Insights into the Mode of Action of Chitosan as an Antibacterial Compound

ABSTRACT Chitosan is a polysaccharide biopolymer that combines a unique set of versatile physicochemical and biological characteristics which allow for a wide range of applications. Although its antimicrobial activity is well documented, its mode of action has hitherto remained only vaguely defined. In this work we investigated the antimicrobial mode of action of chitosan using a combination of approaches, including in vitro assays, killing kinetics, cellular leakage measurements, membrane potential estimations, and electron microscopy, in addition to transcriptional response analysis. Chitosan, whose antimicrobial activity was influenced by several factors, exhibited a dose-dependent growth-inhibitory effect. A simultaneous permeabilization of the cell membrane to small cellular components, coupled to a significant membrane depolarization, was detected. A concomitant interference with cell wall biosynthesis was not observed. Chitosan treatment of Staphylococcus simulans 22 cells did not give rise to cell wall lysis; the cell membrane also remained intact. Analysis of transcriptional response data revealed that chitosan treatment leads to multiple changes in the expression profiles of Staphylococcus aureus SG511 genes involved in the regulation of stress and autolysis, as well as genes associated with energy metabolism. Finally, a possible mechanism for chitosan's activity is postulated. Although we contend that there might not be a single classical target that would explain chitosan's antimicrobial action, we speculate that binding of chitosan to teichoic acids, coupled with a potential extraction of membrane lipids (predominantly lipoteichoic acid) results in a sequence of events, ultimately leading to bacterial death.

[1]  R. Muzzarelli,et al.  Antimicrobial properties of N-carboxybutyl chitosan , 1990, Antimicrobial Agents and Chemotherapy.

[2]  Se-kwon Kim,et al.  Chitosan derivatives killed bacteria by disrupting the outer and inner membrane. , 2006, Journal of agricultural and food chemistry.

[3]  A. Haas,et al.  A method to purify bacteria-containing phagosomes from infected macrophages. , 2000, Methods in cell science : an official journal of the Society for In Vitro Biology.

[4]  Manisha Chawla,et al.  Chitosan: some pharmaceutical and biological aspects ‐ an update , 2001, The Journal of pharmacy and pharmacology.

[5]  S. Ehlers,et al.  Tertiary Structure of Staphylococcus aureus Cell Wall Murein , 2004, Journal of bacteriology.

[6]  V. Singh,et al.  Genome-wide transcriptional profiling of the response of Staphylococcus aureus to cell-wall-active antibiotics reveals a cell-wall-stress stimulon. , 2003, Microbiology.

[7]  T. Lehtimäki,et al.  Cholesterol-lowering Properties and Safety of Chitosan , 2002, Arzneimittelforschung.

[8]  Walter Steurbaut,et al.  Chitosan as antimicrobial agent: applications and mode of action. , 2003, Biomacromolecules.

[9]  I. Booth,et al.  Osmoregulation and its importance to food-borne microorganisms. , 2002, International journal of food microbiology.

[10]  E. Weiler,et al.  Oligogalacturonides and chitosan activate plant defensive genes through the octadecanoid pathway. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[11]  B. Krajewska,et al.  Chitosan as a lipid binder: a langmuir monolayer study of chitosan-lipid interactions. , 2007, Biomacromolecules.

[12]  Kenneth W. Bayles,et al.  The Staphylococcus aureus lrgAB Operon Modulates Murein Hydrolase Activity and Penicillin Tolerance , 2000, Journal of bacteriology.

[13]  H. Sahl,et al.  Physiology and antibiotic susceptibility of Staphylococcus aureus small colony variants. , 2002, Microbial drug resistance.

[14]  N. Ravi,et al.  A Mössbauer study of the interaction of chitosan and D-glucosamine with iron and its relevance to other metalloenzymes. , 2003, Biomacromolecules.

[15]  Tonni Agustiono Kurniawan,et al.  Low-cost adsorbents for heavy metals uptake from contaminated water: a review. , 2003, Journal of hazardous materials.

[16]  Oscar P. Kuipers,et al.  Specific Binding of Nisin to the Peptidoglycan Precursor Lipid II Combines Pore Formation and Inhibition of Cell Wall Biosynthesis for Potent Antibiotic Activity* , 2001, The Journal of Biological Chemistry.

[17]  R. Tharanathan,et al.  Chitin — The Undisputed Biomolecule of Great Potential , 2003, Critical reviews in food science and nutrition.

[18]  S. Meroueh,et al.  Nanomolecular and Supramolecular Paths toward Peptidoglycan Structure , 2006 .

[19]  R. Ahvenainen,et al.  Chitosan disrupts the barrier properties of the outer membrane of gram-negative bacteria. , 2001, International journal of food microbiology.

[20]  H. Sahl,et al.  Autolytic system of Staphylococcus simulans 22: influence of cationic peptides on activity of N-acetylmuramoyl-L-alanine amidase , 1987, Journal of bacteriology.

[21]  L. Illum,et al.  Chitosan and its use as a pharmaceutical excipient. , 1998, Pharmaceutical research.

[22]  Andre Boorsma,et al.  Transcriptional Response of Saccharomyces cerevisiae to the Plasma Membrane-Perturbing Compound Chitosan , 2005, Eukaryotic Cell.

[23]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.

[24]  W. Bentley,et al.  Global Transcriptome Analysis of Staphylococcus aureus Response to Hydrogen Peroxide , 2006, Journal of bacteriology.

[25]  Ø. Langsrud,et al.  Acid-shock responses in Staphylococcus aureus investigated by global gene expression analysis. , 2007, Microbiology.

[26]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[27]  J. Matsuoka,et al.  Antibacterial Properties of Antimicrobial‐Finished Textile Products , 2002, Microbiology and immunology.

[28]  R. Lehrer,et al.  Potassium release, a useful tool for studying antimicrobial peptides. , 2002, Journal of microbiological methods.

[29]  R. Kessler,et al.  Growth characteristics of group A streptococci in a new chemically defined medium , 1980, Infection and immunity.

[30]  H. Kalbacher,et al.  Inactivation of the dlt Operon inStaphylococcus aureus Confers Sensitivity to Defensins, Protegrins, and Other Antimicrobial Peptides* , 1999, The Journal of Biological Chemistry.

[31]  H. Juan Small Colony Variants: a Pathogenic Form of Bacteria that Facilitates Persistent and Recurrent Infections , 2009 .

[32]  K. Leong,et al.  Chitosan nanoparticles for oral drug and gene delivery , 2006, International journal of nanomedicine.

[33]  M. Kanehisa,et al.  Whole genome sequencing of meticillin-resistant Staphylococcus aureus , 2001, The Lancet.

[34]  S. Engelmann,et al.  Physiological Characterization of a Heme-Deficient Mutant of Staphylococcus aureus by a Proteomic Approach , 2003, Journal of bacteriology.

[35]  B. Neumeister,et al.  Role of teichoic acids in Staphylococcus aureus nasal colonization, a major risk factor in nosocomial infections , 2004, Nature Medicine.

[36]  T. Fujinaga,et al.  Topical formulations and wound healing applications of chitosan. , 2001, Advanced drug delivery reviews.

[37]  R. Novick,et al.  Effect of Mild Acid on Gene Expression in Staphylococcus aureus , 2004, Journal of bacteriology.

[38]  Y. Shai,et al.  Analysis of in vitro activities and modes of action of synthetic antimicrobial peptides derived from an alpha-helical 'sequence template'. , 2008, The Journal of antimicrobial chemotherapy.

[39]  S. Fuchs,et al.  Anaerobic Gene Expression in Staphylococcus aureus , 2007, Journal of bacteriology.

[40]  S. Miller,et al.  INTRODUCTORY REMARKS , 1952, Public health reports.

[41]  H. Sahl,et al.  Insights into In Vivo Activities of Lantibiotics from Gallidermin and Epidermin Mode-of-Action Studies , 2006, Antimicrobial Agents and Chemotherapy.

[42]  S. Chirkov The Antiviral Activity of Chitosan (Review) , 2004, Applied Biochemistry and Microbiology.

[43]  A. Tomasz,et al.  Overexpression of Genes of the Cell Wall Stimulon in Clinical Isolates of Staphylococcus aureus Exhibiting Vancomycin-Intermediate- S. aureus-Type Resistance to Vancomycin , 2006, Journal of bacteriology.

[44]  Alessandro Tossi,et al.  Mammalian defensins: structures and mechanism of antibiotic activity , 2005, Journal of leukocyte biology.

[45]  R. Benz,et al.  Lipid II-Mediated Pore Formation by the Peptide Antibiotic Nisin: a Black Lipid Membrane Study , 2004, Journal of bacteriology.

[46]  W. Vollmer,et al.  The Architecture of the Murein (Peptidoglycan) in Gram-Negative Bacteria: Vertical Scaffold or Horizontal Layer(s)? , 2004, Journal of bacteriology.

[47]  W. Fischer Lipoteichoic acid and lipids in the membrane of Staphylococcus aureus , 1994, Medical Microbiology and Immunology.

[48]  H. Sahl,et al.  Mode of action of human beta-defensin 3 against Staphylococcus aureus and transcriptional analysis of responses to defensin challenge. , 2008, International journal of medical microbiology : IJMM.

[49]  H. Sahl,et al.  Mode of action of the peptide antibiotic nisin and influence on the membrane potential of whole cells and on cytoplasmic and artificial membrane vesicles , 1985, Antimicrobial Agents and Chemotherapy.

[50]  J. Rhoades,et al.  Antimicrobial Actions of Degraded and Native Chitosan against Spoilage Organisms in Laboratory Media and Foods , 2000, Applied and Environmental Microbiology.

[51]  V. Varlamov,et al.  Ultrastructural Study of Chitosan Effects on Klebsiella and Staphylococci , 2005, Bulletin of Experimental Biology and Medicine.