This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Arciola CR, Campoccia D, Ravaioli S, Montanaro L. Polysaccharide intercellular adhesin in biofilm: structural and regulatory aspects. Front Cell Infect Microbiol. 2015 Feb;5:7. https://www.doi.org/10.3389/fcimb.2015.00007ArciolaCRCampocciaDRavaioliSMontanaroL.Polysaccharide intercellular adhesin in biofilm: structural and regulatory aspects..2015Feb;5:7. https://www.doi.org/10.3389/fcimb.2015.00007Search in Google Scholar
Chavan T, Muth A. The diverse bioactivity of α-mangostin and its therapeutic implications. Future Med Chem. 2021 Oct;13(19):1679–1694. https://www.doi.org/10.4155/fmc-2021-0146ChavanTMuthA.The diverse bioactivity of α-mangostin and its therapeutic implications..2021Oct;13(19):1679–1694. https://www.doi.org/10.4155/fmc-2021-0146Search in Google Scholar
Chen G, Li Y, Wang W, Deng L. Bioactivity and pharmacological properties of α-mangostin from the mangosteen fruit: a review. Expert Opin Ther Pat. 2018 May;28(5):415–427. https://www.doi.org/10.1080/13543776.2018.1455829ChenGLiYWangWDengL.Bioactivity and pharmacological properties of α-mangostin from the mangosteen fruit: a review..2018May;28(5):415–427. https://www.doi.org/10.1080/13543776.2018.1455829Search in Google Scholar
Cho J, Costa SK, Wierzbicki RM, Rigby WFC, Cheung AL. The extracellular loop of the membrane permease VraG interacts with GraS to sense cationic antimicrobial peptides in Staphylococcus aureus. PLoS Pathog. 2021 Mar;17(3):e1009338. https://www.doi.org/10.1371/journal.ppat.1009338ChoJCostaSKWierzbickiRMRigbyWFCCheungAL.The extracellular loop of the membrane permease VraG interacts with GraS to sense cationic antimicrobial peptides in Staphylococcus aureus..2021Mar;17(3):e1009338. https://www.doi.org/10.1371/journal.ppat.1009338Search in Google Scholar
Ciulla M, Di Stefano A, Marinelli L, Cacciatore I, Di Biase G. RNAIII inhibiting peptide (RIP) and derivatives as potential tools for the treatment of S. aureus biofilm infections. Curr Top Med Chem. 2018;18(24):2068–2079. https://www.doi.org/10.2174/1568026618666181022120711CiullaMDi StefanoAMarinelliLCacciatoreIDi BiaseG.RNAIII inhibiting peptide (RIP) and derivatives as potential tools for the treatment of S. aureus biofilm infections..2018;18(24):2068–2079. https://www.doi.org/10.2174/1568026618666181022120711Search in Google Scholar
CLSI. Performance standards for antimicrobial susceptibility testing. 30th ed. CLSI supplement M100. Wayne (USA): Clinical and Laboratory Standards Institute; 2020.CLSI.Performance standards for antimicrobial susceptibility testing. 30th ed..Wayne (USA):Clinical and Laboratory Standards Institute;2020.Search in Google Scholar
Cyphert EL, von Recum HA. Emerging technologies for long-term antimicrobial device coatings: advantages and limitations. Exp Biol Med (Maywood). 2017 Apr;242(8):788–798. https://www.doi.org/10.1177/1535370216688572CyphertELvon RecumHA.Emerging technologies for long-term antimicrobial device coatings: advantages and limitations..2017Apr;242(8):788–798. https://www.doi.org/10.1177/1535370216688572Search in Google Scholar
Donlan RM. Biofilms and device-associated infections. Emerg Infect Dis. 2001 Mar–Apr;7(2):277–281. https://www.doi.org/10.3201/eid0702.010226DonlanRM.Biofilms and device-associated infections..2001Mar–Apr;7(2):277–281. https://www.doi.org/10.3201/eid0702.010226Search in Google Scholar
Falord M, Karimova G, Hiron A, Msadek T. GraXSR proteins interact with the VraFG ABC transporter to form a five-component system required for cationic antimicrobial peptide sensing and resistance in Staphylococcus aureus. Antimicrob Agents Chemother. 2012 Feb;56(2):1047–1058. https://www.doi.org/10.1128/AAC.05054-11FalordMKarimovaGHironAMsadekT.GraXSR proteins interact with the VraFG ABC transporter to form a five-component system required for cationic antimicrobial peptide sensing and resistance in Staphylococcus aureus..2012Feb;56(2):1047–1058. https://www.doi.org/10.1128/AAC.05054-11Search in Google Scholar
Fan Q, Yan C, Shi C, Xu Y, Ma Y, Zhang C, Peng X, Xia X. Inhibitory effect of coenzyme Q0 on the growth of Staphylococcus aureus. Foodborne Pathog Dis. 2019 May;16(5):317–324. https://www.doi.org/10.1089/fpd.2018.2559FanQYanCShiCXuYMaYZhangCPengXXiaX.Inhibitory effect of coenzyme Q0 on the growth of Staphylococcus aureus..2019May;16(5):317–324. https://www.doi.org/10.1089/fpd.2018.2559Search in Google Scholar
Felix L, Mishra B, Khader R, Ganesan N, Mylonakis E.In vitro and in vivo bactericidal and antibiofilm efficacy of alpha mangostin against Staphylococcus aureus persister cells. Front Cell Infect Microbiol. 2022 Jul;12:898794. https://www.doi.org/10.3389/fcimb.2022.898794FelixLMishraBKhaderRGanesanNMylonakisE.In vitro and in vivo bactericidal and antibiofilm efficacy of alpha mangostin against Staphylococcus aureus persister cells..2022Jul;12:898794. https://www.doi.org/10.3389/fcimb.2022.898794Search in Google Scholar
Ghoreishi FS, Roghanian R, Emtiazi G. Novel chronic wound healing by anti-biofilm peptides and protease. Adv Pharm Bull. 2022 May; 12(3):424–436. https://www.doi.org/10.34172/apb.2022.047GhoreishiFSRoghanianREmtiaziG.Novel chronic wound healing by anti-biofilm peptides and protease..2022May;12(3):424–436. https://www.doi.org/10.34172/apb.2022.047Search in Google Scholar
Gibbons S. Phytochemicals for bacterial resistance – strengths, weaknesses and opportunities. Planta Med. 2008 May;74(6):594–602. https://www.doi.org/10.1055/s-2008-1074518GibbonsS.Phytochemicals for bacterial resistance – strengths, weaknesses and opportunities..2008May;74(6):594–602. https://www.doi.org/10.1055/s-2008-1074518Search in Google Scholar
Gründling A, Schneewind O. Genes required for glycolipid synthesis and lipoteichoic acid anchoring in Staphylococcus aureus. J Bacteriol. 2007 Mar;189(6):2521–2530. https://www.doi.org/10.1128/JB.01683-06GründlingASchneewindO.Genes required for glycolipid synthesis and lipoteichoic acid anchoring in Staphylococcus aureus..2007Mar;189(6):2521–2530. https://www.doi.org/10.1128/JB.01683-06Search in Google Scholar
Hall CW, Mah TF. Molecular mechanisms of biofilm-based antibiotic resistance and tolerance in pathogenic bacteria. FEMS Microbiol Rev. 2017 May;41(3):276–301. https://www.doi.org/10.1093/femsre/fux010HallCWMahTF.Molecular mechanisms of biofilm-based antibiotic resistance and tolerance in pathogenic bacteria..2017May;41(3):276–301. https://www.doi.org/10.1093/femsre/fux010Search in Google Scholar
Hesser AR, Matano LM, Vickery CR, Wood BM, Santiago AG, Morris HG, Do T, Losick R, Walker S. The length of lipoteichoic acid polymers controls Staphylococcus aureus cell size and envelope integrity. J Bacteriol. 2020 Jun;202(16):e00149–20. https://www.doi.org/10.1128/JB.00149-20HesserARMatanoLMVickeryCRWoodBMSantiagoAGMorrisHGDoTLosickRWalkerS.The length of lipoteichoic acid polymers controls Staphylococcus aureus cell size and envelope integrity..2020Jun;202(16):e00149–20. https://www.doi.org/10.1128/JB.00149-20Search in Google Scholar
Iinuma M, Tosa H, Tanaka T, Asai F, Kobayashi Y, Shimano R, Miyauchi K. Antibacterial activity of xanthones from guttiferaeous plants against methicillin-resistant Staphylococcus aureus. J Pharm Pharmacol. 1996 Aug;48(8):861–865. https://www.doi.org/10.1111/j.2042-7158.1996.tb03988.xIinumaMTosaHTanakaTAsaiFKobayashiYShimanoRMiyauchiK.Antibacterial activity of xanthones from guttiferaeous plants against methicillin-resistant Staphylococcus aureus..1996Aug;48(8):861–865. https://www.doi.org/10.1111/j.2042-7158.1996.tb03988.xSearch in Google Scholar
Kali A. Antibiotics and bioactive natural products in treatment of methicillin resistant Staphylococcus aureus: A brief review. Pharmacogn Rev. 2015 Jan–Jun;9(17):29–34. https://www.doi.org/10.4103/0973-7847.156329KaliA.Antibiotics and bioactive natural products in treatment of methicillin resistant Staphylococcus aureus: A brief review..2015Jan–Jun;9(17):29–34. https://www.doi.org/10.4103/0973-7847.156329Search in Google Scholar
Kalil AC, Metersky ML, Klompas M, Muscedere J, Sweeney DA, Palmer LB, Napolitano LM, O’Grady NP, Bartlett JG, Carratalà J, et al. Management of adults with hospital-acquired and ventilator-associated pneumonia: 2016 clinical practice guidelines by the Infectious Diseases Society of America and the American Thoracic Society. Clin Infect Dis. 2016 Sep;63(5):e61–e111. https://www.doi.org/10.1093/cid/ciw353KalilACMeterskyMLKlompasMMuscedereJSweeneyDAPalmerLBNapolitanoLMO’GradyNPBartlettJGCarratalàJ.Management of adults with hospital-acquired and ventilator-associated pneumonia: 2016 clinical practice guidelines by the Infectious Diseases Society of America and the American Thoracic Society..2016Sep;63(5):e61–e111. https://www.doi.org/10.1093/cid/ciw353Search in Google Scholar
Koh JJ, Qiu S, Zou H, Lakshminarayanan R, Li J, Zhou X, Tang C, Saraswathi P, Verma C, Tan DT, et al. Rapid bactericidal action of alpha-mangostin against MRSA as an outcome of membrane targeting. Biochim Biophys Acta. 2013 Feb;1828(2):834–844. https://www.doi.org/10.1016/j.bbamem.2012.09.004KohJJQiuSZouHLakshminarayananRLiJZhouXTangCSaraswathiPVermaCTanDT.Rapid bactericidal action of alpha-mangostin against MRSA as an outcome of membrane targeting..2013Feb;1828(2):834–844. https://www.doi.org/10.1016/j.bbamem.2012.09.004Search in Google Scholar
Lin S, Zhu C, Li H, Chen Y, Liu S. Potent in vitro and in vivo antimicrobial activity of semisynthetic amphiphilic γ-mangostin derivative LS02 against Gram-positive bacteria with destructive effect on bacterial membrane. Biochim Biophys Acta Biomembr. 2020 Sep;1862(9):183353. https://www.doi.org/10.1016/j.bbamem.2020.183353LinSZhuCLiHChenYLiuS.Potent in vitro and in vivo antimicrobial activity of semisynthetic amphiphilic γ-mangostin derivative LS02 against Gram-positive bacteria with destructive effect on bacterial membrane..2020Sep;1862(9):183353. https://www.doi.org/10.1016/j.bbamem.2020.183353Search in Google Scholar
Ma J, Chen T, Wu S, Yang C, Bai M, Shu K, Li K, Zhang G, Jin Z, He F, Hermjakob H, Zhu Y. iProX: An integrated proteome resource. Nucleic Acids Res. 2019 Jan;47(D1):D1211–D1217. https://www.doi.org/10.1093/nar/gky869MaJChenTWuSYangCBaiMShuKLiKZhangGJinZHeFHermjakobHZhuY.iProX: An integrated proteome resource..2019Jan;47(D1):D1211–D1217. https://www.doi.org/10.1093/nar/gky869Search in Google Scholar
Mah TF, O’Toole GA. Mechanisms of biofilm resistance to antimicrobial agents. Trends Microbiol. 2001 Jan;9(1):34–39. https://www.doi.org/10.1016/s0966-842x(00)01913-2MahTFO’TooleGA.Mechanisms of biofilm resistance to antimicrobial agents..2001Jan;9(1):34–39. https://www.doi.org/10.1016/s0966-842x(00)01913-2Search in Google Scholar
Manna AC, Cheung AL.sarU, a sarA homolog, is repressed by SarT and regulates virulence genes in Staphylococcus aureus. Infect Immun. 2003 Jan;71(1):343–53. https://www.doi.org/10.1128/IAI.71.1.343-353.2003MannaACCheungAL.sarU, a sarA homolog, is repressed by SarT and regulates virulence genes in Staphylococcus aureus..2003Jan;71(1):343–53. https://www.doi.org/10.1128/IAI.71.1.343-353.2003Search in Google Scholar
Meah MS, Lertcanawanichakul M, Pedpradab P, Lin W, Zhu K, Li G, Panichayupakaranant P. Synergistic effect on anti-methicillin-resistant Staphylococcus aureus among combinations of α-mangostin-rich extract, lawsone methyl ether and ampicillin. Lett Appl Microbiol. 2020 Nov;71(5):510–519. https://www.doi.org/10.1111/lam.13369MeahMSLertcanawanichakulMPedpradabPLinWZhuKLiGPanichayupakaranantP.Synergistic effect on anti-methicillin-resistant Staphylococcus aureus among combinations of α-mangostin-rich extract, lawsone methyl ether and ampicillin..2020Nov;71(5):510–519. https://www.doi.org/10.1111/lam.13369Search in Google Scholar
Nguyen PTM, Nguyen MTH, Bolhuis A. Inhibition of biofilm formation by alpha-mangostin loaded nanoparticles against Staphylococcus aureus. Saudi J Biol Sci. 2021 Mar;28(3):1615–1621. https://www.doi.org/10.1016/j.sjbs.2020.11.061NguyenPTMNguyenMTHBolhuisA.Inhibition of biofilm formation by alpha-mangostin loaded nanoparticles against Staphylococcus aureus..2021Mar;28(3):1615–1621. https://www.doi.org/10.1016/j.sjbs.2020.11.061Search in Google Scholar
Otto M. Staphylococcal Biofilms. Microbiol Spectr. 2018 Aug;6(4): 6.4.27. https://www.doi.org/10.1128/microbiolspec.GPP3-0023-2018OttoM.Staphylococcal Biofilms..2018Aug;6(4):6.4.27. https://www.doi.org/10.1128/microbiolspec.GPP3-0023-2018Search in Google Scholar
Phuong NTM, Van Quang N, Mai TT, Anh NV, Kuhakarn C, Reutrakul V, Bolhuis A. Antibiofilm activity of α-mangostin extracted from Garcinia mangostana L. against Staphylococcus aureus. Asian Pac J Trop Med. 2017 Dec;10(12):1154–1160. https://www.doi.org/10.1016/j.apjtm.2017.10.022PhuongNTMVan QuangNMaiTTAnhNVKuhakarnCReutrakulVBolhuisA.Antibiofilm activity of α-mangostin extracted from Garcinia mangostana L. against Staphylococcus aureus..2017Dec;10(12):1154–1160. https://www.doi.org/10.1016/j.apjtm.2017.10.022Search in Google Scholar
Roy S, Santra S, Das A, Dixith S, Sinha M, Ghatak S, Ghosh N, Banerjee P, Khanna S, Mathew-Steiner S, et al. Staphylococcus aureus biofilm infection compromises wound healing by causing deficiencies in granulation tissue collagen. Ann Surg. 2020 Jun; 271(6): 1174–1185. https://www.doi.org/10.1097/SLA.0000000000003053RoySSantraSDasADixithSSinhaMGhatakSGhoshNBanerjeePKhannaSMathew-SteinerS.Staphylococcus aureus biofilm infection compromises wound healing by causing deficiencies in granulation tissue collagen..2020Jun;271(6):1174–1185. https://www.doi.org/10.1097/SLA.0000000000003053Search in Google Scholar
Schilcher K, Horswill AR. Staphylococcal biofilm development: Structure, regulation, and treatment strategies. Microbiol Mol Biol Rev. 2020 Aug;84(3):e00026-19. https://www.doi.org/10.1128/MMBR.00026-19SchilcherKHorswillAR.Staphylococcal biofilm development: Structure, regulation, and treatment strategies..2020Aug;84(3):e00026-19. https://www.doi.org/10.1128/MMBR.00026-19Search in Google Scholar
Smit AFA, Hubley R, Green P. RepeatMasker Open-4.0. 2013-2015 [Internet]. Seattle (USA): Institute for Systems Biology; 2013. Available at: http://www.repeatmasker.orgSmitAFAHubleyRGreenP..Seattle (USA):Institute for Systems Biology;2013. Available at: http://www.repeatmasker.orgSearch in Google Scholar
Song M, Liu Y, Huang X, Ding S, Wang Y, Shen J, Zhu K. A broad-spectrum antibiotic adjuvant reverses multidrug-resistant Gram-negative pathogens. Nat Microbiol. 2020 Aug;5(8):1040–1050. https://www.doi.org/10.1038/s41564-020-0723-zSongMLiuYHuangXDingSWangYShenJZhuK.A broad-spectrum antibiotic adjuvant reverses multidrug-resistant Gram-negative pathogens..2020Aug;5(8):1040–1050. https://www.doi.org/10.1038/s41564-020-0723-zSearch in Google Scholar
Stewart PS, Franklin MJ. Physiological heterogeneity in biofilms. Nat Rev Microbiol. 2008 Mar;6(3):199–210. https://www.doi.org/10.1038/nrmicro1838StewartPSFranklinMJ.Physiological heterogeneity in biofilms..2008Mar;6(3):199–210. https://www.doi.org/10.1038/nrmicro1838Search in Google Scholar
Tande AJ, Patel R. Prosthetic joint infection. Clin Microbiol Rev. 2014 Apr;27(2):302–345. https://www.doi.org/10.1128/CMR.00111-13TandeAJPatelR.Prosthetic joint infection..2014Apr;27(2):302–345. https://www.doi.org/10.1128/CMR.00111-13Search in Google Scholar
Tong SY, Davis JS, Eichenberger E, Holland TL, Fowler VG Jr.Staphylococcus aureus infections: epidemiology, pathophysiology, clinical manifestations, and management. Clin Microbiol Rev. 2015 Jul;28(3):603–661. https://www.doi.org/10.1128/CMR.00134-14TongSYDavisJSEichenbergerEHollandTLFowlerVGJr.Staphylococcus aureus infections: epidemiology, pathophysiology, clinical manifestations, and management..2015Jul;28(3):603–661. https://www.doi.org/10.1128/CMR.00134-14Search in Google Scholar
Wang H, Shi Y, Chen J, Wang Y, Wang Z, Yu Z, Zheng J, Shang Y. The antiviral drug efavirenz reduces biofilm formation and hemolysis by Staphylococcus aureus. J Med Microbiol. 2021 Oct;70(10). https://www.doi.org/10.1099/jmm.0.001433WangHShiYChenJWangYWangZYuZZhengJShangY.The antiviral drug efavirenz reduces biofilm formation and hemolysis by Staphylococcus aureus..2021Oct;70(10). https://www.doi.org/10.1099/jmm.0.001433Search in Google Scholar
Wen Z, Zhao Y, Gong Z, Tang Y, Xiong Y, Chen J, Chen C, Zhang Y, Liu S, Zheng J, et al. The mechanism of action of ginkgolic acid (15:1) against Gram-positive bacteria involves cross talk with iron homeostasis. Microbiol Spectr. 2022 Feb;10(1):e0099121. https://www.doi.org/10.1128/spectrum.00991-21WenZZhaoYGongZTangYXiongYChenJChenCZhangYLiuSZhengJ.The mechanism of action of ginkgolic acid (15:1) against Gram-positive bacteria involves cross talk with iron homeostasis..2022Feb;10(1):e0099121. https://www.doi.org/10.1128/spectrum.00991-21Search in Google Scholar
Yang SJ, Bayer AS, Mishra NN, Meehl M, Ledala N, Yeaman MR, Xiong YQ, Cheung AL. The Staphylococcus aureus two-component regulatory system, GraRS, senses and confers resistance to selected cationic antimicrobial peptides. Infect Immun. 2012 Jan;80(1):74–81. https://www.doi.org/10.1128/IAI.05669-11YangSJBayerASMishraNNMeehlMLedalaNYeamanMRXiongYQCheungAL.The Staphylococcus aureus two-component regulatory system, GraRS, senses and confers resistance to selected cationic antimicrobial peptides..2012Jan;80(1):74–81. https://www.doi.org/10.1128/IAI.05669-11Search in Google Scholar
Zheng J, Shang Y, Wu Y, Wu J, Chen J, Wang Z, Sun X, Xu G, Deng Q, Qu D, et al. Diclazuril inhibits biofilm formation and hemolysis of Staphylococcus aureus. ACS Infect Dis. 2021 Jun;7(6):1690–1701. https://www.doi.org/10.1021/acsinfecdis.1c00030ZhengJShangYWuYWuJChenJWangZSunXXuGDengQQuD.Diclazuril inhibits biofilm formation and hemolysis of Staphylococcus aureus..2021Jun;7(6):1690–1701. https://www.doi.org/10.1021/acsinfecdis.1c00030Search in Google Scholar
Zheng JX, Sun X, Lin ZW, Qi GB, Tu HP, Wu Y, Jiang SB, Chen Z, Deng QW, Qu D, et al.In vitro activities of daptomycin combined with fosfomycin or rifampin on planktonic and adherent linezolid-resistant isolates of Enterococcus faecalis. J Med Microbiol. 2019 Mar;68(3):493–502. https://www.doi.org/10.1099/jmm.0.000945ZhengJXSunXLinZWQiGBTuHPWuYJiangSBChenZDengQWQuD.In vitro activities of daptomycin combined with fosfomycin or rifampin on planktonic and adherent linezolid-resistant isolates of Enterococcus faecalis..2019Mar;68(3):493–502. https://www.doi.org/10.1099/jmm.0.000945Search in Google Scholar
Zheng JX, Tu HP, Sun X, Xu GJ, Chen JW, Deng QW, Yu ZJ, Qu D.In vitro activities of telithromycin against Staphylococcus aureus biofilms compared with azithromycin, clindamycin, vancomycin and daptomycin. J Med Microbiol. 2020 Jan;69(1):120–131. https://www.doi.org/10.1099/jmm.0.001122ZhengJXTuHPSunXXuGJChenJWDengQWYuZJQuD.In vitro activities of telithromycin against Staphylococcus aureus biofilms compared with azithromycin, clindamycin, vancomycin and daptomycin..2020Jan;69(1):120–131. https://www.doi.org/10.1099/jmm.0.001122Search in Google Scholar