Evaluation of Some Material to inhibit Biofilm Formed by Acinetobacter baumannii Isolates

Main Article Content

Noor Hussein Ahmad
Ghada A. Mohammad

Abstract

The study has included the ability of Acinetobacter baumannii (isolated from clinical infections and hospital environment) to form a biofilm and investigated the possibility of inhibition this biofilm by using some materials: EDTA, five amino acids and five plant extracts.


The results showed that all isolates of A.baumannii had a good ability to form the biofilm (100%). Four isolates which had strong former of  biofilm which were selected as well as a standard isolate (A. baumannii ATCC19606). The inhibitory effect on biofilm formation was investigated. EDTA had a good inhibitory effect, also, all amino acids showed good inhibitory activity , with the best inhibition in Glutamic acid at a concentration of 50 mM, while plant extracts varied in their inhibition ratio to inhibit the biofilm, turmeric, cloves and rosemary had a good inhibitory effect, Bay leaf has the ability to inhibit the biofilm formation but less than others, while the plant extract of the Myrtle did not show any inhibition activity.

Article Details

How to Cite
Noor Hussein Ahmad, & Ghada A. Mohammad. (2019). Evaluation of Some Material to inhibit Biofilm Formed by Acinetobacter baumannii Isolates. Tikrit Journal of Pure Science, 24(4), 19–24. https://doi.org/10.25130/tjps.v24i4.391
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References

[1] Jung, J., & Park, W. (2015). Acinetobacter species as model microorganisms in environmental microbiology: current state and perspectives. Applied microbiology and biotechnology, 99(6), 2533-2548.

[2] Lee, C. R., Lee, J. H., Park, M., Park, K. S., Bae, I. K., Kim, Y. B. & Lee, S. H. (2017). Biology of Acinetobacter baumannii: pathogenesis, antibiotic resistance mechanisms, and prospective treatment options. Frontiers in cellular and infection microbiology, 7(1): 55-57.

[3] Vasudevan, R. (2014). Biofilms: microbial cities of scientific significance. J Microbiol Exp, 1(3), 00014.

[4] Gentile, V., Frangipani, E., Bonchi, C., Minandri, F., Runci, F., & Visca, P. (2014). Iron and Acinetobacter baumannii biofilm formation. Pathogens, 3(3), 704-719.

[5] Liziana, J. A., Marchal, A., Serrano, Ú., Velasco, D., & Espinosa-Urgel, M. (2013). Use of plant extracts to block bacterial biofilm formation.

[6] AL_Jubori SS, AL_Kadmy IM, Jassim Al_Ani Z. (2016) Emergence of multidrug resistance (MDR) Acinetobacter baumannii isolated from Iraqi hospitals. Adv Environm Biol.10(1):265–76. [7] Lee, H. W., Koh, Y. M., Kim, J., Lee, J. C., Lee, Y. C., Seol, S. Y., & Kim, J. (2008). Capacity of multidrug‐resistant clinical isolates of Acinetobacter baumannii to form biofilm and adhere to epithelial cell surfaces. Clinical microbiology and infection, 14(1), 49-54.

[8] Sasirekha, B., Megha, D. M., Chandra, M. S., & Soujanya, R. (2015). Study on effect of different plant extracts on microbial biofilms. Asian Journal of Biotechnology, 7(1), 1-12.

[9] AL-Kadmy, I. M., Ali, A. N. M., Salman, I. M. A., & Khazaal, S. S. (2018). Molecular characterization of Acinetobacter baumannii isolated from Iraqi hospital environment. New microbes and new infections, 21(1), 51-57.

[10] Al-Dulaimi AA, Al-Taai HR, Al-Bajlany SM.(2017) Virulence Factors of Acinetobacter baumannii isolated from different clinical specimens in Baquba. Diyala Journal of Pure Sciences. 13(1): 13-26.

[11] Fallah, A., Rezaee, M. A., Hasani, A., Barhaghi, M. H. S., & Kafil, H. S. (2017). Frequency of bap and cpaA virulence genes in drug resistant clinical isolates of Acinetobacter baumannii and their role in biofilm formation. Iranian journal of basic medical sciences, 20(8), 849.

[12] Abdi-Ali A, Hendiani S, Mohammadi P, Gharavi S. (2014). Assessment of biofilm formation and resistance to imipenem and ciprofloxacin among clinical isolates of Acinetobacter baumannii in Tehran. Jundishapur J Microbiol. 7(1): 8606-8608.

[13] Farzan Modarresi, Omid Azizi, Mohammad Reza Shakibaie, Mohammad Motamedifar, Shahla Mansouri. (2016). Cloning and expression of quorum sensing N-Acyl-homoserine synthase (luxI) gene detected in Acinetobacter baumannii. Iran J Microbiol. 8 (1): 1-7.

[14] Hassan A, Usman J, Kaleem F, Omair M, Khalid A, Iqbal M. (2011). Evaluation of different detection methods of biofilm formation in the clinical isolates. Braz J Infect Dis. 15(4): 305-11.

[15] Banin, E., Brady, K. M., & Greenberg, E. P. (2006). Chelator-induced dispersal and killing of Pseudomonas aeruginosa cells in a biofilm. Applied and environmental microbiology, 72(3), 2064-2069.

[16] Gawad, W. E., Helmy, O. M., Tawakkol, W. M., & Hashem, A. M. (2017). Effect of EDTA on biofilm formation and antibiotic susceptibility of multidrug resistant uropathogenic Escherichia coli clinical isolates in Egypt.

[17] Sadekuzzaman, M., Yang, S., Mizan, M. F. R., & Ha, S. D. (2015). Current and recent advanced strategies for combating biofilms. Comprehensive Reviews in Food Science and Food Safety, 14(4), 491-509 [18] Ahmad, M. F., & Abas, H. M. (2014). Effect of some amino acids on biofilm for Staphylococcus aureus. Diyala Agricultural Sciences Journal, 6(2), 27-38.

[19] Cava, F., Lam, H., De Pedro, M. A., & Waldor, M. K. (2011). Emerging knowledge of regulatory roles of D-amino acids in bacteria. Cellular and Molecular Life Sciences, 68(5), 817-831.

[20] Kolodkin-Gal, I., Romero, D., Cao, S., Clardy, J., Kolter, R., & Losick, R. (2010). D-amino acids trigger biofilm disassembly. Science, 328(5978), 627-629. [21] Kali, A., Devaraj Bhuvaneshwar, P., Charles, M. V., & Seetha, K. S. (2016). Antibacterial synergy of curcumin with antibiotics against biofilm producing clinical bacterial isolates. Journal of basic and clinical pharmacy, 7(3), 93-96.

[22] Lou, Z., Zhang, J., Chen, W., & Hossen, M. J.(2015). Biofilm inhibitor and its inhibition mechanism: Plant derived agents. European academic research,3(7):7748-7769.