Antimicrobial activity and mode of action of 1,8-cineol against carbapenemase-producing Klebsiella pneumoniae

Antimicrobial resistance remains one of the most challenging issues that threatens the health of people around the world. Plant-derived natural compounds have received considerable attention for their potential role to mitigate antibiotic resistance. This study was carried out to assess the antimicr...

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Main Authors: Moo, Chew Li, Osman, Mohd Azuraidi, Shun, Kai Yang, Wai, Sum Yap, Ismail, Saila, Swee, Hua Erin Lim, Chong, Chou Min, Lai, Kok Song
Format: Article
Published: Nature Research 2021
Online Access:http://psasir.upm.edu.my/id/eprint/95915/
https://www.nature.com/articles/s41598-021-00249-y
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spelling my.upm.eprints.959152023-03-17T08:29:14Z http://psasir.upm.edu.my/id/eprint/95915/ Antimicrobial activity and mode of action of 1,8-cineol against carbapenemase-producing Klebsiella pneumoniae Moo, Chew Li Osman, Mohd Azuraidi Shun, Kai Yang Wai, Sum Yap Ismail, Saila Swee, Hua Erin Lim Chong, Chou Min Lai, Kok Song Antimicrobial resistance remains one of the most challenging issues that threatens the health of people around the world. Plant-derived natural compounds have received considerable attention for their potential role to mitigate antibiotic resistance. This study was carried out to assess the antimicrobial activity and mode of action of a monoterpene, 1,8-cineol (CN) against carbapenemase-producing Klebsiella pneumoniae (KPC-KP). Results showed that resazurin microplate assay and time-kill analysis revealed bactericidal effects of CN at 28.83 mg/mL. Zeta potential showed that CN increased the surface charge of bacteria and an increase of outer membrane permeability was also detected. CN was able to cause leakage of proteins and nucleic acids in KPC-KP cells upon exposure to CN and ethidium bromide influx/efflux experiment showed the uptake of ethidium bromide into the cell; this was attributed to membrane damage. CN was also found to induce oxidative stress in CN-treated KPC-KP cells through generation of reactive oxygen species which initiated lipid peroxidation and thus damaging the bacterial cell membrane. Scanning and transmission electron microscopies further confirmed the disruption of bacterial cell membrane and loss of intracellular materials. In this study, we demonstrated that CN induced oxidative stress and membrane damage resulting in KPC-KP cell death. Nature Research 2021 Article PeerReviewed Moo, Chew Li and Osman, Mohd Azuraidi and Shun, Kai Yang and Wai, Sum Yap and Ismail, Saila and Swee, Hua Erin Lim and Chong, Chou Min and Lai, Kok Song (2021) Antimicrobial activity and mode of action of 1,8-cineol against carbapenemase-producing Klebsiella pneumoniae. Scientific Reports, 11. art. no. 20824. pp. 1-22. ISSN 2045-2322 https://www.nature.com/articles/s41598-021-00249-y
institution Universiti Putra Malaysia
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country Malaysia
content_provider Universiti Putra Malaysia
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description Antimicrobial resistance remains one of the most challenging issues that threatens the health of people around the world. Plant-derived natural compounds have received considerable attention for their potential role to mitigate antibiotic resistance. This study was carried out to assess the antimicrobial activity and mode of action of a monoterpene, 1,8-cineol (CN) against carbapenemase-producing Klebsiella pneumoniae (KPC-KP). Results showed that resazurin microplate assay and time-kill analysis revealed bactericidal effects of CN at 28.83 mg/mL. Zeta potential showed that CN increased the surface charge of bacteria and an increase of outer membrane permeability was also detected. CN was able to cause leakage of proteins and nucleic acids in KPC-KP cells upon exposure to CN and ethidium bromide influx/efflux experiment showed the uptake of ethidium bromide into the cell; this was attributed to membrane damage. CN was also found to induce oxidative stress in CN-treated KPC-KP cells through generation of reactive oxygen species which initiated lipid peroxidation and thus damaging the bacterial cell membrane. Scanning and transmission electron microscopies further confirmed the disruption of bacterial cell membrane and loss of intracellular materials. In this study, we demonstrated that CN induced oxidative stress and membrane damage resulting in KPC-KP cell death.
format Article
author Moo, Chew Li
Osman, Mohd Azuraidi
Shun, Kai Yang
Wai, Sum Yap
Ismail, Saila
Swee, Hua Erin Lim
Chong, Chou Min
Lai, Kok Song
spellingShingle Moo, Chew Li
Osman, Mohd Azuraidi
Shun, Kai Yang
Wai, Sum Yap
Ismail, Saila
Swee, Hua Erin Lim
Chong, Chou Min
Lai, Kok Song
Antimicrobial activity and mode of action of 1,8-cineol against carbapenemase-producing Klebsiella pneumoniae
author_facet Moo, Chew Li
Osman, Mohd Azuraidi
Shun, Kai Yang
Wai, Sum Yap
Ismail, Saila
Swee, Hua Erin Lim
Chong, Chou Min
Lai, Kok Song
author_sort Moo, Chew Li
title Antimicrobial activity and mode of action of 1,8-cineol against carbapenemase-producing Klebsiella pneumoniae
title_short Antimicrobial activity and mode of action of 1,8-cineol against carbapenemase-producing Klebsiella pneumoniae
title_full Antimicrobial activity and mode of action of 1,8-cineol against carbapenemase-producing Klebsiella pneumoniae
title_fullStr Antimicrobial activity and mode of action of 1,8-cineol against carbapenemase-producing Klebsiella pneumoniae
title_full_unstemmed Antimicrobial activity and mode of action of 1,8-cineol against carbapenemase-producing Klebsiella pneumoniae
title_sort antimicrobial activity and mode of action of 1,8-cineol against carbapenemase-producing klebsiella pneumoniae
publisher Nature Research
publishDate 2021
url http://psasir.upm.edu.my/id/eprint/95915/
https://www.nature.com/articles/s41598-021-00249-y
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