ORAL C.ALBICANS COLONIZATION AND NON-CANDIDA ALBICANS CANDIDA COLONIZATION AMONG UNIVERSITY STUDENTS, YEMEN

Abbas M Al-Kebsi1, Arwa M Othman2, Al-Kasem M A Abbas3,  Ebtihal M Madar2, Hassan A. Al-Shamahy2,  Khaled M Al-Gaffari1, Samera M. Naser Daname4, Fuad L. Motareb5.

1Department of  Prosthodontics, Faculty of Dentistry, Sana’a University, Republic of Yemen.

2Medical Microbiology and Clinical Immunology, Faculty of Medicine and Health Sciences, Sana’a University, Yemen.

3Department of Maxillo-Facial, Faculty of Dentistry, Sana’a University, Republic of Yemen.

4Department of Physiology, Faculty of Dentistry, Sana’a University, Republic of Yemen.

5Department of  Orthodontics, Faculty of Dentistry, Sana’a University, Republic of Yemen.

*Corresponding Author’s Email: shmahe@yemen.net.ye

DOI: http://doi.org/10.22270/ujpr.v2i5.R2

ABSTRACT

Candida albicans is diploid yeast that in some circumstances may cause oral or oropharyngeal infections. This investigation aimed to study the oral C. albicans colonization (OCC) and Non-Candida albicans Candida colonization (ONCACC) and risk factors of OCC in healthy University students.  This cross sectional laboratory study was carried between January 2014 and July 2014. A total of 265 healthy students were included in this study, 131 males and 134 females. Demographic and clinical and risk factor variables were registered in predesigned questionnaire. Standard methods were used for collection oral specimens, culturing and identifying Candida species. The crude rate of OCC was 17.7% and the crude rate of ONCACC was 29.1%. C. tropicalis and C. glabrata were the most common species isolated after C. albicans. Statistically significant association of OCC (< 0.05), was identified between the gender (male) (OR=3.7), smoking (OR=14.6), denture wearing (OR=6.2), dental bridge (OR=5.4), orthodontics (OR=2.5), the reduced saliva flow rate (OR=11.3), previous antibiotics users (OR=2.99), and Qat chewers (OR=5.2).Our results are important for the development of strategies to eliminate these indicators of risk and significantly reduce Candida species colonization and oral Candida infections in young healthy adults and in general in Yemen community. The data also suggests that the prevalence rate of OCC was relatively high and it was affected by presence of prostheses, orthodontics, behaviors, xerostomia certain sociodemographic characteristics, which indicate the need for comprehensive, scheduled programs of healthcare educations.

Keywords: Non-Candida albicans Candida colonization (ONCACC), Oral C. albicans colonization (OCC), risk factors, Yemen.

 

INTRODUCTION

Candida albicans is an opportunistic fungal pathogen usually found in the human gastrointestinal and female lower genital tracts. It is a only one of its kind parasite capable of colonizing, infecting, and persisting on mucosal surfaces, and motivating mucosal immune responses1.  Attack of tissues by Candida is aided by hyphal development. The transformation of budding yeasts to hyphal growth is endorsed by physical contact with surfaces and is under genetic control. When fungi colonize an epithelial or epidermal surface, they adhere to host cells and generate depressions in the surface of host cells. As yeast-form cells alter to the hyphal form, these hyphae are capable to diffuse into the surface of the tissue layer. The direction of hyphal growth is resoluted by the topography of the substratum. Hyphae are guided by ridges in the tissue layer. This behavior is known as thigmotropism. It plays an important role in the direction of hyphal growth and in disease progression. Tissue invasion by Candida is made possible by the action of degradative enzymes secreted by the pathogen and by mechanical forces exerted by the hyphae2, 3. C. albicans, is naturally there in the oral cavity in a non-pathogenic state in about one-half of healthy individuals but under favorable situations, has the ability to transform into a pathogenic hyphal form. Conditions that favour this transformation include extremes in age, broad-spectrum antibiotic therapy, corticosteroids, xerostomia, immune dysfunction (especially of cell-mediated immunity), diabetes mellitus, nutritional deficiencies, or the presence of removable prostheses4,5. There are some clinical manifestations of oral candidiasis, the most common being the pseudo membranous, erythematous, angular cheilitis, hyperplastic and mucocutaneous forms6,7. Non-Candida albicans Candida (NCAC) strains, however, are isolated in ever-increasing numbers in medically compromised patients. These strains might cause systemic infections and are frequently resistant to commonly used antifungal agents such as fluconazole8,9.  Candida species may be able of metabolizing ethanol to carcinogenic acetaldehyde and can thus development oral and upper gastrointestinal tract cancer, cconsequently, more focus should be placed on diagnosis and treatment of oral Candida infections, as well on other Candida species than C. albicans10,11.  This investigation aimed to study the prevalence of Candida species and risk factors of oral Candida albicans colonization in healthy students of Sana'a University in Sana'a city, Yemen.

MATERIALS AND METHODS

Sample collection and processing:  The samples were collected aseptically by oral rinse method. The students were asked to rinse the mouth with 10 ml of sterile Phosphate Buffered Saline (PBS, pH 7.2) for 60 seconds and thereafter oral rinse was collected in sterile container. The oral rinse specimen was without delay centrifuged at 3000xg for 10 minute. The supernatant was discarded and sediment was re-suspended in 1 ml of sterile PBS and vortexed for 1 minute. This solution was used for direct microscopic examinations, performed with lactophenol cotton blue and 100 μl of this preparation was inoculated onto Sabouraud’s Dextrose Agar (SDA) plate with and without chloroamphenicol (Oxod, UK). The plates were incubated at 37°C for 48 h. The colonies of Candida were counted to assess CFU/ml of rinse sample12.

Sterile cover-slip, incubated at room temperature for 3 to 5 days in dark to endorse the production of chlamydospores, hyphae, pseudohyphae, and arthroconidia. Biochemical tests were carried out; using API Candida Syste API system ll tests were completed according to the manufacturer’s instructions13. The API Candida system consists of a single-use disposable plastic strip with 10 wells to perform 12 colorimetric biochemical tests: five sugar assimilation tests (for glucose, galactose, sucrose, trehalose, and raffinose) and seven enzymatic tests (for β-maltosidase, α-amylase, β-xylosidase, β-glucuronidase, urea hydrolysis, N-acetyl-β-glucosaminidase, and β-galactosidase). Inoculation of the wells was done by adding a yeast suspension to the dehydrated substrates. The results were read after incubation for 18 to 24 h at 35°C. A four-digit numerical profile was made for each isolate depending upon the reactions it produced. Identifications were made by referring to the list of numerical profiles and a computer program offered by the manufacturer.

The statistical analysis was done using Graph Pad Prism 5. Univariate analyses were performed on all variables of this study using the Fisher’s and Chi squared tests (2-sided tests). The results of this analysis were expressed as an odds ratio (OR) with a 95% confidence interval (CI). A p value of < 0.05 was considered statistically significant. Mouth hygiene determined by the frequency of using oral hygiene measures (as mouth washes, using antiplaque and anti-gingivitis tooth paste per day14. Salivary Flow Rate:  The students asked to chewing paraffin for 5 minutes, and then saliva collected into a measuring container. Then saliva sample was measured and flow rate was calculated on an ml/minute basis15. It is recommended that the tests are performed at least one hour after the person has eaten something (drinking water is allowed), smoked or taken snuff. It is important that the person is relaxed and calm. If the person has any disease, it should be considered if the disease affects the secretion rate, and if it is a temporary condition or a long-lasting disease. If long-lasting, the reduced secretion rate may be regarded as representative for that person and for that period of time.

All relevant data of the students included in this study were obtained though a pre-designed questionnaire. Also laboratory results, measuring of mouth hygiene and salivary flow rate results were collected in the pre-designed questionnaire.

RESULTS

This analytical laboratory study was conducted on 265 students of Sana'a University during the period of two months from January 2014 to February 2014. Their age was ranged from 20–27 years, with mean age±SD equal to 22.1±2.1 years for female students, and for male students the mean age±SD was 23.4±2.3 years. Females represent 49.4% of total and males represent 50.6% of the total.  Most of the students were in age group 20-22 years (43%) and in age groups 22-25 years were 32.8%, and students in age group≥ 26 years count only 24.2% of the total (Table1). The total OCC rate in our students was 17.7%. OCC was 26.7% among male students, higher than that for female students in which it was 9% (Table 2). In addition, there was a highly significant association of OCC with male students (OR=3.7, pv=0.0001) (Table 3). When we study the relation of student age and risk of OCC, a higher rate and risk of colonization found in age group 23-25 years with prevalence rate equal to 23.8%, and risk (OR) equal to 1.65 times comparing to other age groups (Table 2). When we considered predisposing factors of OCC, there was a highly significant association (pv=0.0004) of denture wearing with OCC in which this risk equal to 6.2, and ranged from 1.8-22.2. Also proportional prevalence of 41% oral C. albicans was higher in students who had previously received antibiotics, and there was a highly significant association (pv<0.0001) of  history of recent using antibiotics with colonization of C. albicans in which this risk equal to 2.99, and ranged from 1.8 to 4.9. An inverse correlation between salivary flow rate and OCC is reflected in present study, in which significant relation was found between reduced saliva flow rate and OCC. Proportionally, 58.3% OCC was found with reduced saliva rate (< 1 ml/min) with highly significant OR equal to 14.6 times (pv<0.0001). There was a highly significant association (pv<0.0001) of smoking with OCC in which this risk equal to 14.6, and ranged from 6.5 to 32.9 (Table 4). However, there was no effect for mouth hygiene in occurring of colonization of C. albicans among our students (Table 4).   In this study 29.1% of tested healthy students had oral colonization with Non-Candida albicans Candida colonization (ONCACC). In our study Candida tropicalis accounted for 10.2%, Candida glabrata for 11.7%, and Candida parapsilosis for 2.6% (Table 2).

DISCUSSION

The total OCC rate in our students was 17.7%. This candidal carriage state is not considered a disease, but when Candida species become pathogenic and invade host tissues, oral candidiasis can occur. This change usually constitutes an opportunistic infection of because of local (i.e., mucosal, introducing oral devices as denture, dental bridge etc.), or systemic factors altering host immunity16. Our rate is slightly higher than these findings by Scully in UK in adults (11.5%),  and by Tarcin in USA (13%)17, 18.  Also colonized of C. albicans was about  26.7% among male students, higher than that for female students in which it was  9% (Table 2). In addition, there was a highly significant association of C. albicans colonization with male students (OR= 3.7, pv=0.0001) (Table 3).  Our result is different from that reported by Greenberg et al.3 with high rate (40.9%) in adult females and low rate (12.2%) in adult males. When we study the relation of student age and risk of  mouth colonization of C. albicans, a higher rate and risk of colonization was found in age group 23-25 years with prevalence rate is equal to 23.8%, and risk (OR) equal 1.65 times comparing with other age groups. This result suggested that students in older age are an important risk factor of mouth colonization of C. albicans. Our result is different from that reported from Philadelphia by Bouquot et al19, in which no different in the rate of mouth colonization occurred with age, but similar to that reported from UK by Smaancyake20 in which the highest rate occurred in older adult age groups.

The second aim of the study was to determine other predisposing factors of OCC. There was a highly significant association (pv=0.0004) of denture wearing with OCC in which this risk equal to 6.2, and ranged from 1.8-22.2 (Table 4). This result can be explained by the fact that denture wearing, and poor denture hygiene, particularly wearing the denture continually rather than removing them during sleep16, is another risk factor, both for candidal carriage and for oral candidiasis. Also dentures provide a relative acidic, moist and anaerobic environment because the mucosa coated by the denture is sheltered from oxygen and saliva17.  Other cause for colonization of C. albicans in denture wearing persons is that loose, poorly fitting dentures may also cause minor trauma to the mucosa20, which is thought to enhance the permeability of the mucosa and increase the ability of C. albicans to invade the tissues17, 21.  These situations all favor the growth of C. albicans. Sometimes dentures become much worn, or they have been constructed to allow insufficient lower facial height (occlusal vertical dimension), directed to over-closure of the mouth (an appearance sometimes described as "collapse of the jaws"). This causes pronouncement of the skin folds at the corners of the mouth, in consequence creating an intertriginous areas where another form of candidiasis, angular cheilitis, can develop. Candida species are capable of adhering to the surface of dentures, most of which are made from polymethylacrylate. They exploit micro-fissures and cracks in the surface of dentures to aid their maintenance. Intra-oral prostheses may therefore become covered in a biofilm22, and act as reservoirs of infection23, continually re-infecting the mucosa. For this reason, disinfecting the denture is a vital part of treatment of oral candidiasis in persons who wear dentures, as well as correcting other factors like not enough lower facial height and fit of the dentures17.

   In fact broad-spectrum antibiotics used in the treatment of a wide range of disease conditions have also been recognized as a predisposing factor of  OCC, possibly because of changes in oral environment and/or in the immune response reducing neutrophils candidacidal activity24.  In this study, proportional prevalence of 41% oral C. albicans was higher in students who had previously received antibiotics. Also there was a highly significant association (pv<0.0001) of  history of recent using antibiotics with colonization of C. albicans in which this risk equal to 2.99, and ranged from 1.8 to 4.9 (Table 4). This result can be explained by the fact that broad spectrum antibiotics lead to imbalance of the oral micro-organisms3,25. An inverse correlation between salivary flow rate and OCC has been reported as is reflected in present study26. In this study, significant relation was found between reduced saliva flow rate and OCC. Proportionally, 58.3% OCC was found with reduced saliva rate (< 1 ml/min) with highly significant OR equal to 14.6 times (pv<0.0001) (Table 4). This association can be explained by that both the quantity and quality of saliva are important oral defenses against Candida27. Decreased salivary flow rate or a change in the composition of saliva28 collectively termed salivary hypo function or hypo salivation is an important predisposing factor.  Also xerostomia is frequently listed as a cause of candidias is16 but xerostomia can be subjective or objective, i.e., a symptom present with or without actual changes in the saliva consistency or flow rate16, 28.

There was a highly significant association (pv<0.0001) of smoking with OCC in which this risk equal to 14.6, and ranged from 6.5 to 32.9 (Table 4). Our result is similar to that reported by Tarcin in which a high significant risk of colonization was associated with smoking habit17.  This result can be explained by the fact that smoking, especially heavy smoking, is an important predisposing factor but the reasons for this relationship are unknown. One hypothesis is that cigarette smoke contains nutritional factors for C. albicans, or that local epithelial alterations occur that help colonization of Candida species and smoking lead to kill immune cells and damage mucus membrane of the mouth17, 24. There was no effect for mouth hygiene in occurring of colonization of C. albicans among our students. This result is different from that reported by Rautema et al26 in which a high significant risk of mouth colonization was associated with bad mouth hygiene.

In this study 29.1% of tested healthy students had oral colonization with other Candida species than C. albicans (ONCACC) (Table 2). In our study Candida tropicalis accounted for 10.2%, Candida glabrata for 11.7%, and Candida parapsilosis for 2.6% (Table 2). Our result is similar to that reported elsewhere in which Candida tropicalis was the most common non-albicans species, followed by Candida glabrata while others ad Candida parapsilosis were rare isolated in healthy oral colonization or as cause of illnesses in patients9.  As it is known Candida species may be capable of metabolizing ethanol to carcinogenic acetaldehyde and can thus progress oral and upper gastrointestinal tract cancer so 29.1% of our studied individuals under risk of oral and upper gastrointestinal tract cancer. Consequently, more focus should be placed on diagnosis and treatment of oral Candida infections, also on other Candida species than C. albicans as it has been recommended29,30.

CONCLUSION

In the present study, the higher oral Candida carriage rate in healthy young adults buttresses the importance of oral Candida carriage for identification of individuals with the propensity for progression to clinical cases. Data from our study suggested that OCC was significantly associated with gender (male), smoking, denture wearing, dental bridge, orthodontics, the reduced saliva flow rate, previous antibiotics users, and Qat chewers. Our results are important for the development of strategies to eliminate these indicators of risk and significantly reduce OCC and oral Candida infections in young healthy adults and in general in Yemen community. The data also suggests that the prevalence rate of OCC was relatively high and it was affected by hygiene behaviors and certain socio demographic characteristics, which indicate the need for comprehensive, scheduled programs of healthcare educations.

CONFLICT OF INTERESTS

There are no conflicts of interest.

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Table1:  The distribution of tested students according to their sex and age groups

Total n=265

   Female n=134

           Male n=131

Age groups

 

%

No

%

No.

%

No

43

114

48.5

65

37.4

49

20-22 years

32

87

35.1

47

30.5

40

23 -25 years

24.2

64

6.4

22

32.1

42

≥ 26 years

100

265

50.6

134

49.4

131

Total

 

22.1 years

23.4 years

Mean age

2.1 years

2.3  years

S. D

21 years

22 years

Mode

21 years

21 years

Median

26 years

27 years

Max

20 years

20 years

Min

    

Table 2: The yeast distribution in different sexes of the study population

Organisms

Male n=131

Female n=134

Total n=265

No

%

No

%

No

%

C. albicans

35

26.7

12

9

47

17.7

C. tropicalis

16

12.2

11

8.2

27

10.2

C. glabrata

18

13.7

13

9.7

31

11.7

C. parapsilosis

4

3.1

3

2.2

7

2.6

C. albicans +C. tropicalis

3

2.3

3

2.2

6

2.3

C. albicans+ C. glabrata

2

1.5

4

3

6

2.3

Non-Candida albicans Candida

43

32.8

34

25.4

77

29.1

 

Table 3: The prevalence and associated odds ratio of Candida albicans mouth colonization among different sexes and age groups

Age groups

 

 

Positive C. albicans (n= 47)

No.              %

OR

 

 

CI

 

 

χ2

 

 

Pv

 

 

Male n=131

35

26.7

3.7

1.74-8

14.3

0.0001

Female n=134

12

9

0.27

0.12-0.57

14.3

0.0001

Age groups

20 -22 years n=114

15

13.2

0.56

0.3-1.15

2.9

0.09

23-25 years n=87

20

23

1.67

0.83-33.4

2.5

0.11

≥ 26 years n=65

12

18.5

1.1

0.48-2.3

0.03

0.86

Total n=265

47

17.7

 

OR- odds ratio> 1 (risk)

CI- Confidence intervals 1 to more than 1

X2- Chi-square> 3.9 (significant)

PV- Probability value <0.05 (significant)

 

Table 4: The risk factors of contracting Candida albicans mouth colonization among different student groups

Factors

Positive C. albicans (n= 47)

No.           %

OR

 

 

CI

 

 

χ2

 

 

Pv

 

 

Mouth hygiene

Good n=115

16

13.9

0.67

0.4-1.2

2.03

0.15

Bad n=150

31

20.7

1.6

0.8-3.3

2.03

0.15

Antibiotic use n=39

16

41

2.99

1.8-4.9

17

<0.0001

Smoking n=48

28

58.3

14.6

6.5-32.9

66.2

<0.0001

Denture n=13

7

53.8

6.2

1.8-22.2

12.2

0.0004

Dental  bridge n=19

8

42.1

5.4

1.7-16.99

12.2

0.0004

Orthodontics  n=28

9

32.1

2.5

0.95-6.3

4.5

0.03

Qat chewing n=101

33

32.7

5.2

2.5-10.9

24.9

<0.0001

Saliva flow rate

< 1ml/min n=63

 

31

 

49.2

 

11.3

 

5.2-24.5

 

56

 

<0.0001

> 2ml/min n=202

16

7.9

0.09

0.04-0.19

56

<0.0001

Halitosis (bad breath) n=67

22

32.8

3.4

1.7-6.9

14

0.0001

OR- odds ratio > 1 (risk)

CI- Confidence intervals 1 to more than 1

X2- Chi-square > 3.9 (significant)

PV- Probability value < 0.05 (significant)