期刊论文详细信息
BMC Complementary and Alternative Medicine
In vitro effect of bergamot (Citrus bergamia) juice against cagA-positive and-negative clinical isolates of Helicobacter pylori
Michele Navarra1  Giuseppina Mandalari1  Santa Cirmi1  Nadia Ferlazzo1  Carlo Bisignano2  Angela Filocamo1 
[1] Dipartimento di Scienze del Farmaco e Prodotti per la Salute, University of Messina, Viale Annunziata, 98168, Messina, Italy;Dipartimento di Scienze Biologiche e Ambientali, University of Messina, Sal. Sperone 31, Messina, 98166, Italy
关键词: Complementary and alternative medicines;    Synergism;    Antibiotic resistance;    Natural products;    Citrus bergamia;    Antimicrobial;    H. pylori;    Bergamot;   
Others  :  1221537
DOI  :  10.1186/s12906-015-0769-2
 received in 2015-02-05, accepted in 2015-07-07,  发布年份 2015
PDF
【 摘 要 】

Background

Helicobacter pylori infection has been associated with chronic gastritis, peptic ulcer and gastric carcinoma as over half of the world's population is colonized with this gram-negative bacterium. Due to the increasing antibiotic resistance, its eradication rates fails in a great portion of patients. A number of studies showed that molecules largely distributed in commonly consumed fruits and vegetables may have antimicrobial activity. The aim of the present study was to investigate the effect of bergamot juice (BJ) against Helicobacter pylori in vitro. The potential therapeutic combination between BJ and the antibiotics amoxicillin (AMX), clarithromycin (CLA) and metronidazole (MTZ) has also been evaluated.

Methods

The minimum inhibitory concentration (MIC) of BJ, AMX, CLA and MTZ against 2 ATCC and 32 clinical isolates of H. pylori was assayed according to CLSI. The checkerboard method was used to determine the efficacy of the association BJ with the three reference antibiotics.

Killing curves were performed on the two cagA-positive ATCC strains of H. pylori (ATCC 43504 and ATCC 49503), on the clinical isolate cagA-positive HP6 strain of H. pylori and on the clinical isolate cagA-negative HP61 strain of H. pylori.

Results

BJ (2.5 %, v/v) inhibited the growth of 50 % of the H. pylori clinical isolates, whereas 5 % (v/v) inhibited 90 %. AMX was the most effective antibiotic against the reference strains and the clinical isolates, followed by CLA and MTZ. In the combination assays, synergism was observed between BJ and AMX and between BJ and MTZ against both the reference strains and the clinical isolates. Indifference was observed between BJ and CLA.

Conclusions

BJ was effective in vitro against H. pylori and the genotype status of the clinical strains may have an impact on its susceptibility. The synergistic combination of BJ and antibiotics could be used to prevent or treat resistance.

【 授权许可】

   
2015 Filocamo et al.

【 预 览 】
附件列表
Files Size Format View
20150802011441653.pdf 748KB PDF download
Fig. 2. 31KB Image download
Fig. 1. 32KB Image download
【 图 表 】

Fig. 1.

Fig. 2.

【 参考文献 】
  • [1]Covacci A, Telford JL, Del Giudice G, Parsonnet J, Rappuoli R. Helicobacter pylori virulence and genetic geography. Science. 1999; 284(5418):1328-33.
  • [2]Momtaz H, Souod N, Dabiri H. Comparison of the virulence factors of Helicobacter pylori isolated in stomach and saliva in Iran. Am J Med Sci. 2010; 340(5):345-9.
  • [3]Hunt RH, Xiao SD, Megraud F, Leon-Barua R, Bazzoli F, van der Merwe S, et al. Helicobacter pylori in developing countries. World Gastroenterology Organisation Global Guideline. J Gastrointestin Liver Dis. 2011;20(3):299–304.
  • [4]Atherton JC, Cao P, Peek RM, Tummuru MK, Blaser MJ, Cover TL. Mosaicism in vacuolating cytotoxin alleles of Helicobacter pylori. Association of specific vacA types with cytotoxin production and peptic ulceration. J Biol Chem. 1995; 270(30):17771-7.
  • [5]Akopyants NS, Clifton SW, Kersulyte D, Crabtree JE, Youree BE, Reece CA, et al. Analyses of the cag pathogenicity island of Helicobacter pylori. Mol Microbiol. 1998;28(1):37–53.
  • [6]Peek Jr RM, Blaser MJ, Mays DJ, Forsyth MH, Cover TL, Song SY, et al. Helicobacter pylori strain-specific genotypes and modulation of the gastric epithelial cell cycle. Cancer Res. 1999;59(24):6124–31.
  • [7]Rudi J, Kolb C, Maiwald M, Kuck D, Sieg A, Galle PR, et al. Diversity of Helicobacter pylori vacA and cagA genes and relationship to VacA and CagA protein expression, cytotoxin production, and associated diseases. J Clin Microbiol. 1998;36(4):944–8.
  • [8]Mishra S. Is Helicobacter pylori good or bad? Eur J Clin Microbiol Infect Dis. 2013; 32(3):301-4.
  • [9]Graham DY. Therapy of Helicobacter pylori: current status and issues. Gastroenterology. 2000; 118(2 Suppl 1):S2-8.
  • [10]Gerrits MM, van Vliet AH, Kuipers EJ, Kusters JG. Helicobacter pylori and antimicrobial resistance: molecular mechanisms and clinical implications. Lancet Infect Dis. 2006; 6(11):699-709.
  • [11]Fukai T, Marumo A, Kaitou K, Kanda T, Terada S, Nomura T. Anti-Helicobacter pylori flavonoids from licorice extract. Life Sci. 2002; 71(12):1449-63.
  • [12]Shin JE, Kim JM, Bae EA, Hyun YJ, Kim DH. In vitro inhibitory effect of flavonoids on growth, infection and vacuolation of Helicobacter pylori. Planta Med. 2005; 71(3):197-201.
  • [13]Nostro A, Cellini L, Di Bartolomeo S, Di Campli E, Grande R, Cannatelli MA, et al. Antibacterial effect of plant extracts against Helicobacter pylori. Phytother Res. 2005;19(3):198–202.
  • [14]Bisignano C, Filocamo A, La Camera E, Zummo S, Fera MT, Mandalari G. Antibacterial activities of almond skins on cagA-positive and-negative clinical isolates of Helicobacter pylori. BMC Microbiol. 2013; 13:103. BioMed Central Full Text
  • [15]Navarra M, Mannucci C, Delbo M, Calapai G. Citrus bergamia essential oil: from basic research to clinical application. Front Pharmacol. 2015; 6:36.
  • [16]Delle Monache S, Sanita P, Trapasso E, Ursino MR, Dugo P, Russo M, et al. Mechanisms Underlying the Anti-Tumoral Effects of Citrus bergamia Juice. PLoS One. 2013;8(4):e61484.
  • [17]Navarra M, Ursino MR, Ferlazzo N, Russo M, Schumacher U, Valentiner U. Effect of Citrus bergamia juice on human neuroblastoma cells in vitro and in metastatic xenograft models. Fitoterapia. 2014; 95:83-92.
  • [18]Visalli G, Ferlazzo N, Cirmi S, Campiglia P, Gangemi S, Di Pietro A, et al. Bergamot Juice Extract Inhibits Proliferation by Inducing Apoptosis in Human Colon Cancer Cells. Anti-Cancer Agent Me. 2014;14(10):1402–13.
  • [19]Ferlazzo N, Visalli G, Smeriglio A, Cirmi S, Lombardo GE, Campiglia P, et al. Flavonoid fraction of orange and bergamot juice protect human lung epithelial cells from hydrogen peroxide-induced oxidative stress. Evid-Based Compl Altern Med. 2015;1: 14.
  • [20]Risitano R, Curro M, Cirmi S, Ferlazzo N, Campiglia P, Caccamo D, et al. Flavonoid Fraction of Bergamot Juice Reduces LPS-Induced Inflammatory Response through SIRT1-Mediated NF-kappa B Inhibition in THP-1 Monocytes. PLoS One. 2014;9(9):e107431.0.
  • [21]Impellizzeri D, Bruschetta G, Di Paola R, Ahmad A, Campolo M, Cuzzocrea S, et al. The anti-inflammatory and antioxidant effects of bergamot juice extract (BJe) in an experimental model of inflammatory bowel disease. Clin Nutr. 2014. doi:10.1016/j.clnu.2014.11.012.
  • [22]Marino A, Paterniti I, Cordaro M, Morabito R, Campolo M, Navarra M, et al. Role of natural antioxidants and potential use of bergamot in treating rheumatoid arthritis. Pharma Nutrition. 2015;3(2):53–9.
  • [23]Mollace V, Sacco I, Janda E, Malara C, Ventrice D, Colica C, et al. Hypolipemic and hypoglycaemic activity of bergamot polyphenols: From animal models to human studies. Fitoterapia. 2011;82(3):309–16.
  • [24]Miceli N, Mondello MR, Monforte MT, Sdrafkakis V, Dugo P, Crupi ML, et al. Hypolipidemic effects of Citrus bergamia Risso et Poieteau juice in rats fed a hypercholesterolemic diet. J Agric Food Chem. 2007;55(26):10671–7.
  • [25]Clinical and Laboratory Standards Institute. Performance standards for antimicrobial susceptibility testing; twentieth informational supplement. M100-S22. Wayne: PA: CLSI; 2012.
  • [26]White RL, Burgess DS, Manduru M, Bosso JA. Comparison of three different in vitro methods of detecting synergy: time-kill, checkerboard, and E test. Antimicrob Agents Chemother. 1996;40(8):1914–8.
  • [27]Filocamo A, Bisignano C, D'Arrigo M, Ginestra G, Mandalari G, Galati EM. Norfloxacin and ursolic acid: in vitro association and postantibiotic effect against Staphylococcus aureus. Lett Appl Microbiol. 2011;53(2):193–7.
  • [28]Trombetta D, Castelli F, Sarpietro MG, Venuti V, Cristani M, Daniele C, et al. Mechanisms of antibacterial action of three monoterpenes. Antimicrob Agents Chemother. 2005;49(6):2474–8.
  • [29]Xiao ZP, Shi DH, Li HQ, Zhang LN, Xu C, Zhu HL. Polyphenols based on isoflavones as inhibitors of Helicobacter pylori urease.Bioorgan Med Chem. 2007;15(11):3703–10.
  • [30]Ansari FL, Umbreen S, Hussain L, Makhmoor T, Nawaz SA, Lodhi MA, et al. Syntheses and biological activities of chalcone and 1,5-benzothiazepine derivatives: promising new free-radical scavengers, and esterase, urease, and alpha-glucosidase inhibitors. Chem Biodivers. 2005;2(4):487–96.
  • [31]Tombola F, Campello S, De Luca L, Ruggiero P, Del Giudice G, Papini E, et al. Plant polyphenols inhibit VacA, a toxin secreted by the gastric pathogen Helicobacter pylori. FEBS Lett. 2003;543(1–3):184–9.32.
  • [32]Mandalari G, Bennett RN, Bisignano G, Trombetta D, Saija A, Faulds CB, et al. Antimicrobial activity of flavonoids extracted from bergamot (Citrus bergamia Risso) peel, a byproduct of the essential oil industry. J Appl Microbiol. 2007;103(6):2056–64.
  文献评价指标  
  下载次数:28次 浏览次数:10次