Red Light‐Triggered Intracellular Carbon Monoxide Release Enables Selective Eradication of MRSA Infection
Carbon monoxide (CO) is an important gaseous signaling molecule. The use of CO‐releasing molecules such as metal carbonyls enables the elucidation of the pleiotropic functions of CO. Although metal carbonyls show a broad‐spectrum antimicrobial activity, it remains unclear whether the bactericidal pr...
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Published in | Angewandte Chemie International Edition Vol. 60; no. 24; pp. 13513 - 13520 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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WEINHEIM
Wiley
07.06.2021
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Abstract | Carbon monoxide (CO) is an important gaseous signaling molecule. The use of CO‐releasing molecules such as metal carbonyls enables the elucidation of the pleiotropic functions of CO. Although metal carbonyls show a broad‐spectrum antimicrobial activity, it remains unclear whether the bactericidal property originates from the transition metals or the released CO. Here, we develop nonmetallic CO‐releasing micelles via a photooxygenation mechanism of 3‐hydroxyflavone derivatives, enabling CO release under red light irradiation (e.g., 650 nm). Unlike metal carbonyls that non‐specifically internalize into both Gram‐positive and Gram‐negative bacteria, the nonmetallic micelles are selectively taken up by S. aureus instead of E. coli cells, exerting a selective bactericidal effect. Further, we demonstrate that the CO‐releasing micelles can cure methicillin‐resistant S. aureus (MRSA)‐infected wounds, simultaneously eradicating MRSA pathogens and accelerating wound healing.
Metal‐free CO‐releasing micelles can be selectively taken up by Gram‐positive bacteria, exerting a narrow‐spectrum bactericidal activity toward only Gram‐positive bacteria under red light irradiation. The CO‐releasing micelles synergistically eradicate MRSA pathogens and accelerate MRSA‐infected wound healing. |
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AbstractList | Carbon monoxide (CO) is an important gaseous signaling molecule. The use of CO-releasing molecules such as metal carbonyls enables the elucidation of the pleiotropic functions of CO. Although metal carbonyls show a broad-spectrum antimicrobial activity, it remains unclear whether the bactericidal property originates from the transition metals or the released CO. Here, we develop nonmetallic CO-releasing micelles via a photooxygenation mechanism of 3-hydroxyflavone derivatives, enabling CO release under red light irradiation (e.g., 650 nm). Unlike metal carbonyls that non-specifically internalize into both Gram-positive and Gram-negative bacteria, the nonmetallic micelles are selectively taken up by S. aureus instead of E. coli cells, exerting a selective bactericidal effect. Further, we demonstrate that the CO-releasing micelles can cure methicillin-resistant S. aureus (MRSA)-infected wounds, simultaneously eradicating MRSA pathogens and accelerating wound healing.Carbon monoxide (CO) is an important gaseous signaling molecule. The use of CO-releasing molecules such as metal carbonyls enables the elucidation of the pleiotropic functions of CO. Although metal carbonyls show a broad-spectrum antimicrobial activity, it remains unclear whether the bactericidal property originates from the transition metals or the released CO. Here, we develop nonmetallic CO-releasing micelles via a photooxygenation mechanism of 3-hydroxyflavone derivatives, enabling CO release under red light irradiation (e.g., 650 nm). Unlike metal carbonyls that non-specifically internalize into both Gram-positive and Gram-negative bacteria, the nonmetallic micelles are selectively taken up by S. aureus instead of E. coli cells, exerting a selective bactericidal effect. Further, we demonstrate that the CO-releasing micelles can cure methicillin-resistant S. aureus (MRSA)-infected wounds, simultaneously eradicating MRSA pathogens and accelerating wound healing. Carbon monoxide (CO) is an important gaseous signaling molecule. The use of CO‐releasing molecules such as metal carbonyls enables the elucidation of the pleiotropic functions of CO. Although metal carbonyls show a broad‐spectrum antimicrobial activity, it remains unclear whether the bactericidal property originates from the transition metals or the released CO. Here, we develop nonmetallic CO‐releasing micelles via a photooxygenation mechanism of 3‐hydroxyflavone derivatives, enabling CO release under red light irradiation (e.g., 650 nm). Unlike metal carbonyls that non‐specifically internalize into both Gram‐positive and Gram‐negative bacteria, the nonmetallic micelles are selectively taken up by S. aureus instead of E. coli cells, exerting a selective bactericidal effect. Further, we demonstrate that the CO‐releasing micelles can cure methicillin‐resistant S. aureus (MRSA)‐infected wounds, simultaneously eradicating MRSA pathogens and accelerating wound healing. Metal‐free CO‐releasing micelles can be selectively taken up by Gram‐positive bacteria, exerting a narrow‐spectrum bactericidal activity toward only Gram‐positive bacteria under red light irradiation. The CO‐releasing micelles synergistically eradicate MRSA pathogens and accelerate MRSA‐infected wound healing. Carbon monoxide (CO) is an important gaseous signaling molecule. The use of CO‐releasing molecules such as metal carbonyls enables the elucidation of the pleiotropic functions of CO. Although metal carbonyls show a broad‐spectrum antimicrobial activity, it remains unclear whether the bactericidal property originates from the transition metals or the released CO. Here, we develop nonmetallic CO‐releasing micelles via a photooxygenation mechanism of 3‐hydroxyflavone derivatives, enabling CO release under red light irradiation (e.g., 650 nm). Unlike metal carbonyls that non‐specifically internalize into both Gram‐positive and Gram‐negative bacteria, the nonmetallic micelles are selectively taken up by S. aureus instead of E. coli cells, exerting a selective bactericidal effect. Further, we demonstrate that the CO‐releasing micelles can cure methicillin‐resistant S. aureus (MRSA)‐infected wounds, simultaneously eradicating MRSA pathogens and accelerating wound healing. |
Author | Zhang, Guoying Gao, Lei Shen, Zhiqiang Gan, Guihai Hu, Jinming Cheng, Jian |
Author_xml | – sequence: 1 givenname: Jian surname: Cheng fullname: Cheng, Jian organization: University of Science and Technology of China, Hefei – sequence: 2 givenname: Guihai surname: Gan fullname: Gan, Guihai organization: University of Science and Technology of China, Hefei – sequence: 3 givenname: Zhiqiang surname: Shen fullname: Shen, Zhiqiang organization: University of Science and Technology of China, Hefei – sequence: 4 givenname: Lei surname: Gao fullname: Gao, Lei organization: University of Science and Technology of China, Hefei – sequence: 5 givenname: Guoying surname: Zhang fullname: Zhang, Guoying organization: University of Science and Technology of China, Hefei – sequence: 6 givenname: Jinming orcidid: 0000-0002-6969-1343 surname: Hu fullname: Hu, Jinming email: jmhu@ustc.edu.cn organization: University of Science and Technology of China, Hefei |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33829616$$D View this record in MEDLINE/PubMed |
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Keywords | carbon monoxide wound healing photooxidation antibacterial agents MRSA |
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Snippet | Carbon monoxide (CO) is an important gaseous signaling molecule. The use of CO‐releasing molecules such as metal carbonyls enables the elucidation of the... Carbon monoxide (CO) is an important gaseous signaling molecule. The use of CO-releasing molecules such as metal carbonyls enables the elucidation of the... |
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SubjectTerms | antibacterial agents Antiinfectives and antibacterials Antimicrobial activity Carbon monoxide Carbonyl compounds Carbonyls Chemistry Chemistry, Multidisciplinary Drug resistance E coli Gram-negative bacteria Irradiation Light irradiation Metal carbonyls Metals Methicillin Micelles MRSA photooxidation Physical Sciences Releasing Science & Technology Staphylococcus aureus Transition metals Wound healing |
Title | Red Light‐Triggered Intracellular Carbon Monoxide Release Enables Selective Eradication of MRSA Infection |
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