Kurkcuoglu, M. & Baser, Okay. H. C. Research on Turkish rose concrete, absolute, and hydrosol. Chem. Nat. Compd. 39, 457–464 (2003).
D’Amato, S., Serio, A., Lopez, C. C. & Paparella, A. Hydrosols: Organic exercise and potential as antimicrobials for meals purposes. Meals Management 86, 126–137 (2018).
Zekri, N., Handaq, N., El Caidi, A., Zair, T. & El Belghiti, M. A. Insecticidal impact of Mentha pulegium L. and Mentha suaveolens Ehrh. hydrosols towards a pest of citrus, Toxoptera aurantii (Aphididae). Res. Chem. Intermed. 42, 1639–1649 (2016).
Politi, M. et al. Reconsidering hydrosols as major merchandise of fragrant vegetation manufactory: The Lavandin (Lavandula x intermedia) case examine in Tuscany. Molecules 25, 2225 (2020).
Andres, M. F. et al. Nematicidal potential of hydrolates from the semi industrial vapor-pressure extraction of Spanish fragrant vegetation. Environ. Sci. Pollut. Res. 25, 29834–29840 (2018).
Marino, A. et al. Analysis of antimicrobial exercise of the hydrolate of Coridothymus capitatus (L.) Reichenb fil. (Lamiaceae) alone and together with antimicrobial brokers. Bmc Complement. Med. Ther. 20, 1–11 (2020).
Prusinowska, R., Smigielski, Okay., Stobiecka, A. & Kunicka-Styczynska, A. Hydrolates from lavender (Lavandula angustifolia): Their chemical composition in addition to fragrant, antimicrobial and antioxidant properties. Nat. Prod. Res. 30, 386–393 (2016).
Garzoli, S. et al. Lavandula x intermedia important oil and hydrolate: Analysis of chemical composition and antibacterial exercise earlier than and after formulation in nanoemulsion. Ind. Crops Prod. 145, 112068 (2020).
Wawrzynczak, Okay., Sadowska, B., Wieckowska-Szakiel, M. & Kalemba, D. Composition and antimicrobial exercise of Myrica gale L. leaf and flower important oils and hydrolates. Rec. Nat. Prod. 15, 35–45 (2021).
Sagdic, O., Ozturk, I. & Tornuk, F. Inactivation of non-toxigenic and toxigenic Escherichia coli O157:H7 inoculated on minimally processed tomatoes and cucumbers: Utilization of hydrosols of Lamiaceae spices as pure meals sanitizers. Meals Management 30, 7–14 (2013).
Gil, M. I., Selma, M. V., Lopez-Galvez, F. & Allende, A. Contemporary-cut product sanitation and wash water disinfection: Issues and options. Int. J. Meals Microbiol. 134, 37–45 (2009).
Al-Turki, A. I. Antibacterial impact of thyme, peppermint, sage, black pepper and garlic hydrosols towards Bacillus subtilis and Salmonella enteritidis. J. Meals Agric. Environ. 5, 92–94 (2007).
Tornuk, F. et al. Efficacy of assorted plant hydrosols as pure meals sanitizers in decreasing Escherichia coli O157:H7 and Salmonella typhimurium on contemporary minimize carrots and apples. Int. J. Meals Microbiol. 148, 30–35 (2011).
Lewis, Okay. & Ausubel, F. M. Prospects for plant-derived antibacterials. Nat. Biotechnol. 24, 1504–1507 (2006).
Zarshenas, M. M. & Krenn, L. Phytochemical and pharmacological facets of Salvia mirzayanii Rech F. & Esfand. J. Evid.-Primarily based Integr. Med. 20, 65–72 (2015).
Rustaiyan, A., Feizbakhsh, A., Masoudi, S. & Ameri, N. Comparability of the unstable oils of Satureja atropatana Bung. and Satureja mutica Fisch et CA Mey. from Iran. J. Essent. Oil Res. 16, 594–596 (2004).
Cabana, R., Silva, L. R., Valentao, P., Viturro, C. I. & Andrade, P. B. Impact of various extraction methodologies on the restoration of bioactive metabolites from Satureja parvifolia (Phil.) Epling (Lamiaceae). Ind. Crops Prod. 48, 49–56 (2013).
Amanlou, M., Dadkhah, F., Salehnia, A., Farsam, H. & Dehpour, A. R. An anti-inflammatory and anti-nociceptive results of hydroalcoholic extract of Satureja khuzistanica Jamzad extract. J. Pharm. Pharm. Sci. 8, 102–106 (2005).
Caprioli, G., Lupidi, G. & Maggi, F. Comparability of chemical composition and antioxidant actions of two Winter savory subspecies (Satureja montana subsp. variegata and Satureja montana subsp. montana) cultivated in Northern Italy. Nat. Prod. Res. 33, 3143–3147 (2019).
Tepe, B. & Cilkiz, M. A pharmacological and phytochemical overview on Satureja. Pharm. Biol. 54, 375–412 (2016).
Sagdic, O. & Ozcan, M. Antibacterial exercise of Turkish spice hydrosols. Meals Management 14, 141–143 (2003).
Sahan, N. & Tornuk, F. Utility of plant hydrosols for decontamination of wheat, lentil and mung bean seeds previous to sprouting. Qual. Assur. Saf. Crops Meals 8, 575–582 (2016).
Chorianopoulos, N. G., Giaouris, E. D., Skandamis, P. N., Haroutounian, S. A. & Nychas, G. J. E. Disinfectant take a look at towards monoculture and mixed-culture biofilms composed of technological, spoilage and pathogenic micro organism: Bactericidal impact of important oil and hydrosol of Satureja thymbra and comparability with commonplace acid-base sanitizers. J. Appl. Microbiol. 104, 1586–1596 (2008).
Djenane, D., Yanguela, J., Montanes, L., Djerbal, M. & Roncales, P. Antimicrobial exercise of Pistacia lentiscus and Satureja montana important oils towards Listeria monocytogenes CECT 935 utilizing laboratory media: Efficacy and synergistic potential in minced beef. Meals Management 22, 1046–1053 (2011).
Boyraz, N. & Ozcan, M. Inhibition of phytopathogenic fungi by important oil, hydrosol, floor materials and extract of summer time savory (Satureja hortensis L.) rising wild in Turkey. Int. J. Meals Microbiol. 107, 238–242 (2006).
Di Vito, M. et al. Is the antimicrobial exercise of hydrolates decrease than that of important oils?. Antibiotics-Basel 10, 88 (2021).
Walczak, M., Michalska-Sionkowska, M., Olkiewicz, D., Tarnawska, P. & Warzynska, O. Potential of carvacrol and thymol in decreasing biofilm formation on technical surfaces. Molecules 26, 2723 (2021).
Badawy, M. E. I., Marei, G. I. Okay., Rabea, E. I. & Taktak, N. E. M. Antimicrobial and antioxidant actions of hydrocarbon and oxygenated monoterpenes towards some foodborne pathogens by way of in vitro and in silico research. Pestic. Biochem. Physiol. 158, 185–200 (2019).
Garcia-Salinas, S., Elizondo-Castillo, H., Arruebo, M., Mendoza, G. & Irusta, S. Analysis of the antimicrobial exercise and cytotoxicity of various parts of pure origin current in important oils. Molecules 23, 1399 (2018).
Zhang, J. H., Ma, S., Du, S. L., Chen, S. Y. & Solar, H. L. Antifungal exercise of thymol and carvacrol towards postharvest pathogens Botrytis cinerea. J. Meals Sci. Technol.-Mysore 56, 2611–2620 (2019).
Ghosh, C., Sarkar, P., Issa, R. & Haldar, J. Options to standard antibiotics within the period of antimicrobial resistance. Tendencies Microbiol. 27, 323–338 (2019).
World Well being Group. International Motion Plan on Antimicrobial Resistance. World Well being Group. https://apps.who.int/iris/deal with/10665/193736 (2016).
Magnusson, U. A. & Landin, H. Tips on how to Use Antibiotics Successfully and Responsibly in Dairy Manufacturing for the Sake of Human and Animal Well being (FAO, 2021).
Kummerer, Okay. Antibiotics within the aquatic atmosphere: A overview—Half II. Chemosphere 75, 435–441 (2009).
Ternes, T. A., Joss, A. & Siegrist, H. Scrutinizing prescription drugs and private care merchandise in wastewater therapy. Environ. Sci. Technol. 38, 392A-399A (2004).
Yu, Y. et al. Prevalence and conduct of prescription drugs, steroid hormones, and endocrine-disrupting private care merchandise in wastewater and the recipient river water of the Pearl River Delta, South China. J. Environ. Monit. 13, 871–878 (2011).
Fytili, D. & Zabaniotou, A. Utilization of sewage sludge in EU software of outdated and new strategies: A overview. Renew. Maintain. Power Rev. 12, 116–140 (2008).
Lishman, L. et al. Prevalence and reductions of prescription drugs and private care merchandise and estrogens by municipal wastewater therapy vegetation in Ontario, Canada. Sci. Complete Environ. 367, 544–558 (2006).
Martin, J., Camacho-Munoz, D., Santos, J. L., Aparicio, I. & Alonso, E. Prevalence of pharmaceutical compounds in wastewater and sludge from wastewater therapy vegetation: Elimination and ecotoxicological impression of wastewater discharges and sludge disposal. J. Hazard. Mater. 239, 40–47 (2012).
Radjenovic, J., Petrovic, M. & Barcelo, D. Destiny and distribution of prescription drugs in wastewater and sewage sludge of the standard activated sludge (CAS) and superior membrane bioreactor (MBR) therapy. Water Res. 43, 831–841 (2009).
Hamscher, G., Sczesny, S., Hoper, H. & Nau, H. Willpower of persistent tetracycline residues in soil fertilized with liquid manure by high-performance liquid chromatography with electrospray ionization tandem mass spectrometry. Anal. Chem. 74, 1509–1518 (2002).
Kovalakova, P. et al. Prevalence and toxicity of antibiotics within the aquatic atmosphere: A overview. Chemosphere 251, 126351 (2020).
Carvalho, I. T. & Santos, L. Antibiotics within the aquatic environments: A overview of the European situation. Environ. Int. 94, 736–757 (2016).
Janecko, N., Pokludova, L., Blahova, J., Svobodova, Z. & Literak, I. Implications of fluoroquinolone contamination for the aquatic atmosphere: A overview. Environ. Toxicol. Chem. 35, 2647–2656 (2016).
Du, L. F. & Liu, W. Okay. Prevalence, destiny, and ecotoxicity of antibiotics in agro-ecosystems A overview. Agron. Maintain. Dev. 32, 309–327 (2012).
Pino, M. R., Muniz, S., Val, J. & Navarro, E. Phytotoxicity of 15 widespread prescription drugs on the germination of Lactuca sativa and photosynthesis of Chlamydomonas reinhardtii. Environ. Sci. Pollut. Res. 23, 22530–22541 (2016).
Pino, M. R. et al. Acute toxicological results on the earthworm Eisenia fetida of 18 widespread prescription drugs in synthetic soil. Sci. Complete Environ. 518, 225–237 (2015).
Pino-Otin, M. R., Muniz, S., Val, J. & Navarro, E. Results of 18 prescription drugs on the physiological range of edaphic microorganisms. Sci. Complete Environ. 595, 441–450 (2017).
Pino-Otin, M. R. et al. Ecotoxicity of a novel biopesticide from Artemisia absinthium on non-target aquatic organisms. Chemosphere 216, 131–146 (2019).
Pino-Otin, M. R. et al. Impression of Artemisia absinthium hydrolate extracts with nematicidal exercise on non-target soil organisms of various trophic ranges. Ecotoxicol. Environ. Saf. 180, 565–574 (2019).
Pino-Otin, M. R. et al. Ecotoxicity of a brand new biopesticide produced by Lavandula luisieri on non-target soil organisms from completely different trophic ranges. Sci. Complete Environ. 671, 83–93 (2019).
Pino-Otin, M. R. et al. Spanish Satureja montana L. hydrolate: Ecotoxicological examine in soil and water non-target organisms. Ind. Crops Prod. 178, 114553 (2022).
Julio, L. F., Gonzalez-Coloma, A., Burillo, J., Diaz, C. E. & Andres, M. F. Nematicidal exercise of the hydrolate byproduct from the semi industrial vapor strain extraction of domesticated Artemisia absinthium towards Meloidogyne javanica. Crop Prot. 94, 33–37 (2017).
Gonzalez-Torralba, A., Garcia-Esteban, C. & Alos, J.-I. Enteropathogens and antibiotics. Enferm. Infect. Microbiol. Clin. 36, 47–54 (2018).
Ronveaux, O., Gheldre, Y., Glupczynski, Y., Struelens, M. & Mol, P. Emergence of Enterobacter aerogenes as a serious antibiotic-resistant nosocomial pathogen in Belgian hospitals. Clin. Microbiol. Infect. 5, 622–627 (1999).
Canton, R. et al. Antimicrobial susceptibility of Gram-negative organisms from intra belly infections and evolution of isolates with prolonged spectrum beta-lactamases within the SMART examine in Spain (2002–2010). Rev. Espanola De Quimioterapia 24, 223–232 (2011).
Ghadiri, H., Vaez, H., Khosravi, S. & Soleymani, E. The antibiotic resistance profiles of bacterial strains remoted from sufferers with hospital-acquired bloodstream and urinary tract infections. Crit. Care Res. Pract. 2012, 890797–890797 (2012).
Peman, J. et al. Epidemiology of candidemia in Spain: Multicenter examine. Rev. Iberoamericana Micol. 19, 30–35 (2002).
Strategies for Dilution Antimicrobial Susceptibility Checks for Micro organism That Develop Aerobically; Accredited Customary—Ninth Version. M07-A9. 32 No. 2 (2012)
Centurión-Hidalgo, D., Espinosa-Moreno, J., Mayo-Mosqueda, A., Frías-Jiménez, A. & Velázquez-Martínez, J. R. Evaluación de la actividad antibacteriana de los extractos hexánicos de las inflorescencias de palmas comestibles de la Sierra de Tabasco, Mexico. Polibotánica 35, 133–142 (2013).
Tortora, G. J., Funke, B. R. & Case, C. L. Introduccion a la Microbiología (Médica. Panamericana, 2007).
Adrar, N., Oukil, N. & Bedjou, F. Antioxidant and antibacterial actions of Thymus numidicus and Salvia officinalis important oils alone or together. Ind. Crops Prod. 88, 112–119 (2016).
Pino-Otin, M. R., Langa, E., Val, J., Mainar, A. M. & Ballestero, D. Impression of citronellol on river and soil environments utilizing non-target mannequin organisms and pure populations. J. Environ. Manag. 287, 112303 (2021).
Garland, J. L. & Mills, A. L. Classification and characterization of heterotrophic microbial communities on the premise of patterns of community-level sole-carbon-source utilization. Appl. Environ. Microbiol. 57, 2351–2359 (1991).
Lehman, R. M., Colwell, F. S., Ringelberg, D. B. & White, D. C. Mixed microbial community-level analyses for high quality assurance of terrestrial subsurface cores. J. Microbiol. Strategies 22, 263–281 (1995).
Weber, Okay. P. & Legge, R. L. One-dimensional metric for monitoring bacterial group divergence utilizing sole carbon supply utilization patterns. J. Microbiol. Strategies 79, 55–61 (2009).
Caporaso, J. G. et al. International patterns of 16S rRNA range at a depth of thousands and thousands of sequences per pattern. Proc. Natl. Acad. Sci. U.S.A. 108, 4516–4522 (2011).
Caporaso, J. G. et al. Extremely-high-throughput microbial group evaluation on the Illumina HiSeq and MiSeq platforms. ISME J. 6, 1621–1624 (2012).
Farag, R. S., Daw, Z. Y., Hewedi, F. M. & Elbaroty, G. S. A. Antimicrobial exercise of some egyptian spice important oils. J. Meals Prot. 52, 665–667 (1989).
Pardavella, I., Nasiou, E., Daferera, D., Trigas, P. & Giannakou, I. The usage of important oil and hydrosol extracted from Satureja hellenica for the management of Meloidogyne incognita and M. javanica. Vegetation-Basel 9, 856 (2020).
Silva, F. V. et al. Anti-Inflammatory and anti-ulcer actions of Carvacrol, a monoterpene current within the important oil of oregano. J. Med. Meals 15, 984–991 (2012).
Elshafie, H. S. et al. Cytotoxic exercise of Origanum Vulgare L. on hepatocellular carcinoma cell line HepG2 and analysis of its organic exercise. Molecules 22, 1435 (2017).
Lombrea, A. et al. A current perception relating to the phytochemistry and bioactivity of Origanum vulgare L. important oil. Int. J. Mol. Sci. 21, 9653 (2020).
Memar, M. Y., Raei, P., Alizadeh, N., Aghdam, M. A. & Kafil, H. S. Carvacrol and thymol: Robust antimicrobial brokers towards resistant isolates. Rev. Med. Microbiol. 28, 63–68 (2017).
Kachur, Okay. & Suntres, Z. The antibacterial properties of phenolic isomers, carvacrol and thymol. Crit. Rev. Meals Sci. Nutr. 60, 3042–3053 (2020).
Eftekhar, F., Raei, F., Yousefzadi, M., Ebrahimi, S. N. & Hadian, J. Antibacterial exercise and important oil composition of Satureja spicigera from Iran. Z. Fur Naturforschung Part C-a Journal of Biosciences 64, 20–24 (2009).
Pei, R. S., Zhou, F., Ji, B. P. & Xu, J. Analysis of mixed antibacterial results of eugenol, cinnamaldehyde, thymol, and carvacrol towards E. coli with an improved methodology. J. Meals Sci. 74, M379–M383 (2009).
Xu, J., Zhou, F., Ji, B. P., Pei, R. S. & Xu, N. The antibacterial mechanism of carvacrol and thymol towards Escherichia coli. Lett. Appl. Microbiol. 47, 174–179 (2008).
Miladi, H. et al. Use of carvacrol, thymol, and eugenol for biofilm eradication and resistance modifying susceptibility of Salmonella enterica serovar Typhimurium strains to nalidixic acid. Microb. Pathog. 104, 56–63 (2017).
Trevisan, D. A. C. et al. Antibacterial and antibiofilm exercise of carvacrol towards Salmonella enterica serotype Typhimurium. Braz. J. Pharm. Sci. https://doi.org/10.1590/s2175-97902018000117229 (2018).
Zhou, F. et al. The antibacterial impact of cinnamaldehyde, thymol, carvacrol and their combos towards the foodborne pathogen Salmonella typhimurium. J. Meals Saf. 27, 124–133 (2007).
Raei, P. et al. Thymol and carvacrol strongly inhibit biofilm formation and progress of carbapenemase-producing Gram adverse bacilli. Cell Mol. Biol. 63, 108–112 (2017).
Lambert, R. J. W., Skandamis, P. N., Coote, P. J. & Nychas, G. J. E. A examine of the minimal inhibitory focus and mode of motion of oregano important oil, thymol and carvacrol. J. Appl. Microbiol. 91, 453–462 (2001).
Churklam, W., Chaturongakul, S., Ngamwongsatit, B. & Aunpad, R. The mechanisms of motion of carvacrol and its synergism with nisin towards Listeria monocytogenes on sliced bologna sausage. Meals Management 108, 106864 (2020).
da Luz, I. S. et al. Lack of induction of direct safety or cross-protection in Staphylococcus aureus by sublethal concentrations of Origanum vulgare L. important oil and carvacrol in a meat-based medium. Arch. Microbiol. 195, 587–593 (2013).
Gutierrez-Fernandez, J. et al. Antimicrobial exercise of binary combos of pure and artificial phenolic antioxidants towards Enterococcus faecalis. J. Dairy Sci. 96, 4912–4920 (2013).
Maccelli, A. et al. Satureja montana L. Important oils: Chemical profiles/phytochemical screening, antimicrobial exercise and O/W nanoemulsion formulations. Pharmaceutics 12, 7 (2020).
de Souza, E. L., Montenegro Stamford, T. L., Lima, E. D. O., Barbosa Filho, J. M. & Mayo Marques, M. O. Interference of heating on the antimicrobial exercise and chemical composition of Origanum vulgare L. (Lamiaceae) important oil. Ciencia E Tecnol. De Alimentos 28, 418–422 (2008).
Askun, T., Tumen, G., Satil, F. & Ates, M. Characterization of the phenolic composition and antimicrobial actions of Turkish medicinal vegetation. Pharm. Biol. 47, 563–571 (2009).
Amaral, S. C. et al. Origanum vulgare important oil: Antibacterial actions and synergistic impact with polymyxin B towards multidrug-resistant Acinetobacter baumannii. Mol. Biol. Rep. 47, 9615–9625 (2020).
Mauriello, E., Ferrari, G. & Donsi, F. Impact of formulation on properties, stability, carvacrol launch and antimicrobial exercise of carvacrol emulsions. Colloids Surf. B 197, 111424 (2021).
Marinelli, L., Di Stefano, A. & Cacciatore, I. Carvacrol and its derivatives as antibacterial brokers. Phytochem. Rev. 17, 903–921 (2018).
Man, A., Santacroce, L., Jacob, R., Mare, A. & Man, L. Antimicrobial exercise of six important oils towards a bunch of human pathogens: A comparative examine. Pathogens 8, 15 (2019).
El-Mentioned, H. et al. Important oil evaluation and antimicrobial analysis of three fragrant plant species rising in Saudi Arabia. Molecules 26, 959 (2021).
Khoshbakht, T., Karami, A., Tahmasebi, A. & Maggi, F. The variability of thymol and carvacrol contents reveals the extent of antibacterial exercise of the important oils from completely different accessions of Oliveria decumbens. Antibiotics-Basel 9, 409 (2020).
Botelho, M. A. et al. Antimicrobial exercise of the important oil from Lippia sidoides, carvacrol and thymol towards oral pathogens. Braz. J. Med. Biol. Res. 40, 349–356 (2007).
Mirjana, S. & Nada, B. Chemical composition and antimicrobial variability of Satureja montana, L. important oils produced throughout ontogenesis. J. Essent. Oil Res. 16, 387–391 (2004).
Fathi-Moghadam, E., Shakerian, A., Chaleshtori, R. S. & Rahimi, E. Chemical composition and antioxidant properties and antimicrobial results of Satureja bachtiarica Bunge and Echinophora platyloba DC. Important oils towards listeria monocytogenes. J. Med. Vegetation By-Prod. 9, 47–58 (2020).
Gill, T. A., Li, J., Saenger, M. & Scofield, S. R. Thymol-based submicron emulsions exhibit antifungal exercise towards Fusarium graminearum and inhibit Fusarium head blight in wheat. J. Appl. Microbiol. 121, 1103–1116 (2016).
Vardar-Unlu, G., Yagmuroglu, A. & Unlu, M. Analysis of in vitro exercise of carvacrol towards Candida albicans strains. Nat. Prod. Res. 24, 1189–1193 (2010).
Shaban, S., Patel, M. & Ahmad, A. Improved efficacy of antifungal medication together with monoterpene phenols towards Candida auris. Sci. Rep. 10, 1–8 (2020).
Lima, I. O. et al. Antifungal exercise and mode of motion of carvacrol towards Candida albicans strains. J. Essent. Oil Res. 25, 138–142 (2013).
Marcos-Arias, C., Eraso, E., Madariaga, L. & Quindos, G. In vitro actions of pure merchandise towards oral Candida isolates from denture wearers. Bmc Complement. Altern. Med. 11, 1–7 (2011).
Baj, T., Biernasiuk, A., Wrobel, R. & Malm, A. Chemical composition and in vitro exercise of Origanum vulgare L., Satureja hortensis L., Thymus serpyllum L. and Thymus vulgaris L. important oils in direction of oral isolates of Candida albicans and Candida glabrata. Open Chem. 18, 108–118 (2020).
Duran, N. & Kaya, D.A. Antifungal exercise of Origanum syriacum L. important oils towards Candida spp. In seventh Worldwide Convention on Superior Supplies and Programs 81–85 (2018).
Tampieri, M. P. et al. The inhibition of Candida albicans by chosen important oils and their main parts. Mycopathologia 159, 339–345 (2005).
Ben Arfa, A., Combes, S., Preziosi-Belloy, L., Gontard, N. & Chalier, P. Antimicrobial exercise of carvacrol associated to its chemical construction. Lett. Appl. Microbiol. 43, 149–154 (2006).
Garvey, M. I., Rahman, M. M., Gibbons, S. & Piddock, L. J. V. Medicinal plant extracts with efflux inhibitory exercise towards Gram-negative micro organism. Int. J. Antimicrob. Brokers 37, 145–151 (2011).
Hyldgaard, M., Mygind, T. & Meyer, R. L. Important oils in meals preservation: Mode of motion, synergies, and interactions with meals matrix parts. Entrance. Microbiol. 3, 12 (2012).
Reynolds, C. S. Variability within the provision and performance of mucilage in phytoplankton: Facultative responses to the atmosphere. Hydrobiologia 578, 37–45 (2007).
Saikaly, P. E. & Oerther, D. B. Variety of dominant bacterial taxa in activated sludge promotes practical resistance following poisonous shock loading. Microb. Ecol. 61, 557–567 (2011).
Raza, S., Matula, Okay., Karon, S. & Paczesny, J. Resistance and adaptation of micro organism to non-antibiotic antibacterial brokers: Bodily stressors, nanoparticles, and bacteriophages. Antibiotics-Basel 10, 435 (2021).
Ramos, J. L. et al. Mechanisms of solvent tolerance in gram-negative micro organism. Annu. Rev. Microbiol. 56, 743–768 (2002).
Nguyen, U. T. et al. Small-molecule modulators of listeria monocytogenes biofilm growth. Appl. Environ. Microbiol. 78, 1454–1465 (2012).
Lynn, N., Garcia, J., Gruenberg, Okay. & MacDougall, C. Multidrug-resistant pseudomonas infections: Arduous to deal with, however hope on the horizon?. Curr. Infect. Dis. Rep. 20, 1–10 (2018).
Tetard, A., Zedet, A., Girard, C., Plesiat, P. & Llanes, C. Cinnamaldehyde induces expression of efflux pumps and multidrug resistance in Pseudomonas aeruginosa. Antimicrob. Brokers Chemother. 63, e1081-19 (2019).
Ratajczak, M., Kaminska, D., Dlugaszewska, J. & Gajecka, M. Antibiotic resistance, biofilm formation, and presence of genes encoding virulence elements in strains remoted from the pharmaceutical manufacturing atmosphere. Pathogens 10, 130 (2021).
Ali, F., Kamal, S., Shakeela, Q. & Ahmed, S. Prolonged-spectrum and Metallo-beta lactamase enzymes mediated resistance in Pseudomonas aeruginosa in clinically remoted specimens. Kuwait Journal of Science https://doi.org/10.48129/kjs.v48i2.8495 (2021).
Mallea, M. et al. Porin alteration and energetic efflux: Two in vivo drug resistance methods utilized by Enterobacter aerogenes. Microbiology 144, 3003–3009 (1998).
Chevalier, J. et al. Identification and evolution of drug efflux pump in scientific Enterobacter aerogenes strains remoted in 1995 and 2003. PLoS ONE 3, e3203 (2008).
Chevalier, J., Pages, J. M. & Mallea, M. In vivo modification of porin exercise conferring antibiotic resistance to Enterobacter aerogenes. Biochem. Biophys. Res. Commun. 266, 248–251 (1999).
Xu, H. X., Delling, M., Jun, J. C. & Clapham, D. E. Oregano, thyme and clove-derived flavors and pores and skin sensitizers activate particular TRP channels. Nat. Neurosci. 9, 628–635 (2006).
Pino-Otin, M. R. et al. Impression of eight extensively consumed antibiotics on the expansion and physiological profile of pure soil microbial communities. Chemosphere 305, 135473 (2022).