Volume 54, Issue 21 pp. 6278-6282
Communication

Amphiphilic Tobramycins with Immunomodulatory Properties

Dr. Goutam Guchhait

Dr. Goutam Guchhait

Department of Chemistry, University of Manitoba, Winnipeg, MB, R3T 2N2 (Canada)

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Anthony Altieri

Anthony Altieri

Department of Internal Medicine and Immunology, University of Manitoba, Winnipeg, MB, R3T 2N2 (Canada)

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Dr. Balakishan Gorityala

Dr. Balakishan Gorityala

Department of Chemistry, University of Manitoba, Winnipeg, MB, R3T 2N2 (Canada)

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Xuan Yang

Xuan Yang

Department of Chemistry, University of Manitoba, Winnipeg, MB, R3T 2N2 (Canada)

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Dr. Brandon Findlay

Dr. Brandon Findlay

Department of Chemistry, University of Manitoba, Winnipeg, MB, R3T 2N2 (Canada)

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Prof. George G. Zhanel

Prof. George G. Zhanel

Department of Medical Microbiology and Medicine, Health Science Centre, Winnipeg, Manitoba, R3T 1R9 (Canada)

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Prof. Neeloffer Mookherjee

Prof. Neeloffer Mookherjee

Department of Internal Medicine and Immunology, University of Manitoba, Winnipeg, MB, R3T 2N2 (Canada)

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Prof. Frank Schweizer

Corresponding Author

Prof. Frank Schweizer

Department of Chemistry, University of Manitoba, Winnipeg, MB, R3T 2N2 (Canada)

Department of Chemistry, University of Manitoba, Winnipeg, MB, R3T 2N2 (Canada)Search for more papers by this author
First published: 01 April 2015
Citations: 52

Funding for this project was provided by CIHR (MOP 119335) Research Manitoba and NSERC.

Graphical Abstract

Double duty: Amphiphilic antibacterial aminoglycosides with additional immunomodulatory properties similar to those of host-defense peptides can be generated by appending a lipophilic R group (blue oval) to tobramycin. These amphiphilic tobramycin analogues can boost innate immune responses and control inflammatory responses related to septic shock.

Abstract

Amphiphilic aminoglycosides (AAGs) are an emerging source of antibacterials to combat infections caused by antibiotic-resistant bacteria. Mode-of-action studies indicate that AAGs predominately target bacterial membranes, thereby leading to depolarization and increased permeability. To assess whether AAGs also induce host-directed immunomodulatory responses, we determined the AAG-dependent induction of cytokines in macrophages in the absence or presence of lipopolysaccharide (LPS). Our results show for the first time that AAGs can boost the innate immune response, specifically the recruitment of immune cells such as neutrophils required for the resolution of infections. Moreover, AAGs can selectively control inflammatory responses induced in the presence of endotoxins to prevent septic shock. In conclusion, our study demonstrates that AAGs possess multifunctional properties that combine direct antibacterial activity with host-directed clearance effects reminiscent of those of host-defense peptides.

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