Oral Antimicrobial Peptides and Biological Control of Caries
© Dale et al.. 2006
Published: 15 June 2006
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© Dale et al.. 2006
Published: 15 June 2006
The presence of antimicrobial peptides (AMPs) in saliva may be a biological factor that contributes to susceptibility or resistance to caries. This manuscript will review AMPs in saliva, consider their antimicrobial and immunomodulatory functions, and evaluate their potential role in the oral cavity for protection of the tooth surface as well as the oral mucosa. These AMPs are made in salivary gland and duct cells and have broad antimicrobial activity. Alpha-defensins and LL37 are also released by neutrophils into the gingival crevicular fluid. Both sources may account for their presence in saliva. A recent study in middle school children aimed to determine a possible correlation between caries prevalence in children and salivary concentrations of the antimicrobial peptides human beta-defensin-3 (hBD-3), the cathelicidin, LL37, and the alpha-defensins. The levels of these AMPs were highly variable in the population. While levels of LL37 and hBD-3 did not correlate with caries experience, the mean alpha-defensin level was significantly higher in children with no caries than in children with caries (p < 0.005). We conclude that several types of AMPs that may have a role in oral health are present in unstimulated saliva. Low salivary levels of alpha-defensin may represent a biological factor that contributes to caries susceptibility. Our observation could lead to new ways to prevent caries and to a new tool for caries risk assessment.
This manuscript will review oral AMPs, consider their role as genetically inherited factors that may be among the biological controls that influence caries risk, briefly describe a study of AMPs in children with and without caries, and discuss the potential utility of one particular AMP in caries risk assessment and prevention.
Oral AMPs provide a first line of defense against a wide spectrum of pathogens [1–3]. Members of the three main AMP families are found in the oral cavity. These are defined by biochemical and structural characteristics: 1) α-helical peptides without cysteine (the cathelicidin, LL37) ; 2) peptides with three disulphide bonds (the α- and β- defensins) [1, 5]; and 3) peptides with an unusually high proportion of specific amino acids; for example, the histatins .
Recent research suggests the importance of the defensins and the cathelicidin LL37 as antibacterial agents in the oral cavity , while histatins are primarily antifungal agents . The human β-defensins (hBDs) are widely expressed in oral tissues including gingival epithelium [8, 9], salivary glands and ducts and saliva [10, 11]. The neutrophil alpha-defensins, (human neutrophil peptides 1–3 (HNP1–3)), are one of the mechanisms for non-oxidative microbial killing  and are found in gingival crevicular fluid . The human cathelicidin peptide, LL37, is in neutrophils, inflamed epithelia, submandibular salivary glands and saliva [13, 14].
With antimicrobial peptides now strongly implicated in the host innate immune response, in particular in the oral cavity (reviewed by Dale and Fredericks, Ganz) [7, 1], their availability in unstimulated saliva implies their potential role in protecting tooth structure from bacterially-induced caries, either by direct killing or by prevention of biofilm formation on the tooth surface.
Antimicrobial Peptides in Saliva
Major Oral Microbial Targets
Alpha-defensins HNP 1–4
Neutrophils, gingival sulcus, sites of inflammation, salivary duct cells
Antibacterial, antifungal, antiviral. Present in GCF
Candida albicans HIV S. mutans (poor)
(Raj et al., 2000; Zhang et al., 2002) [43, 44]
Neutrophils, gingival sulcus, salivary glands and ducts
S. mutans F. nucleatum A. actinomycetemcomitans Capnocytophaga sputigena
(Ouhara et al., 2005; Tanaka et al., 2000) [17, 19]
Beta-defensins hBD1 hBD2 hBD3
Epithelia, salivary ducts
Antibacterial, antifungal, antiviral. Part of the protective barrier function of epithelium. Secreted
hBD1: Poor antibacterial hBD2, hBD3: S. mutans S. sanguis F. nucleatum P. gingivalis Candida albicans HIV
(Joly et al., 2004; Maisetta et al., 2003; Quinones-Mateu et al., 2003)[15, 20, 18]
(Oppenheim et al., 1988) 
The amount of AMPs expressed in saliva varies between individuals. This has been previously demonstrated for alpha- and beta-defensins, histatin, and proline-rich proteins [6, 22, 23]. Our initial studies in children show that the levels of these peptides in unstimulated saliva vary greatly between individuals, even when differences in total salivary protein are considered (see below). The large variation in concentration of defensins in saliva and in their mRNA in oral tissues could be attributed to the organization of their genes. The genes for the alpha- and beta-defensins lie in a cluster on human chromosome 8. Several genes in this region can occur as multiple repeated copies. This is known as copy number polymorphism [24, 25]. We do not yet know if individuals with multiple copies of a particular gene, for example, HNP1, make more of the protein, but this seems quite likely. In other words, individual differences in the amount of alpha- and beta-defensins may be genetically determined. In contrast, there is only one copy of the LL37 gene, which is located on chromosome 3.
There is also evidence for genetically determined factors in susceptibility to caries. Anecdotal evidence suggests individual differences in caries experience in children even within the same family . These individual differences suggest that biological factors, which may be genetically determined, have a role in caries resistance and susceptibility. Studies of twins offer the strongest evidence to date for the importance of biologically inherited factors contributing to caries susceptibility [27–29]. Twins show significantly greater similarity of caries experience in monozygotic (MZ, identical) than in dizygotic (DZ, fraternal) twins (reviewed by Shuler) .
Salivary constituents are potential candidates as biological factors influencing caries risk. Many salivary protein components, such as proline-rich glycoprotein, mucins, immunoglobulins, agglutinin, lactoferrin, cystatins and lysozyme are thought to have a role in defense in the oral cavity . Numerous studies have investigated the correlation among these salivary proteins and glycoproteins and caries experience, but no studies have shown reliable association between a single salivary component and caries experience [32, 33]. The expression of AMPs in saliva and throughout the oral cavity suggests that they may have a role in protecting tooth structure from caries as well as protecting oral mucosa. Several reasons for this proposal are 1) AMPs have broad antimicrobial activity; 2) their action is synergystic with other antimicrobials in saliva; co-expression of cathelicidins and defensins with peptides such as histatin, proline-rich proteins may enhance antimicrobial function; 3) they stimulate the acquired immune system and could function to enhance IgA production as well as IgG production ; 4) these AMPs may function to keep overall bacteria in check and to help prevent biofilm formation. Thus, oral AMPs may provide a natural antibiotic barrier.
To investigate the possible relationship between AMP levels in saliva and caries experience, we conducted a study in middle school children located in a rural area in Washington state . One hundred and forty-nine children (88 females, 61 males) participated in the study. All children were between 11 and 15 years of age. Most of the population was Hispanic with some Native Americans and Caucasians. A brief health history survey was completed by parents of the subjects. Oral examinations were performed by trained calibrated clinicians using standardized procedures. Overall, the children were healthy with 92% having no history of major illness or disease. The study was conducted with permission of school officials and informed consent of subjects and parents obtained through an educational session and written bilingual consent in accordance with a protocol approved by the University of Washington Institutional Review Board. A brief health history was taken, and unstimulated saliva samples collected and stored in a frozen state for later analysis. Examiners were instructed to rank subjects separately for active caries and for filled surfaces as 0, no decayed or filled surfaces; 1, mild (1–2 affected surfaces); 2, moderate (3–6 affected surfaces); and 3, severe (>6 affected surfaces). Final caries experience score was determined as the sum of the scores for active decay and filled surfaces. Fifty-three subjects (36%) had no decay, 37 (24%), 39 (27%), and 20 (13%) had caries scores of 1, 2, and 3 or greater, respectively.
For analysis, saliva samples were thawed and cleared by centrifugation twice at 15,000 rpm for 10 min. Cleared saliva samples were assayed for total protein concentration by the BCA assay (Pierce Inc., Rockford, IL, USA) and for alpha-defensin HNP1–3 ELISA assay according to manufacturer's instructions (HyCult Biotechnology, Uden, Netherlands). This assay measures HNP1, 2, and 3 because the antibody does not distinguish between these closely related peptides. Aliquots of cleared saliva were acid-extracted for assay of LL37 and hBD3 by slot immunoblot analysis (LL37 by assay from Phoenix Pharmaceuticals Inc., Belmont, CA and hBD3 using polyclonal antibody from Orbigen Inc, San Diego, CA). The mean protein concentration of unstimulated saliva samples was 1633 ± 908 μg/ml (range from 421 to 7052 μg/ml). This value agrees with previously reported total protein concentration for this age group . The salivary protein concentration showed no correlation with age, gender, or caries score. Antimicrobial peptide (AMP) concentrations were in the μg/ml range. AMP levels were also normalized to the protein concentration in whole saliva for each sample. HNP1–3, hBD3 and LL37 all showed extensive variation in concentration in our population, even when normalized to total salivary protein levels. Mean values for HNP1–3, hBD3 and LL37 were 0.94, 0.73, 3.36 μg/ml, respectively, with the range extending 10-fold up and down from the mean. The concentration of AMPs in unstimulated saliva of children has not been previously reported, although normal adults have a mean value of 0.8 μg/ml HNP .
Caries Free Children by HNP score
Caries Free (n)
Caries Free (%)
There were two major findings from our study. First, there was extensive variation in AMP levels between individuals; levels varied by 100 fold from the lowest to highest even when adjusted for total salivary protein. Second, the level of alpha-defensins HNP1–3 was inversely correlated with caries (Figure 2). Our findings suggest that low salivary levels of HNP1–3 may contribute to caries susceptibility and could be a new and useful measure of the risk for caries in children.
The most obvious source for salivary AMPs is secretion by salivary gland and duct cells. LL-37 and beta-defensins are expressed in salivary glands [7, 8, 10, 13, 14]. In addition, we have shown HNP1–3 by immunohistochemistry in submandibular salivary duct cells . The submandibular glands are the major source of unstimulated saliva, suggesting that these cells may be a source of AMPs in saliva. However, an important alternative source for HNP1–3 and LL37 are the neutrophils that migrate into the oral cavity via gingival crevicular fluid. In normal individuals it has been estimated that 30,000 neutrophils per minute enter the oral cavity via this route through the junctional epithelium surrounding the teeth . This flow of neutrophils is required for periodontal health, and defects in neutrophil function and chemotatsis are associated with early onset periodontal disease in children [38, 39]. Our findings suggest that this flow of neutrophils may also be important for protection from caries.
HNP1–3 in saliva could contribute to resistance to caries by direct antimicrobial properties (either alone or in combination with other saliva components) or by preventing biofilm formation on the surface of the tooth via its ability to bind bacterial outer membranes. The AMP levels found in saliva in this study are in the range of effective antimicrobial function for beta-defensins vs. S. mutans  although effectiveness of HNPs against S. mutans has not been reported. The low ionic strength in saliva is conducive to antimicrobial activity and thus may impact the flora of the oral cavity and exert a beneficial effect on dental health. In addition, alpha- and beta-defensins as well as LL37 have other immunomodulatory and chemoattractant effects, and individuals with high expression may benefit from these effects. The inverse correlation of HNP1–3 with caries experience suggests its possible protective effect. Conversely, low levels of HNP1–3 may result in increased susceptibility to caries.
We have many follow-up questions. Based on our study design, we cannot yet determine if the level of salivary alpha-defensin is predictive of future caries, but we have shown that children with caries have significantly lower levels of alpha-defensins based both on their concentration in saliva and their relationship to total salivary protein. Can this finding be replicated in younger children? This is important because of the need for new approaches for caries risk assessment in young children, when preventive measures are likely to have the greatest impact. Identifying those children who are at highest risk for disease will enable limited resources to be targeted toward individualized, aggressive and pro-active interventions to prevent caries. Can the level of AMPs be replicated over time? Could alpha-defensins be used therapeutically or in a prospective manner in mouthwash or toothpaste or chewing gum? Is the effect primarily an antimicrobial effect, or is it also due to immunomodulatory functions of these peptides? Do children with very low alpha-defensin levels have different flora than children with high alpha-defensin levels? Is there a relationship between the intensity of tooth brushing and levels of salivary AMPs? Perhaps vigorous brushing could stimulate outflow of the neutrophils via the gingival sulcus. In addition, the junctional epithelium is innervated with substance P expressing nerve fibers. Irritation provoked by vigorous brushing might stimulate local release of this neuropeptide, which in turn has profound chemoattractive activity for neutrophils [40, 41].
The prediction of caries risk has been of long-standing interest and is very important for development of new preventive strategies. This is especially significant for young children and for children with special health care needs. Saliva is an easily available fluid which can be collected non-invasively and used to measure and monitor the risk for caries . The assay for HNP1–3 is easy to perform and can be done using less than 0.2 ml crude whole saliva. Low salivary levels of alpha-defensins (HNP1–3) could be a new and useful measure of the risk for caries in children. Future studies could lead to development of means to enhance endogenous oral peptide expression, to utilization of these peptides as therapeutics, and to the development of a simple test for clinical evaluation of caries risk.
This study was supported by grants from the national Institute of Dental and Craniofacial Research via the Northwest/Alaska Center for Research to Reduce Oral Health Disparities (U54 DE14254).
This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.