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Quaternized chitosan derivatives inhibit growth and affect biofilm formation of Staphylococcus aureus

  • Ahmed, S. K. et al. Antimicrobial resistance: impacts, challenges, and future prospects. J. Med. Surg. Public. Health. 2, 100081 (2024).


    Google Scholar
     

  • Tang, K. W. K., Millar, B. C. & Moore, J. E. Antimicrobial resistance (AMR). Br. J. Biomed. Sci. 80, 11387 (2023).

    PubMed 
    PubMed Central 

    Google Scholar
     

  • Salam, M. A. et al. Antimicrobial resistance: A growing serious threat for global public health. Healthc. 11, 1946 (2023).


    Google Scholar
     

  • Llor, C. & Bjerrum, L. Antimicrobial resistance: risk associated with antibiotic overuse and initiatives to reduce the problem. 5, 229–241. http://dx.doi.org/10.1177/2042098614554919 (2014)

  • Prestinaci, F., Pezzotti, P. & Pantosti, A. Antimicrobial resistance: a global multifaceted phenomenon. Pathog. Glob. Health. 109, 309–318 (2015).

    PubMed 
    PubMed Central 

    Google Scholar
     

  • Cosgrove, S. E. The relationship between antimicrobial resistance and patient outcomes: mortality, length of hospital stay, and health care costs. Clin. Infect. Dis. 42, S82–S89 (2006).

    PubMed 

    Google Scholar
     

  • Thompson, T. The staggering death toll of drug-resistant bacteria. Nature. https://doi.org/10.1038/D41586-022-00228-X (2022).

    PubMed 
    PubMed Central 

    Google Scholar
     

  • Turner, N. A. et al. Methicillin-resistant Staphylococcus aureus: an overview of basic and clinical research. Nat. Rev. Microbiol. 17, 203–218 (2019).

  • Singh, S., Datta, S., Narayanan, K. B. & Rajnish, K. N. Bacterial exo-polysaccharides in biofilms: role in antimicrobial resistance and treatments. J. Genetic Eng. Biotechnol. 19, 140 (2021).


    Google Scholar
     

  • Shree, P., Singh, C. K., Sodhi, K. K., Surya, J. N. & Singh, D. K. Biofilms: Understanding the structure and contribution towards bacterial resistance in antibiotics. Med. Microecol. 16, 100084 (2023).


    Google Scholar
     

  • Zhao, A., Sun, J. & Liu, Y. Understanding bacterial biofilms: from definition to treatment strategies. Front. Cell. Infect. Microbiol. 13, 1137947 (2023).

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Young, M. H., Upchurch, G. R. & Malani, P. N. Vascular graft infections. Infect. Dis. Clin. N. Am. 26, 41–56 (2012).


    Google Scholar
     

  • Tello-Díaz, C. et al. Methicillin-Susceptible Staphylococcus aureus biofilm formation on vascular grafts: an in vitro study. Microbiol. Spectr. 11, (2023).

  • Towne, J. B., Seabrook, G. R., Bandyk, D., Freischlag, J. A. & Edmiston, C. E. In situ replacement of arterial prosthesis infected by bacterial biofilms: Long-term follow-up. J. Vasc. Surg. 19, 226–235 (1994).

    CAS 
    PubMed 

    Google Scholar
     

  • Ju, G. et al. Comparative effectiveness and safety of six antibiotics in treating MRSA infections: A network meta-analysis. Int. J. Infect. Dis. 146, 107109 (2024).

    CAS 
    PubMed 

    Google Scholar
     

  • Kawasuji, H. et al. Effectiveness and safety of linezolid versus vancomycin, teicoplanin, or daptomycin against methicillin-resistant Staphylococcus aureus bacteremia: A systematic review and meta-analysis. Antibiotics. 12, 697 (2023).

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Huang, V., Clayton, N. A. & Welker, K. H. Glycopeptide hypersensitivity and adverse reactions. Pharm. 8, 70 (2020).


    Google Scholar
     

  • Minhas, J. S., Wickner, P. G., Long, A. A., Banerji, A. & Blumenthal, K. G. Immune-mediated reactions to Vancomycin A systematic case review and analysis. Ann. Allergy Asthma Immunol. 116, 544–553 (2016).

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Uda, K., Suwa, J., Ito, K., Hataya, H. & Horikoshi, Y. Ototoxicity and nephrotoxicity with elevated serum concentrations following Vancomycin overdose: A retrospective case series. J. Pediatr. Pharmacol. Ther. 24, 450–455 (2019).

    PubMed 
    PubMed Central 

    Google Scholar
     

  • Shariati, A. et al. Global prevalence and distribution of vancomycin resistant, vancomycin intermediate and heterogeneously vancomycin intermediate Staphylococcus aureus clinical isolates: a systematic review and meta-analysis. Sci. Rep. 10, 1–16 (2020).

  • Alemu, D., Getachew, E. & Mondal, A. K. Study on the physicochemical properties of chitosan and their applications in the biomedical sector. Int. J. Polym. Sci. 2023, 5025341 (2023).

  • Ke, C. L., Deng, F. S., Chuang, C. Y. & Lin, C. H. Antimicrobial actions and applications of Chitosan. Polym. 13, 904 (2021).

    CAS 

    Google Scholar
     

  • Zhao, D. et al. Biomedical applications of Chitosan and its derivative nanoparticles. Polym. 10, 462 (2018).


    Google Scholar
     

  • Hong, F. et al. Chitosan-based hydrogels: from preparation to applications, a review. Food Chem. X. 21, 101095 (2024).

    CAS 
    PubMed 

    Google Scholar
     

  • Hoque, J., Prakash, R. G., Paramanandham, K., Shome, B. R. & Haldar, J. Biocompatible injectable hydrogel with potent wound healing and antibacterial properties. Mol. Pharm. 14, 1218–1230 (2017).

    CAS 
    PubMed 

    Google Scholar
     

  • Feng, P. et al. Chitosan-based functional materials for skin wound repair: mechanisms and applications. Front. Bioeng. Biotechnol. 9, 650598 (2021).

    PubMed 
    PubMed Central 

    Google Scholar
     

  • Le, L. T. T. et al. Enhancement of wound healing efficacy by Chitosan-based hydrocolloid on Sprague Dawley rats. Vivo 37, 1052–1064 (2023).

    CAS 

    Google Scholar
     

  • Wang, L. et al. Quarternized chitosan/quercetin/polyacrylamide semi-interpenetrating network hydrogel with recoverability, toughness and antibacterial properties for wound healing. Int. J. Biol. Macromol. 228, 48–58 (2023).

    CAS 
    PubMed 

    Google Scholar
     

  • Ueno, H., Mori, T. & Fujinaga, T. Topical formulations and wound healing applications of Chitosan. Adv. Drug Deliv. Rev. 52, 105–115 (2001).

    CAS 
    PubMed 

    Google Scholar
     

  • Chen, X. et al. Peptide-modified Chitosan hydrogels promote skin wound healing by enhancing wound angiogenesis and inhibiting inflammation. Am. J. Transl. Res. 9, 2352 (2017).

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Augustine, R. et al. Electrospun Chitosan membranes containing bioactive and therapeutic agents for enhanced wound healing. Int. J. Biol. Macromol. 156, 153–170 (2020).

    CAS 
    PubMed 

    Google Scholar
     

  • Tien, N. D. et al. Solution blow spinning of highly deacetylated Chitosan nanofiber scaffolds for dermal wound healing. Biomater. Adv. 137, 212871 (2022).

    CAS 
    PubMed 

    Google Scholar
     

  • Ishihara, M. et al. Photocrosslinkable Chitosan as a dressing for wound occlusion and accelerator in healing process. Biomaterials. 23, 833–840 (2002).

    CAS 
    PubMed 

    Google Scholar
     

  • Kossovich, L. Y., Salkovskiy, Y. & Kirillova, I. V. Electrospun Chitosan nanofiber materials as burn dressing BT—6th world Congress of biomechanics (WCB 2010). August 1–6, 2010 Singapore. (eds Lim, C. T. & Goh, J. C. H.) 1212–1214. https://doi.org/10.1007/978-3-642-14515-5_307 (Springer Berlin Heidelberg, 2010).


    Google Scholar
     

  • Perrin, N., Mohammadkhani, G., Homayouni Moghadam, F., Delattre, C. & Zamani, A. Biocompatible fibers from fungal and shrimp chitosans for suture application. Curr. Res. Biotechnol. 4, 530–536 (2022).

    CAS 

    Google Scholar
     

  • Aussel, A. et al. Chitosan-based hydrogels for developing a small-diameter vascular graft: in vitro and in vivo evaluation. Biomed. Mater. 12, (2017).

  • Maleki, S., Shamloo, A. & Kalantarnia, F. Tubular TPU/SF nanofibers covered with chitosan-based hydrogels as small-diameter vascular grafts with enhanced mechanical properties. Sci. Rep. 12, 1–15 (2022).

  • Ibrahim, A. G., Hamodin, A. G., Fouda, A., Eid, A. M. & Elgammal, W. E. Fabrication and characterization of a new eco-friendly sulfonamide-chitosan derivative with enhanced antimicrobial and selective cytotoxicity properties. Sci. Rep. 14, (2024).

  • Rahayu, D. P. et al. Enhancing the antibacterial effect of Chitosan to combat orthopaedic implant-associated infections. Carbohydr. Polym. 289, (2022).

  • Nicolle, L., Journot, C. M. A. & Gerber-Lemaire, S. Chitosan functionalization: covalent and non-covalent interactions and their characterization. Polymers (Basel) 13, (2021).

  • Dhlamini, K. S., Selepe, C. T., Ramalapa, B., Tshweu, L. & Ray, S. S. Reimagining chitosan-based antimicrobial biomaterials to mitigate antibiotic resistance and alleviate antibiotic overuse: A review. Macromol. Mater. Eng. 2400018 https://doi.org/10.1002/MAME.202400018 (2024).

  • Yilmaz Atay, H. Antibacterial activity of chitosan-based systems. In Functional Chitosan: Drug Delivery and Biomedical Applications, 457–489 (eds Jana, S. & Jana, S.) https://doi.org/10.1007/978-981-15-0263-7_15. (Springer Singapore, 2019).


    Google Scholar
     

  • Sadykov, M. R. et al. Inactivation of the Pta-AckA pathway causes cell death in Staphylococcus aureus. J. Bacteriol. 195, 3035–3044 (2013).

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Salkovskiy, Y. & Fadeev, A. High-efficiency retention of ultrafine aerosols by electrospun nanofibers. Sci. Rep. 12, (2022).

  • Laliwala, A. et al. Machine learning assisted identification of antibiotic-resistant Staphylococcus aureus strains using a paper-based ratiometric sensor array. Microchem. J. 206, 111395 (2024).

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Thomas, V. C. et al. A central role for carbon-overflow pathways in the modulation of bacterial cell death. PLoS Pathog. 10, e1004205 (2014).

    PubMed 
    PubMed Central 

    Google Scholar
     

  • Heydorn, A. et al. Quantification of biofilm structures by the novel computer program COMSTAT. Microbiol. (N Y). 146, 2395–2407 (2000).

    CAS 

    Google Scholar
     

  • Li, P. et al. A polycationic antimicrobial and biocompatible hydrogel with microbe membrane suctioning ability. Nat. Mater. 10, 149–156 (2011).

    ADS 
    CAS 
    PubMed 

    Google Scholar
     

  • Andreica, B. I., Cheng, X. & Marin, L. Quaternary ammonium salts of chitosan. A critical overview on the synthesis and properties generated by quaternization. Eur. Polym. J. 139, 110016 (2020).

    CAS 

    Google Scholar
     

  • Babij, N. R. et al. NMR chemical shifts of trace impurities: industrially preferred solvents used in process and green chemistry. Org. Process. Res. Dev. 20, 661–667 (2016).

    CAS 

    Google Scholar
     

  • Chang, S. H., Lin, H. T. V., Wu, G. J. & Tsai, G. J. pH effects on solubility, zeta potential, and correlation between antibacterial activity and molecular weight of Chitosan. Carbohydr. Polym. 134, 74–81 (2015).

    CAS 
    PubMed 

    Google Scholar
     

  • Somerville, G. A. et al. Correlation of acetate catabolism and growth yield in Staphylococcus aureus: implications for host-pathogen interactions. Infect. Immun. 71, 4724–4732 (2003).

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Ke, C. L., Deng, F. S., Chuang, C. Y. & Lin, C. H. Antimicrobial actions and applications of Chitosan. Polymers (Basel). 13, (2021).

  • Raafat, D. & Sahl, H. G. Chitosan and its antimicrobial potential—a critical literature survey. Microb. Biotechnol. 2, 186–201 (2009).

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Yan, D. et al. Antimicrobial properties of Chitosan and Chitosan derivatives in the treatment of enteric infections. Molecules 2021. 26, 7136 (2021).

    CAS 

    Google Scholar
     

  • Yan, D. et al. Antimicrobial properties of Chitosan and Chitosan derivatives in the treatment of enteric infections. Molecules. 26, (2021).

  • Hoque, J. et al. Chitosan derivatives active against multidrug-resistant bacteria and pathogenic fungi: in vivo evaluation as topical antimicrobials. Mol. Pharm. 13, 3578–3589 (2016).

    CAS 
    PubMed 

    Google Scholar
     

  • Qiu, H. et al. The mechanisms and the applications of antibacterial polymers in surface modification on medical devices. Front. Bioeng. Biotechnol. 8, 910 (2020).

    PubMed 
    PubMed Central 

    Google Scholar
     

  • Juan, C. A., de la Lastra, J. M. P., Plou, F. J. & Pérez-Lebeña, E. The chemistry of reactive oxygen species (ROS) revisited: outlining their role in biological macromolecules (DNA, lipids and Proteins) and induced pathologies. Int. J. Mol. Sci. 22, 4642 (2021).

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Marshall, D. D., Sadykov, M. R., Thomas, V. C., Bayles, K. W. & Powers, R. A redox imbalance underlies the fitness defect associated with inactivation of the Pta-AckA pathway in Staphylococcus aureus. J. Proteome Res. 15, 1205 (2016).

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Desnues, B. et al. Differential oxidative damage and expression of stress defence Regulons in culturable and non-culturable Escherichia coli cells. EMBO Rep. 4, 400–404 (2003).

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Sadykov, M. R. et al. Tricarboxylic acid cycle-dependent regulation of Staphylococcus epidermidis polysaccharide intercellular adhesin synthesis. J. Bacteriol. 190, 7621–7632 (2008).

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Wang, Y. et al. Inactivation of TCA cycle enhances Staphylococcus aureus persister cell formation in stationary phase. Sci. Rep. 8, 1–13 (2018).

  • Venkova, T. et al. Molecular basis of stationary phase survival and applications. Front. Microbiol. 8, 2000 (2017).


    Google Scholar
     

  • Behbahani, S. B. et al. pH variation in medical implant biofilms: causes, measurements, and its implications for antibiotic resistance. Front. Microbiol. 13, 1028560 (2022).

    PubMed 
    PubMed Central 

    Google Scholar
     

  • Melro, E. et al. Chitosan films in food applications. Tuning film properties by changing acidic dissolution conditions. Polym. (Basel). 13, 1 (2020).


    Google Scholar
     

  • Haktaniyan, M. & Bradley, M. Polymers showing intrinsic antimicrobial activity. Chem. Soc. Rev. 51, 8584–8611 (2022).

    CAS 
    PubMed 

    Google Scholar
     

  • Ardean, C. et al. Factors influencing the antibacterial activity of Chitosan and Chitosan modified by functionalization. Int. J. Mol. Sci. 22, (2021).

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