Anti-microbial Effects of Rhizome Extracts of Alpinia officinarum Hance against VRE (vancomycin-resistant enterococci) and Other Pathogenic Microorganisms

  • Received : 2011.04.17
  • Accepted : 2011.06.10
  • Published : 2011.06.30

Abstract

The purpose of this investigation was to extract the bioactive agents from Alpinia officinarum Hance. The methanol with ethylacetate extracts alone and combined were examined for their activities against VRE (vancomycin-resistant enterococci) and pathogenic yeast in vitro. The incidence of infections caused by VRE and other pathogenic microorganisms and the importance of using novel synergistic drug combinations has become important. Previously, we reported the antimicrobial effects of the butanol extract from Lonicera japonica and have evaluated combinations of solvent extracts, with a focus on the MeOH and EtOAc extracts from A. officinarum. In the present study, enhanced inhibitory effects were achieved by employing a combination of the two solvent extracts. The MeOH and EtOAc combination was especially effective against four VRE strains: E. faecalis (K-10-22), E. faecaium (K-11-212), E. faecalis (K-10-57) and E. faecalis (K-10-361) with MIC values of 12.5, 12.5, 6.25 and 25 ${\mu}g/ml$, respectively. Thus, the combination was more effective than other antibiotics such as kanamycin, gentamicin or tetracycline against bacteria including E. coli, Staphylococcus aureus, and Micrococcus luteus. In addition, the combination was effective against yeasts such as Candida albicans, Candida tropicalis and Cryptococcus neoformans.

Keywords

References

  1. Aeschlimann, J.R., Zerves, M.J., and Raybak, J., Treatment of vancomycin-resistant Enterococcus faecium with RP5900 (quinupristindalfipristin) administered by intermittent or continuous infusion, alone or in combination with doxycycline, in an in vitro pharmacodynamic infection model with simulated endocardial vegetations. Antimicrob. Agents Chemother. 42, 2710-2717 (1998).
  2. Arvind, M., Dhople, A.M., and Kenji, N., In vivo susceptibility of Mycobacterium leprae to sitafloxacin (DU-6859a), either singly or in combination with rifampicin analogues. Int. J. Antimicrob. Agents. 21, 251-255 (2002).
  3. Athamaprasangsa, S., Buntrarongroj, U., Dampawan, P., Ongkavoranan, N., Rukachaisirikul, V., and Sethijinda, S., A 1,7-diarylheptanoids from Alpinia conchigera. Phytochemistry 37, 871-873 (1994). https://doi.org/10.1016/S0031-9422(00)90374-1
  4. Claeson, P., Pongprayyoon, U., Sematong, T., Tuchinda, and P., and Reutrakul, V., Non-phenolic linear diarylheptanoids from Curcuma xanthorrhiza. A novel type of topical anti-inflammator agents. Structure-activity relationship. Planta Med. 62, 236-240 (1996). https://doi.org/10.1055/s-2006-957867
  5. Frandgerg, E., Petesson, C., Lundgren, L.N., and Schunrer, J., Streptomyces halstedii K122 produces the antifungal compounds bafilomycin B1 and C1. Can. J. Microbiol. 46, 753-758 (2000). https://doi.org/10.1139/w00-050
  6. Grey, D., Hamiliton - Miller, J.M., and Brumfitt, W., Combined action of sulphamethoxazole and trimethoprim against clinically - isolated sulphonamide - resistant bacteria. Chemotherapy 25, 296-302 (1979). https://doi.org/10.1159/000237854
  7. Iotaka, H., Morita, H., Midorikawa, I., Aiyama, R., and Morita, M., Diarylheptanoids from the rhizome of Alpinia officinarum Hance. Chem. Pharm. Bull. 33, 4889-4893 (1985). https://doi.org/10.1248/cpb.33.4889
  8. King, T.C., Schlessinger, D., and Krogstad, D.J., The assessment of antimicrobial combinations. Rev. Infect. Dis. 3, 627-633 (1981). https://doi.org/10.1093/clinids/3.3.627
  9. Lambert RJ, Johnston MD, Hanlon GW, Denyer, SP., Theory of antimicrobial combinations: biocide mixtures - synergy or addition? J. Appl. Microbiol. 94, 747-759(2003). https://doi.org/10.1046/j.1365-2672.2003.01908.x
  10. Kim, W.J., Weinstein, R.A., and Hayden, M.K., The changing molecular epidemiology and establishment of endemicity of vancomycin resistance enterococci at one hospital over a 6-year period. J. Infect. Dis. 179, 163-171 (1999). https://doi.org/10.1086/314564
  11. Livornese, L.L., Dias, S., and Samuel, C., Hospital-acquired infection with vancomycin- resistant Enterococcus faecium transmitted by electronic ear prove thermometer. Infect. Control Hosp. Epidemiol. 18, 771-773 (1997). https://doi.org/10.1086/647535
  12. Matsuda, H., Ando, S., Kato, T., Morikawa, T., and Yoshikawa, M., Inhibitors from the rhizomes of Alpinia officinarum on production of nitric oxide in lipopolysaccharide-activated macrophages and the structure requirement of diarylheptanoids for the activity. Bioorg. Med. Chem. 14, 138-142 (2006). https://doi.org/10.1016/j.bmc.2005.08.003
  13. National Committee for Clinical Laboratory Standards. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically; approved standard M7-A3. Villanova, PA:NCCLS (1997).
  14. Newman, D.J., Cragg, G.M., and Snader, K.M., Natural products as sources of new drugs over the period. Nat. Prod. 66, 1022-1037 (2003). https://doi.org/10.1021/np030096l
  15. Niku-Paavola, M.L., Laitila, A., Mattila-Sandholm, T., and Haikara, A., New types of antimicrobial compounds produced by Lactobacillus plantarum. J. Appl. Microbiol. 87, 29-35 (1999). https://doi.org/10.1046/j.1365-2672.1999.00786.x
  16. Rhee, K.H. and Lee, K.H., Antimicrobial effects of Lonicera japonica against gram positive and gram negative anaerobic bacteria. Nat. Prod. Sci. 17, 23-25 (2011).
  17. Saito, H., Tomioka, H., Sato, K., and Dekio, S., Therapuetic efficacy of benzoxazinorifamycin, KRM-1648, in combination with other antimicrobial against Mycobacterium lepraae infection induced in nude mice. Int. J. Lepr. Other. Mycobact. Dis. 62, 43-47 (1994).
  18. Shlaes, D.M., Etter, L., and Gutmann, L., Synergistic killing of vancomycin-resistant enterococci of classes A, B, and C by combinations of vancomycin, penicillin, and gentamicin. Antimicrob. Agents Chemother. 35, 776-779 (1991). https://doi.org/10.1128/AAC.35.4.776
  19. Yokosuka, A., Mimaki, Y., Sakagami, H., and Sashida, Y., New diarylheptanoids and diarylheptanoid glucosides from the rhizomes of Tacca chantrieri and their cytotoxic activity. J. Nat. Prod. 65, 283-289 (2002). https://doi.org/10.1021/np010470m
  20. Yang, Y., Kinoshita, K., Koyama, K., Takahashi, T., and Kondo, S., Watanabe K. Structure-antiemetic-activity of some diarylheptanoids and their analogues. Phytomedicine 9, 146-152 (2002). https://doi.org/10.1078/0944-7113-00091