Regulation of Staphylococcus aureus Virulence and Application of Nanotherapeutics to Eradicate S. aureus Infection
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Staphylococcus aureus is a versatile pathogen known to cause hospital- and community-acquired, foodborne, and zoonotic infections. The clinical infections by S. aureus cause an increase in morbidity and mortality rates and treatment costs, aggravated by the emergence of drug-resistant strains. As a multi-faceted pathogen, it is imperative to consolidate the knowledge on its pathogenesis, including the mechanisms of virulence regulation, development of antimicrobial resistance, and biofilm formation, to make it amenable to different treatment strategies. Nanomaterials provide a suitable platform to address this challenge, with the potential to control intracellular parasitism and multidrug resistance where conventional therapies show limited efficacy. In a nutshell, the first part of this review focuses on the impact of S. aureus on human health and the role of virulence factors and biofilms during pathogenesis. The second part discusses the large diversity of nanoparticles and their applications in controlling S. aureus infections, including combination with antibiotics and phytochemicals and the incorporation of antimicrobial coatings for biomaterials. Finally, the limitations and prospects using nanomaterials are highlighted, aiming to foster the development of novel nanotechnology-driven therapies against multidrug-resistant S. aureus.
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The cell wall of S. aureus is the main target of the active substance in the gel extract of bay leaf and Saba banana peel.
“Therefore, the cell wall of S. aureus is the main target of the active substance in the gel extract of bay leaf and Saba banana peel 18 .”
From Evaluating the synergistic antibacterial and anti-inflammatory effects of Kapok banana peel (Musa acuminata balbisiana colla) and Bay leaf (Syzygium polyanthum) extract gel formulation on wound healing (2025) · cites this paper as [18]
The Introduction says conventional antibiotics can target bacterial cell walls, and section 3.3 describes liposomes that interact with the S. aureus cell wall. Neither passage addresses the active substances in bay leaf and Saba banana peel gel extract or establishes their main target. Searches for those extracts and for plant extracts targeting the cell wall found no passage that verifies the claim. (LLM, conf=0.75)
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Nanotechnology approaches for global infectious diseases
Kirtane, A. R., Verma, M., Karandikar, P., Furin, J., Langer, R., & Traverso, G. (2021) · Nature Nanotechnology · doi:10.1038/s41565-021-00866-8 · Cited by 520 · see citing works
Vancomycin-Resistant Staphylococcus aureus in the United States, 2002-2006
Sievert, D. M., Rudrik, J. T., Patel, J. B., McDonald, L. C., Wilkins, M. J., & Hageman, J. C. (2008) · Clinical Infectious Diseases · doi:10.1086/527392 · Cited by 483 · see citing works
Antibiotic-loaded nanoparticles targeted to the site of infection enhance antibacterial efficacy
Hussain, S., Joo, J., Kang, J., Kim, B., Braun, G. B., She, Z.-G., Kim, D., Mann, A. P., Mölder, T., Teesalu, T., et al. (2018) · Nature Biomedical Engineering · doi:10.1038/s41551-017-0187-5 · Cited by 399 · see citing works
Host defense and pathogenesis in Staphylococcus aureus infections
DeLeo, F. R., Diep, B. A., & Otto, M. (2009) · Infectious Disease Clinics of North America · doi:10.1016/j.idc.2008.10.003 · Cited by 269 · cited 1× · see citing works
“In parallel, PMNs also activate phagocytosis to eradicate the free-living planktonic cells by reactive oxygen species (ROS) generation [26], and has a significant role in reducing the biofilms of S.”
BackgroundA Staphylococcus aureus Regulatory System that Responds to Host Heme and Modulates Virulence
Torres, V. J., Stauff, D. L., Pishchany, G., Bezbradica, J. S., Gordy, L. E., Iturregui, J., Anderson, K. L., Dunman, P. M., Joyce, S., & Skaar, E. P. (2007) · Cell Host & Microbe · doi:10.1016/j.chom.2007.03.001 · Cited by 241 · see citing works
Antibacterial Activity of TiO2 Nanoparticles Prepared by One-Step Laser Ablation in Liquid
Khashan, K. S., Sulaiman, G. M., Abdulameer, F. A., Albukhaty, S., Ibrahem, M. A., Al-Muhimeed, T., & AlObaid, A. A. (2021) · Applied Sciences · doi:10.3390/app11104623 · Cited by 182 · see citing works
Magnetic Nanoparticle Targeted Hyperthermia of Cutaneous Staphylococcus aureus Infection
Kim, M.-H., Yamayoshi, I., Mathew, S., Lin, H., Nayfach, J., & Simon, S. I. (2013) · Annals of Biomedical Engineering · doi:10.1007/s10439-012-0698-x · Cited by 135 · see citing works
Formulation and pharmacology of long-acting rilpivirine
Williams, P. E., Crauwels, H. M., & Basstanie, E. D. (2015) · Current Opinion in HIV and AIDS · doi:10.1097/coh.0000000000000164 · Cited by 86 · see citing works
Immune evasion by Staphylococcus aureus conferred by iron-regulated surface determinant protein IsdH
Visai, L., Yanagisawa, N., Josefsson, E., Tarkowski, A., Pezzali, I., Rooijakkers, S. H. M., Foster, T. J., & Speziale, P. (2009) · Microbiology · doi:10.1099/mic.0.025684-0 · Cited by 73 · see citing works
Flagged first, then by citations
Research works printed but not linked: 286
- [1]Wright G.D. Mechanisms of resistance to antibiotics Curr. Opin. Chem. Biol. 2003 7 563 569 10.1016/j.cbpa.2003.08.004 14580559 · DOI
- [2]Römling U. Kjelleberg S. Normark S. Nyman L. Uhlin B.E. Åkerlund B. Microbial biofilm formation: A need to act J. Intern. Med. 2014 276 98 110 10.1111/joim.12242 24796496 · DOI
- [3]Alonso B. Pérez-Granda M.J. Latorre M.C. Sánchez-Carrillo C. Bouza E. Muñoz P. Guembe M. Production of biofilm by Staphylococcus aureus: Association with infective endocarditis? Enferm. Infecc. Y Microbiol. Clín. 2021 40 418 422 10.1016/j.eimc.2021.03.012 36195405 · DOI
- [4]Gittins D.I. Bethell D. Schiffrin D.J. Nichols R.J. A nanometre-scale electronic switch consisting of a metal cluster and redox-addressable groups Nature 2000 408 67 69 10.1038/35040518 11081506 · DOI
- [5]Sathishkumar M. Sneha K. Yun Y.-S. Immobilization of silver nanoparticles synthesized using Curcuma longa tuber powder and extract on cotton cloth for bactericidal activity Bioresour. Technol. 2010 101 7958 7965 10.1016/j.biortech.2010.05.051 20541399 · DOI
- [6]Elegbede J.A. Lateef A. Green synthesis of silver (Ag), gold (Au), and silver–gold (Ag–Au) alloy nanoparticles: A review on recent advances, trends, and biomedical applications Nanotechnology and Nanomaterial Applications in Food, Health, and Biomedical Sciences Apple Academic Press Palm Bay, FI, USA 2019 3 89
- [8]Pinto R.M. Lopes-de-Campos D. Martins M.C.L. Van Dijck P. Nunes C. Reis S. Impact of nanosystems in Staphylococcus aureus biofilms treatment FEMS Microbiol. Rev. 2019 43 622 641 10.1093/femsre/fuz021 31420962 PMC8038934 · DOI
- [9]Alavi M. Rai M. Recent advances in antibacterial applications of metal nanoparticles (MNPs) and metal nanocomposites (MNCs) against multidrug-resistant (MDR) bacteria Expert Rev. Anti-Infect. Ther. 2019 17 419 428 10.1080/14787210.2019.1614914 31046483 · DOI
- [10]Boswell G.W. Buell D. Bekersky I. AmBisome (Liposomal Amphotericin B): A Comparative Review J. Clin. Pharmacol. 1998 38 583 592 10.1002/j.1552-4604.1998.tb04464.x 9702842 · DOI
- [11]Gupta N. Rai D.B. Jangid A.K. Kulhari H. Chapter 7—Use of nanotechnology in antimicrobial therapy Methods in Microbiology Gurtler V. Ball A.S. Soni S. Academic Press Cambridge, UK 2019 Volume 46 143 172
- [12]Bassetti M. Vena A. Russo A. Peghin M. Inhaled liposomal antimicrobial delivery in lung infections Drugs 2020 80 1309 1318 10.1007/s40265-020-01359-z 32691293 PMC7479014 · DOI
- [13]Shimanovich U. Gedanken A. Nanotechnology solutions to restore antibiotic activity J. Mater. Chem. B 2016 4 824 833 10.1039/C5TB01527H 32263154 · DOI
- [14]Kaur K. Reddy S. Barathe P. Shriram V. Anand U. Proćków J. Kumar V. Combating Drug-Resistant Bacteria Using Photothermally Active Nanomaterials: A Perspective Review Front. Microbiol. 2021 12 747019 10.3389/fmicb.2021.747019 34867863 PMC8633304 · DOI
- [15]Alavi M. Jabari E. Jabbari E. Functionalized carbon-based nanomaterials and quantum dots with antibacterial activity: A review Expert Rev. Anti-Infect. Ther. 2021 19 35 44 10.1080/14787210.2020.1810569 32791928 · DOI
- [16]Wagner A.M. Knipe J.M. Orive G. Peppas N.A. Quantum dots in biomedical applications Acta Biomater. 2019 94 44 63 10.1016/j.actbio.2019.05.022 31082570 PMC6642839 · DOI
- [17]Herold B.C. Immergluck L.C. Maranan M.C. Lauderdale D.S. Gaskin R.E. Boyle-Vavra S. Leitch C.D. Daum R.S. Community-acquired methicillin-resistant Staphylococcus aureus in children with no identified predisposing risk JAMA 1998 279 593 598 10.1001/jama.279.8.593 9486753 · DOI · Paper page
- [20]Rowe S.E. Beam J.E. Conlon B.P. Recalcitrant Staphylococcus aureus infections: Obstacles and solutions Infect. Immun. 2021 89 e00694-20 10.1128/IAI.00694-20 33526569 PMC8090968 · DOI
- [21]Cruz A.R. van Strijp J.A.G. Bagnoli F. Manetti A.G.O. Virulence Gene Expression of Staphylococcus aureus in Human Skin Front. Microbiol. 2021 12 692023 10.3389/fmicb.2021.692023 34177874 PMC8231915 · DOI
- [22]Kannappan A. Gowrishankar S. Srinivasan R. Pandian S.K. Ravi A.V. Antibiofilm activity of Vetiveria zizanioides root extract against methicillin-resistant Staphylococcus aureus Microb. Pathog. 2017 110 313 324 10.1016/j.micpath.2017.07.016 28710012 · DOI
- [23]Algharib S.A. Dawood A. Xie S. Nanoparticles for treatment of bovine Staphylococcus aureus mastitis Drug Deliv. 2020 27 292 308 10.1080/10717544.2020.1724209 32036717 PMC7034104 · DOI
- [24]Meyle E. Stroh P. Günther F. Hoppy-Tichy T. Wagner C. Hänsch G.M. Destruction of bacterial biofilms by polymorphonuclear neutrophils: Relative contribution of phagocytosis, DNA release, and degranulation Int. J. Artif. Organs 2010 33 608 620 10.1177/039139881003300906 20890882 · DOI
- [25]Stroh P. Günther F. Meyle E. Prior B. Wagner C. Hänsch G.M. Host defence against Staphylococcus aureus biofilms by polymorphonuclear neutrophils: Oxygen radical production but not phagocytosis depends on opsonisation with immunoglobulin G Immunobiology 2011 216 351 357 10.1016/j.imbio.2010.07.009 20850891 · DOI
- [27]Guenther F. Stroh P. Wagner C. Obst U. Hänsch G.M. Phagocytosis of staphylococci biofilms by polymorphonuclear neutrophils: S. aureus and S. epidermidis differ with regard to their susceptibility towards the host defense Int. J. Artif. Organs 2009 32 565 573 19856266
- [28]Faurschou M. Borregaard N. Neutrophil granules and secretory vesicles in inflammation Microb. Infect. 2003 5 1317 1327 10.1016/j.micinf.2003.09.008 14613775 · DOI · Paper page
- [29]Alegre M.-L. Chen L. David M.Z. Bartman C. Boyle-Vavra S. Kumar N. Chong A.S. Daum R.S. Impact of Staphylococcus aureus USA300 colonization and skin infections on systemic immune responses in humans J. Immunol. 2016 197 1118 1126 10.4049/jimmunol.1600549 27402695 PMC4976020 · DOI
- [30]Brinkmann V. Reichard U. Goosmann C. Fauler B. Uhlemann Y. Weiss D.S. Weinrauch Y. Zychlinsky A. Neutrophil extracellular traps kill bacteria Science 2004 303 1532 1535 10.1126/science.1092385 15001782 · DOI · Paper page
- [31]Pastacaldi C. Lewis P. Howarth P. Staphylococci and staphylococcal superantigens in asthma and rhinitis: A systematic review and meta-analysis Allergy 2011 66 549 555 10.1111/j.1398-9995.2010.02502.x 21087214 · DOI
- [32]Kim M.R. Hong S.W. Choi E.B. Lee W.H. Kim Y.S. Jeon S. Jang M. Gho Y. Kim Y.K. Staphylococcus aureus-derived extracellular vesicles induce neutrophilic pulmonary inflammation via both T h1 and T h17 cell responses Allergy 2012 67 1271 1281 10.1111/all.12001 22913540 · DOI
- [33]Zhang R. Shebes M.A. Kho K. Scaffidi S.J. Meredith T.C. Yu W. Spatial regulation of protein A in Staphylococcus aureus Mol. Microbiol. 2021 116 589 605 10.1111/mmi.14734 33949015 PMC8403129 · DOI
- [35]Sharp J.A. Echague C.G. Hair P.S. Ward M.D. Nyalwidhe J.O. Geoghegan J.A. Foster T.J. Cunnion K.M. Staphylococcus aureus surface protein SdrE binds complement regulator factor H as an immune evasion tactic PLoS ONE 2012 7 e38407 10.1371/journal.pone.0038407 22675461 PMC3364985 · DOI
- [36]Hallett A. Cooper R. Complement activation in Staphylococcus aureus bacteraemia Clin. Exp. Immunol. 1980 40 306 6904257 PMC1536978
- [37]Diep B.A. Sensabaugh G.F. Somboona N.S. Carleton H.A. Perdreau-Remington F. Widespread skin and soft-tissue infections due to two methicillin-resistant Staphylococcus aureus strains harboring the genes for Panton-Valentine leucocidin J. Clin. Microbiol. 2004 42 2080 2084 10.1128/JCM.42.5.2080-2084.2004 15131173 PMC404676 · DOI
- [38]de Jong N. van Kessel K. van Strijp J. Immune evasion by Staphylococcus aureus Microbiol. Spectr. 2019 7 7.2.20 10.1128/microbiolspec.GPP3-0061-2019 30927347 PMC11590434 · DOI
- [39]See I. Wesson P. Gualandi N. Dumyati G. Harrison L.H. Lesher L. Nadle J. Petit S. Reisenauer C. Schaffner W. Socioeconomic factors explain racial disparities in invasive community-associated methicillin-resistant Staphylococcus aureus disease rates Clin. Infect. Dis. 2017 64 597 604 10.1093/cid/ciw808 28362911 PMC5656382 · DOI · Paper page
- [41]Khatoon Z. McTiernan C.D. Suuronen E.J. Mah T.-F. Alarcon E.I. Bacterial biofilm formation on implantable devices and approaches to its treatment and prevention Heliyon 2018 4 e01067 10.1016/j.heliyon.2018.e01067 30619958 PMC6312881 · DOI
- [42]Wang R. Braughton K.R. Kretschmer D. Bach T.-H.L. Queck S.Y. Li M. Kennedy A.D. Dorward D.W. Klebanoff S.J. Peschel A. Identification of novel cytolytic peptides as key virulence determinants for community-associated MRSA Nat. Med. 2007 13 1510 1514 10.1038/nm1656 17994102 · DOI · Paper page
- [43]Nurjadi D. Friedrich-Jänicke B. Schäfer J. Van Genderen P.J. Goorhuis A. Perignon A. Neumayr A. Mueller A. Kantele A. Schunk M. Skin and soft tissue infections in intercontinental travellers and the import of multi-resistant Staphylococcus aureus to Europe Clin. Microbiol. Infect. 2015 21 567.e1 567.e10 10.1016/j.cmi.2015.01.016 25753191 · DOI
- [44]Walter J. Haller S. Quinten C. Kärki T. Zacher B. Eckmanns T. Sin M.A. Plachouras D. Kinross P. Suetens C. Healthcare-associated pneumonia in acute care hospitals in European Union/European Economic Area countries: An analysis of data from a point prevalence survey, 2011 to 2012 Eurosurveillance 2018 23 1700843 10.2807/1560-7917.ES.2018.23.32.1700843 30107871 PMC6092912 · DOI
- [45]Stauffer B.S. aureus Sphingomyelinase is a state-dependent inhibitor of the cystic fibrosis transmembrane conductance regulator (CFTR) Biophys. J. 2017 112 254a 10.1016/j.bpj.2016.11.1384 PMC5462758 28592822 · DOI
- [46]Bauer T. Torres A. Ferrer R. Heyer C. Schultze-Werninghaus C. Rasche K. Biofilm formation in endotracheal tubes. Association between pneumonia and the persistence of pathogens Monaldi Arch. Chest Dis. 2002 57 84 87 12174708
- [47]Viola G.M. Darouiche R.O. Cardiovascular implantable device infections Curr. Infect. Dis. Rep. 2011 13 333 342 10.1007/s11908-011-0187-7 21484218 · DOI
- [48]Brien L. Kerrigan S.W. Kaw G. Hogan M. Penadés J. Litt D. Fitzgerald D.J. Foster T.J. Cox D. Multiple mechanisms for the activation of human platelet aggregation by Staphylococcus aureus: Roles for the clumping factors ClfA and ClfB, the serine–aspartate repeat protein SdrE and protein A Mol. Microbiol. 2002 44 1033 1044 12010496
- [49]Yakut N. Soysal A. Kepenekli Kadayifci E. Dalgic N. Yılmaz Ciftdogan D. Karaaslan A. Akkoc G. Ocal Demir S. Cagan E. Celikboya E. Ventriculoperitoneal shunt infections and re-infections in children: A multicentre retrospective study Br. J. Neurosurg. 2018 32 196 200 10.1080/02688697.2018.1467373 29706112 · DOI
- [50]Bhatia P.L. Lilani S. Shirpurkar R. Chande C. Joshi S. Chowdhary A. Coagulase-negative staphylococci: Emerging pathogen in central nervous system shunt infection Indian J. Med. Microbiol. 2017 35 120 123 10.4103/ijmm.IJMM_16_157 28303832 · DOI
- [51]Kulkarni A.V. Drake J.M. Lamberti-Pasculli M. Cerebrospinal fluid shunt infection: A prospective study of risk factors J. Neurosurg. 2001 94 195 201 10.3171/jns.2001.94.2.0195 11213954 · DOI
- [52]Chang Y. Tai C. Hsieh P. Ueng S. Gentamicin in bone cement: A potentially more effective prophylactic measure of infection in joint arthroplasty Bone Jt. Res. 2013 2 220 226 10.1302/2046-3758.210.2000188 PMC3809714 24128666 · DOI
- [53]Beam E. Osmon D. Prosthetic joint infection update Infect. Dis. Clin. 2018 32 843 859 30241717
- [54]Gad G.F.M. El-Feky M.A. El-Rehewy M.S. Hassan M.A. Abolella H. Abd El-Baky R.M. Detection of icaA, icaD genes and biofilm production by Staphylococcus aureus and Staphylococcus epidermidis isolated from urinary tract catheterized patients J. Infect. Dev. Ctries. 2009 3 342 351 19759503
- [55]Gjødsbøl K. Christensen J.J. Karlsmark T. Jørgensen B. Klein B.M. Krogfelt K.A. Multiple bacterial species reside in chronic wounds: A longitudinal study Int. Wound J. 2006 3 225 231 10.1111/j.1742-481X.2006.00159.x 16984578 PMC7951738 · DOI
- [56]Stoodley P. Sauer K. Davies D.G. Costerton J.W. Biofilms as complex differentiated communities Annu. Rev. Microbiol. 2002 56 187 209 10.1146/annurev.micro.56.012302.160705 12142477 · DOI
- [57]Kannappan A. Durgadevi R. Srinivasan R. Lagoa R.J.L. Packiavathy I.A.S.V. Pandian S.K. Veera Ravi A. 2-Hydroxy-4-methoxybenzaldehyde from Hemidesmus indicus is antagonistic to Staphylococcus epidermidis biofilm formation Biofouling 2020 36 549 563 10.1080/08927014.2020.1777989 32586125 · DOI
- [58]Lister J.L. Horswill A.R. Staphylococcus aureus biofilms: Recent developments in biofilm dispersal Front. Cell. Infect. Microbiol. 2014 4 178 10.3389/fcimb.2014.00178 25566513 PMC4275032 · DOI
- [59]Srinivasan R. Santhakumari S. Poonguzhali P. Geetha M. Dyavaiah M. Xiangmin L. Bacterial biofilm inhibition: A focused review on recent therapeutic strategies for combating the biofilm mediated infections Front. Microbiol. 2021 12 1106 10.3389/fmicb.2021.676458 34054785 PMC8149761 · DOI
- [60]Kostakioti M. Hadjifrangiskou M. Hultgren S.J. Bacterial biofilms: Development, dispersal, and therapeutic strategies in the dawn of the postantibiotic era Cold Spring Harb. Perspect. Med. 2013 3 a010306 10.1101/cshperspect.a010306 23545571 PMC3683961 · DOI
- [61]Yan J. Bassler B.L. Surviving as a community: Antibiotic tolerance and persistence in bacterial biofilms Cell Host Microbe 2019 26 15 21 10.1016/j.chom.2019.06.002 31295420 PMC6629468 · DOI
- [62]Lewis K. Persister cells and the riddle of biofilm survival Biochemistry 2005 70 267 274 10.1007/s10541-005-0111-6 15807669 · DOI
- [63]Srivastava S. Bhargava A. Biofilms and human health Biotechnol. Lett. 2016 38 1 22 10.1007/s10529-015-1960-8 26386834 · DOI
- [64]Wang Z. Gong X. Xie J. Xu Z. Liu G. Zhang G. Investigation of formation of bacterial biofilm upon dead siblings Langmuir 2018 35 7405 7413 10.1021/acs.langmuir.8b01962 30084644 · DOI
- [65]Hassanzadeh S. Ganjloo S. Pourmand M.R. Mashhadi R. Ghazvini K. Epidemiology of efflux pumps genes mediating resistance among Staphylococcus aureus; A systematic review Microb. Pathog. 2020 139 103850 10.1016/j.micpath.2019.103850 31706002 · DOI
- [66]Rumbaugh K.P. Sauer K. Biofilm dispersion Nat. Rev. Microbiol. 2020 18 571 586 10.1038/s41579-020-0385-0 32533131 PMC8564779 · DOI
- [67]Blair J.M.A. Webber M.A. Baylay A.J. Ogbolu D.O. Piddock L.J.V. Molecular mechanisms of antibiotic resistance Nat. Rev. Microbiol. 2015 13 42 51 10.1038/nrmicro3380 25435309 · DOI · Paper page
- [68]Gao P. Wang Y. Villanueva I. Ho P.L. Davies J. Kao R.Y.T. Construction of a multiplex promoter reporter platform to monitor Staphylococcus aureus virulence gene expression and the identification of usnic acid as a potent suppressor of psm gene expression Front. Microbiol. 2016 7 1344 10.3389/fmicb.2016.01344 27625639 PMC5004274 · DOI
- [69]Bronesky D. Wu Z. Marzi S. Walter P. Geissmann T. Moreau K. Vandenesch F. Caldelari I. Romby P. Staphylococcus aureus RNAIII and its regulon link quorum sensing, stress responses, metabolic adaptation, and regulation of virulence gene expression Annu. Rev. Microbiol. 2016 70 299 316 10.1146/annurev-micro-102215-095708 27482744 · DOI
- [70]Tiwari S. Jamal S.B. Hassan S.S. Carvalho P.V. Almeida S. Barh D. Ghosh P. Silva A. Castro T.L. Azevedo V. Two-component signal transduction systems of pathogenic bacteria as targets for antimicrobial therapy: An overview Front. Microbiol. 2017 8 1878 10.3389/fmicb.2017.01878 29067003 PMC5641358 · DOI
- [71]Felden B. Vandenesch F. Bouloc P. Romby P. The Staphylococcus aureus RNome and its commitment to virulence PLoS Pathog. 2011 7 e1002006 10.1371/journal.ppat.1002006 21423670 PMC3053349 · DOI
- [72]Reyes D. Andrey D.O. Monod A. Kelley W.L. Zhang G. Cheung A.L. Coordinated regulation by AgrA, SarA, and SarR to control agr expression in Staphylococcus aureus J. Bacteriol. 2011 193 6020 6031 10.1128/JB.05436-11 21908676 PMC3194896 · DOI
- [73]Valle J. Toledo-Arana A. Berasain C. Ghigo J.M. Amorena B. Penadés J.R. Lasa I. SarA and not σB is essential for biofilm development by Staphylococcus aureus Mol. Microbiol. 2003 48 1075 1087 10.1046/j.1365-2958.2003.03493.x 12753197 · DOI
- [74]Tan L. Li S.R. Jiang B. Hu X.M. Li S. Therapeutic targeting of the Staphylococcus aureus accessory gene regulator (agr) system Front. Microbiol. 2018 9 55 10.3389/fmicb.2018.00055 29422887 PMC5789755 · DOI
- [75]Karthik L. Kumar G. Keswani T. Bhattacharyya A. Chandar S.S. Bhaskara Rao K. Protease inhibitors from marine actinobacteria as a potential source for antimalarial compound PLoS ONE 2014 9 e90972 10.1371/journal.pone.0090972 24618707 PMC3949715 · DOI
- [76]Boles B.R. Horswill A.R. Agr-mediated dispersal of Staphylococcus aureus biofilms PLoS Pathog. 2008 4 e1000052 10.1371/journal.ppat.1000052 18437240 PMC2329812 · DOI
- [77]Tiwari N. López-Redondo M. Miguel-Romero L. Kulhankova K. Cahill M.P. Tran P.M. Kinney K.J. Kilgore S.H. Al-Tameemi H. Herfst C.A. The SrrAB two-component system regulates Staphylococcus aureus pathogenicity through redox sensitive cysteines Proc. Natl. Acad. Sci. USA 2020 117 10989 10999 10.1073/pnas.1921307117 32354997 PMC7245129 · DOI
- [78]Kolar S.L. Nagarajan V. Oszmiana A. Rivera F.E. Miller H.K. Davenport J.E. Riordan J.T. Potempa J. Barber D.S. Koziel J. NsaRS is a cell-envelope-stress-sensing two-component system of Staphylococcus aureus Microbiology 2011 157 2206 2219 10.1099/mic.0.049692-0 21565927 PMC3167884 · DOI
- [79]Kraus D. Herbert S. Kristian S.A. Khosravi A. Nizet V. Götz F. Peschel A. The GraRS regulatory system controls Staphylococcus aureus susceptibility to antimicrobial host defenses BMC Microbiol. 2008 8 85 10.1186/1471-2180-8-85 18518949 PMC2430206 · DOI
- [80]Hall J.W. Yang J. Guo H. Ji Y. The AirSR two-component system contributes to Staphylococcus aureus survival in human blood and transcriptionally regulates sspABC operon Front. Microbiol. 2015 6 682 10.3389/fmicb.2015.00682 26191060 PMC4490255 · DOI
- [82]Wu S. Lin K. Liu Y. Zhang H. Lei L. Two-component signaling pathways modulate drug resistance of Staphylococcus aureus (Review) Biomed. Rep. 2020 13 5 10.3892/br.2020.1312 32607234 PMC7323452 · DOI
- [83]Rapun-Araiz B. Haag A.F. Solano C. Lasa I. The impact of two-component sensorial network in staphylococcal speciation Curr. Opin. Microbiol. 2020 55 40 47 10.1016/j.mib.2020.02.004 32199334 PMC7322546 · DOI
- [84]O’Gara J.P. ica and beyond: Biofilm mechanisms and regulation in Staphylococcus epidermidis and Staphylococcus aureus FEMS Microbiol. Lett. 2007 270 179 188 10.1111/j.1574-6968.2007.00688.x 17419768 · DOI
- [85]Cue D. Lei M.G. Luong T.T. Kuechenmeister L. Dunman P.M. O’Donnell S. Rowe S. O’Gara J.P. Lee C.Y. Rbf promotes biofilm formation by Staphylococcus aureus via repression of icaR, a negative regulator of icaADBC J. Bacteriol. 2009 191 6363 6373 10.1128/JB.00913-09 19684134 PMC2753044 · DOI
- [86]Vuong C. Kocianova S. Voyich J.M. Yao Y. Fischer E.R. DeLeo F.R. Otto M. A crucial role for exopolysaccharide modification in bacterial biofilm formation, immune evasion, and virulence J. Biol. Chem. 2004 279 54881 54886 10.1074/jbc.M411374200 15501828 · DOI
- [87]Corrigan R.M. Rigby D. Handley P. Foster T.J. The role of Staphylococcus aureus surface protein SasG in adherence and biofilm formation Microbiology 2007 153 2435 2446 10.1099/mic.0.2007/006676-0 17660408 · DOI
- [88]Gruszka D.T. Wojdyla J.A. Bingham R.J. Turkenburg J.P. Manfield I.W. Steward A. Leech A.P. Geoghegan J.A. Foster T.J. Clarke J. Staphylococcal biofilm-forming protein has a contiguous rod-like structure Proc. Natl. Acad. Sci. USA 2012 109 E1011 10.1073/pnas.1119456109 22493247 PMC3340054 · DOI
- [89]Yu D. Zhao L. Xue T. Sun B. Staphylococcus aureus autoinducer-2 quorum sensing decreases biofilm formation in an icaR-dependent manner BMC Microbiol. 2012 12 288 10.1186/1471-2180-12-288 23216979 PMC3539994 · DOI
- [90]Houston P. Rowe S.E. Pozzi C. Waters E.M. O’Gara J.P. Essential role for the major autolysin in the fibronectin-binding protein-mediated Staphylococcus aureus biofilm phenotype Infect. Immun. 2011 79 1153 1165 10.1128/IAI.00364-10 21189325 PMC3067512 · DOI
- [91]Nair S.P. Bischoff M. Senn M.M. Berger-Bächi B. The σB regulon influences internalization of Staphylococcus aureus by osteoblasts Infect. Immun. 2003 71 4167 4170 10.1128/IAI.71.7.4167-4170.2003 12819110 PMC161998 · DOI
- [92]Chongtrakool P. Ito T. Ma X.X. Kondo Y. Trakulsomboon S. Tiensasitorn C. Jamklang M. Chavalit T. Song J.-H. Hiramatsu K. Staphylococcal cassette chromosome mec (SCCmec) typing of methicillin-resistant Staphylococcus aureus strains isolated in 11 Asian countries: A proposal for a new nomenclature for SCC mec elements Antimicrob. Agents Chemother. 2006 50 1001 1012 10.1128/AAC.50.3.1001-1012.2006 16495263 PMC1426434 · DOI
- [93]Kuroda M. Ohta T. Uchiyama I. Baba T. Yuzawa H. Kobayashi I. Cui L. Oguchi A. Aoki K.-i. Nagai Y. Whole genome sequencing of methicillin-resistant Staphylococcus aureus Lancet 2001 357 1225 1240 10.1016/S0140-6736(00)04403-2 11418146 · DOI
- [94]Malachowa N. DeLeo F.R. Mobile genetic elements of Staphylococcus aureus Cell. Mol. Life Sci. 2010 67 3057 3071 10.1007/s00018-010-0389-4 20668911 PMC2929429 · DOI
- [95]Otto M. Staphylococcus aureus toxin gene hitchhikes on a transferable antibiotic resistance element Virulence 2010 1 49 51 10.4161/viru.1.1.10453 21178414 PMC3080199 · DOI
- [96]Zhu W. Murray P.R. Huskins W.C. Jernigan J.A. McDonald L.C. Clark N.C. Anderson K.F. McDougal L.K. Hageman J.C. Olsen-Rasmussen M. Dissemination of an Enterococcus Inc18-Like vanA plasmid associated with vancomycin-resistant Staphylococcus aureus Antimicrob. Agents Chemother. 2010 54 4314 4320 10.1128/AAC.00185-10 20660665 PMC2944587 · DOI
- [97]Shallcross L.J. Fragaszy E. Johnson A.M. Hayward A.C. The role of the Panton-Valentine leucocidin toxin in staphylococcal disease: A systematic review and meta-analysis Lancet Infect. Dis. 2013 13 43 54 10.1016/S1473-3099(12)70238-4 23103172 PMC3530297 · DOI
- [98]CheungGY W. Role of the accessory gene regulator agr in community-associated methicillin-resistant Staphylococcus aureus pathogenesis Infect. Immun. 2011 79 1927 1935 10.1128/IAI.00046-11 21402769 PMC3088142 · DOI
- [99]Genestier A.-L. Michallet M.-C. Prévost G. Bellot G. Chalabreysse L. Peyrol S. Thivolet F. Etienne J. Lina G. Vallette F.M. Staphylococcus aureus Panton-Valentine leukocidin directly targets mitochondria and induces Bax-independent apoptosis of human neutrophils J. Clin. Investig. 2005 115 3117 3127 10.1172/JCI22684 16276417 PMC1265849 · DOI · Paper page
- [100]Joo H.-S. Cheung G.Y. Otto M. Antimicrobial activity of community-associated methicillin-resistant Staphylococcus aureus is caused by phenol-soluble modulin derivatives J. Biol. Chem. 2011 286 8933 8940 10.1074/jbc.M111.221382 21278255 PMC3059065 · DOI
- [103]Fulaz S. Vitale S. Quinn L. Casey E. Nanoparticle–biofilm interactions: The role of the EPS matrix Trends Microbiol. 2019 27 915 926 10.1016/j.tim.2019.07.004 31420126 · DOI
- [104]Singh B. Vuddanda P.R. Vijayakumar M. Kumar V. Saxena P.S. Singh S. Cefuroxime axetil loaded solid lipid nanoparticles for enhanced activity against S. Aureus Biofilm Colloids Surf. B Biointerfaces 2014 121 92 98 10.1016/j.colsurfb.2014.03.046 24945607 · DOI
- [105]Lagoa R. Silva J. Rodrigues J.R. Bishayee A. Advances in phytochemical delivery systems for improved anticancer activity Biotechnol. Adv. 2020 38 107382 10.1016/j.biotechadv.2019.04.004 30978386 · DOI
- [106]Rane A.V. Kanny K. Abitha V. Thomas S. Methods for synthesis of nanoparticles and fabrication of nanocomposites Synthesis of Inorganic Nanomaterials Elsevier Amsterdam, The Netherlands 2018 121 139
- [107]Sajid M. Płotka-Wasylka J. Nanoparticles: Synthesis, characteristics, and applications in analytical and other sciences Microchem. J. 2020 154 104623 10.1016/j.microc.2020.104623 · DOI
- [108]Xiao X. Zhu Y. Liao J. Wang T. Sun W. Tong Z. High-efficient and synergetic antibacterial nanocomposite hydrogel with quaternized chitosan/Ag nanoparticles prepared by one-pot UV photochemical synthesis Biopolymers 2020 111 e23354 10.1002/bip.23354 32449971 · DOI
- [109]Alothman A.A. Albaqami M.D. Nano-sized Cu(II) and Zn(II) complexes and their use as a precursor for synthesis of CuO and ZnO nanoparticles: A study on their sonochemical synthesis, characterization, and DNA-binding/cleavage, anticancer, and antimicrobial activities Appl. Organomet. Chem. 2020 34 e5827 10.1002/aoc.5827 · DOI
- [110]Goswami S. Sahareen T. Singh M. Kumar S. Role of biogenic silver nanoparticles in disruption of cell–cell adhesion in Staphylococcus aureus and Escherichia coli biofilm J. Ind. Eng. Chem. 2015 26 73 80 10.1016/j.jiec.2014.11.017 · DOI
- [111]Lozhkomoev A. Bakina O. Pervikov A. Kazantsev S. Glazkova E. Synthesis of CuO–ZnO composite nanoparticles by electrical explosion of wires and their antibacterial activities J. Mater. Sci. Mater. Electron. 2019 30 13209 13216 10.1007/s10854-019-01684-4 · DOI
- [112]Tharchanaa S. Priyanka K. Preethi K. Shanmugavelayutham G. Facile synthesis of Cu and CuO nanoparticles from copper scrap using plasma arc discharge method and evaluation of antibacterial activity Mater. Technol. 2021 36 97 104 10.1080/10667857.2020.1734721 · DOI
- [114]Zhang S. Li R. Huang D. Ren X. Huang T.-S. Antibacterial modification of PET with quaternary ammonium salt and silver particles via electron-beam irradiation Mater. Sci. Eng. C 2018 85 123 129 10.1016/j.msec.2017.12.010 29407140 · DOI
- [115]Kankala R.K. Wang S.B. Chen A.Z. Nanoarchitecting Hierarchical Mesoporous Siliceous Frameworks: A New Way Forward Iscience 2020 23 101687 10.1016/j.isci.2020.101687 33163941 PMC7607446 · DOI
- [116]Rónavári A. Igaz N. Adamecz D.I. Szerencsés B. Molnar C. Kónya Z. Pfeiffer I. Kiricsi M. Green silver and gold nanoparticles: Biological synthesis approaches and potentials for biomedical applications Molecules 2021 26 844 10.3390/molecules26040844 33562781 PMC7915205 · DOI · Paper page
- [117]De Souza C.D. Nogueira B.R. Rostelato M.E.C. Review of the methodologies used in the synthesis gold nanoparticles by chemical reduction J. Alloys Compd. 2019 798 714 740 10.1016/j.jallcom.2019.05.153 · DOI
- [118]Kherde Y. Aguilar Z.P. Zystein L. Rodgers H.M. Hamilton W. Gold nanoparticles: Various methods of synthesis and antibacterial applications Front. Biosci. 2014 19 1320 1344 24896353
- [119]Shamaila S. Zafar N. Riaz S. Sharif R. Nazir J. Naseem S. Gold nanoparticles: An efficient antimicrobial agent against enteric bacterial human pathogen Nanomaterials 2016 6 71 10.3390/nano6040071 28335198 PMC5302575 · DOI
- [120]Dasari T.S. Zhang Y. Yu H. Antibacterial activity and cytotoxicity of gold (I) and (III) ions and gold nanoparticles Biochem. Pharmacol. 2015 4 199 10.4172/2167-0501.1000199 PMC4807878 27019770 · DOI
- [121]Boda S.K. Broda J. Schiefer F. Weber-Heynemann J. Hoss M. Simon U. Basu B. Jahnen-Dechent W. Cytotoxicity of ultrasmall gold nanoparticles on planktonic and biofilm encapsulated Gram-positive staphylococci Small 2015 11 3183 3193 10.1002/smll.201403014 25712910 · DOI
- [122]Gouyau J. Duval R.E. Boudier A. Lamouroux E. Investigation of nanoparticle metallic core antibacterial activity: Gold and silver nanoparticles against Escherichia coli and Staphylococcus aureus Int. J. Mol. Sci. 2021 22 1905 10.3390/ijms22041905 33672995 PMC7918116 · DOI
- [123]Singh P. Kim Y.J. Wang C. Mathiyalagan R. El-Agamy Farh M. Yang D.C. Biogenic silver and gold nanoparticles synthesized using red ginseng root extract, and their applications Artif. Cells Nanomed. Biotechnol. 2016 44 811 816 10.3109/21691401.2015.1008514 25706249 · DOI
- [124]Khan F. Park S.-K. Bamunuarachchi N.I. Oh D. Kim Y.-M. Caffeine-loaded gold nanoparticles: Antibiofilm and anti-persister activities against pathogenic bacteria Appl. Microbiol. Biotechnol. 2021 105 3717 3731 10.1007/s00253-021-11300-3 33900427 · DOI
- [125]Bar H. One pot green synthesis of gold nanoparticles using Piper betle leaf extract and their antibacterial activities Adv. Mater. Res. 2021 1163 106 116 10.4028/www.scientific.net/AMR.1163.106 · DOI
- [126]Hameed S. Wang Y. Zhao L. Xie L. Ying Y. Shape-dependent significant physical mutilation and antibacterial mechanisms of gold nanoparticles against foodborne bacterial pathogens (Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus) at lower concentrations Mater. Sci. Eng. C 2020 108 110338 10.1016/j.msec.2019.110338 31923994 · DOI
- [127]Penders J. Stolzoff M. Hickey D.J. Andersson M. Webster T.J. Shape-dependent antibacterial effects of non-cytotoxic gold nanoparticles Int. J. Nanomed. 2017 12 2457 2468 10.2147/IJN.S124442 28408817 PMC5383085 · DOI
- [128]Vanlalveni C. Lallianrawna S. Biswas A. Selvaraj M. Changmai B. Rokhum S.L. Green synthesis of silver nanoparticles using plant extracts and their antimicrobial activities: A review of recent literature RSC Adv. 2021 11 2804 2837 10.1039/D0RA09941D 35424248 PMC8694026 · DOI
- [129]Hamad A. Khashan K.S. Hadi A. Silver nanoparticles and silver ions as potential antibacterial agents J. Inorg. Organomet. Polym. Mater. 2020 30 4811 4828 10.1007/s10904-020-01744-x · DOI
- [130]Franci G. Falanga A. Galdiero S. Palomba L. Rai M. Morelli G. Galdiero M. Silver nanoparticles as potential antibacterial agents Molecules 2015 20 8856 8874 10.3390/molecules20058856 25993417 PMC6272636 · DOI
- [131]Hussein E.A.M. Mohammad A.A.-H. Harraz F.A. Ahsan M.F. Biologically synthesized silver nanoparticles for enhancing tetracycline activity against Staphylococcus aureus and Klebsiella pneumoniae Braz. Arch. Biol. Technol. 2019 62 10.1590/1678-4324-2019180266 · DOI
- [132]Zautner A.E. Krause M. Stropahl G. Holtfreter S. Frickmann H. Maletzki C. Kreikemeyer B. Pau H.W. Podbielski A. Intracellular persisting Staphylococcus aureus is the major pathogen in recurrent tonsillitis PLoS ONE 2010 5 e9452 10.1371/journal.pone.0009452 20209109 PMC2830486 · DOI
- [133]Kang J. Dietz M.J. Hughes K. Xing M. Li B. Silver nanoparticles present high intracellular and extracellular killing against Staphylococcus aureus J. Antimicrob. Chemother. 2019 74 1578 1585 10.1093/jac/dkz053 30778552 PMC6524480 · DOI
- [134]Parveen F. Sannakki B. Mandke M.V. Pathan H.M. Copper nanoparticles: Synthesis methods and its light harvesting performance Sol. Energy Mater. Sol. Cells 2016 144 371 382 10.1016/j.solmat.2015.08.033 · DOI
- [135]Varghese B. Kurian M. Krishna S. Athira T. Biochemical synthesis of copper nanoparticles using Zingiber officinalis and Curcuma longa: Characterization and antibacterial activity study Mater. Today Proc. 2020 25 302 306 10.1016/j.matpr.2020.01.476 · DOI
- [136]Elsayed M.M. Elgohary F.A. Zakaria A.I. Elkenany R.M. El-Khateeb A.Y. Novel eradication methods for Staphylococcus aureus biofilm in poultry farms and abattoirs using disinfectants loaded onto silver and copper nanoparticles Environ. Sci. Pollut. Res. 2020 27 30716 30728 10.1007/s11356-020-09340-9 32468379 · DOI
- [137]Chen J. Mao S. Xu Z. Ding W. Various antibacterial mechanisms of biosynthesized copper oxide nanoparticles against soilborne Ralstonia solanacearum RSC Adv. 2019 9 3788 3799 10.1039/C8RA09186B 35518060 PMC9060243 · DOI
- [138]Spirescu V.A. Chircov C. Grumezescu A.M. Vasile B.Ș. Andronescu E. Inorganic nanoparticles and composite films for antimicrobial therapies Int. J. Mol. Sci. 2021 22 4595 10.3390/ijms22094595 33925617 PMC8123905 · DOI
- [139]Kadiyala U. Turali-Emre E.S. Bahng J.H. Kotov N.A. VanEpps J.S. Unexpected insights into antibacterial activity of zinc oxide nanoparticles against methicillin resistant Staphylococcus aureus (MRSA) Nanoscale 2018 10 4927 4939 10.1039/C7NR08499D 29480295 PMC5847298 · DOI
- [140]Liu Y. Li Y. Deng L. Zou L. Feng F. Zhang H. Hydrophobic Ethylcellulose/Gelatin Nanofibers Containing Zinc Oxide Nanoparticles for Antimicrobial Packaging J. Agric. Food Chem. 2018 66 9498 9506 10.1021/acs.jafc.8b03267 30138556 · DOI
- [142]Fang C.-H. Tsai P.-I. Huang S.-W. Sun J.-S. Chang J.Z.-C. Shen H.-H. Chen S.-Y. Lin F.H. Hsu L.-T. Chen Y.-C. Magnetic hyperthermia enhance the treatment efficacy of peri-implant osteomyelitis BMC Infect. Dis. 2017 17 516 10.1186/s12879-017-2621-4 28743235 PMC5526269 · DOI
- [144]Ekielski A. Interactions Between Food Ingredients and Nanocomponents Used for Composite Packaging Encyclopedia of Food Chemistry Melton L. Shahidi F. Varelis P. Academic Press Oxford, UK 2019 669 674
- [145]Cai L. Chen J. Liu Z. Wang H. Yang H. Ding W. Magnesium oxide nanoparticles: Effective agricultural antibacterial agent against Ralstonia Solanacearum Front. Microbiol. 2018 9 790 10.3389/fmicb.2018.00790 29922237 PMC5996892 · DOI
- [146]Akhtar S. Shahzad K. Mushtaq S. Ali I. Rafe M.H. Fazal-ul-Karim S.M. Antibacterial and antiviral potential of colloidal Titanium dioxide (TiO2) nanoparticles suitable for biological applications Mater. Res. Express 2019 6 105409 10.1088/2053-1591/ab3b27 · DOI
- [147]Shkodenko L. Kassirov I. Koshel E. Metal oxide nanoparticles against bacterial biofilms: Perspectives and limitations Microorganisms 2020 8 1545 10.3390/microorganisms8101545 33036373 PMC7601517 · DOI
- [148]Gao W. Thamphiwatana S. Angsantikul P. Zhang L. Nanoparticle approaches against bacterial infections Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. 2014 6 532 547 10.1002/wnan.1282 25044325 PMC4197093 · DOI
- [149]Wang L. Hu C. Shao L. The antimicrobial activity of nanoparticles: Present situation and prospects for the future Int. J. Nanomed. 2017 12 1227 10.2147/IJN.S121956 28243086 PMC5317269 · DOI · Paper page
- [150]Zaidi S. Misba L. Khan A.U. Nano-therapeutics: A revolution in infection control in post antibiotic era Nanomed. Nanotechnol. Biol. Med. 2017 13 2281 2301 10.1016/j.nano.2017.06.015 28673854 · DOI
- [151]Niemirowicz K. Swiecicka I. Wilczewska A.Z. Misztalewska I. Kalska-Szostko B. Bienias K. Bucki R. Car H. Gold-functionalized magnetic nanoparticles restrict growth of Pseudomonas aeruginosa Int. J. Nanomed. 2014 9 2217 PMC4020905 24855358
- [152]Su Y. Zheng X. Chen Y. Li M. Liu K. Alteration of intracellular protein expressions as a key mechanism of the deterioration of bacterial denitrification caused by copper oxide nanoparticles Sci. Rep. 2015 5 15824 10.1038/srep15824 26508362 PMC4623765 · DOI
- [153]Jung W.K. Koo H.C. Kim K.W. Shin S. Kim S.H. Park Y.H. Antibacterial activity and mechanism of action of the silver ion in Staphylococcus aureus and Escherichia coli Appl. Environ. Microbiol. 2008 74 2171 2178 10.1128/AEM.02001-07 18245232 PMC2292600 · DOI
- [154]Lesniak A. Salvati A. Santos-Martinez M.J. Radomski M.W. Dawson K.A. Åberg C. Nanoparticle adhesion to the cell membrane and its effect on nanoparticle uptake efficiency J. Am. Chem. Soc. 2013 135 1438 1444 10.1021/ja309812z 23301582 · DOI
- [155]Bharti C. Nagaich U. Pal A.K. Gulati N. Mesoporous silica nanoparticles in target drug delivery system: A review Int. J. Pharm. Investig. 2015 5 124 10.4103/2230-973X.160844 PMC4522861 26258053 · DOI
- [156]Gounani Z. Asadollahi M.A. Pedersen J.N. Lyngsø J. Pedersen J.S. Arpanaei A. Meyer R.L. Mesoporous silica nanoparticles carrying multiple antibiotics provide enhanced synergistic effect and improved biocompatibility Colloids Surf. B Biointerfaces 2019 175 498 508 10.1016/j.colsurfb.2018.12.035 30572158 · DOI
- [157]Slomberg D.L. Lu Y. Broadnax A.D. Hunter R.A. Carpenter A.W. Schoenfisch M.H. Role of size and shape on biofilm eradication for nitric oxide-releasing silica nanoparticles ACS Appl. Mater. Interfaces 2013 5 9322 9329 10.1021/am402618w 24006838 · DOI
- [158]Joyce P. Ulmefors H. Maghrebi S. Subramaniam S. Wignall A. Jõemetsa S. Höök F. Prestidge C.A. Enhancing the cellular uptake and antibacterial activity of rifampicin through encapsulation in mesoporous silica nanoparticles Nanomaterials 2020 10 815 10.3390/nano10040815 32344619 PMC7221943 · DOI
- [160]Wu C. Zhu Y. Wu T. Wang L. Yuan Y. Chen J. Hu Y. Pang J. Enhanced functional properties of biopolymer film incorporated with curcurmin-loaded mesoporous silica nanoparticles for food packaging Food Chem. 2019 288 139 145 10.1016/j.foodchem.2019.03.010 30902273 · DOI
- [161]Tamanna T. Landersdorfer C.B. Ng H.J. Bulitta J.B. Wood P. Yu A. Prolonged and continuous antibacterial and anti-biofilm activities of thin films embedded with gentamicin-loaded mesoporous silica nanoparticles Appl. Nanosci. 2018 8 1471 1482 10.1007/s13204-018-0807-8 · DOI
- [162]Vijayan V. Uthaman S. Park I.-K. Cell membrane coated nanoparticles: An emerging biomimetic nanoplatform for targeted bioimaging and therapy Biomim. Med. Mater. 2018 1064 45 59 30471025
- [163]Gao W. Zhang L. Coating nanoparticles with cell membranes for targeted drug delivery J. Drug Target. 2015 23 619 626 10.3109/1061186X.2015.1052074 26453159 · DOI
- [164]Yang S. Han X. Yang Y. Qiao H. Yu Z. Liu Y. Wang J. Tang T. Bacteria-targeting nanoparticles with microenvironment-responsive antibiotic release to eliminate intracellular Staphylococcus aureus and associated infection ACS Appl. Mater. Interfaces 2018 10 14299 14311 10.1021/acsami.7b15678 29633833 · DOI
- [165]Tan Y. Ma S. Leonhard M. Moser D. Haselmann G.M. Wang J. Eder D. Schneider-Stickler B. Enhancing antibiofilm activity with functional chitosan nanoparticles targeting biofilm cells and biofilm matrix Carbohydr. Polym. 2018 200 35 42 10.1016/j.carbpol.2018.07.072 30177175 · DOI
- [166]Singh A.K. Prakash P. Singh R. Nandy N. Firdaus Z. Bansal M. Singh R.K. Srivastava A. Roy J.K. Mishra B. Curcumin quantum dots mediated degradation of bacterial biofilms Front. Microbiol. 2017 8 1517 10.3389/fmicb.2017.01517 28848526 PMC5552728 · DOI
- [167]Meikhail M. Abdelghany A. Awad W. Role of CdSe quantum dots in the structure and antibacterial activity of chitosan/poly ε-caprolactone thin films Egypt. J. Basic Appl. Sci. 2018 5 138 144 10.1016/j.ejbas.2018.05.003 · DOI
- [168]Wansapura P.T. Dassanayake R.S. Hamood A. Tran P. Moussa H. Abidi N. Preparation of chitin-CdTe quantum dots films and antibacterial effect on Staphylococcus aureus and Pseudomonas aeruginosa J. Appl. Polym. Sci. 2017 134 10.1002/app.44904 · DOI
- [169]Openda Y.I. Sen P. Managa M. Nyokong T. Acetophenone substituted phthalocyanines and their graphene quantum dots conjugates as photosensitizers for photodynamic antimicrobial chemotherapy against Staphylococcus aureus Photodiagnosis Photodyn. Ther. 2020 29 101607 10.1016/j.pdpdt.2019.101607 31775056 · DOI
- [170]Xu X. Ray R. Gu Y. Ploehn H.J. Gearheart L. Raker K. Scrivens W.A. Electrophoretic analysis and purification of fluorescent single-walled carbon nanotube fragments J. Am. Chem. Soc. 2004 126 12736 12737 10.1021/ja040082h 15469243 · DOI
- [171]Saravanan A. Maruthapandi M. Das P. Luong J.H. Gedanken A. Green synthesis of multifunctional carbon dots with antibacterial activities Nanomaterials 2021 11 369 10.3390/nano11020369 33540607 PMC7912860 · DOI
- [172]Lu F. Ma Y. Wang H. Zhang M. Wang B. Zhang Y. Huang H. Liao F. Liu Y. Kang Z. Water-solvable carbon dots derived from curcumin and citric acid with enhanced broad-spectrum antibacterial and antibiofilm activity Mater. Today Commun. 2021 26 102000 10.1016/j.mtcomm.2020.102000 · DOI
- [173]Salam F.D. Vinita M.N. Puja P. Prakash S. Yuvakkumar R. Kumar P. Anti-bacterial and anti-biofilm efficacies of bioinspired gold nanoparticles Mater. Lett. 2020 261 126998 10.1016/j.matlet.2019.126998 · DOI
- [174]Zhang W. Wu Y. Liu L. Xiao X. Cong Z. Shao N. Qiao Z. Chen K. Liu S. Zhang H. The membrane-targeting mechanism of host defense peptides inspiring the design of polypeptide-conjugated gold nanoparticles exhibiting effective antibacterial activity against methicillin-resistant Staphylococcus aureus J. Mater. Chem. B 2021 9 5092 5101 10.1039/D1TB00533B 34128037 · DOI
- [175]Hamida R.S. Ali M.A. Goda D.A. Khalil M.I. Al-Zaban M.I. Novel biogenic silver nanoparticle-induced reactive oxygen species inhibit the biofilm formation and virulence activities of methicillin-resistant Staphylococcus aureus (MRSA) strain Front. Bioeng. Biotechnol. 2020 8 433 10.3389/fbioe.2020.00433 32548095 PMC7270459 · DOI
- [176]Lara H.H. Lopez-Ribot J.L. Inhibition of mixed biofilms of Candida albicans and methicillin-resistant Staphylococcus aureus by positively charged silver nanoparticles and functionalized silicone elastomers Pathogens 2020 9 784 10.3390/pathogens9100784 32992727 PMC7600790 · DOI · Paper page
- [177]Romero-Urbina D.G. Lara H.H. Velázquez-Salazar J.J. Arellano-Jiménez M.J. Larios E. Srinivasan A. Lopez-Ribot J.L. Yacamán M.J. Ultrastructural changes in methicillin-resistant Staphylococcus aureus induced by positively charged silver nanoparticles Beilstein J. Nanotechnol. 2015 6 2396 2405 10.3762/bjnano.6.246 26734530 PMC4685924 · DOI
- [178]Jusuf S. Hui J. Dong P.-T. Cheng J.-X. Staphyloxanthin photolysis potentiates low concentration silver nanoparticles in eradication of methicillin-resistant Staphylococcus aureus J. Phys. Chem. C 2020 124 5321 5330 10.1021/acs.jpcc.9b10209 · DOI
- [179]Huang H. Shan K. Liu J. Tao X. Periyasamy S. Durairaj S. Jiang Z. Jacob J.A. Synthesis, optimization and characterization of silver nanoparticles using the catkin extract of Piper longum for bactericidal effect against food-borne pathogens via conventional and mathematical approaches Bioorg. Chem. 2020 103 104230 10.1016/j.bioorg.2020.104230 32916540 PMC7449118 · DOI
- [180]Attallah N.G.M. Elekhnawy E. Negm W.A. Hussein I.A. Mokhtar F.A. Al-Fakhrany O.M. In vivo and in vitro antimicrobial activity of biogenic silver nanoparticles against Staphylococcus aureus clinical isolates Pharmaceuticals 2022 15 194 10.3390/ph15020194 35215306 PMC8878289 · DOI
- [181]Taifa S. Muhee A. Bhat R.A. Nabi S.U.I. Roy A. Rather G.A. Khan A.A. Bashir S.M. Patwekar M. Wahab S. Evaluation of therapeutic efficacy of copper nanoparticles in Staphylococcus aureus-induced rat mastitis model J. Nanomater. 2022 2022 7124114 10.1155/2022/7124114 · DOI
- [182]Mohd Yusof H. Abdul Rahman N.A. Mohamad R. Hasanah Zaidan U. Samsudin A.A. Antibacterial potential of biosynthesized zinc oxide nanoparticles against poultry-associated foodborne pathogens: An in vitro study Animals 2021 11 2093 10.3390/ani11072093 34359225 PMC8300380 · DOI
- [183]Banerjee S. Vishakha K. Das S. Dutta M. Mukherjee D. Mondal J. Mondal S. Ganguli A. Antibacterial, anti-biofilm activity and mechanism of action of pancreatin doped zinc oxide nanoparticles against methicillin resistant Staphylococcus aureus Colloids Surf. B Biointerfaces 2020 190 110921 10.1016/j.colsurfb.2020.110921 32172163 · DOI
- [184]Malakar C. Kashyap B. Kalita M.C. Deka S. Wound healing efficacy of rhamnolipid-coated zinc oxide nanoparticle along with its in vivo antibacterial efficacy against Staphylococcus aureus Exp. Dermatol. 2022 10.1111/exd.14692 36270963 · DOI
- [185]Malakar C. Patowary K. Deka S. Kalita M.C. Synthesis, characterization, and evaluation of antibacterial efficacy of rhamnolipid-coated zinc oxide nanoparticles against Staphylococcus aureus World J. Microbiol. Biotechnol. 2021 37 193 10.1007/s11274-021-03160-w 34642826 · DOI
- [186]Saied E. Eid A.M. Hassan S.E.-D. Salem S.S. Radwan A.A. Halawa M. Saleh F.M. Saad H.A. Saied E.M. Fouda A. The catalytic activity of biosynthesized magnesium oxide nanoparticles (MgO-NPs) for inhibiting the growth of pathogenic microbes, tanning effluent treatment, and chromium ion removal Catalysts 2021 11 821 10.3390/catal11070821 · DOI
- [187]Altaf M. Zeyad M.T. Hashmi M.A. Manoharadas S. Hussain S.A. Abuhasil M.S.A. Almuzaini M.A.M. Effective inhibition and eradication of pathogenic biofilms by titanium dioxide nanoparticles synthesized using Carum copticum extract RSC Adv. 2021 11 19248 19257 10.1039/D1RA02876F 35478667 PMC9033554 · DOI
- [188]Zubair M. Husain F.M. Qais F.A. Alam P. Ahmad I. Albalawi T. Ahmad N. Alam M. Baig M.H. Dong J.-J. Bio-fabrication of titanium oxide nanoparticles from Ochradenus arabicus to obliterate biofilms of drug-resistant Staphylococcus aureus and Pseudomonas aeruginosa isolated from diabetic foot infections Appl. Nanosci. 2021 11 375 387 10.1007/s13204-020-01630-5 · DOI
- [189]Devlin H. Fulaz S. Hiebner D.W. O’Gara J.P. Casey E. Enzyme-functionalized mesoporous silica nanoparticles to target Staphylococcus aureus and disperse biofilms Int. J. Nanomed. 2021 16 1929 1942 10.2147/IJN.S293190 33727807 PMC7954034 · DOI
- [190]Aguilera-Correa J.J. Gisbert-Garzarán M. Mediero A. Fernández-Aceñero M.J. de-Pablo-Velasco D. Lozano D. Esteban J. Vallet-Regí M. Antibiotic delivery from bone-targeted mesoporous silica nanoparticles for the treatment of osteomyelitis caused by methicillin-resistant Staphylococcus aureus Acta Biomater. 2022 154 608 625 10.1016/j.actbio.2022.10.039 36341887 · DOI
- [191]Nie B.e. Huo S. Qu X. Guo J. Liu X. Hong Q. Wang Y. Yang J. Yue B. Bone infection site targeting nanoparticle-antibiotics delivery vehicle to enhance treatment efficacy of orthopedic implant related infection Bioact. Mater. 2022 16 134 148 10.1016/j.bioactmat.2022.02.003 35386313 PMC8958424 · DOI
- [192]Zulkarnain M.Z. Tong W.Y. Tan W.-N. Leong C.R. Md Yusof F.A. Wahidin S. Attifah N.R. Zubaidah S. p-Coumaric acid quantum dots inhibit beta lactam resistant foodborne microorganisms Mater. Today Proc. 2020 31 48 53 10.1016/j.matpr.2020.01.104 · DOI
- [193]Li P. Liu S. Cao W. Zhang G. Yang X. Gong X. Xing X. Low-toxicity carbon quantum dots derived from gentamicin sulfate to combat antibiotic resistance and eradicate mature biofilms Chem. Commun. 2020 56 2316 2319 10.1039/C9CC09223D 31990011 · DOI
- [194]Wang H. Lu F. Ma C. Ma Y. Zhang M. Wang B. Zhang Y. Liu Y. Huang H. Kang Z. Carbon dots with positive surface charge from tartaric acid and m-aminophenol for selective killing of Gram-positive bacteria J. Mater. Chem. B 2021 9 125 130 10.1039/D0TB02332A 33225328 · DOI
- [195]Liang J. Li W. Chen J. Huang X. Liu Y. Zhang X. Shu W. Lei B. Zhang H. Antibacterial activity and synergetic mechanism of carbon dots against Gram-positive and -negative bacteria ACS Appl. Bio. Mater. 2021 4 6937 6945 10.1021/acsabm.1c00618 35006993 · DOI
- [196]Kung J.-C. Tseng I.T. Chien C.-S. Lin S.-H. Wang C.-C. Shih C.-J. Microwave assisted synthesis of negative-charge carbon dots with potential antibacterial activity against multi-drug resistant bacteria RSC Adv. 2020 10 41202 41208 10.1039/D0RA07106D 35519222 PMC9057765 · DOI
- [197]Kumar R. Chapter 8—Lipid-based nanoparticles for drug-delivery systems Nanocarriers for Drug Delivery Mohapatra S.S. Ranjan S. Dasgupta N. Mishra R.K. Thomas S. Elsevier Amsterdam, The Netherlands 2019 249 284
- [198]Walduck A. Sangwan P. Vo Q.A. Ratcliffe J. White J. Muir B.W. Tran N. Treatment of Staphylococcus aureus skin infection in vivo using rifampicin loaded lipid nanoparticles RSC Adv. 2020 10 33608 33619 10.1039/D0RA06120D 35515067 PMC9056717 · DOI
- [199]Sercombe L. Veerati T. Moheimani F. Wu S.Y. Sood A.K. Hua S. Advances and challenges of liposome assisted drug delivery Front. Pharmacol. 2015 6 286 10.3389/fphar.2015.00286 26648870 PMC4664963 · DOI
- [200]Chang H.-I. Yeh M.-K. Clinical development of liposome-based drugs: Formulation, characterization, and therapeutic efficacy Int. J. Nanomed. 2012 7 49 PMC3260950 22275822
- [201]Mitchell S.L. Carlson E.E. Tiny things with enormous impact: Nanotechnology in the fight against infectious disease ACS Infect. Dis. 2018 4 1432 1435 10.1021/acsinfecdis.8b00138 30070819 PMC9701496 · DOI · Paper page
- [202]Pinheiro M. Magalhães J. Reis S. Antibiotic interactions using liposomes as model lipid membranes Chem. Phys. Lipids 2019 222 36 46 10.1016/j.chemphyslip.2019.05.002 31078558 · DOI
- [203]Dong D. Thomas N. Thierry B. Vreugde S. Prestidge C.A. Wormald P.-J. Distribution and inhibition of liposomes on Staphylococcus aureus and Pseudomonas aeruginosa biofilm PLoS ONE 2015 10 e0131806 10.1371/journal.pone.0131806 26125555 PMC4488362 · DOI
- [204]Akbarzadeh A. Rezaei-Sadabady R. Davaran S. Joo S.W. Zarghami N. Hanifehpour Y. Samiei M. Kouhi M. Nejati-Koshki K. Liposome: Classification, preparation, and applications Nanoscale Res. Lett. 2013 8 102 10.1186/1556-276X-8-102 23432972 PMC3599573 · DOI
- [206]Berti I.R. Dell’Arciprete M.L. Dittler M.L. Miñan A. de Mele M.F.L. Gonzalez M. Delivery of fluorophores by calcium phosphate-coated nanoliposomes and interaction with Staphylococcus aureus biofilms Colloids Surf. B Biointerfaces 2016 142 214 222 10.1016/j.colsurfb.2016.03.003 26954088 · DOI
- [207]Cui H. Li W. Li C. Vittayapadung S. Lin L. Liposome containing cinnamon oil with antibacterial activity against methicillin-resistant Staphylococcus aureus biofilm Biofouling 2016 32 215 225 10.1080/08927014.2015.1134516 26838161 · DOI
- [208]Zomorodian K. Veisi H. Mousavi S.M. Ataabadi M.S. Yazdanpanah S. Bagheri J. Mehr A.P. Hemmati S. Veisi H. Modified magnetic nanoparticles by PEG-400-immobilized Ag nanoparticles (Fe(3)O(4)@PEG-Ag) as a core/shell nanocomposite and evaluation of its antimicrobial activity Int. J. Nanomed. 2018 13 3965 3973 10.2147/IJN.S161002 30022820 PMC6042532 · DOI
- [209]Hu H. Zhong D. Li W. Lin X. He J. Sun Y. Wu Y. Shi M. Chen X. Xu F. Microalgae-based bioactive hydrogel loaded with quorum sensing inhibitor promotes infected wound healing Nano Today 2022 42 101368 10.1016/j.nantod.2021.101368 · DOI · Paper page
- [210]Ferreira M. Pinto S. Aires-da-Silva F. Bettencourt A. Aguiar S. Gaspar M. Liposomes as a nanoplatform to improve the delivery of antibiotics into Staphylococcus aureus biofilms Pharmaceutics 2021 13 321 10.3390/pharmaceutics13030321 33801281 PMC7999762 · DOI
- [211]Hsu C.-Y. Sung C.T. Aljuffali I.A. Chen C.-H. Hu K.-Y. Fang J.-Y. Intravenous anti-MRSA phosphatiosomes mediate enhanced affinity to pulmonary surfactants for effective treatment of infectious pneumonia Nanomed. Nanotechnol. Biol. Med. 2018 14 215 225 10.1016/j.nano.2017.10.006 29128664 · DOI
- [212]Silva N.C. Silva S. Sarmento B. Pintado M. Chitosan nanoparticles for daptomycin delivery in ocular treatment of bacterial endophthalmitis Drug Deliv. 2015 22 885 893 10.3109/10717544.2013.858195 24266551 PMC11132849 · DOI
- [213]Vyas S. Sihorkar V. Jain S. Mannosylated liposomes for bio-film targeting Int. J. Pharm. 2007 330 6 13 10.1016/j.ijpharm.2006.08.034 16997519 · DOI
- [214]Rani N.N.I.M. Chen X.Y. Al-Zubaidi Z.M. Azhari H. Khaitir T.M.N. Ng P.Y. Buang F. Tan G.C. Wong Y.P. Said M.M. Surface-engineered liposomes for dual-drug delivery targeting strategy against methicillin-resistant Staphylococcus aureus (MRSA) Asian J. Pharm. Sci. 2022 17 102 119 10.1016/j.ajps.2021.11.004 35261647 PMC8888183 · DOI
200 of 286 shown
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Muniroh, N. A. N., Cahyaningrum, W. R., Sarinastiti, D. D., Putranti, R. A. D., Hanifa, N., Dhanti, K. R., Wardani, D. P. K., & Mulyanto, A. (2025) · Jurnal Teknologi Laboratorium · doi:10.29238/teknolabjournal.v14i1.483
“Therefore, the cell wall of S. aureus is the main target of the active substance in the gel extract of bay leaf and Saba banana peel 18 . pg. 67 The antibacterial mechanism inhibits bacterial growth by inhibiting cell wall synthesis, metabolism synthesis, disrupting cell membrane integrity,…”
- Authors
- Arunachalam, K., Pandurangan, P., Shi, C., & Lagoa, R.
- Affiliations
- MOST-USDA Joint Research Center for Food Safety, Department of Food Science and Technology, School of Agriculture and Biology, and State Key Laboratory of Microbial Metabolism, Shanghai Jiao Tong University, Minhang, Shanghai 200240, China
- Department of Microbiology, M.R. Government Arts College, Mannargudi, Coimbatore 614001, Tamil Nadu, India
- United States Department of Agriculture (US)
- Universidade de Leiria e Oeste (PT)
- Corresponding author
- Shi, Chunlei
- Lagoa, Ricardo
- Venue
- Pharmaceutics
- Publisher
- MDPI AG
- Published
- 2023-01-17
- Volume
- 15
- Issue
- 2
- Pages
- 310
- ISSN
- 1999-4923 (ISSN-L)
- PMC
- PMC9960757
- OpenAlex
- W4317036207
- Cited by
- 48
- References
- 9
- Citations by year
- 2026: 12 · 2025: 15 · 2024: 17 · 2023: 4
- FWCI
- 2.28
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Pharmaceutics (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Science and Technology Commission of Shanghai Municipality of China (21N31900200, 32001798, 31972169, UIDP/04378/2020, UIDB/04378/2020)
- Natural Science Foundation of China (21N31900200, 32001798, 31972169, UIDP/04378/2020, UIDB/04378/2020)
- FCT-Foundation for Science and Technology (21N31900200, 32001798, 31972169, UIDP/04378/2020, UIDB/04378/2020)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Antimicrobial Resistance in Staphylococcus
- Physical Sciences › Materials Science › Materials Chemistry › Nanoparticles: synthesis and applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
- Keywords
- Staphylococcus aureus, virulence regulation, virulence factors, biofilm formation, multidrug resistance, nanotherapeutics, nanoparticles, antimicrobial resistance, phytochemicals, antimicrobial coatings, biomaterials, combination therapy, intracellular parasitism, drug-resistant infections
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