ANTIBACTERIAL ACTIVITY OF TAMARIX APHYLLA L. LEAVES EXTRACT ON HETEROGENEOUS VANCOMYCIN ITERMEDIATED STAPHYLOCOCCUS AUREUS (hVISA)
DOI:
https://doi.org/10.36103/hwm37e61Keywords:
Antimicrobial activity, chemical composition, essential oil, gene expressionAbstract
This study was aimed to examine the antibacterial activity of the T. aphylla leaves ethanolic extract in vitro against the locally strain heterogeneous vancomycin intermediated Staphylococcus aureus (hVISA) at different concentrations starting from 0.03 to 200 mg/ml. T.aphylla leaves were extracted by ethanol 96% in the Soxhlet extraction unit. Using both gas chromatography and mass spectrometry (GC/MS), the results indicated that the composition of T. aphylla extract was oil and include a variety of chemicals, including 9,12-Octadecadienoic acid, methyl ester (20.06%), followed by Phytol, acetate (18.93%) and Hexadecanoic acid, methyl ester (12.14%), were in leaves. The concentration of 1.5 (mg/ml.) was determined as a minimum inhibitory concentration (MIC) for hVISA antibacterial activity. Gene expression was detected using the Quantitative Real-Time PCR technique; before and after treatment with T. aphylla leaves extracts; the gene expression was low after treatment with T. aphylla leaves extracts. In conclusion, T. aphylla leaves extract is a promising alternative medication that can treat the infection caused by hVISA.
References
Al-salmany, A.S.M., and A. M. S. AL-Rubeii. 2020. Effect of cinnamon and turmeric nanoparticles extract in quality characteristics of fresh ground beef during cold storage. Annals of Tropical Medicine and Public Health, 23(2): 200–213.
Adnan, M., A. Tariq, R. Bibi, N.M. AbdElsalam, H. Rehman, W. Murad, S. Ahmad, M. Israr, S. Sabahat, R. Ullah, A. Akber, J. Ud Din, and M.A. Aziz, 2015. Antimicrobial potential of alkaloids and flavonoids extracted from Tamarix aphylla leaves against common human pathogenic bacteria. African Journal of Traditional. Complementary and Alternative Medicines. 12(2): 27-31. 10.4314/ajtcam.v12i2.6
Al Sobeai SM., 2018. Anticancer, cytotoxic effect of Tamarix aphylla, and antibacterial screening efficiency against multidrug-resistant human pathogens. Asian Journal of Pharmaceutical and Clinical Research. 11(11): 241-246. 10.22159/ajpcr.2018.v11i11.27309
Al-salmany, A.S.M., and A. M. S. AL-Rubeii. 2020. Effect of cinnamon and turmeric nanoparticles extract in quality characteristics of ground beef during freeze storage. Plant Archives, 20, 350–356.
Alhourani N., V. Kasabri, Y. Bustanji, R. Abbassi, and M. Hudaib, 2018. Potential antiproliferative activity and evaluation of essential oil composition of the aerial parts of Tamarix aphylla (L.) H. Karst.: a wild grown medicinal plant in Jordan. Evidence-Based Complementary and Alternative Medicine. 2018(9363868): 1-7. 10.1155/2018/9363868
Aljoubory, H.M., and M.F. Altaee, 2021. Correlation study between three different genes expression and chronic myeloid leukemia in Iraq. Iraqi Journal of Agricultural Science. 52(3): 611-619. https://doi.org/10.36103/ijas.v52i3.1350
Alrumman, S.A. 2016. Phytochemical and antimicrobial properties of Tamarix aphylla L. leaves growing naturally in the Abha Region, Saudi Arabia. Arabian Journal for Science and Engineering. 41: 2123-2129.
1007/s13369-015-1900-x
Asadzadeh, R., N. Abbasi, and M. Bahmani, 2021. Extraction and identification of chemical compounds of Peganum harmala L. seed essential oil by HS-SPME and GC-MS methods. Traditional and Integrative Medicine. 6(3): 229-235.
https://doi.org/10.18502/tim.v6i3.7310
Chaudhari, C.N., K. Tandel, N. Grover, S. Sen, P. Bhatt, A.K. Sahni, and A.K. Praharaj, 2015. Heterogeneous vancomycin-intermediate among methicillin resistant Staphylococcus aureus. Medical Journal Forces India. 71(1): 15-18. 10.1016/j.mjafi.2014.03.008
Chon, J.W., U.J. Lee, R. Bensen, S. West, A. Paredes, J. Lim, S. Khan, M.E. Hart, K.S. Phillips, and K. Sung, 2020. Virulence characteristics of mecA-positive multidrug-resistant clinical coagulase negative Staphylococci. Microorganisms. 8(5):659.
3390/microorganisms8050659
Cilliam, B. W., D. V. paul, M. G. George, J. Dorothy, R. K Noel, L. Wolfgang, A. R. Fred and S. Karl, 2009. Bergey's Manual of Systematic. 2nd edition. Com. pp: 392-433.
https://doi.org/10.1007/978-0-387-68233-4
Eleaume, H., and S. Jabbouri, 2004. Comparison of two standardisation methods in real-time quantitative RT-PCR to follow Staphylococcus aureus genes expression during in vitro growth. Journal of microbiological methods. 59(3):363-370.
1016/j.mimet.2004.07.015
Farjadmand, F., M. Khanavi, M. Eftekhari, A. Hosseinsalari, T. Akbarzadeh, M. Safavi, R. Asatouri, M. Mirabzadeh, and M.R. Shams Ardekani, 2018. The effect of extraction method on the major constituents and biological effects of Trachyspermum ammi L. fruits. Research Journal of Pharmacognosy. 5(1): 55-61.
https://api.semanticscholar.org/CorpusID:59129579
Hai, N.V., 2015. The Use of Medicinal Plants as Immunostimulants in Aquaculture: A review. Aquacul. 446:88-96.
https://doi.org/10.1016/j.aquaculture.2015.03.014
Hameda, A.A., D.M. Eskanderb, and M.S.E. Badawyc, 2022. Isolation of secondary metabolites from marine Streptomyces sparsus ASD203 and evaluation its bioactivity. Egypt. J. Chem. 65(3): 539–547.
21608/EJCHEM.2021.95284.4489
Howden, B.P., J.K. Davies, P.D. Johnson, T.P. Stinear, and M. L. Grayson, 2010. Reduced vancomycin susceptibility in Staphylococcus aureus, including vancomycin-intermediate and heterogeneous vancomycin-intermediate strains: resistance mechanisms, laboratory detection, and clinical implications. Clinical Microbiology Reviews. 23(1): 99-139.
1128/CMR.00042-09
Haneen H K Alkhafaji, H. J M Altameme, and S. M H Alsharifi. 2022. Detection of bioactive chemical compounds in the methanolic extract of azolla filiculoides lamark fern by gc-ms technique. Iraqi Journal of Agricultural Sciences, 53(4):922-930. https://doi.org/10.36103/ijas.v53i4.1604
Iyer, R.N., and V. Hittinahalli, 2008. Modified PAP method to detect heteroresistance to vancomycin among methicillin resistant Staphylococcus aureus isolates at a tertiary care hospital. Indian Journal of Medical Microbiology. 26(2): 176-179.
4103/0255-0857.40537
Jaddoa, N.T.M. and L.A. Gharb, 2021. The antibiofilm activity of Hibiscus sabdriffa L. against methicillin resistant staphylococcus aureus. Iraqi Journal of Agricultural Sciences. 52(3):626-631. https://doi.org/10.36103/ijas.v52i3.1352
Jomehpour, N., G. Eslami, and M.B. Khalili, 2016. The effect of Ferula assa-foetida L and Carum copticum hydroalcoholic extract on the expression levels of Staphylococcus aureus genes involved in quorum sensing. Jundishapur Journal of Microbiology. 9(10): e33879. 10.5812/jjm.33879
Jouda, M.M., T. Elbashiti, A. Masad, and M. Albayoumi, 2016. The antibacterial effect of some medicinal plant extracts and their synergistic effect with antibiotic. World Journal of Pharmacy and Pharmaceutical Science. 5(2): 23-33.
20959/wjpps201612-8160
Koh, C.L., C.K. Sam, W.F. Yin, L.Y. Tan, T. Krishnan, Y.M. Chong, and K.G. Chan, 2013. Plant-derived natural products as sources of anti-quorum sensing compounds. Sensors. 13(5): 6217-6228. https://doi.org/10.3390/s130506217
Kőszegi, K., G. Vatai, and E. Békássy-Molnár, 2015. Comparison the soxhlet and supercritical fluid extraction of nettle root (Urtica dioica L.). Periodica Polytechnica Chemical Engineering. 59(3): 168-173. https://doi.org/10.3311/PPch.7582
Lo, S.F., T.D. Ho, Y. Liu, M. Jiang, K. Hsieh, K. Chen, L. Yu, M. Lee, C. Chen, T. Huang, M. Kojima, H. Sakakibara, L. Chen and S. Yu, 2017. Ectopic expression of specific GA2 oxidase mutants promotes yield and stress tolerance in rice. Plant Biotechnol. J.15(7):850–864. 10.1111/pbi.12681
Malhotra-Kumar, S., K. Haccuria, M. Michiels, M Ieven, C. Poyart, W. Hryniewicz, and H. Goossens, 2008. Current trends in rapid diagnostics for Methicillin Resistance Staphylococcus aureus and glycopeptides resistant Enterococcus species. J. Clin. Microbiol. 46(5):1577-1587.
1128/JCM.00326-08
Maor, Y., M. Hagin, N. Belausov, N. Keller, D. Ben-David, and G. Rahav, 2009. Clinical features of heteroresistant vancomycin-intermediate Staphylococcus aureus bacteremia versus those of methicillin-resistant S. aureus bacteremia. Journal of Infectious Diseases. 199(5): 619-624. 10.1086/596629
Marchese, A., G. Balistreri, E. Tonoli, E. A. Debbia, and G.C. Schito, 2000. Heterogeneous vancomycin resistance in methicillin-resistant Staphylococcus aureus strains isolated in a large Italian hospital. Journal of Clinical Microbiology. 38(2): 866-869. 10.1128/jcm.38.2.866-869.2000
Moore, M.R., F. Perdreau-Remington, and H.F. Chambers, 2003. Vancomycin treatment failure associated with heterogeneous vancomycin-intermediate Staphylococcus aureus in a patient with endocarditis and in the rabbit model of endocarditis. Antimicrobial Agents and Chemotherapy. 47(4): 1262-1266. 10.1128/AAC.47.4.1262-1266.2003
Quave, C.L., L.R. Plano, and B.C. Bennett, 2011. Quorum sensing inhibitors of Staphylococcus aureus from Italian medicinal plants. Planta medica. 77(2): 188-195. 10.1055/s-0030-1250145
Rahman, M.Z., 2014. Antimicrobial compounds from leaf extracts of Jatropha curcas, Psidium guajava, and Andrographis paniculata. The Scientific World Journal. 2014(635240): 1-8.
https://doi.org/10.1155/2014/635240
Reverdy, M., S. Jarraud, S. Bohin-Duhreux, E. Buret, P. Girardo, G. Lina, F. Vandenesch, and J. Etienne, 2001. Incidence of Staphylococcus aureus with reduced susceptibility to glycopeptides in two French hospitals. Clinical microbiology and infection. 7(5): 267-272.https://doi.org/10.1046/j.1198-743x.2001.00256.x
Rose, W. E., S. N. Leonard, K. L. Rossi, G. W. Kaatz, and M. J. Rybak, 2009. Impact of inoculum size and heterogeneous vancomycin-intermediate Staphylococcus aureus (hVISA) on vancomycin activity and emergence of VISA in an in vitro pharmacodynamic model. Antimicrobial Agents and Chemotherapy. 53(2): 805-807. 10.1128/AAC.01009-08
Sajith Khan A.K., P.J. Shetty, L.Y. Sarayu. A. Chidambaram, and R. Ranganathan, 2012. Detection of mecA gene of methicillin-resistant Staphylococcus aureus by polymerase chain reaction. International Journal of Health and Rehabilitation Sciences. 1(2): 64-68.
5455/ijhrs.000000011
Salmerón-Manzano, E., J.A. Garrido-Cardenas, and F. Manzano-Agugliaro, 2020. Worldwide research trends on medicinal plants. International Journal of Environmental Research and Public Health, 17(10): 3376. https://doi.org/10.3390/ijerph17103376
Sancak, B., S. Ercis, D. Menemenlioğlu, S. Çolakoğlu, and G. Hasçelik, 2005. Methicillin-resistant Staphylococcus aureus heterogeneously resistant to vancomycin in a Turkish University Hospital. Journal of Antimicrobial Chemotherapy. 56(3): 519-523 10.1093/jac/dki272
Shaaban, M.T., M.F. Ghaly, and S.M. Fahmi, 2021. Antibacterial activities of hexadecanoic acid methyl ester and green‐synthesized silver nanoparticles against multidrug‐resistant bacteria. Journal of Basic Microbiology. 61(6): 557-568.
1002/jobm.202100061
Shabani, Z., and A. Sayadi, 2014. The antimicrobial in vitro effects of different concentrations of some plant extracts including tamarisk, march, acetone and mango kernel. Journal of Applied Pharmaceutical Science. 4(5): 75-79.
7324/JAPS.2014.40514
Sharifi, A., A. Mohammadzadeh, T. Zahraei Salehi, and P. Mahmoodi, 2018. Antibacterial, antibiofilm and antiquorum sensing effects of Thymus daenensis and Satureja hortensis essential oils against Staphylococcus aureus isolates. Journal of Applied Microbiology. 124(2): 379-388. 10.1111/jam.13639
Van Griethuysen, A., A. Van't Veen, A. Buiting, T. Walsh and J. Kluytmans, 2003. High percentage of methicillin-resistant Staphylococcus aureus isolates with reduced susceptibility to glycopeptides in the Netherlands. Journal of Clinical Microbiology. 41(6): 2487-2491. 10.1128/JCM.41.6.2487-2491.2003
Vattem, D., K. Mihalik, S. Crixell, and R. McLean, 2007. Dietary phytochemicals as quorum sensing inhibitors. Fitoterapia. 78(4): 302-310. 10.1016/j.fitote.2007.03.009
Wright, J.S., G.L. Lyon, E. A. George, T.W. Muir, and R.P. Novick, 2004. Hydrophobic interactions drive ligand-receptor recognition for activation and inhibition of staphylococcal quorum sensing. Proceedings of the National Academy of Sciences. 101(46): 16168-16173. 10.1073/pnas.0404039101
Yassin, H.Y., A.K. Melconian and S.S. Mahmood, 2022. Prevalence of exfoliative toxin genes among clinical isolates of staphylococcus aureus in Iraq. Iraqi Journal of Agricultural Sciences. 53(2), 465-470. https://doi.org/10.36103/ijas.v53i2.1554
Zhang, S., X. Sun, W. Chang, Y. Dai and X. Ma, 2015. Systematic review and meta-analysis of the epidemiology of vancomycin-intermediate and heterogeneous vancomycin-intermediate Staphylococcus aureus isolates. PloS One. 10(8): e0136082.
1371/journal.pone.0136082
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