EFFECT OF APC ON KILLING OF STAPHYLOCOCCUS AUREUS BY OXIDATIVE STRESS AGENTS

Authors

  • Noor Faradilla Abdullah Department of Medical Laboratory Technology, Faculty of Health Sciences, Universiti Teknologi MARA, Puncak Alam, Selangor, Malaysia
  • Roslinah Mohamad Hussain Department of Medical Laboratory Technology, Faculty of Health Sciences, Universiti Teknologi MARA, Puncak Alam, Selangor, Malaysia
  • Zulkhairi Amom Department of Medical Laboratory Technology, Faculty of Health Sciences, Universiti Teknologi MARA, Puncak Alam, Selangor, Malaysia

DOI:

https://doi.org/10.11113/jt.v78.8573

Keywords:

Allylpyrocatechol, oxidative stress

Abstract

Allylpyrocatechol (APC) which consists of benzene ring with hydroxyl groups, is a major phenolic constituent in Piper betle L. leaves extract.  Antimicrobial activity of APC against S. aureus (ATCC 25923) was tested by determination of Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) using the broth microdilution method. In addition, oxidative stress resistance assay was performed to determine the antioxidant activity of APC against hydrogen peroxide (10 mM), diamide(10 mM) and methyl viologen (10 mM) in relation to its toxicity against S. aureus. MIC and MBC values of APC against S. aureus were both 2000 µg/ml. Exposure of S. aureus cells to hydrogen peroxide, diamide and methyl viologen for 1 hour caused reduction of cells with percentage of survival of 87%, 15% and 10% respectively. Treatment of S. aureus cells with APC was found to increase killing compared to treatment with oxidative stress agent alone. Further research is recommended to investigate the effect of oxidative stress induced by hydrogen peroxide, diamide and methyl viologen on the production of reactive oxygen species (ROS) and antioxidant enzyme activities in S. aureus to elucidate the mechanism involved. This study potentially leads to discover and develop new antibiotic agents against all types of MRSA and in particular, novel phytochemicals of antimicrobial potential from natural products.

References

Chakraborty, D. And Shah, B. 2011. Antimicrobial, Antioxidative And Antihemolytic Activity Of Piper Betle Leaf Extracts. Int. J. Pharm. Pharm. Sci. 3(1923).

Shimeld, A. T., & L. A. Rodgers. 1999. Essentials Of Diagnostic Microbiology. New York: Delmar Publishers.

Roslinah, M. N., M. H., Nurul Adzuani, M. D. & Noor Anis Nadhirah. 2013. Piper Betle Ethanolic Extract Reduces Neutrophil Scavenging Ability And Possibly Catalase Activity In S. Aureus. Int J. Pharm. Sci. Rev. Res. 22: 135-40.

Nalina, Z. H. A., T. A. R., 2007. The Crude Aqueous Extract Of Piper Betle L. And Its Antibacterial Effect Towards Streptococcus Mutans. Am. J. Biotechnol. Biochem. 3: 10-15.

Sarkar, D., Kundu S., De S., Hariharan C., Saha P., Manna A., Chattopadhyay S., And Chatterjee M., 2013. The Antioxidant Activity Of Allylpyrocatechol Is Mediated Via Decreased Generation Of Free Radicals Along With Escalation Of Antioxidant Mechanisms. Phytother. Res. 27(3): 324-9.

Poole, K. 2012. Bacterial Stress Responses As Determinants Of Antimicrobial Resistance., J. Antimicrob. Chemother. 67, 9: 2069-89.

Chung, P. Y., Chung, L. Y., And Navaratnam, P. 2013. Identification, By Gene Expression Profiling Analysis, Of Novel Gene Targets In Staphylococcus Aureus Treated With Betulinaldehyde. Res. Microbiol. 164(4): 319-26.

Sharma, S., Khan, I. A., Ali, I., Ali, F., Kumar, M., Kumar, A., Johri, R. K., Abdullah, S. T., Bani, S., Pandey, A., Suri, K. A., Gupta, B. D., Satti, N. K., Dutt, P., And Qazi, G. N. 2009. Evaluation Of The Antimicrobial, Antioxidant, And Anti-Inflammatory Activities Of Hydroxychavicol For Its Potential Use As An Oral Care Agent. Antimicrob. Agents Chemother. 53(1): 216-22

Jesonbabu, J., Spandana, N., And Lakshmi, K. A. 2011. The Potential Activity Of Hydroxychavicol Against Pathogenic Bacteria, J. Bacteriol. Parasitol. 02(06): 2-5.

Abdullah, N. F. And Mohamad Hussain, R. 2014. Isolation Of Allylpyrocatechol From Piper Betle L. Leaves By Using High Performance Liquid Chromatography. J. Liq. Chromatogr. Relat. Technol.

Bhattacharya, S., Subramanian, M., Roychowdhury, S., Bauri, A. K., Kamat, J. P., Chattopadhyay, S., And Bandyopadhyay, S. K. 2005. Radioprotective Property Of The Ethanolic Extract Of Piper Betel Leaf. J. Radiat. Res. 46(2): 165-71.

Sarkar, D., Saha, P., Gamre, S., Bhattacharjee, S., Hariharan, C., Ganguly, S., Sen, R., Mandal, G., Chattopadhyay, S., Majumdar, S., And Chatterjee, M., 2008. Anti-Inflammatory Effect Of Allylpyrocatechol In LPS-Induced Macrophages Is Mediated By Suppression Of Inos And COX-2 Via The NF-Kappab Pathway. Int. Immunopharmacol. 8(9): 1264-71.

Kehrer, J. P. 2000. The Haber-Weiss Reaction And Mechanisms Of Toxicity. Toxicology. 149: 43-50.

Abrashev, M., Krumova, R., Dishliska, E., Eneva, V., Engibarov, R., Abrashev, S. I., & Angelova. 2011. Differential Effect Of Paraquat And Hydrogen Peroxide On The Oxidative Stress Response In Vibrio Cholerae Non 01 26/06. Biotechnol. Biotechnol. Eq. 25(4): 72-76.

Kosower, N. S. And Kosower, E. M. 1995. Biothiols Part A Monothiols And Dithiols, Protein Thiols, And Thiyl Radicals, Elsevier. 251.

Hasset, M. S., D. J. & Cohen. 1989. Bacterial Adaptation To Oxidative Stress: Implications For Pathogenesis And Interaction With Phagocytic Cells. FASEB J. 3: 2574-2582.

National Committee For Clinical Laboratory Standards. 1999. National Committee Of Clinical Laboratory Standards Performance Standards For Antimicrobial Disk Susceptibility Testing. Wayne, PA.

Halliwell, J. M. C., B & Gutteridge. 1984. Oxygen Toxicity, Oxygen Radicals, Transition Metals And Disease. Biochem. J. 219: 1-14.

Lynch, M. And Kuramitsu, H. 2000. Expression And Role Of Superoxide Dismutases (SOD) In Pathogenic Bacteria. Microbes Infect. 2(10): 1245-55.

Rawat, M., Jheys., And Av-Gay Y. 2003. Identification And Characterization Of A Diamide Sensitive Mutant Of Mycobacterium Smegmatis. FEMS Microbiol. Lett. 220(2): 161-169.

Hibberd, J. A., Berget, K. A., Warner, P. B., & Fuchs, H. R. 1978. Role Of Glutathione In Reversing The Deleterious Effects Of A Thiol-Oxidizing Agent In Escherichia Coli, J. Bacteriol. 133(3): 1150-1155.

Bus, J. S., Aust, S. D., And Gibson, J. E. 1976. Paraquat Toxicity: Proposed Mechanism Of Action Involving Lipid Peroxidation. Environ. Health Perspect. 16: 139-46.

Suntres, Z. 2002. Role Of Antioxidants In Paraquat Toxicity. Toxicology. 180(1): 65-77.

Peterson, T., Fairshter, E., Morrison, R., & Cesario, J. 1981. Effects Of The Herbicide Paraquat Dichloride On Bacteria Of Human Origin. Appl. Environ. Microbiol. 327-328.

Nakonieczna, J., Michta, E., Rybicka, M., Grinholc, M., Gwizdek-Wiśniewska, A., And Bielawski, K. P. 2010. Superoxide Dismutase Is Upregulated In Staphylococcus Aureus Following Protoporphyrin-Mediated Photodynamic Inactivation And Does Not Directly Influence The Response To Photodynamic Treatment. BMC Microbiol. 10(1): 323.

Paterson, G. K., Blue, C. E., And Mitchell, T. J. 2006. An Operon In Streptococcus Pneumoniae Containing A Putative Alkylhydroperoxidase D Homologue Contributes To Virulence And The Response To Oxidative Stress. Microb. Pathog. 40(4): 152-160.

Sunanda Kundu, S. C. & M. C., Asis Bala, Parasar Ghosh, Debanjan Mukhopadhyay, Anupam Mitra, Avijit Sarkar, Ajay K. Bauri, Alakendu Ghosh. 2011. Attenuation Of Oxidative Stress By Allylpyrocatechol In Synovial Cellular Infiltrate Of Patients With Rheumatoid Arthritis. Free Radic. Res. 45(5): 518-526.

Downloads

Published

2016-05-09

How to Cite

EFFECT OF APC ON KILLING OF STAPHYLOCOCCUS AUREUS BY OXIDATIVE STRESS AGENTS. (2016). Jurnal Teknologi, 78(5-5). https://doi.org/10.11113/jt.v78.8573