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Oral candidosis by Candida albicans in normal and xerostomic mice

Candidose oral por Candida albicans em camundongos normais e xerostômicos

Abstracts

The aim of this study was to analyze the effect of sialoadenectomy on the development of oral candidosis after one or four inoculations of Candida albicans. Initially, a suspension containing 10(8) cells/ml of C. albicans ATCC 36801 was prepared. Seventy-eight sialoadenectomized mice and a similar amount of mice with normal salivary flow received a single inoculation of C. albicans suspension. Another group with a similar number of mice received 4 inoculations. The control group consisted of 6 sialoadenectomized mice and 6 mice with normal salivary flow that were not inoculated with C. albicans. Candidosis development was studied histologically in the tongue of the animals 1, 2, 3, 5, and 8 days after inoculation and at 15-day intervals up to 165 days. According to the results obtained, it could be concluded that sialoadenectomy and a higher frequency of yeast inoculation influenced the presence and extension of candidosis lesions.

Candidiasis, oral; Candida albicans; Xerostomia


O objetivo deste estudo foi analisar o efeito da sialoadenectomia sobre o desenvolvimento da candidose oral após uma ou quatro inoculações de Candida albicans. Inicialmente, uma suspensão contendo 10(8) células/ml de C. albicans ATCC 36801 foi preparada. Setenta e oito camundongos sialoadenectomizados e mesma quantidade de camundongos com fluxo salivar normal receberam uma única inoculação de suspensão de C. albicans. Outro grupo, com o mesmo número de camundongos, recebeu 4 inoculações. O grupo controle consistiu de 6 camundongos sialoadenectomizados e 6 com fluxo salivar normal que não foram inoculados com C. albicans. O desenvolvimento de candidose foi estudado histologicamente na língua dos animais em períodos de 1, 2, 3, 5 e 8 dias após a inoculação e em intervalos de 15 dias até 165 dias. De acordo com os resultados obtidos, conclui-se que a sialoadenectomia e uma maior freqüência de inoculação influenciaram na presença e extensão das lesões de candidose.

Candidíase bucal; Candida albicans; Xerostomia


MICROBIOLOGY

Oral candidosis by Candida albicans in normal and xerostomic mice

Candidose oral por Candida albicans em camundongos normais e xerostômicos

Marilda Aparecida Gonçalves TottiI; Elisabete Brasil dos SantosII; Oslei Paes de AlmeidaIII; Cristiane Yumi Koga-ItoIV; Antonio Olavo Cardoso JorgeV

IPhD in Oral Biopathology, School of Dentistry of Piracicaba, State University of Campinas

IIPhD, Assistant Professor, Department of Dentistry, University of Ponta Grossa

IIIHead Professor, Department of Oral Pathology, School of Dentistry of Piracicaba, State University of Campinas

IVPhD, Assistant Professor, Department of Biosciences and Oral Diagnosis, School of Dentistry of São José dos Campos, São Paulo State University

VHead Professor, Department of Dentistry, University of Taubaté

ABSTRACT

The aim of this study was to analyze the effect of sialoadenectomy on the development of oral candidosis after one or four inoculations of Candida albicans. Initially, a suspension containing 108 cells/ml of C. albicans ATCC 36801 was prepared. Seventy-eight sialoadenectomized mice and a similar amount of mice with normal salivary flow received a single inoculation of C. albicans suspension. Another group with a similar number of mice received 4 inoculations. The control group consisted of 6 sialoadenectomized mice and 6 mice with normal salivary flow that were not inoculated with C. albicans. Candidosis development was studied histologically in the tongue of the animals 1, 2, 3, 5, and 8 days after inoculation and at 15-day intervals up to 165 days. According to the results obtained, it could be concluded that sialoadenectomy and a higher frequency of yeast inoculation influenced the presence and extension of candidosis lesions.

Descriptors: Candidiasis, oral; Candida albicans; Xerostomia.

RESUMO

O objetivo deste estudo foi analisar o efeito da sialoadenectomia sobre o desenvolvimento da candidose oral após uma ou quatro inoculações de Candida albicans. Inicialmente, uma suspensão contendo 108 células/ml de C. albicans ATCC 36801 foi preparada. Setenta e oito camundongos sialoadenectomizados e mesma quantidade de camundongos com fluxo salivar normal receberam uma única inoculação de suspensão de C. albicans. Outro grupo, com o mesmo número de camundongos, recebeu 4 inoculações. O grupo controle consistiu de 6 camundongos sialoadenectomizados e 6 com fluxo salivar normal que não foram inoculados com C. albicans. O desenvolvimento de candidose foi estudado histologicamente na língua dos animais em períodos de 1, 2, 3, 5 e 8 dias após a inoculação e em intervalos de 15 dias até 165 dias. De acordo com os resultados obtidos, conclui-se que a sialoadenectomia e uma maior freqüência de inoculação influenciaram na presença e extensão das lesões de candidose.

Descritores: Candidíase bucal; Candida albicans; Xerostomia.

INTRODUCTION

Candidosis is the most common infection of the oral cavity caused by fungi and C. albicans is the main species related to its development. The genus Candida belongs to the indigenous oral flora of 20 to 40% of healthy subjects7,18 and its pathogenicity is observed in the presence of predisposing conditions such as immunodepression, use of denture or orthodontic appliances and diabetes mellitus. The transformation from the saprophytic to the parasitic form is related to various factors, including not only the virulence of these yeasts, but also host-related variables19. Among the host-related factors, the modification of the oral microbiota balance is considered a very important factor6.

Xerostomia is one of the main factors related to the development of oral candidosis, since the lack of or decrease in salivary flow causes changes in the resident oral microbiota. Also, food and microorganisms are poorly mechanically removed from the oral cavity and subjects lack the protector effect of saliva constituents, such as lactoferrin and lysozyme20.

In a previous study, Totti et al.22,23 (1996, 2002) observed that xerostomia helps in the appearance, proliferation and persistency of five Candida species in the oral cavity of rats. Similar results were observed by Jorge et al.11,12 (2000, 2002). Xerostomia is also related to the longer permanence of yeasts in the mouth of mice12 and to a higher Candida albicans transmissibility11. Takakura et al.21 (2003) correlated the number of candidosis lesions with the increased number of Candida in the oral cavity.

Rats have been used as an experimental model in studies on oral candidosis and also to evaluate the influence of local and systemic factors1,4,10. The use of mice as an experimental model in studies on oral candidosis is relevant, since Candida is not part of their indigenous oral microbiota14.

The influence of several inoculations of C. albicans on the development of candidosis in mice has not been discussed yet. The aim of this study was to analyze the effect of sialoadenectomy on the development of oral candidosis in mice after one or four inoculations of Candida albicans suspensions.

MATERIAL AND METHODS

Three-hundred and twenty four male mice (Mus musculus, albinos, Swiss; School of Dentistry of São José dos Campos, University of São Paulo), weighting from 25 to 30 g were included in this study. The animals were divided into three groups as follows: 156 xerostomic mice, 156 mice with normal salivary flow and 12 controls.

Xerostomia was obtained by surgical removal of the major salivary glands, according to Cheyne4 (1939), with modifications. Before the beginning of the experiment, the presence of Candida in the oral cavity of the normal and sialoadenectomized animals was analyzed by plating the collected material from the oral cavity of the mice with a sterile swab (CB Products, SP, Brazil) in Sabouraud dextrose agar with chloramphenicol (quemicetina succinato, Carlo Erba, 0.1 mg/ml, SP, Brazil). After incubation at 37ºC for 48 h, the presence of Candida ssp. was analyzed. This procedure was repeated two weeks later. All mice were initially negative to Candida.

C. albicans ATCC 36801 was subcultured in Sabouraud agar slants (Difco, Detroit, USA) and incubated for 24 h at 35°C. The cells of C. albicans were resuspended in phosphate-buffered saline (PBS, pH 7.4, Sigma, St. Louis, USA) and washed three times. From these cells, a suspension containing 108 viable cells/ml of C. albicans was standardized using a Neubauer chamber (Assistent, München, Germany) and 0.05% methylene blue (Dr. Theodor Schuchardt GMBH & Co., München, Germany). The inoculations were performed using this cell suspension as follows:

  • Single-inoculation group: 78 sialoadenectomized mice and 78 mice with normal salivary flow received a single inoculation of 0.1 ml of the

    C. albicans suspension containing 10

    8 viable cells/ml using a 1 ml syringe and a 30 x 8 mm needle.

  • Four-inoculation group: 78 sialoadenectomized mice and 78 mice with normal salivary flow received a total of 4 intraoral inoculations of the

    C. albicans suspension containing 10

    8 viable cells/ml, performed during 4 consecutive days.

  • Control group: 6 sialoadenectomized mice and 6 mice with normal salivary flow that were not inoculated with the

    C. albicans suspension.

All the animals did not receive water for at least 1 h after inoculation. Candidosis was studied in the tongue of normal and sialoadenectomized mice at 1, 2, 3, 5 and 8 days after inoculation and at 15-day intervals up to 165 days. Six animals of each group were sacrificed at each studied time and the tongue was surgically removed, fixed in a 10% formalin solution (Synth, SP, Brazil) and processed for histological examination. For the histological processing, the tongue was divided longitudinally and the two portions were included in paraffin. Semi serial slices of 5 µm were obtained, which allowed the analysis of the central, lateral and edge part of the tongue (designed sites A, B and C, respectively) on the left and right sides. The slides were dyed using PAS (periodic acid - Sigma, St. Louis, USA; Schiff's reagent - Merck, Darmstadt, Germany), H & E (Merck, Darmstadt, Germany) and Gomori-Grocott stains (Sigma, St. Louis, USA). The tongue was thoroughly examined for presence of candidosis, with a total of 18 sections examined for each animal. All the sections were analyzed by one examiner previously trained. The description of the candidosis areas was performed considering the localization, extension, alterations in the tissues, and candidal hyphae presence.

Statistical analysis

Data on the mean and standard deviation of the number of animals with candidosis after one and four inoculations were compared statistically by means of the Student's t-test (a = 5%).

RESULTS

Presence of candidosis

According to the histological analysis of the tongues, it could be observed that the development of candidosis occurred more frequently among sialoadenectomized mice submitted to both one and four inoculations of the yeast suspension.

Table 1 presents the number of sialoadenectomized and normal salivary flow mice that presented candidosis according to the period of time analyzed. Amont the xerostomic animals that received 1 inoculation of C. albicans, candidosis was observed in 33.33% of the animals, after a period of 15 days. This value decreased to 16.6% 75 days after the inoculation. After this period, no animal presented candidosis.

Among the animals that received 4 inoculations of Candida albicans suspension, candidosis was observed in 83.3% to 100% of the xerostomic animals after the period of eight days. This number decreased to 33.33% after 15 days, and 115 days after the last inoculation only 1 (16.6%) animal presented candidosis.

Considering the mice with normal salivary flow, no difference could be observed in relation to the number of animals with candidosis after 1 or 4 inoculations of C. albicans. Eight days after a single inoculation, only one animal presented candidosis in the tongue dorsum. After 4 C. albicans inoculations, candidosis was observed in one animal after 45 days.

Candidosis was not observed in animals from the control group, which were not inoculated with C. albicans.

Mean and standard deviations values of the number of candidosis areas observed among normal and xerostomic mice after 1 and 4 inoculations are presented in Table 2. Statistically significant differences were observed between the 4-inoculation normal salivary flow group and the 4-inoculation sialoadenectomized mice group at 2, 3 and 45 days. Considering the single-inoculation group, a statistically significant difference between sialoadenectomized and normal salivary flow mice was observed at day 8.

Histological analysis

8 days after C. albicans inoculation

After this period of time, considering the animals that received only a single inoculation, candidosis was observed in the dorsum of the tongue of 2 sialoadenectomized and of 1 normal mouse. The tongue of sialoadenectomized mice presented flatting of the papillae, acanthosis, parakeratosis, and lymphocytic infiltration.

Observations performed after 4 inoculations of C. albicans, showed necrotic areas on the dorsum of the tongue of normal mice. Sialoadenectomized animals presented extensive areas with intense candidosis, mainly in the papillae regions. Figure 1 shows the histologic examination of a sialoadenectomized animal 3 days after the last inoculation.


15 to 60 days after the C. albicans inoculation

The epithelium of the dorsum of the tongue of normal salivary flow mice had normal histological aspect 15 days after a single inoculation. Candidosis lesions were observed in 2 sialoadenectomized animals 15 days after the inoculation and in 1 animal 30 days after the inoculation. Forty-five and 60 days after the inoculation, no candidosis lesions were registered. The lesions in the interior of the epithelium's keratine in the dorsum of the tongue presented few candidal hyphae. No alterations in the epithelium were observed.

After 4 inoculations of the C. albicans suspension, one normal and 2 sialoadenectomized mice presented candidosis in the dorsum of the tongue. Fifteen and 30 days after the inoculation, 2 sialoadenectomized animals presented candidosis in the dorsum of the tongue and 60 days after the inoculations just one animal presented signs of candidosis. The observed candidosis areas were extensive, mainly in the lingual papillae region, and were found in all the extension of the dorsum of the tongue. Candidal hyphae could be observed penetrating the epithelium.

Among the mice without candidosis, flattening of lingual papillae, hiperkeratosis, acanthosis, lymphocitic infiltrate and areas of necrosis in the epithelium could be observed.

75 to 165 days after the inoculation

Only one sialoadenectomized mouse presented candidosis in this period. Extensive areas of candidosis with similar histologic aspects to those described previously were observed. In the other animals, the histologic aspect of the dorsum of the tongue was normal.

DISCUSSION

It is well known that infections caused by Candida species have a multifactorial etiology. The transformation from the saprophytic to the parasitic form is related to several factors including not only the virulence of these yeasts but also host-related variables. Among the host-related factors, the salivary anti-Candida immunoglobulins and cellular defenses play an essential role for controlling the infection13,18. When these defenses are compromised, such as in cases of xerostomia, candidosis can occur. In fact, Brown et al.3 (1975) observed an increase in the prevalence of Candida spp., mainly C. albicans, in patients with xerostomia induced by head and neck radiation.

In this study, it could be observed that the surgical removal of the major salivary glands produced deep xerostomia in mice. The volume of saliva was reduced by approximately 75%. In human beings, the symptoms of xerostomia can be observed when the salivary flow is reduced by 40 to 50%5,8. After surgery, the oral cavity of the mice was dry, presenting only residual viscous saliva and food on mucous tissue and teeth. The residual salivary flow present in the mouth of sialoadenectomized mice was probably produced by the minor salivary glands.

Our results showed that xerostomia induced by sialoadenectomy itself did not promote the appearance of C. albicans in the oral cavity. This fact is probably because these yeasts are not part of their indigenous oral microbiota. Candida was not isolated from the mice's oral cavity before the experiment. The cultures remained negative for Candida 1 and 2 weeks after surgery.

Sialoadenectomy was the technique selected to produce xerostomia in mice because it is a simple method and it causes a permanent reduction in the salivary flow. The use of chemical agents can also produce xerostomia16. However, their effects are transient and they can produce side effects that can interfere on the results.

In human beings, xerostomia is associated with atrophy of the oral mucosa, especially in the dorsum of the tongue24. In the present study, this alteration was not observed. On the other hand, alterations in the oral microbiota have also been reported in patients with xerostomia17.

Mice have been used in studies on the pathogenicity of C. albicans in the oral cavity. These animals do not harbor Candida in their oral cavity and can be considered more adequate for these studies, since other microbial species do not interfere with the tested microorganism1,2,9,14,20. This way, the infection by Candida spp. is considered as a transient colonization in the oral cavity of these animals.

The development of candidosis, after 1 and 4 inoculations of the C. albicans suspension occurred more frequently in sialoadenectomized mice in comparison with the normal ones. Eight days after the last inoculation, 83.3% of the animals presented extensive candidosis lesions, particularly in the true papillae region.

In relation to the animals with normal salivary flow that received 1 inoculation, only one presented lesions in the dorsum of the tongue. This number was lower than that observed by Lacasse et al.15 (1990). Among the animals that received 4 inoculations, 33.33% presented candidosis and this number decreased with time.

Candidosis on the dorsum of the tongue was characterized by the presence of pseudohyphaes inside the epithelium, flattening of the lingual papillae, hyperkeratosis, akanthosis and neutrophilic infiltrate, forming intraepithelial micro abscesses. There were no differences among lesions found in the central, lateral or edge regions of the tongue; however, a slightly higher prevalence of the lesions in the true and conical papillae was observed.

CONCLUSION

According to the results obtained, it could be concluded that sialoadenectomy and a higher number of C. albicans inoculations influenced the frequency and extension of candidosis lesions in mice.

Received for publication on Mar 01, 2004

Sent for alterations on Apr 22, 2004

Accepted for publication on May 26, 2004

  • 1. Adams D, Jones JH. Life history of experimentally induced acute oral candidiasis in the rat. J Dent Res 1971;50:643-4.
  • 2. Allen CM. Animal models of oral candidiasis. A review. Oral Surg Oral Med Oral Pathol 1994;78:216-21.
  • 3. Brown LR, Dreizen S, Handler S, Johnston DA. Effect of radiation-induced xerostomia on human oral microflora. J Dent Res 1975;54:740-50.
  • 4. Cheyne VD. A description of the salivary glands of the rat and a procedure for their extirpation. J Dent Res 1939;18:457-68.
  • 5. Dawes C. Physiological factors affecting salivary flow rate, oral sugar clearance, and the sensation of dry mouth in man. J Dent Res 1987;66:648-53.
  • 6. do Rego MA, Koga-Ito CY, Jorge AOC. Effects of oral environment stabilization procedures on counts of Candida spp. in children. Pesqui Odontol Bras 2003;17(4):332-6.
  • 7. Farah CS, Ashman RB, Challacombe SJ. Oral candidosis. Clin Dermatol 2000;18:553-62.
  • 8. Fox CP, van der Ven PF, Sonies BC, Weiffenbach JM, Baum BJ. Xerostomia: evaluation of a symptom with increasing significance. J Am Dent Assoc 1985;110:519-25.
  • 9. Hassan OE, Jones JH, Russell C. Experimental oral candidal infection and carriage of oral bacteria in rats subjected to a carbohydrate-rich diet and tetracycline treatment. J Med Microbiol 1985;20:291-8.
  • 10. Jones JH, Russell C. The histology of chronic candidal infection of the rat's tongue. J Pathol 1974;113:97-100.
  • 11. Jorge AOC, Batista JA, Rego MA. Influência da xerostomia na transmissibilidade de Candida albicans na cavidade bucal de ratos. Rev Odontol UNICID 2000;12:121-8.
  • 12. Jorge AOC, Rego MA, Santos EB, Almeida OP. Efeitos da aplicação de Candida albicans na língua de ratos normais e sialoadenectomizados. Rev Odontol UNICID 2002;14:35-44.
  • 13. Jorge AOC, Totti MAG, de Almeida OP, Scully C. Effect of sialoadenectomy on the carriage of Candida albicans in the mouths of rats. J Oral Pathol Med 1993;22:138-40.
  • 14. Lacasse M, Fortier C, Chankir J, Cote L, Deslauriers N. Acquired resistance and persistence of Candida albicans following oral candidiasis in the mouse: a model of the carrier state in humans. Oral Microbiol Immunol 1993;8: 313-8.
  • 15. Lacasse M, Fortier C, Trudel L, Collet AJ, Deslauriers N. Experimental oral candidosis in the mouse: microbiologic and histologic aspects. J Oral Pathol Med 1990;19:136-41.
  • 16. Lekholm U, Wallenius K. Experimental oral cancer in rats with xerostomia. Odontol Revy 1976;27:11-8.
  • 17. Llory H, Dammron A, Frank RM. Les modifications de la flore buccale aerobie apres radiotherapie bucco-pharynge. Arch Oral Biol 1971;16:617-30.
  • 18. Odds FC. Candida infections: an overview. Crit Rev Microbiol 1987;15:1-5.
  • 19. Samaranayake LP, MacFarlane TW. Oral candidosis. Cambridge: Wright; 1990.
  • 20. Samaranayake YH, Samaranayake LP. Experimental oral candidiasis in animal models. Clin Microbiol Rev 2001;14:398-429.
  • 21. Takakura N, Sato Y, Ishibashi H, Oshima H, Uchida K, Yamaguchi H, et al A novel murine model of oral candidiasis with local symptoms characteristic of oral thrush. Microbiol Immunol 2003,47:321-6.
  • 22. Totti MAG, Jorge AOC, dos Santos EB, de Almeida OP, Scully C. Implantation of Candida albicans and other Candida species in the oral cavity of rats. J Oral Pathol Med 1996;25:308-10.
  • 23. Totti MAG, Santos EB, Almeida OP, Jorge AOC. Implantation and permanency of Candida albicans in the oral cavity of normal and sialoadenectomized mice after a single inoculation of yeast. Braz J Oral Sci 2002,1:133-6.
  • 24. Wallace MC, Petrusneck F. The dental implications of xerostomia. A review of the literature. J Ala Dent Assoc 1985;69:44-7.

Publication Dates

  • Publication in this collection
    29 Sept 2004
  • Date of issue
    Sept 2004

History

  • Reviewed
    22 Apr 2004
  • Received
    01 Mar 2004
  • Accepted
    26 May 2004
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