Implications of oral biofilms in medically at risk persons☆

2012-10-27 09:20KevinYipRogerSmles
THE JOURNAL OF BIOMEDICAL RESEARCH 2012年1期

Kevin H.-K. Yip, Roger J. Smles

aSchool of Dentistry, Charles Sturt University, Orange, New South Wales, Australia;bCollege of Stomatology, Nanjing Medical University, Nanjing, Jiangsu 210029 China;cSchool of Dentistry, Faculty of Health Sciences, the University of Adelaide, Adelaide, Australia.Received 07 July 2011, Revised 23 September 2011, Accepted 15 November 2011

INTRODUCTION

The significant relationship between oral and general health is increasingly recognized by both medical and dental health care personnel[1]. Persons with compromised general health from chronic diseases, and perhaps also their associated treatments, are at high risk for oral disease. In addition, as has been reviewed elsewhere[1-3], several epidemiological and many clinical reports have linked, to varying degrees, oral infections and their products of inflammation with increasing rates of septicemia and several cardiovascular, central nervous system, respiratory and skeletal infections.Poor glycemic control in diabetics, and low-weight preterm births perhaps may also be associated with poor plaque control and resultant poor oral health.Unlike other body environments, the nonshedding surfaces of teeth, restorations and prostheses allow oral biofilms to maintain their attachments if left undisturbed[3].

Investigations of the links between oral and systemic diseases have focused largely on oral biofilm associated with chronic periodontitis, and on damage to the highly vascular periodontal tissues. There have been few investigations on the possible association of systemic diseases with other oral diseases and related biofilms such as carious tissue, mucosal and nonvital root canal biofilms. In particular, in persons at high risk for dental caries, investigation of possible links between carious tissue biofilms and systemic diseases should be pursued.

The purposes of the present article are to review the association between oral biofilms and systemic dis-ease, to review relevant information regarding carious tissue biofilms and possible systemic disease, and to emphasize the critical importance of effective preventive oral care for reducing the potential for oral and systemic diseases.

THE RELATIONSHIP BETWEEN ORAL AND GENERAL HEALTH

Medically compromised at risk persons

Because of their deteriorating health, increasing numbers of elderly persons will reside in long-term care institutions. The presence of physical and mental disabilities, compounded by communal living, leads frequently to the neglect of oral hygiene and to major changes in diets with an increased ingestion of refined sugars. These changes, in addition to impaired saliva flow and buffering capacity arising from hyposalivation caused by many medications and dehydration,greatly increase the risk of plaque-related dental caries, periodontal disease, candidosis and associated morbidity in old age[4]. Moreover, the negative impacts of poor oral health extend well beyond the mouth[5,6].For example, pathogenic microorganisms that are frequently found in dental biofilms have been associated with coronary heart disease, and with chronic obstructive pulmonary disease and aspiration pneumonia in particular[7-14]. The latter was reported to be the leading cause of death from nosocomial infections in longterm care facilities[15].

Apart from the institutionalized, other medically at risk groups of persons include those with impaired host defense systems and pre-existing respiratory conditions who are at risk for hospital-acquired and ventilator-associated pneumonia[16]. As in nursing homes,elderly persons in hospitals also have an increased risk for pneumonia, which is not unusual and again is the leading cause of death from nosocomial infections[17].

Bacterial biofilms

Bacterial biofilms consist of dynamic, complex three-dimensional aggregations of heterogeneous microorganisms and their sticky extracellular polysaccharide matrix, which adheres to moist mucosal and tooth surfaces and to foreign surfaces such as indwelling catheters and tubes, and dental prostheses.Biofilms are associated with, for example, brochiectasis, chronic rhinosinusitis, tonsillitis and otitis media,recurrent urinary tract infections, chronic periodontitis and dental caries[18]. Thick, persistent biofilms protect embedded slow-growing microorganisms from physical dislodgement and the effective actions of antibodies, phagocytes, and antimicrobials and antibiotics,which may then promote selective bacterial resistance[18,19]. In some instances, biofilm aggregates may reside in a mucus layer or within the cytoplasm of epithelial cells that also could protect the microorganisms.

Oral biofilms and systemic diseases

A recent review of possible systemic diseases linked to chronic periodontal disease concluded that although there were definite epidemiological associations, particularly for cardiovascular disease and poor glycemic control in diabetics, the associations for other medical conditions such as preterm births were not always strong[12]. Another recent systematic review and metaanalysis confirmed previous meta-analytical studies that periodontal disease is an independent, though relatively weak, risk factor or marker for coronary heart disease[14].

A microorganism found in dental plaque, Streptococcus sanguinis, has been reported to correlate with coronary heart disease in a Chinese population[20], and another microorganism, Strep. mutans, has been detected in the heart valves and blood of persons with infective endocarditis[21]. A recent study that evaluated the DNA serotype distribution of Strep. mutans,detected the microorganism in approximately 64% of defective heart valves and atheromatous plaques, and in 95% of dental plaques obtained from patients undergoing cardiovascular surgery[13]. High agreement was found in particular for the single serotype e of Strep. mutans from dental plaques and from defective heart valves, which contrasted with the usual serotype c found in the dental plaques of healthy individuals[13].

Dental plaque also has long been implicated as an important biofilm reservoir for respiratory pathogens such as Staphylococcus aureus, enteric Gram-negative bacilli and Pseudomonas aeruginosa, especially in persons with poor oral and denture hygiene and who are at high risk for aspiration pneumonia[22,23]. Several studies have confirmed similar chromosomal DNA patterns present between microorganisms found in dental plaque, and subsequently in the lungs of many patients who developed ventilator-associated pneumonia[17,24-26].

The implication from these studies is that the control of pathogens in oral biofilms may prevent such microorganisms from reaching cardiovascular and pulmonary tissues, and from potentially causing or exacerbating existing diseases.

Oral biofilms from low and high caries risk persons

The treatment needs for high caries risk adults are approximately four times that of low caries risk adults,but current methods of prevention appear unable to effect a significant caries reduction[27]. Additionally,caries risk in the elderly is approximately twice that in children[28]. Of concern is the presence of possibly virulent pathogenic microorganisms from oral biofilms in persons having poor general health. A significantly increased risk for pneumonia has been observed in elderly persons with many carious teeth[29,30]. Another study also reported that adults with systemic lupus erythematosus and having large carious lesions were at a significantly higher risk (odds ratio 7.5)for pneumonia compared with a similar group of adults having much better oral health[31]. From a multivariate logistic regression analysis, the numbers of carious teeth, as well as increased periodontal disease and serum lipid levels, were found to be significantly associated with acute myocardial infarction[32].

Since high caries risk persons may be linked potentially with several systemic diseases, it is important to differentiate oral biofilms formed by low caries risk persons from oral biofilms formed by high caries risk persons that may contain possible virulent pathogens.Hence, the composition of oral biofilms in the initiation and progression of caries in low and high caries risk persons requires re-evaluation[33].

Though oral biofilms are found on intact tooth surfaces, they are also implicated in the etiology of one of the most prevalent diseases, namely, dental caries[34].The relationship between the microbiota in the biofilm and the demineralization of tooth surface suggests that certain species or combinations of species are more cariogenic than others, and that the dominance of single acidogenic species in particular is conducive to high caries activity[35].

Oral biofilms fromin vitromicrobial models

It is necessary to investigate oral biofilms more closely in an attempt to identify at different ages the pathogenic microorganisms that contribute to significant differences in caries risk (Fig. 1). Though in vivo studies of artificial caries have the advantage of the actual oral environment, in vitro studies of artificial caries can be advantageous because most of the oral environmental conditions and the microbiota can be controlled and changed[36]. When using an artificial mouth, the development of a four species consortia biofilm of oral bacteria in a bovine enamel and dentin model system successfully reproduced dentin caries[37].A further study using in vitro microbial models examined oral biofilm formed by a few known cariogenic oral microorganisms, and how they affected carbohydrate consumption and the demineralization of salivary protein-coated calcified tooth tissue[38]. Bacteria from human tooth root surface caries have also been used in an artificial mouth to investigate the effect of oral biofilms on calcified tooth tissue and restorative materials[39].

Fig. 1 Mature oral biofilms photographed at the same magnification on d5. A: From a low caries risk person (scale bar= 50 μm). B: From a high caries risk person, showing increased live bacteria concentrations compared with those in A. Live bacteria are stained fluorescent green by SYTOR 9 stain, and dead bacteria are stained fluorescent red by propidium iodide. Note the high density of the live and dead bacteria. (scale bar = 10 μm).

Fig. 2 FTIR spectra of sound and demineralized root surface dentin with 1-, 2-, and 3-bacterial culture species. A: Actino. israelii [NT6-2A], L: Lact. acidophilus[ND7-2A], and S: Strep. mutans [ND16-6A].

There are significant limitations when using traditional culture, direct microscopic and biochemical methods to identify oral bacteria. Not all bacteria are cultivable or have immunological characteristics that fit into the patterns of any known genus and species[46,47]. The use of the 16S ribosomal RNA gene in quantitative gene cloning and sequencing techniques has resulted in the reclassification and renaming of numerous bacterial genera and species and the identification of many novel bacteria. The oral cavity and the gastrointestinal tract have been the most significant sites for the discovery of potentially pathogenic novel species, including Strep. sinensis and many Prevotella species in saliva and dental plaque[46]. With at least 800 known bacterial species inhabiting the oral cavity,considerably more metagenomic research, including the use of pyrosequencing, is required to determine species significance in polymicrobial consortia infections[44,45,47].

The importance of effective preventive oral care

Institutionalized persons encounter substantial barriers to dental care compared to their independent peers[48]. These include cognitive and functional disabilities, transportation problems, financial costs and anxiety[48-50], compounded by a lack of professional interest from physicians, dentists and dental hygienists, and a lack of facilities to treat such institutionalized persons[51]. Increased tooth retention leads to increased dental calculus and periodontal disease, and increased numbers of coronal and root surface carious lesions[52]. Consequently, studies of elderly long-term care residents in nursing homes have continued to report an increasing need for urgent preventive dental services[53-56].

Immunosuppressive agents and head and neck tumor irradiation may result in severe damage to the oral mucosa and salivary glands, resulting in mucosal lesions that offer a portal for systemic infection[1]. Such treatments will compromise the normal protective mechanisms of the oral cavity, creating an ecological imbalance that allows the proliferation of opportunistic microorganisms, with possible life-threatening results. A thorough oral examination of all patients, and the elimination/reduction of all sources of infection and inflammation, should be done before any medical procedures that may result in, or be compromised by,oral bacteremias.

In several studies, the use of antimicrobials such as chlorhexidine, and the application of high concentration fluorides in high caries risk elderly persons either failed to show their effectiveness in the prevention of caries[57], or met with limited success[58-60]. Fortunately, the oral cavity is one of the few regions of the body where thick biofilms can be readily accessed and physically disrupted. Hence, a recent review found that the focused use of tooth brushing combined with chlorhexidine rinses and gels effectively reduced the prevalence of respiratory pathogens in dental biofilms,and the rate of pneumonia in persons at high risk by approximately 40%-50%[16]. Alternatively, essentialoils containing rinses also have been shown to be very effective for the long-term reduction of oral biofilms and, unlike chlorhexidine, without staining teeth and esthetic restorations, altering taste or forming supragingival calculi[61,62]. Additional preventive methods include the gentle use of electric tooth brushes and tongue scrapers, and the use of sugarless chewing gums and casein-derived pastes/cremes. It is essential also that adequate hydration and saliva flow be maintained.Good denture hygiene is also very important for reducing potential pathogens present in oral biofilms[63].

CONCLUSION

There is increasing evidence of the important relationship between oral biofilms and systemic diseases such as cardiovascular, central nervous system, respiratory and skeletal infections, and to nosocomial infections that are associated with a high morbidity in institutionalized and hospitalized elderly persons in particular. Microorganisms from oral biofilms have also been identified by DNA genotyping in defective heart valves and atheromatous plaques. Persons who have many, acute carious lesions caused by virulent microorganisms may be at a greater potential risk for several systemic diseases, particularly if their general health is poor. This possible high risk association requires further metagenomic and clinical research. The physical disruption of thick oral biofilms is necessary to allow the effective action of antimicrobials.

ACKNOWLEDGMENT

The assistance for the experience from Dr. Tong Zheng, Associate Professor in Environmental Engineering, University of Hong Kong is gratefully acknowledged.

[1]Rautemaa R, Lauhio A, Cullinan MP, Seymour GJ. Oral infections and systemic diseae – an emerging problem in medicine. Clin Microbiol Infect 2007;13:1041-7.

[2]Duval X, Leport C. Prophylaxis of infective endocarditis:current tendencies, continuing controversies. Lancet Infect Dis 2008; 8: 225-32.

[3]Parahitiyawa NB, Jin LJ, Leung WK, Yam WC, Samaranayake LP. Microbiology of odontogenic bacteremia:beyond endodcarditis. Clin Microbiol Rev 2009; 22: 46-64.

[4]Murtaugh CM, Kemper P, Spillman BC. The risk of nursing home use in later life. Med Care 1990; 28: 952-62.

[5]Nordström G. The impact of socio-medical factors and oral status on dietary intake in the eighth decade of life.Ageing 1990; 2: 371-85.

[6]Dorminval V, Budtz-Jørgensen E, Mojon P, Bruyere A,Rapin CH. Association between malnutrition, poor general health and oral dryness in hospitalized elderly patients. Ageing 1998; 27: 123-8.

[7]DeStefano F, Anda RF, Kahn HS, Williamson DF, Russell CM. Dental disease and risk of coronary heart disease and mortality. Br Med J 1993; 306: 688-91.

[8]Terpenning M, Bretz W, Lopatin D, Langmore S,Dominguez B, Loesche W. Bacterial colonisation of saliva and plaque in the elderly. Clin Infect Dis 1993; 16(S4): 314-6.

[9]Scannapieco FA, Mylotte JM. Relationship between periodontal disease and bacterial pneumonia. J Periodontol 1996; 67: 1114-22.

[10]Mojon P, Budtz-Jørgensen E, Michel J-P, Limeback H.Oral health and history of respiratory tract infection in frail institutionalised elders. Gerontology 1997; 14: 1-16.

[11]Scannapieco FA, Bush RB, Paju S. Associations between periodontal disease and risk for nosocomial bacterial pneumonia and chronic obstructive pulmonary disease.A systematic review. Ann Periodontol 2003; 8: 54-69.

[12]Cullin MP, Ford PJ, Seymour GJ. Periodontal disease and systemic health: current status. Aust Dent J 2009;54(S1):62-9.

[13]Nakano K, Nemoto H, Nomura R, Homma H, Yoshoka H, Shudo Y, et al. Serotype distribution of Streptococcus mutans a pathogen of dental caries in cardiovascular specimens from Japanese patients. J Med Microbiol 2007: 56: 551-6.

[14]Humphrey LL, Fu R, Buckley DI, Freeman M, Helfand M. Periodontal disease and coronary heart disease incidence: a systematic review and meta-analysis. J Gen Intern Med 2008; 23: 2079-86.

[15]Scheld WM, Mandell GL. Nosocomial pneumonia:Pathogenesis and recent advances and therapy. Rev Infect Dis 1991; 13: 743-51.

[16]Raghavendran K, Mylotte JM, Scannapieco FA. Nursing home-associated pneumonia, hospital-acquired pneumonia and ventilator-assisted pneumonia: the contribution of dental biofilms and periodontal inflammation. Periodontol 2000 2007; 44: 164-77.

[17]Pesola GR. Ventilator-associated pneumonia in institutionalized elders. Are teeth a reservoir for respiratory pathogens? Chest 2004; 126: 1401-3.

[18]Hall-Stoodley L, Stoodley P. Evolving concepts in biofilm infections. Cellular Microbiol 2009; 11: 1034-43.

[19]Gander S. Bacterial biofilms: Resistance to antimicrobial agents. J Antimicrob Chemother 1996; 37: 1047-50.

[20]Deng S, Chen H, Zhang W. The relationship between the Streptococcus sanguis group and coronary heart disease.Chinese J Dent Res (in Chinese)2002; 5: 65-9.

[21]Moreillon P, Que YA. Infective endocarditis. Lancet 2004: 363: 139-49.

[22]Russell SL, Boylan RJ, Kaslick RS, Scannapieco FA,Katz RV. Respiratory pathogen colonization of the dental plaque of institutionalized elders. Spec Care Dent 1999; 19: 128-34.

[23]Scannapieco FA. Pneumonia in nonambulatory patients.The role of oral bacteria and oral hygiene. J Am Dent Assoc 2006; 137(S): 21-5.

[24]El-Sohl AA, Pietrantoni C, Bhat A, Okada M, Zambon J, Aquilina A, et al. Colonization of dental plaques. A reservoir of respiratory pathogens for hospital-acquired pneumonia in institutionalized elders. Chest 2004; 126:1575-82.

[25]Didilescu AC, Skaug N, Marica C, Didilescu C. Respiratory pathogens in dental plaque of hospitalized patients with chronic lung diseases. Clin Oral Invest 2005;9:141-7.

[26]Heo S-M, Haase EM, Lesse AJ, Gill SR, Scannapieco FA. Genetic relationships between respiratory pathogens isolated from dental plaque and bronchoalveolar lavage fluid from patients in the intensive care unit undergoing mechanical ventilation. Clin Infect Dis 2008; 47: 1562-70.

[27]Rindal DB, Rush WA, Perrin NA, Maupome G, Bader JD. Outcomes associated with dentists’ risk assessment.Community Dent Oral Epidemiol 2006; 34: 381-6.

[28]Petersson GH, Fure S, Twetman S, Bratthall D. Comparing caries risk factors and risk profiles between children and elderly. Swed Dent J 2004; 28: 119-28.

[29]Langmore SE, Terpenning MS, Schork A, Chen Y, Murray JT, Lopatin D, et al. Predictors of aspiration pneumonia: how important is dysphagia? Dysphagia 1998;13: 69-81.

[30]Terpenning M, Taylor GW, Lopatin DE, Kerr CK,Dominguez BL, Loesche WJ. Aspiration pneumonia:dental and oral risk factors in an older veteran population. J Am Geriatr Soc 2001; 49: 557-63.

[31]Pascual-Ramos V, Hernández-Hernández C, Soto-Rojas AE, Celis-Aguilar E, Sánchez-Guerrero J. Association between dental caries and pneumonia in patients with systemic lupus erythematosus. J Rheumatol 2006; 33:1996-2002.

[32]Kaisare S, Rao J, Dubashi N. Periodontal disease as a risk factor for acute myocardial infarction. A case-control study in Goans highlighting a review of the literature. Br Dent J 2007; 203: E5; discussion 144-5.

[33]Beighton D. The complex oral microbiota of high risk individuals and groups and its role in the caries process.Community Dent Oral Epidemiol 2005; 33: 248-55.

[34]Kidd EAM, Fejerskov O. What constitutes dental caries? Histopathology of carious enamel and dentin related to the action of cariogenic biofilm. J Dent Res 2004;83(Spec No. C): 35-8.

[35]Nyvad B, Kilian M. Microflora associated with experimental root surface caries in humans. Infect Immun 1990; 58: 1628-33.

[36]Sissons CH. Artificial dental plaque biofilm model system. Adv Dent Res 1997; 11: 111-26.

[37]Shu M, Wong L, Miller JH, Sissons CH. Development of multi-species consortia biofilms of oral bacteria as an enamel and root caries model system. Arch Oral Biol 2000; 45: 27-40.

[38]Fontana M, Haider A, Gonzălez-Cebezas C. Caries lesion development and biofilm composition responses to varying demineralization times and sucrose exposures.Biofilm 2004; 1: 229-37.

[39]Tang GY, Yip HK, Cutress T, Samaranayake LP. Artificial mouth model systems and their contribution to caries research. J Dent 2003; 31: 161-71.

[40]Shen S, Samaranayake LP, Yip HK, Dyson JE. Bacterial and yeast flora of root surface caries in elderly, ethnic Chinese. Oral Dis 2002; 8: 207-17.

[41]Shen S, Samaranayake LP, Yip HK. Coaggregation profiles of microflora from root surface caries lesions. Arch Oral Biol 2005; 50: 23-32.

[42]Shen S, Samaranayake LP, Yip HK. In vitro growth, acidogenicity and cariogenicity of predominant bacteria in root caries. J Dent 2004; 32: 667-78.

[43]Yip HK, Guo J, Wong WHS. Incipient caries lesions on cementum by mono- and co-culture oral biofilms. J Dent 2007; 35: 377-82.

[44]Aas JA, Griffin AL, Dardis SR, Lee AM, Olsen I, Dewhirst FE, et al. Bacteria of dental caries in primary and permanent teeth in children and young adults. J Clin Microbiol 2008; 46: 1407-1417.

[45]Parahitiyawa NB, Scully C, Leung WK, Yam WC, Jin LJ, Samaranayake LP. Exploring the oral bacterial flora:current status and future directions. Oral Dis 2010; 16:136-145.

[46]Woo PCY, Lau SKP, Teng JLL, Tse H, Yuen K-Y. Then and now: use of 16S rDNA gene sequencing for bacterial identification and discovery of novel bacteria in clinical microbiology laboratories. Clin Microbiol Infect 2008;14: 908-934.

[47]Filoche S, Wong L, Sissons CH. Oral biofilms: emerging concepts in microbial ecology. J Dent Res 2010; 89:8-18.

[48]Dolan TA, Atchison KA. Implications of access, utilization and need for oral health care by the non-institutionalized and institutionalized elderly on the dental delivery system. J Dent Educ 1993; 57: 876-87.

[49]Kent GG, Blinkhorn AS. The Psychology of Dental Care.2nd edition. Bristol: John Wright, 1991: 55-121.

[50]Locker D, Liddell AM. Correlates of dental anxiety among older adults. J Dent Res 1991; 70: 198-203.

[51]Wyatt CC, MacEntee MI. Dental caries in chronically disabled elders. Spec Care Dent 1997; 17: 196-202.

[52]Joshi A, Douglass CW, Feldman H, Mitchell P, Jette A.Consequences of success: do more teeth translate into more disease and utilization? J Public Health Dent 1996;56: 190-7.

[53]Chalmers JM, Carter KD, Fuss JM, Spencer AJ, Hodge CP. Caries experience in existing and new nursing home residents in Adelaide, Australia. Gerodontol 2002; 19:30-40.

[54]Wardh I, Berggren U, Andersson L, Sorensen S. Assessments of oral health care in dependent older persons in nursing facilities. Acta Odontol Scand 2002; 60: 330-6.

[55]Wyatt CC. Elderly Canadians residing in long-term care hospitals: Part I. Medical and dental status. J Can Dent Assoc 2002; 68: 353-8.

[56]Yip KH-K, Smales RJ. Root surface caries in elderly people in residential care. J Disability Oral Health 2004;5: 70-6.

[57]van Strijp AJ, van Steenbergen TJ, ten Cate JM. Effects of chlorhexidine on the bacterial colonization and deg-radation of dentin and completely demineralized dentin in situ. Eur J Oral Sci 1997; 105: 27-35.

[58]Lynch E, Baysan A, Ellwood R, Davies R, Petersson L,Borsboom P. Effectiveness of two fluoride dentifrices to arrest root carious lesions. Am J Dent 2000; 13: 218-20.

[59]Baysan A, Lynch E, Ellwood R, Davies R, Petersson L,Borsboom P. Reversal of primary root caries using dentifrices containing 5,000 and 1,100 ppm fluoride. Caries Res 2001; 35: 41-6.

[60]Lynch E, Baysan A. Reversal of primary root caries using a dentifrice with a high fluoride content. Caries Res 2001; 35(S1): 60-4.

[61]Stoeken JE, Paraskevas S, van der Weijden GA. The long-term effect of a mouthrinse containing essential oils on dental plaque and gingivitis: A systematic review. J Periodontol 2007; 78: 1218-28.

[62]Gunsolley JC. Clinical efficacy of antimicrobial mouthrinses. J Dent 2010; 38: S6-S10.

[63]Drinka P. Preventing aspiration in the nursing home: the role of biofilm and data from the ICU. J Am Med Dir Assoc 2010; 11: 70-7.