Planta Med 2010; 76(1): 47-52
DOI: 10.1055/s-0029-1185947
Pharmacology
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Ceanothane and Lupane Type Triterpenes from Zizyphus joazeiro – An Anti-Staphylococcal Evaluation[*]

Ivana Correa Ramos Leal1 , Kátia Regina Netto dos Santos2 , Ivaldo Itabaiana Júnior1 , Octávio Augusto Ceva Antunes4 , Andrea Porzel3 , Ludger Wessjohann3 , Ricardo Machado Kuster1
  • 1Núcleo de Pesquisas de Produtos Naturais, Bloco H, Centro de Ciências da Saúde, Ilha do Fundão, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
  • 2Instituto de Microbiologia Prof. Paulo de Góes, Bloco J, Centro de Ciências da Saúde, Ilha do Fundão – Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
  • 3Department of Bioorganic Chemistry, Leibniz Institute of Plant Biochemistry, Halle/Saale, Germany
  • 4Departamento de Química Inorgânica, Bloco A, Centro de Tecnologia, Ilha do Fundão – Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
Further Information

Publication History

received January 2, 2009 revised June 10, 2009

accepted June 16, 2009

Publication Date:
28 July 2009 (online)

Abstract

The present paper describes the phytochemical and anti-staphylococcal activity investigation of the dichloromethane extract of the Brazilian plant Zizyphus joazeiro Mart. The purification steps were guided by bioassays against 17 bacterial strains of clinical sources, including methicillin-resistant (MRSA) and ‐sensitive (MSSA) Staphylococcus aureus as well as MRSA (ATCC 33591) and MSSA (ATCC 29213) reference strains. One of the more active fractions is comprised of three lupane-type triterpenes, the methylbetulinate (1) as well as the known betulinic (2) and alphitolic (3) acids and, for the first time in the Z. joazeiro, two ceanothane type triterpenes, the methylceanothate (4) and the epigouanic acid A (5). These substances were assayed against one clinical (PVL+) and the reference strains of S. aureus as well as the ATTC 12228 strain of S. epidermidis, in concentrations that varied from 128 to 0.125 µg/mL in order to establish the minimum inhibitory concentration (MIC) of the drugs. The minimum bactericide concentration (MBC) was also evaluated to distinguish the bactericidal from bacteriostatic activity of the crude fractions and single compounds. Compounds 3 and 4 possess the highest antibacterial activity. They inhibit all bacteria tested at 32 µg/mL and 16 µg/mL, respectively, while the other compounds showed no activity at 128 µg/mL. In contrast to single compounds, the triterpenoid fraction showed bactericidal activity at 256 µg/mL. Structural elucidations are based on 1D and 2D NMR spectroscopy as well as HR‐FT‐ICR‐MS experiments.

1 Dedication: This paper is dedicated to Professor Octavio A. C. Antunes, in memory of his wide interdisciplinary interests.

References

  • 1 Schühly W, Heilmann J, Çalis I, Sticher O. New triterpenoids with antibacterial activity from Zizyphus joazeiro.  Planta Med. 1999;  65 740-743
  • 2 Nunes P H, Marinho L C, Nunes M L, Soares E O. Antipyretic activity of an aqueous extract of Zizyphus joazeiro Mart. (Rhamnaceae).  Braz J Med Biol Res. 1987;  20 599-601
  • 3 Chambers H F. The changing epidemiology of Staphylococcus aureus?.  Emerg Infect Dis. 2001;  7 178-182
  • 4 Maranan C M, Moreira B, Boyle-Vavra S, Daum R S. Antimicrobial resistance in Staphylococci epidemiology, molecular mechanisms, and clinical relevance.  Infect Dis Clin North Am. 1997;  4 813-849
  • 5 Genestier A L, Michallet M C, Prévost G, Bellot G, Chalabreysse L, Peyrol S, Thivolet F, Etienne J, Lina G, Vallette F M, Vandenesch F, Genestier L. Staphylococcus aureus Panton-Valentine leukocidin directly targets mitochondria and induces Bax-independent apoptosis of human neutrophils.  J Clin Invest. 2005;  115 3117-3127
  • 6 Costa S F, Miceli M H, Anaissie E J. Mucosa or skin as source of coagulase-negative staphylococcal bacteraemia?.  Lancet Infect Dis. 2004;  4 278-286
  • 7 Von Eiff C, Peters G, Heilmann C. Pathogenesis of infections due to coagulase-negative staphylococci.  Lancet Infect Dis. 2002;  2 677-685
  • 8 Bannerman T L. Staphylococcus, Micrococcus, and other catalase-positive cocci that grow aerobically, 8th edition. Murray PR, Baron EJ, Jorgensen JH, Pfaller MA, Yolken RH Manual of clinical microbiology. Washington; ASM Press 2003: 384-404
  • 9 Clinical and Laboratory Standards Institute .Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically. Approved standards: M7-A6. Wayne, Pennsylvania; CLSI 2003
  • 10 Machado T B, Leal I CR, Amaral A CF, Santos K RN, Silva M G, Kuster R M. Antimicrobial ellagitannin of Punica granatum fruits.  J Braz Chem Soc. 2002;  13 606-610
  • 11 Machado T B, Leal I CR, Kuster R M, Amaral A CF, Kokis V, Silva M G, Santos K RN. Brazilian phytopharmaceuticals – evaluation against hospital bacteria.  Phytother Res. 2005;  19 519-525
  • 12 Pereira E M, Machado T B, Leal I CR, Jesus D M, Damaso C RA, Pinto A V, Giambiagi-de-Marval M, Kuster R M, Santos K RN. Tabebuia avellanedae naphthoquinones: activity against methicillin-resistant staphylococcal strains, cytotoxic activity and in vivo dermal irritability analysis.  Ann Clin Microbiol Antimicrob. 2006;  5 5
  • 13 Giacomelli S R, Maldaner G, Stücker C, Marasciulo C, Schmidt J, Wessjohann L, Dalcol I I, Morel A F. Triterpenoids from Gouania ulmifolia.  Planta Med. 2007;  73 499-501
  • 14 Suksamrarn S, Panseeta P, Kunchanawatia S, Distaporn T, Ruktasing S, Suksamrarn A. Ceanothane- and lupane-type triterpenes with antiplasmodial and antimycobacterial activities from Zizyphus cambodiana. .  Chem Pharm Bull. 2006;  54 535-537
  • 15 Li X C, Cai L, Wu C D. Antimicrobial compounds from Ceanothus americanus against oral pathogens.  Phytochemistry. 1997;  46 97-102
  • 16 Eade R A, Grant P K, Mcgrath M JA, Simes J JH, Wootton M. The stereochemistry of ceanothic acid.  Chem Commun. 1967;  1204
  • 17 Aguierre M C, Delporte C, Backhouse N, Eraso S, Letelier M E, Cassels B K, Silva X, Alegria S, Negrete R. Topical anti-inflamatory activity of 2-α-hydroxypentacyclic triterpene acids from the leaves of Ugni molinae.  Bioorg Med Chem. 2006;  14 5673-5677
  • 18 Chatterjee P, Kouzi S A, Pezzuto J M, Hamann M T. Biotransformation of the antimelanoma agent betulinic acid by Bacillus megaterium ATCC 13368.  Appl Envir Microbiol. 2000;  66 3850-3855
  • 19 Lee S-S, Shy S-N, Liu K C. Triterpenes from Paliurus Hemsleyanus.  Phytochemistry. 1997;  46 549-554

1 Dedication: This paper is dedicated to Professor Octavio A. C. Antunes, in memory of his wide interdisciplinary interests.

Dr. Ivana Correa Ramos Leal

Núcleo de Pesquisas de Produtos Naturais – NPPN
Bloco H
Laboratório H-30 (Sub-solo)
Centro de Ciências da Saúde
Universidade Federal do Rio de Janeiro, UFRJ

Ilha do Fundão 21921-590

Rio de Janeiro – RJ

Brazil

Phone: + 55 21 25 62 67 95

Email: ivanafarma@yahoo.com.br

>