<i>In Vitro</i> Efficacy of <i>Crataegus oxycantha</i> L. (Hawthorn) and Its Major Components against ATCC and Clinical Strains of <i>Ureaplasma urealyticum</i> — Oak Academic Publishing
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<i>In Vitro</i> Efficacy of <i>Crataegus oxycantha</i> L. (Hawthorn) and Its Major Components against ATCC and Clinical Strains of <i>Ureaplasma urealyticum</i>
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Messina, Italy
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Section of Microbiology, Department of Biomedical and Biotechnological Sciences-BIOMETEC, University of Catania, Catania, Italy
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Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Messina, Italy
1 Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Messina, Italy
2 Section of Microbiology, Department of Biomedical and Biotechnological Sciences-BIOMETEC, University of Catania, Catania, Italy
3 Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Messina, Italy
Crataegus oxycantha L., commonly known as hawthorn , has traditionally been used for its beneficial effect on cardiovascular health, which is related to its flavonoid content. The aim of the present study was to evaluate the antibacterial properties of a fluid extract and a hydro-ethanolic macerate from buds of Crataegus oxycantha against clinical isolates of Ureaplasma urealyticum . The major purified flavonoids present in the extracts were also tested against ATCC strains and clinical isolates. Both the fluid extract and the hydro-ethanolic macerate were active agains t thirty-due clinical strains of U. urealyticum , with MIC ranges between 15.6 and 250 μg/ml and 15.6 and 62.5 μg/ml, respectively. All pure organic compounds, with the exception of rutin, showed activity against the strains tested, luteolin 3,7-diglucoside being the most active compound (MICs in the range of 0.48 and 1.95 μg/ml), followed by apigenin-7- O -glucoside (MICs in the range of 0.48 and 3.9 μg/ml). The activity of the pure flavonoids was greater against the clinical isolates compared to the ATCC strains. The data presented here demonstrate that flavonoids present in Crataegus oxycantha are effective against clinical isolates of U. urealyticum and could be used in combination with antibiotics in order to combat resistance.
Redelinghuys, M.J., Ehlers, M.M., Dreyer, A.W., Lombaard, H.A. and Kock, M.M. (2014) Antimicrobial Susceptibility Patterns of Ureaplasma Species and Mycoplasma hominis in Pregnant Women. BMC Infectious Diseases, 14, 171. http://dx.doi.org/10.1186/1471-2334-14-171
Beuchat, L.R. and Golden, D.A. (1989) Antimicrobials Occurring Naturally in Foods. Food Technology, 43, 134-142.
Gould, G.W. (1996) Industry Perspectives on the Use of Natural Antimicrobials and Inhibitors for Food Applications. Journal of Food Protection, 59, 82-86.
Cushnie, T.P.T. and Lamb, A.J. (2011) Recent Advances in Understanding the Antibacterial Properties of Flavonoids. International Journal of Antimicrobial Agents, 38, 99-107. http://dx.doi.org/10.1016/j.ijantimicag.2011.02.014
Zuo, G.-Y., Zhang, X.-J., Yang, C.-X., Han, J., Wang, G.-C. and Bian, Z.-Q. (2012) Evaluation of Traditional Chinese Medicinal Plants for Anti-MRSA Activity with Reference to the Treatment Record of Infectious Diseases. Molecules, 17, 2955-2967. http://dx.doi.org/10.3390/molecules17032955
Mandalari, G., Bisignano, C., D’Arrigo, M., Ginestra, G., Arena, A., Tomaino, A. and Wickham, M.S.J. (2010) Antimicrobial Potential of Polyphenols Extracted from Almond Skins. Letters in Applied Microbiology, 51, 83-89. http://dx.doi.org/10.1111/j.1472-765x.2010.02862.x
Bisignano, C., Filocamo, A., La Camera, E., Zummo, S., Fera, M.T. and Mandalari, G. (2013) Antibacterial Activities of Almond Skins on cagA-Positive and -Negative Clinical Isolates of Helicobacter pylori. BMC Microbiology, 13, 103. http://dx.doi.org/10.1186/1471-2180-13-103
Bisignano, C., Filocamo, A., Faulks, R.M. and Mandalari, G. (2013) In Vitro Antimicrobial Activity of Pistachio (Pistacia vera L.) Polyphenols. FEMS Microbiology Letters, 341, 62-67. http://dx.doi.org/10.1111/1574-6968.12091
Mandalari, G., Bennett, R.N., Bisignano, G., Trombetta, D., Saija, A., Faulds, C.B., Gasson, M. and Narbad, A. (2007) Antimicrobial Activity of Flavonoids Extracted from Bergamot (Citrus bergamia Risso) Peel, a Byproduct of the Essential Oil Industry. Journal of Applied Microbiology, 103, 2056-2064. http://dx.doi.org/10.1111/j.1365-2672.2007.03456.x
Filocamo, A., Bisignano, C., Mandalari, G. and Navarra, M. (2015) In Vitro Antimicrobial Activity and Effect on Biofilm Production of a White Grape Juice (Vitis vinifera) Extract. Evidence-Based Complementary and Alternative Medicine, 2015, 856243. http://dx.doi.org/10.1155/2015/856243
Bisignano, C., Filocamo, A., Ginestra, G., Giofre’, S.V., Navarra, M., Romeo, R. and Mandalari, G. (2004) 3,4-DHPEA-EA from Olea europaea L. Is Effective against Standard and Clinical Isolates of Staphylococcus sp. Annals of Clinical Microbiology and Antimicrobials, 13, 24. http://dx.doi.org/10.1186/1476-0711-13-24
Furneri, P.M., Mondello, L., Mandalari, G., Paolino, D., Dugo, P., Garrozzo, A. and Bisignano, G. (2012) In Vitro Antimycoplasmal Activity of Citrus bergamia Essential Oil and Its Major Components. European Journal of Medicinal Chemistry, 52, 66-69. http://dx.doi.org/10.1016/j.ejmech.2012.03.005
Filocamo, A., Bisignano, C., Ferlazzo, N., Cirmi, S., Mandalari, G. and Navarra, M. (2015) In Vitro Effect of Bergamot (Citrus bergamia) Juice against cagA-Positive and -Negative Clinical Isolates of Helicobacter pylori. BMC Complementary and Alternative Medicine, 15, 256. http://dx.doi.org/10.1186/s12906-015-0769-2
Mills, S. and Bone, K. (2000) Principles and Practice of Phytotherapy: Modern Herbal Medicine. Churchill Livingdtone, Edinburg, 439-447.
Jayalakshmi, R., Thirupurasundari, C.J. and Devaraj, S.N. (2006) Pretreatment with Alchoholic Extract of Crataegus oxycantha (AEC) Activates Mitochondrial Infacrtion during Isoproterenol-Induced Myocardial Infarction in Rats. Molecular Cellular Biochemistry, 292, 59-67. http://dx.doi.org/10.1007/s11010-006-9218-3
Ficarra, P., Ficarra, R., De Pasquale, A., Monforte, M.T. and Calabro’ M.L. (1990) High-Performance Liquid Chromatography of Flavonoids in Crataegus oxycantha L. Il Farmaco, 45, 247-255.
Bisignano, G., Jauk, I. and Galati, E.M. (1983) In "LE DROGHE VEGETALI NELLA MEDICINA TRADIZIONALE E NELLA MEDICINA MODERNA”, Todi.
Caschetto, S., Bisignano, G., Maugeri, G., Strano, V. and Albanese, A. (1983) Incidenza e ruole dei micoplasmi nelle vaginiti. Attual Ost Gin., 29, 111.
Shepard, M.C. (1983) Culture Media for Ureaplasmas. In: Razin, S. and Tully, J.G., Eds., Methods in Mycoplasmology, Vol. 1, Academic Press, Inc., New York, 137-146. http://dx.doi.org/10.1016/b978-0-12-583801-6.50030-5
Clinical and Laboratory Standards Institute (CLSI) (2012) Clinical and Laboratory Standards Institute Performance Standards for Antimicrobial Susceptibility Testing; Twentieth Informational Supplement. CLSI, Wayne.
Furneri, P.M., Bisignano, G., Cerniglia, G., Nicoletti, G., Cesana, M. and Tempera, G. (1994) In Vitro Antimycoplasmal Activities of Rufloxacin and Its Metabolite MF922. Antimicrobial Agents and Chemotherapy, 38, 2651-2654. http://dx.doi.org/10.1128/AAC.38.11.2651
Benmalek, Y., AitYahia, O., Belkebir, A. and Fardeau, M.-L. (2013) Anti-Microbial and Anti-Oxidant Activities of Illicium verum, Crataegus oxyacantha spp monogyna and Allium cepa Red and Qhite Varieties. Bioengineered, 4, 244-248. http://dx.doi.org/10.4161/bioe.24435
Su, Y., Ma, L., Wen, Y., Wang, H. and Zhang S. (2014) Studies of the in Vitro Antibacterial Activities of Several Polyphenols against Clinical Isolates of Methicillin-Resistant Staphylococcus aureus. Molecules, 19, 12630-12639. http://dx.doi.org/10.3390/molecules190812630
Taguri, T., Tanaka, T. and Kouno, I. (2004) Antimicrobial Activity of 10 Different Plant polYphenols against Bacteria Causing Food-Borne Disease. Biological and Pharmacological Bulletin, 27, 1965-1969. http://dx.doi.org/10.1248/bpb.27.1965
Diniz-Silva, H., Magnani, M., de Siqueira, S., Leite de Souza, E. and de Siqueira-Junior, J.P. (2016) Fruit Flavonoids as Modulators of Norfloxacin Resistance in Staphylococcus aureus That Overexpressed NorA. LWT—Food Science and Technology, 1-12.
Pereira, A.P., Ferreira, I.C.F.R., Marcelino, F., Valentao, P. Andrade, P.B., Seabra, R., Estevinho, L., Bento, A. and Pereira, J.A. (2007) Phenolic Compounds and Antimicrobial Activity of Olive (Olea europaea L. Cv. Cobrancosa) Leaves. Molecules, 12, 1153-1162. http://dx.doi.org/10.3390/12051153
Nayaka, H.B., Londonkar, R.L., Umesh, M.K. and Tukappa, A. (2014) Antibacterial Attributes of Apigenin, Isolated from Portulaca oleracea L. International Journal of Bacteriology, 2014, Article ID: 175851.
Siriwong, S., Thumanu, K., Hengpratom, T. and Eumkeb, G. (2015) Synergy and Mode of Action of Ceftazidime plus Quercetin or Luteolin on Streptococcus pyogenes. Evidence-Based Complementary and Alternative Medicine, 2015, Article ID: 759459. http://dx.doi.org/10.1155/2015/759459