This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Falkinham JO, 3rd Surrounded by mycobacteria: nontuberculous mycobacteria in the human environment. J Appl Microbiol 2009;107:356–67. doi: 10.1111/j.1365-2672.2009.04161.xFalkinhamJO3rdSurrounded by mycobacteria: nontuberculous mycobacteria in the human environmentJ Appl Microbiol20091073566710.1111/j.1365-2672.2009.04161.x19228258Open DOISearch in Google Scholar
De Groote MA, Huitt G. Infections due to rapidly growing mycobacteria. Clin Infect Dis 2006;42:1756–63. doi: 10.1086/504381De GrooteMAHuittGInfections due to rapidly growing mycobacteriaClin Infect Dis20064217566310.1086/50438116705584Open DOISearch in Google Scholar
Steed KA, Falkinham JO, 3rd Effect of growth in biofilms on chlorine susceptibility of Mycobacterium avium and Mycobacterium intracellulare. Appl Environ Microbiol 2006;72:4007–11. doi: 10.1128/AEM.02573-05SteedKAFalkinhamJO3rdEffect of growth in biofilms on chlorine susceptibility of Mycobacterium avium and Mycobacterium intracellulareAppl Environ Microbiol20067240071110.1128/AEM.02573-05148966016751509Open DOISearch in Google Scholar
Falkinham JO, 3rdMycobacterium avium complex: Adherence as a way of life. AIMS Microbiol 2018;4:428–38. doi: 10.3934/microbiol.2018.3.428FalkinhamJO3rdMycobacterium avium complex: Adherence as a way of lifeAIMS Microbiol201844283810.3934/microbiol.2018.3.428660493731294225Open DOISearch in Google Scholar
Falkinham JO, 3rd Common features of opportunistic premise plumbing pathogens. Int J Environ Res Public Health 2015;12:4533–45. doi: 10.3390/ijerph120504533FalkinhamJO3rdCommon features of opportunistic premise plumbing pathogensInt J Environ Res Public Health20151245334510.3390/ijerph120504533445492425918909Open DOISearch in Google Scholar
Greub G, Raoult D. Microorganisms resistant to free-living amoebae. Clin Microbiol Rev 2004;17:413–33. doi: 10.1128/cmr.17.2.413-433.2004GreubGRaoultDMicroorganisms resistant to free-living amoebaeClin Microbiol Rev2004174133310.1128/cmr.17.2.413-433.200438740215084508Open DOISearch in Google Scholar
Guimaraes AJ, Gomes KX, Cortines JR, Peralta JM, Peralta RH. Acanthamoeba spp. as a universal host for pathogenic microorganisms: One bridge from environment to host virulence. Microbiol Res 2016;193:30–8. doi: 10.1016/j.micres.2016.08.001GuimaraesAJGomesKXCortinesJRPeraltaJMPeraltaRH.Acanthamoeba spp. as a universal host for pathogenic microorganisms: One bridge from environment to host virulenceMicrobiol Res201619330810.1016/j.micres.2016.08.00127825484Open DOISearch in Google Scholar
Salah IB, Ghigo E, Drancourt M. Free-living amoebae, a training field for macrophage resistance of mycobacteria. Clin Microbiol Infect 2009;15:894–905. doi: 10.1111/j.1469-0691.2009.03011.xSalahIBGhigoEDrancourtMFree-living amoebae, a training field for macrophage resistance of mycobacteriaClin Microbiol Infect20091589490510.1111/j.1469-0691.2009.03011.x19845701Open DOISearch in Google Scholar
Lamrabet O, Mba Medie F, Drancourt M. Acanthamoeba polyphaga-enhanced growth of Mycobacterium smegmatis. PLoS One 2012;7:e29833. doi: 10.1371/journal.pone.0029833LamrabetOMbaMedie FDrancourtM.Acanthamoeba polyphaga-enhanced growth of Mycobacterium smegmatisPLoS One20127e2983310.1371/journal.pone.0029833325620122253795Open DOISearch in Google Scholar
Cirillo JD, Falkow S, Tompkins LS, Bermudez LE. Interaction of Mycobacterium avium with environmental amoebae enhances virulence. Infect Immun 1997;65:3759–67. PMCID: PMC175536CirilloJDFalkowSTompkinsLSBermudezLEInteraction of Mycobacterium avium with environmental amoebae enhances virulenceInfect Immun199765375967PMCID: PMC17553610.1128/iai.65.9.3759-3767.19971755369284149Search in Google Scholar
Peruč D, Gobin I, Abram M, Broznić D, Svalina T, Štifter S, Malenica Staver M, Tićac B. Antimycobacterial potential of the juniper berry essential oil in tap water. Arh Hig Rada Toksikol 2018;69:46–54. doi: 10.2478/aiht-2018-69-3085PeručDGobinIAbram MBroznićDSvalinaTŠtifterSMalenica StaverMTićacBAntimycobacterial potential of the juniper berry essential oil in tap waterArh Hig Rada Toksikol201869465410.2478/aiht-2018-69-308529604199Open DOISearch in Google Scholar
Mastelić J, Miloš M, Kuštrak D, Radonić A. Essential Oil and Glycosidically Bound Volatile Compounds from the Needles of Common Juniper Juniperus communis L.). Croat Chem Acta 2000;73:585–93.MastelićJMilošMKuštrakDRadonićAEssential Oil and Glycosidically Bound Volatile Compounds from the Needles of Common Juniper Juniperus communis L.)Croat Chem Acta20007358593Search in Google Scholar
Sela F, Karapandzova M, Stefkov G, Cvetkovikj I, Kulevanova S. Chemical composition and antimicrobial activity of essential oils of Juniperus excelsa Bieb. (Cupressaceae) grown in R. Macedonia. Pharmacognosy Res 2015;7:74–80. doi: 10.4103/0974-8490.147212SelaFKarapandzovaMStefkovGCvetkovikjIKulevanovaSChemical composition and antimicrobial activity of essential oils of Juniperus excelsa Bieb. (Cupressaceae) grown in R. MacedoniaPharmacognosy Res20157748010.4103/0974-8490.147212428565325598638Open DOISearch in Google Scholar
Angioni A, Barra A, Russo MT, Coroneo V, Dessiä S, Cabras P. Chemical composition of the essential oils of Juniperus from ripe and unripe berries and leaves and their antimicrobial activity. J Agric Food Chem 2003;51:3073–8. doi: 10.1021/jf026203jAngioniABarraARussoMTCoroneoVDessiäSCabrasPChemical composition of the essential oils of Juniperus from ripe and unripe berries and leaves and their antimicrobial activityJ Agric Food Chem2003513073810.1021/jf026203j12720394Open DOISearch in Google Scholar
Mastelic J, Politeo O, Jerkovic I. Contribution to the analysis of the essential oil of Helichrysum italicum (Roth) G. Don. Determination of ester bonded acids and phenols. Molecules 2008;13:795–803. doi: 10.3390/molecules13040795MastelicJPoliteoOJerkovicIContribution to the analysis of the essential oil of Helichrysum italicum (Roth) G. Don. Determination of ester bonded acids and phenolsMolecules20081379580310.3390/molecules13040795624482918463581Open DOISearch in Google Scholar
Bezić N, Vuko E, Ruščić M, Dunkić V. Helichrysum italicum (Roth) G. Don - essential oil composition and activity on tobacco mosaic virus infection. J Plant Physiol Pathol 2016;4:1–3. doi: 10.4172/2329-955X.1000144BezićNVukoERuščićMDunkićV.Helichrysum italicum (Roth) G. Don - essential oil composition and activity on tobacco mosaic virus infectionJ Plant Physiol Pathol201641310.4172/2329-955X.1000144Open DOISearch in Google Scholar
Mancini E, De Martino L, Marandino A, Scognamiglio MR, De Feo V. Chemical composition and possible in vitro phytotoxic activity of Helichrsyum italicum (Roth) Don ssp. italicum. Molecules 2011;16:7725–35. doi: 10.3390/molecules16097725ManciniEDe MartinoLMarandinoAScognamiglioMRDe FeoVChemical composition and possible in vitro phytotoxic activity of Helichrsyum italicum (Roth) Don ssp. italicumMolecules20111677253510.3390/molecules16097725626476921904272Open DOISearch in Google Scholar
Malenica Staver M, Gobin I, Ratkaj I, Petrović M, Vulinović A, Dinarina-Sablić M, Broznić D. In vitro antiproliferative and antimicrobial activity of the essential oil from the flowers and leaves of Helichrysum italicum (Roth) G. Don growing in Central Dalmatia (Croatia). J Essent Oil Bear Pl 2018;21:77–91. doi: 10.1080/0972060X.2018.1433071MalenicaStaver MGobinIRatkajIPetrovićMVulinovićADinarina-SablićMBroznićD.In vitro antiproliferative and antimicrobial activity of the essential oil from the flowers and leaves of Helichrysum italicum (Roth) G. Don growing in Central Dalmatia (Croatia)J Essent Oil Bear Pl201821779110.1080/0972060X.2018.1433071Open DOISearch in Google Scholar
Peruc D, Ticac B, Broznic D, Maglica Z, Sarolic M, Gobin I. Juniperus communis essential oil limit the biofilm formation of Mycobacterium avium and Mycobacterium intracellulare on polystyrene in a temperature-dependent manner. Int J Environ Health Res 2020:1–14. doi: 10.1080/09603123.2020.1741519PerucDTicacBBroznicDMaglicaZSarolicMGobinI.Juniperus communis essential oil limit the biofilm formation of Mycobacterium avium and Mycobacterium intracellulare on polystyrene in a temperature-dependent mannerInt J Environ Health Res202011410.1080/09603123.2020.174151932196364Open DOISearch in Google Scholar
Peruč D, Tićac B, Abram M, Broznić D, Štifter S, Malenica Staver M, Gobin I. Synergistic potential of Juniperus communis and Helichrysum italicum essential oils against nontuberculous mycobacteria. J Med Microbiol 2019;68:703–10. doi: 10.1099/jmm.0.000962PeručDTićacBAbramMBroznićDŠtifterSMalenica StaverMGobinISynergistic potential of Juniperus communis and Helichrysum italicum essential oils against nontuberculous mycobacteriaJ Med Microbiol2019687031010.1099/jmm.0.00096230916640Open DOISearch in Google Scholar
Doll-Boscardin PM, Sartoratto A, Sales Maia BH, Padilha de Paula J, Nakashima T, Farago PV, Kanunfre CC. In vitro cytotoxic potential of essential oils of Eucalyptus benthamii and its related terpenes on tumor cell lines. Evid Based Complement Alternat Med 2012;2012:342652. doi: 10.1155/2012/342652Doll-BoscardinPMSartorattoASalesMaia BHPadilhade Paula JNakashimaTFaragoPVKanunfreCC.In vitro cytotoxic potential of essential oils of Eucalyptus benthamii and its related terpenes on tumor cell linesEvid Based Complement Alternat Med2012201234265210.1155/2012/342652335689122645627Open DOISearch in Google Scholar
Broznic D, Ratkaj I, Malenica Staver M, Kraljevic Pavelic S, Zurga P, Bubalo D, Gobin I. Evaluation of the antioxidant capacity, antimicrobial and antiproliferative potential of fir Abies alba Mill.) honeydew honey collected from Gorski Kotar (Croatia). Food Technol Biotechnol 2018;56:533–45. doi: 10.17113/ftb.56.04.18.5666BroznicDRatkajIMalenica StaverMKraljevic PavelicSZurgaPBubaloDGobinIEvaluation of the antioxidant capacity, antimicrobial and antiproliferative potential of fir Abies alba Mill.) honeydew honey collected from Gorski Kotar (Croatia)Food Technol Biotechnol2018565334510.17113/ftb.56.04.18.5666639971030923450Open DOISearch in Google Scholar
Gazivoda T, Plevnik M, Plavec J, Kraljevic S, Kralj M, Pavelic K, Balzarini J, De Clercq E, Mintas M, Raic-Malic S. The novel pyrimidine and purine derivatives of L-ascorbic acid: synthesis, one- and two-dimensional 1H and 13C NMR study, cytostatic and antiviral evaluation. Bioorg Med Chem 2005;13:131–9. doi: 10.1016/j.bmc.2004.09.052GazivodaTPlevnikMPlavecJKraljevicSKraljMPavelicKBalzariniJDe ClercqEMintasMRaic-MalicSThe novel pyrimidine and purine derivatives of L-ascorbic acid: synthesis, one- and two-dimensional 1H and 13C NMR study, cytostatic and antiviral evaluationBioorg Med Chem200513131910.1016/j.bmc.2004.09.05215582458Open DOISearch in Google Scholar
Sarker SD, Nahar L, Kumarasamy Y. Microtitre plate-based antibacterial assay incorporating resazurin as an indicator of cell growth, and its application in the in vitro antibacterial screening of phytochemicals. Methods 2007;42:321–4. doi: 10.1016/j.ymeth.2007.01.006SarkerSDNaharLKumarasamyYMicrotitre plate-based antibacterial assay incorporating resazurin as an indicator of cell growth, and its application in the in vitro antibacterial screening of phytochemicalsMethods200742321410.1016/j.ymeth.2007.01.006189592217560319Open DOISearch in Google Scholar
Andrejak C, Almeida DV, Tyagi S, Converse PJ, Ammerman NC, Grosset JH. Characterization of mouse models of Mycobacterium avium complex infection and evaluation of drug combinations. Antimicrob Agents Chemother 2015;59:2129–35. doi: 10.1128/AAC.04841-14AndrejakCAlmeidaDVTyagiSConversePJAmmermanNCGrossetJHCharacterization of mouse models of Mycobacterium avium complex infection and evaluation of drug combinationsAntimicrob Agents Chemother20155921293510.1128/AAC.04841-14435682725624335Open DOISearch in Google Scholar
Vasiljević B, Knežević-Vučković J, Mitić-Ćulafić D, Orčić D, Francišković M, Srdic-Rajic T, Jovanović M, Nikolić B. Chemical characterization, antioxidant, genotoxic and in vitro cytotoxic activity assessment of Juniperus communis var. saxatilis. Food Chem Toxicol 2018;112:118–25. doi: doi.org/10.1016/j.fct.2017.12.044VasiljevićBKnežević-VučkovićJMitić-ĆulafićDOrčićDFranciškovićMSrdic-RajicTJovanovićMNikolićBChemical characterization, antioxidant, genotoxic and in vitro cytotoxic activity assessment of Juniperus communis var. saxatilisFood Chem Toxicol201811211825doi.org/10.1016/j.fct.2017.12044Open DOISearch in Google Scholar
Bassole IH, Juliani HR. Essential oils in combination and their antimicrobial properties. Molecules 2012;17:3989–4006. doi: 10.3390/molecules17043989BassoleIHJulianiHREssential oils in combination and their antimicrobial propertiesMolecules2012173989400610.3390/molecules17043989626892522469594Open DOISearch in Google Scholar
White RL, Burgess DS, Manduru M, Bosso JA. Comparison of three different in vitro methods of detecting synergy: time-kill, checkerboard, and E test. Antimicrob Agents Chemother 1996;40:1914–8. doi: 10.1128/AAC.40.8.1914WhiteRLBurgessDSManduruMBossoJAComparison of three different in vitro methods of detecting synergy: time-kill, checkerboard, and E testAntimicrob Agents Chemother1996401914810.1128/AAC.40.8.19141634398843303Open DOISearch in Google Scholar
Balouiri M, Sadiki M, Ibnsouda SK. Methods for in vitro evaluating antimicrobial activity: A review. J Pharm Anal 2016;6:71–9. doi: 10.1016/j.jpha.2015.11.005BalouiriMSadikiMIbnsoudaSKMethods for in vitro evaluating antimicrobial activity: A reviewJ Pharm Anal2016671910.1016/j.jpha.2015.11.005576244829403965Open DOISearch in Google Scholar
Teanpaisan R, Kawsud P, Pahumunto N, Puripattanavong J. Screening for antibacterial and antibiofilm activity in Thai medicinal plant extracts against oral microorganisms. J Tradit Complement Med 2017;7:172–7. doi: 10.1016/j.jtcme.2016.06.007TeanpaisanRKawsudPPahumuntoNPuripattanavongJScreening for antibacterial and antibiofilm activity in Thai medicinal plant extracts against oral microorganismsJ Tradit Complement Med20177172710.1016/j.jtcme.2016.06.007538808228417087Open DOISearch in Google Scholar
Pfyffer GE, Brown-Elliott BA, Wallace RJJ. Mycobacterium: general characteristics, isolation, and staining procedures. In: Murray PR, editor. Manual of Clinical Microbiology. 8th editon. Washington, DC: American Society of Microbiology; 2003. p. 532–84.PfyfferGEBrown-ElliottBAWallaceRJJMycobacterium: general characteristics, isolation, and staining proceduresInMurrayPReditorManual of Clinical Microbiology8th editonWashington, DCAmerican Society of Microbiology2003p53284Search in Google Scholar
Ovrutsky AR, Chan ED, Kartalija M, Bai X, Jackson M, Gibbs S, Falkinham JO, 3rd Iseman MD, Reynolds PR, McDonnell G, Thomas V. Cooccurrence of free-living amoebae and nontuberculous Mycobacteria in hospital water networks, and preferential growth of Mycobacterium avium in Acanthamoeba lenticulata. Appl Environ Microbiol 2013;79:3185–92. doi: 10.1128/AEM.03823-12OvrutskyARChanEDKartalijaMBaiXJacksonMGibbsSFalkinhamJO3rdIsemanMDReynoldsPRMcDonnellGThomasVCooccurrence of free-living amoebae and nontuberculous Mycobacteria in hospital water networks, and preferential growth of Mycobacterium avium in Acanthamoeba lenticulataAppl Environ Microbiol20137931859210.1128/AEM.03823-12368524923475613Open DOISearch in Google Scholar
Miltner EC, Bermudez LE. Mycobacterium avium grown in Acanthamoeba castellanii is protected from the effects of antimicrobials. Antimicrob Agents Chemother 2000;44:1990–4. doi: 10.1128/aac.44.7.1990-1994.2000MiltnerECBermudezLE.Mycobacterium avium grown in Acanthamoeba castellanii is protected from the effects of antimicrobialsAntimicrob Agents Chemother2000441990410.1128/aac.44.7.1990-1994.2000Open DOISearch in Google Scholar
Ohno A, Kato N, Sakamoto R, Kimura S, Yamaguchi K. Temperature-dependent parasitic relationship between Legionella pneumophila and a free-living amoeba Acanthamoeba castellanii Appl Environ Microbiol 2008;74:4585–8. doi: 10.1128/AEM.00083-08OhnoAKatoNSakamotoRKimuraSYamaguchiKTemperature-dependent parasitic relationship between Legionella pneumophila and a free-living amoeba Acanthamoeba castellaniiAppl Environ Microbiol2008744585810.1128/AEM.00083-08249314718502936Open DOISearch in Google Scholar
Khan NA. Acanthamoeba biology and increasing importance in human health. FEMS Microbiol Rev 2006;30:564–95. doi: 10.1111/j.1574-6976.2006.00023.xKhanNA.Acanthamoeba biology and increasing importance in human healthFEMS Microbiol Rev2006305649510.1111/j.1574-6976.2006.00023.x16774587Open DOISearch in Google Scholar
Berry D, Horn M, Xi C, Raskin L. Mycobacterium avium infections of Acanthamoeba strains: host strain variability, grazing-acquired infections, and altered dynamics of inactivation with monochloramine. Appl Environ Microbiol 2010;76:6685–8. doi: 10.1128/AEM.00644-10BerryDHornMXiCRaskinL.Mycobacterium avium infections of Acanthamoeba strains: host strain variability, grazing-acquired infections, and altered dynamics of inactivation with monochloramineAppl Environ Microbiol2010766685810.1128/AEM.00644-10295045320709834Open DOISearch in Google Scholar
Mackowiak PA, Marling-Cason M, Cohen RL. Effects of temperature on antimicrobial susceptibility of bacteria. J Infect Dis 1982;145:550–3. doi: 10.1093/infdis/145.4.550MackowiakPAMarling-CasonMCohenRLEffects of temperature on antimicrobial susceptibility of bacteriaJ Infect Dis1982145550310.1093/infdis/145.4.5507069235Open DOISearch in Google Scholar