In vitro bactericidal activity of recombinant human β-defensin-3 against pathogenic bacterial strains in human tooth root canal

被引:27
作者
Song, Wei [1 ]
Shi, Yong [1 ]
Xiao, Mingzhen [1 ]
Lu, Hong [1 ]
Qu, Tiejun [1 ]
Li, Ping [1 ]
Wu, Gang [1 ]
Tian, Yu [1 ]
机构
[1] Fourth Mil Med Univ, Sch Stomatol, Xian 710032, Peoples R China
关键词
Human beta-defensin-3; Recombinant protein; Antimicrobial activity; Pathogenic microbes; Infected root canals; ANTIMICROBIAL PEPTIDES; STAPHYLOCOCCUS-AUREUS; CALCIUM HYDROXIDE; DENTINAL TUBULES; BETA-DEFENSINS; ORAL BACTERIA; RESISTANT; FUNGI; SUSCEPTIBILITY; CYTOTOXICITY;
D O I
10.1016/j.ijantimicag.2008.05.022
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Human beta-defensin-3 (HBD3), an endogenous antimicrobial peptide, has strong broad-spectrum antimicrobial activity. This study aimed to obtain recombinant HBD3 (rHBD3) and to test the hypothesis that the antimicrobial characteristics of HBD3 may offer an advantage over conventional medicine in reducing intracanal bacteria. Genetic engineering was used to obtain active rHBD3 and analysis revealed that it exhibited a broad spectrum of antibacterial activity at low micromolar concentrations against not only Staphylococcus aureus and Escherichia coli but also against some critical pathogenic microbes in infected root canals, including Fusobacterium nucleatum, Prevotella melaninogenica, Peptostreptococcus anaerobius, Streptococcus mutans, Actinomyces naeslundii, Enterococcus faecalis and Candida albicans. In an in vitro antibacterial experiment, rHBD3 significantly eliminated pathogenic bacteria in root canals. The ratio of bacterial death was up to 98%. We conclude that HBD3 has the potential to eliminate bacteria effectively and rapidly in the local microenvironment of the root canal system and that it may contribute to successful endodontic treatment. (C) 2008 Elsevier B. V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:237 / 243
页数:7
相关论文
共 35 条
  • [1] Human β-defensin 2 is a salt-sensitive peptide antibiotic expressed in human lung
    Bals, R
    Wang, XR
    Wu, ZR
    Freeman, T
    Bafna, V
    Zasloff, M
    Wilson, JM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (05) : 874 - 880
  • [2] Human beta-defensin-3: A promising antimicrobial peptide
    Batoni, G.
    Maisetta, G.
    Esin, S.
    Campa, M.
    [J]. MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2006, 6 (10) : 1063 - 1073
  • [3] Lipid-specific membrane activity of human β-defensin-3
    Böhling, A
    Hagge, SO
    Roes, S
    Podschun, R
    Sahly, H
    Harder, J
    Schröder, JM
    Grötzinger, J
    Seydel, U
    Gutsmann, T
    [J]. BIOCHEMISTRY, 2006, 45 (17) : 5663 - 5670
  • [4] Comparison of the antimicrobial activity of six Irrigants on primary endodontic pathogens
    Carson, KR
    Goodell, GG
    McClanahan, SB
    [J]. JOURNAL OF ENDODONTICS, 2005, 31 (06) : 471 - 473
  • [5] THE ROLE OF INTRACANAL MEDICATION IN ROOT-CANAL TREATMENT
    CHONG, BS
    FORD, TRP
    [J]. INTERNATIONAL ENDODONTIC JOURNAL, 1992, 25 (02) : 97 - 106
  • [6] DALE BA, 2006, BMC ORAL HLTH S1, V15, pS13
  • [7] A REVIEW OF CALCIUM HYDROXIDE
    FOREMAN, PC
    BARNES, IE
    [J]. INTERNATIONAL ENDODONTIC JOURNAL, 1990, 23 (06) : 283 - 297
  • [8] Detection of bacteria in endodontic samples by polymerase chain reaction assays and association with defined clinical signs in Italian patients
    Foschi, F
    Cavrini, F
    Montebugnoli, L
    Stashenko, P
    Sambri, V
    Prati, C
    [J]. ORAL MICROBIOLOGY AND IMMUNOLOGY, 2005, 20 (05): : 289 - 295
  • [9] Molecular detection of Enterococcus species in root canals of therapy-resistant endodontic infections
    Fouad, AF
    Zerella, J
    Barry, J
    Spångberg, LS
    [J]. ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTOLOGY, 2005, 99 (01): : 112 - 118
  • [10] Defensins and other antimicrobial peptides: A historical perspective and an update
    Ganz, T
    [J]. COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING, 2005, 8 (03) : 209 - 217