Combinatorial Antimicrobial Efficacy and Mechanism of Linalool Against Clinically Relevant Klebsiella pneumoniae

被引:20
|
作者
Yang, Shun-Kai [1 ]
Yusoff, Khatijah [2 ,3 ]
Ajat, Mokrish [4 ]
Wee, Chien-Yeong [5 ]
Yap, Polly-Soo-Xi [6 ]
Lim, Swee-Hua-Erin [7 ]
Lai, Kok-Song [7 ]
机构
[1] Univ Putra Malaysia, Fac Biotechnol & Biomol Sci, Dept Cell & Mol Biol, Serdang, Malaysia
[2] Univ Putra Malaysia, Fac Biotechnol & Biomol Sci, Dept Microbiol, Serdang, Malaysia
[3] Univ Putra Malaysia, Inst Biosci, UPM MAKNA Canc Res Lab, Serdang, Malaysia
[4] Univ Putra Malaysia, Dept Vet Preclin Sci, Fac Vet Med, Serdang, Malaysia
[5] Malaysian Agr Res & Dev Inst MARDI, Biotechnol & Nanotechnol Res Ctr, Kuala Lumpur, Malaysia
[6] Univ Malaya, Dept Med Microbiol, Fac Med, Kuala Lumpur, Malaysia
[7] Abu Dhabi Womens Coll, Higher Coll Technol, Hlth Sci Div, Abu Dhabi, U Arab Emirates
关键词
adjuvant– antibiotic combinatory therapy; carbapenemase-producing Klebsiella pneumoniae; linalool; membrane disruption; oxidative stress;
D O I
10.3389/fmicb.2021.635016
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Antibiotic-adjuvant combinatory therapy serves as a viable treatment option in addressing antibiotic resistance in the clinical setting. This study was carried out to assess and characterize the adjuvant potential and mode of action of linalool against carbapenemase-producing Klebsiella pneumoniae (KPC-KP). Linalool exhibited bactericidal activity alone (11,250 mu g/ml) and in combination with meropenem (5,625 mu g/ml). Comparative proteomic analysis showed significant reduction in the number of cytoplasmic and membrane proteins, indicating membrane damage in linalool-treated KPC-KP cells. Upregulation of oxidative stress regulator proteins and downregulation of oxidative stress-sensitive proteins indicated oxidative stress. Zeta potential measurement and outer membrane permeability assay revealed that linalool increases the bacterial surface charge as well as the membrane permeability. Intracellular leakage of nucleic acid and proteins was detected upon linalool treatment. Scanning and transmission electron microscopies further revealed the breakage of bacterial membrane and loss of intracellular materials. Linalool induced oxidative stress by generating reactive oxygen species (ROS) which initiates lipid peroxidation, leading to damage of the bacterial membrane. This leads to intracellular leakage, eventually killing the KPC-KP cells. Our study demonstrated that linalool possesses great potential in future clinical applications as an adjuvant along with existing antibiotics attributed to their ability in disrupting the bacterial membrane by inducing oxidative stress. This facilitates the uptake of antibiotics into the bacterial cells, enhancing bacterial killing.
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页数:10
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