μg/mL and a minimum bactericidal concentration (MBC) of 64 μg/mL. Bacterial reactive oxygen species (ROS) increased 3.5-fold upon treatment with actinomycin D, as was measured with the oxidation-sensitive fluorescent probe DCFH-DA, and H<sub>2</sub>O<sub>2</sub> increased 3.5 times with treatment by actinomycin D. Proteomics and metabolomics, respectively, identified differentially expressed proteins in control and treatment groups, and the co-mapped correlation network of proteomics and metabolomics annotated five major pathways that were potentially related to disrupting the energy metabolism and oxidative stress of <i>S. aureus</i>. All findings contributed to providing new insight into the mechanisms of the anti-<i>S. aureus</i> effects of actinomycin D originating from <i>S. parvulus.</i>
format article
author Yuqi Lin
Li Huang
Xiaoyong Zhang
Jiajia Yang
Xiaodan Chen
Fengming Li
Jun Liu
Riming Huang
author_facet Yuqi Lin
Li Huang
Xiaoyong Zhang
Jiajia Yang
Xiaodan Chen
Fengming Li
Jun Liu
Riming Huang
author_sort Yuqi Lin
title Multi-Omics Analysis Reveals Anti-<i>Staphylococcus aureus</i> Activity of Actinomycin D Originating from <i>Streptomyces parvulus</i>
title_short Multi-Omics Analysis Reveals Anti-<i>Staphylococcus aureus</i> Activity of Actinomycin D Originating from <i>Streptomyces parvulus</i>
title_full Multi-Omics Analysis Reveals Anti-<i>Staphylococcus aureus</i> Activity of Actinomycin D Originating from <i>Streptomyces parvulus</i>
title_fullStr Multi-Omics Analysis Reveals Anti-<i>Staphylococcus aureus</i> Activity of Actinomycin D Originating from <i>Streptomyces parvulus</i>
title_full_unstemmed Multi-Omics Analysis Reveals Anti-<i>Staphylococcus aureus</i> Activity of Actinomycin D Originating from <i>Streptomyces parvulus</i>
title_sort multi-omics analysis reveals anti-<i>staphylococcus aureus</i> activity of actinomycin d originating from <i>streptomyces parvulus</i>
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/157df331543e4d0fba439efa1cb4055e
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