Research Article | Open Access

Derick Erl P. Sumalapao1,2 , Pauline Bridgette D. Salazar2,3, Frederico Martin D. Alegre2,3, Nelson R. Villarante4 and Nina G. Gloriani5

1Department of Epidemiology and Biostatistics, College of Public Health, University of the Philippines Manila, Manila, Philippines.
2Biology Department, College of Science, De La Salle University, Manila, Philippines.
3College of Medicine, De La Salle Medical and Health Sciences Institute, Cavite, Philippines.
4Department of Physical Sciences and Mathematics, College of Arts and Sciences, University of the Philippines Manila, Manila, Philippines.
5Department of Medical Microbiology, College of Public Health, University of the Philippines Manila, Manila, Philippines.
J. Pure Appl. Microbiol., 2019, 13 (4):1881-1891 | Article Number: 5862 | © The Author(s). 2019
Received: 06/09/2019 | Accepted: 10/10/2019 | Published: 14/12/2019

Prolonged use of implanted medical devices has been linked with device-associated infections. Since enteral tube feeding is increasing worldwide, the present study described the morphology of Candida albicans biofilms on the surface of silicone nasogastric tube (NGT) using fluorescence microscopy. With the emergence of multidrug-resistant fungal infections, the present study assessed the susceptibility profile of the biofilms to antifungal azoles namely fluconazole, miconazole, voriconazole, and posaconazole using the standard disc diffusion method. Microscopic studies of C. albicans biofilms revealed a complex heterogeneous structure with yeast cells and hyphal elements entrenched within a polysaccharide matrix. Planktonic C. albicans cells remained susceptible with posaconazole, fluconazole, miconazole, and voriconazole. However, the fungal biofilms exhibited resistance with miconazole. There was a significant reduction in the zone of inhibition on the 24-h, 48-h, and 72-h biofilm formation with posaconazole, voriconazole, and fluconazole, respectively. Kinetic investigation on C. albicans biofilm with posaconazole revealed a zero-order kinetic profile (R2=0.9774) whereas with voriconazole exhibited a first-order kinetic profile (R2=0.9974). These findings can possibly provide information regarding the resistance of fungal biofilms with antifungal azoles. Demonstration of common biofilm features will extend the findings of this study beyond fungi to polymicrobial infections, as new information and insights will influence several disciplines ranging from environmental microbiology to pharmaceutical drug design intended for biofilm-associated infections.


Posaconazole, Fluconazole, Miconazole, Voriconazole, Feeding tube, Kinetic equations.


Enteral tube feeding is a standard of practice for patients who have functional gastrointestinal tracts but cannot acquire their nutritional needs through normal oral intake (De Legge, 2017). One type of tube that is used for short term enteral tube feeding is the nasogastric tube (NGT). This fine tube is inserted through the nostril of the patient, passes along nasopharynx and esophagus, and finally, into the stomach (Best, 2016). Thus, feeding tubes are usually made of either silicone or polyurethane because they can withstand the gastric acid of the stomach and are able to maintain their position for more than 10-14 d (Dougherty & Lister, 2015). However, the increasing usage of implanted medical devices also increases device-associated infections, such as biofilm formation of fungal species. Candida is the most common genus of fungi that colonizes medical devices by forming resilient biofilm (Desai et al., 2014). Center for Disease Control recognizes C. albicans as the third most commonly isolated bloodstream pathogen in hospitalized patients where mortality rate is up to 50% (Tsui et al., 2016). Pathogenesis of C. albicans is a consequence of its biofilm formation on host or abiotic surfaces. Silva and colleagues (2017) reported that an estimate of 100,000 deaths annually were caused by biofilm infection. Furthermore, Nobile and Johnson (2015) reported in their study that National Institutes of Health identified biofilm formation of C. albicans to be the cause of 80% of all microbial infections, ranging from superficial mycoses to more serious infections with higher mortality rates. Among the different major classes of antifungal drugs available for treating mucosal or systemic candidiasis, azoles are frequently used because of its availability for oral administration, economical price, and less toxicity (Whaley et al., 2016). The utility of enteral tube feeding for patients with complications such as poor voluntary intake or gut dysfunction is increasing worldwide (Blumenstein et al., 2014). The present study described the morphology of C. albicans biofilm on the surface of silicone NGT using fluorescence microscopy. One of the major concerns in fungal infections today is the development of multidrug-resistant strains due to broad-spectrum antibiotics (Perlin et al., 2015). Hence, the present study assessed the antifungal activity of fluconazole, miconazole, voriconazole, and posaconazole to C. albicans biofilms using the standard disc diffusion method. Moreover, the susceptibility profile of the sessile cells to antifungal azoles was described using different kinetic rate equations. Findings of this study will provide additional information on the biofilm formation of C. albicans on silicone NGT with emphasis on its morphological features and susceptibility kinetic profile with the selected antifungal azoles.

Materials and Methods

Organism, Culture Conditions, and Inoculum
Candida albicans (ATCC 14053) isolate was kindly provided by the Department of Medical Microbiology, College of Public Health, University of the Philippines Manila. The organism was maintained, grown, and subcultured at 37°C on Sabouraud dextrose agar (SDA) plates 48 h prior to use. The inoculum was prepared by placing three distinct 1.5-mm 48-h colonies into 10 mL of sterile distilled water warmed to 37°C as modified from Andes et al. (2004). The final inoculum was adjusted to 7.46 (±0.07) log10 CFU/mL using serial dilution and the viable fungal counts of the inoculum were confirmed by plating on SDA. Alternatively, the suspension was vortexed for 15 s and its turbidity was adjusted to have the final stock suspension of 1.0 to 5.0 x 106 cells/mL. The turbidity was adjusted by adding saline solution or more colonies in order to achieve the turbidity produced by the 0.5 McFarland standard at 530 nm wavelength (National Committee for Clinical Laboratory Standards (NCCLS), 2004).

Candida albicans Biofilm Formation on Silicone Nasogastric Tube
A modified method (Hawser & Douglas, 1994; Chandra et al., 2001) for growing biofilms was employed in this study. Disks with surface area of 0.16 cm2 (0.2 cm x 0.8 cm) from the silicone NGT (Fr5, Medline®, NeoMed, Inc.) were prepared. These disks were placed in glass culture plates for sterilization. Once oven-dried, these strips were individually placed in 96-well tissue culture plates. Standardized cell suspensions (100µL) of the final inoculum was applied to the surface of each disk, supplemented with 50 mM glucose (200µL), and then incubated for up to 72 h at 37°C for the biofilm formation. All experimental setups were carried out in triplicates.

Microscopic Examination of Candida albicans Biofilms
Assessment on the morphological structure and appearance of the biofilms on the surface of silicone NGT was performed using fluorescence microscopy. To remove the nonadherent cells, disks were individually submerged in a new 96-well plate containing 0.15 M phosphate buffer solution (PBS, 300µL) as modified from Chandra et al. (2001). The surfaces of the disks with biofilms were stained for 15 min with 2 mL Sypro® Ruby (Invitrogen, USA) and were subsequently transferred to microscope slides. The dye was used to stain the fungal cell wall, revealing a dense matrix between the hyphae and biofilm (Steinberg et al., 1996). The stained disks were examined under a fluorescence microscope (lmax = 450 nm).

Susceptibility Kinetic Profile of Candida albicans Biofilms to Antifungal Azoles
Antifungal susceptibility of C. albicans planktonic cells and sessile cells (24, 48, and 72 h) was monitored using the Clinical and Laboratory Standards Institute (CLSI, 2017) standard disc diffusion method. Following biofilm formation, the disc diffusion method was employed to determine zone of inhibition of the antifungal azoles. A standard test tube was prepared by inoculating three colonies of C. albicans in 10 mL sterile distilled water adjusted to 107 cells/mL. Moreover, the disks were individually submerged in a new 96-well plate with 0.15 M PBS (300µL). Varied number of strips were transferred to a test tube containing 2 mL of sterile distilled water until similar turbidity was obtained with the established standard test tube and confirmed by standard plating procedure. A sterile cotton swab was dipped in the suspension and streaked in many directions over the entire surface of the Mueller-Hinton agar (MHA) plate supplemented with 2% glucose and 0.5µg/mL methylene blue. The inoculated agar was air dried for 30 min. With a pair of forceps, each disc containing antifungal drug was dispensed on the surface of the agar distributed in such a way that their distance from one another is no less than 24 mm from the center (NCCLS, 2004). The four antifungal discs, fluconazole (25µg) (Oxoid Ltd.), posaconazole (5µg) (Liofilchem Diagnostic), voriconazole (1µg) (Oxoid Ltd.), and miconazole (10µg) (Liofilchem Diagnostic), were placed in the MHA plates, incubated for 24 h at 37oC, and then the zone of inhibition (mm) was measured. The zone of inhibition was measured at the transitional phase wherein apparent decrease in the growth and size of colonies was observed. In addition to the Clinical and Laboratory Standards Institute (CLSI, 2017) guidelines, reference obtained from the Susceptibility Testing of Yeasts (STY, 2011) was also considered in the interpretation of the measured zone of inhibition (Table 1).

Table (1):
Clinical and Laboratory Standards Institute (CLSI) and Susceptibility Testing of Yeasts (STY) interpretive guidelines on antifungal susceptibility testing.

Antifungal Azole Zone of inhibition diameter (mm) interpretation Reference
Resistant Intermediate Susceptible-Dose Dependent Susceptible
Posaconazole (5 μg) < 13 14 – 16 > 17 STY, 2011
Fluconazole (25 μg) < 14 15 – 18 > 19 STY, 2011
Fluconazole (25 μg) < 13 14 – 16 > 17 CLSI, 2017
Miconazole (10 μg) < 11 12 – 19 > 20 STY, 2011
Voriconazole (1 μg) < 14 15 – 16 > 17 CLSI, 2017
Voriconazole (1 μg) < 13 14 – 16 > 17 STY, 2011

Numerical Calculations and Data Analyses
Quantitative measures were subjected to analysis of variance and made use of Bonferroni test in the post hoc analysis. Several kinetic equations including zero-order, first-order, and second-order models were employed in elucidating the rate mechanisms regarding the susceptibility kinetic profile of C. albicans biofilms with the selected antifungal azoles. The parameters of these kinetic equations were estimated employing the linearized forms of the kinetic equations (Table 2) using linear regression analysis (Sumalapao, 2017; Sumalapao, 2018).

Table (2):
Nonlinear and linearized forms of the susceptibility kinetic models.

Kinetic Model Nonlinear Model Linearized Form

zt (mm): zone of inhibition at time t (hour); z0 (mm): zone of inhibition at t=0; k0 (mm/hour): zero-order rate constant; k1 (mm/hour): first-order rate constant; k2 (mm-1hour-1): second-order rate constant


Examination of the biofilm formation via fluorescence microscopy revealed a dense matrix in the areas between the hyphae in a biofilm (Fig. 1). In the initial adherence stage, which occurred during the first 12 h, colonization of C. albicans on the surface of the device was observed microscopically. The aggregation complexity increases as the biofilm matures with time. A mature biofilm on the 72-h formation was observed to be embedded in a matrix of exopolysaccharide (Fig. 1C). However, biofilms with less cell density were observed on 72 h suggesting biofilm detachment and reduction which can lead to possible accumulation of biochemical metabolites and waste products. Microscopic studies of C. albicans biofilms on the surface of silicone NGT revealed a complex heterogeneous structure with yeast cells and hyphal elements entrenched within a polysaccharide matrix. Microscopic images revealed a highly heterogeneous architecture of mature C. albicans biofilms in terms of the distribution of fungal cells and polysaccharide matrix.

Fig. 1. Fluorescence microscopy of Candida albicans biofilms (in white arrows) on the surface of silicone nasogastric tube at (A) 24 h, (B) 48 h, and (C) 72 h. Magnification: X40.

Table (3):
Antifungal susceptibility of Candida albicans biofilm on the surface of silicone nasogastric tube to azoles.

Azoles Zone of inhibition diameter (mean ± standard deviation, mm)
Plankton cells 24-hr biofilm 48-hr biofilm 72-hr biofilm
Fluconazole (25 μg) 28.33 ± 0.58a 25.67 ± 1.53a 26.33 ± 0.58a 21.33 ± 1.15b
Miconazole (10 μg) 21.33 ± 0.58a 11.67 ± 0.58b 10.33 ± 0.58bc 9.67 ± 0.58c
Posaconazole (5 μg) 24.00 ± 1.00a 20.33 ± 0.58b 18.67 ± 0.58b 18.67 ± 1.53b
Voriconazole (1 μg) 23.67 ± 0.58a 21.67 ± 0.58ab 21.00 ± 1.00b 17.67 ± 0.58c

Values with identical superscript letters in a given row do not differ at 5% level of significance using Bonferroni test
In vitro susceptibility testing of C. albicans planktonic cells and biofilms revealed varying profiles with the different antifungal azoles. Some of these representative test plates are presented in Fig. 2. The planktonic C. albicans cells were susceptible to posaconazole, fluconazole, miconazole, and voriconazole (Table 3). However, for the susceptibility profile of fungal biofilms with the antifungal azoles, resistance to miconazole was identified (Table 3). Zone of inhibition with miconazole significantly differed between the planktonic cells and the 24-h biofilms (p<0.05). Despite of the resistance profile identified with miconazole, the mean zone of inhibition in the 24-h and 48-h biofilms did not differ (Table 3). However, the 72-h biofilms had a significant reduction in the zone of inhibition when compared with the 24-h biofilms and planktonic cells (p<0.05). Moreover, the fungal biofilms remained susceptible to other antifungal azoles. Although these fungal biofilms were susceptible to fluconazole, a significant reduction in the zone of inhibition on the 72-h biofilm formation was observed (Table 3). Significant reductions in the zone of inhibition were also observed as early as 24 h and 48 h to posaconazole and voriconazole, respectively (Table 3). Zone of inhibition of sessile cells with posaconazole did not differ across the entire biofilm formation (p>0.05). The susceptibility pattern of C. albicans biofilms with posaconazole exhibits a zero-order kinetic profile (R2=0.9774, Table 4) with a mean reduction rate of 0.0972 mm/h in the zone of inhibition (p=0.0114). Had resistance pattern of biofilms with voriconazole behaved in the same zero-order kinetics (R2=0.9955), there is an average of 0.0830 mm/h reduction in the zone of inhibition. However, susceptibility of sessile cells with voriconazole exhibited a first-order kinetic profile (R2=0.9974, Table 4). The mean reduction in the zone of inhibition is 0.0041 mm/h under the first-order kinetic model (p=0.0013) with a significant difference in the susceptibility profile between the 48-h and 72-h biofilm formation (Table 3).

Table (4):
Parameter estimates of the different kinetic rate equations describing the susceptibility of Candida albicans biofilms on the surface of silicone nasogastric tube to antifungal azoles.

Kinetic Model Parameter Antifungal Azole  
Posaconazole Fluconazole Miconazole Voriconazole
Zero-order -0.0972 -0.1398 -0.0655 -0.0830
28.4275 17.5836 22.4480 23.5742
R2 0.9774 0.5290 0.6113 0.9955
SSE 0.5892 36.3623 7.3658 0.0846
p 0.0114 0.2306 0.2181 0.0023
First-order -0.0040 -0.0096 -0.0031 -0.0041
28.5932 16.9328 22.3590 23.7013
R2 0.9744 0.6398 0.6188 0.9974
SSE 0.0002 0.0267 0.0030 2.20e-5
p 0.0129 0.2001 0.2134 0.0013
Second-order 0.0002 0.0007 0.0001 0.0002
28.8082 16.2800 22.2670 23.8681
R2 0.9688 0.6941 0.6254 0.9954
SSE 2.32e-6 0.0006 3.54e-5 5.08e-7
p 0.0157 0.1669 0.2092 0.0023

z0 (mm): zone of inhibition at t=0; k0 (mm/hour): zero-order rate constant; k1 (mm/hour): first-order rate constant; k2 (mm-1.hour-1): second-order rate constant; R2: coefficient of determination; SSE: sum of squares of the error; p: p-value

Fig. 2. Susceptibility profile of (A) 24-h, (B) 48-h, and (C) 72-h Candida albicans biofilm: fluconazole (FCA), miconazole (MCL), posaconazole (POS), and voriconazole (VO).


Candida albicans, a commensal microorganism, can be found on mucosal surfaces such as oral cavity, gut, and vagina (Williams et al., 2013). However, its asymptomatic colonization becomes pathogenic when its local environment is altered because of a change in the immune response of the host. Its development as a pathogenic fungi is caused by its capability to switch morphology and its ability to form biofilm, the latter is considered as an important factor in the contribution of C. albicans to human diseases (Tsui et al., 2016). Growth of C. albicans biofilm begins with the formation of basal layer by adhesion of yeast cells on a surface. This basal layer is composed of long tubular cells which can extend to form hyphae, and eventually a mature biofilm can form after addition of proteins and carbohydrates, forming an extracellular matrix (Xu et al., 2019). In the present study, biofilm formation by C. albicans initially involved adhesion of yeast cells to the surface of NGT. With the dimorphic switching of the organism from yeast cells to hyphal form, it resulted to matrix formation and complex biofilm architectural structure. As a dimorphic organism, C. albicans morphogenetic conversions, the ability to reversibly switch between yeast and filamentous forms, are important for multiple aspects of C. albicans biology and pathogenicity. Filamentation seems to play a critical role in the development of the spatially organized architecture observed in mature and highly structured C. albicans biofilm. Hyphae are essential elements for providing structural integrity to fully developed biofilms. When representative microscopic images of the biofilms at varying magnifications were obtained, the thickness of the mature biofilm appears varied over the different areas on the surfaces of the medical device. Individual yeast cells appeared discernible with the less dense biofilm matrix. Moreover, imaging of the biofilms using fluorescence microscopy revealed a heterogeneous structure, a network of extracellular matrix strands, characterized by the presence of yeast cells and hyphal forms. These C. albicans hyphal elements were implicated in fungal infections (Gale et al., 1998; Yaar et al., 1997; Yamada-Okabe et al., 1999).

Fungal infections, device-related biofilm infections caused by C. albicans in particular, had been linked with an increase use of medical device among immunocompromised patients or for surgical advances (Shinde et al., 2012). In 2015, it was reported that these caused 65% of infections in catheterized patients (Yousif et al., 2015). Recurring infections and death can result from such fungal biofilms (Pandolfi et al., 2019) and these clinical problems are further aggravated by resistance to antifungal drugs. The use of these antifungal drugs depends on the sensitivity profile of species, anatomical site it was found, and the type of infection (De Oliveria Santos et al., 2018). Azoles, which include triazoles and imidazoles, remain to be the largest family of antifungal drugs. Triazoles, which include posaconazole, fluconazole, and voriconazole, are considered in the treatment of superficial and systemic fungal infections (Sheehan et al., 1999). Triazoles inhibit lanosterol 14-a-demethylase, an important enzyme in ergosterol biosynthesis pathway, resulting in aberrant sterol intermediates accumulation and subsequent fungal growth restriction (Fera et al., 2009). Similarly, imidazoles such as miconazole respond to induce membrane damage by inhibiting ergosterol synthesis leading to the accumulation of lanosterol. Imidazoles were observed to have fungistatic activity, but a leak in membranes from sterol perturbations has eventually resulted in fungal death (Sud & Feingold, 1981). Azoles inhibit lanosterol 14-a-sterol demethylase encoded in ERG11 gene, a gene responsible for ergosterol biosynthesis. Ergosterol is the largest component of fungal cell wall, therefore, its downregulation leads to increased membrane fluidity. Increased membrane fluidity makes the cell vulnerable to toxic 14-a-methylated sterol that when accumulates inside the cell would result in growth arrest and apoptosis (Musu et al., 2014). In the present study, planktonic C. albicans remained susceptible to antifungal azoles, namely posaconazole, fluconazole, miconazole, and voriconazole. Biofilms on the surface of NGT exhibited consistent susceptibility profile to fluconazole. Fluconazole is a broad-spectrum antifungal that is the first choice of drug because of its high efficiency, safety profile, and bioavailability (Liu et al., 2015). Fluconazole, most commonly prescribed antifungal drug for Candida albicans infection, is a triazole antifungal used to treat cryptococcal meningitis in AIDS and oropharyngeal candidiasis. It has been extensively used over the years because of its efficacy as first line drug which is also the principal reason of increasing resistance of C. albicans to fluconazole and change of etiological agent of infection from albicans to non-albicans species (Musu et al., 2014). Fluconazole resistance to C. albicans (14.1%) was reported in 2014 due to repeated use of the drug (Liu et al., 2015). Fluconazole and other triazoles target C. albicans by inhibiting cytochrome P450 enzyme lanosterol demethylase in the ergosterol biosynthesis pathway, preventing activation of oxygen and demethylation of lanosterol to become ergosterol. Such inhibition promotes toxic accumulation of methylated sterols in fungal cell which eventually leads to cell death (Berkow & Lockhart, 2017).

In addition to fluconazole, planktonic cells and biofilms on the surface of NGT also exhibited consistent susceptibility profile to voriconazole. Voriconazole is also an active triazole derived from fluconazole with enhanced antifungal spectrum (Saravolatz et al., 2003). Furthermore, voriconazole and other second-generation azoles were also reported to be fungicidal for some filamentous organisms. Unlike fungistatic drugs, voriconazole completely interrupts ergosterol synthesis resulting to cell death (Saravolatz et al., 2003). However, a study conducted by Flowers and colleagues (2015) showed that when wild-type azole-susceptible strain of C. albicans were exposed to ERG11 alleles carrying an amino acid substitution and tested for susceptibility to voriconazole, substantial decrease in susceptibility was observed. In addition, Wiebusch & colleagues (2014) tested susceptibility of 24 samples of C. albicans against fluconazole and voriconazole. They found out that 54.16% of C. albicans were sensitive to fluconazole while 45.83% were resistant. A similar result was observed with voriconazole.

Moreover, both the planktonic and sessile cells remained susceptible with posaconazole. Posaconazole is a broad-spectrum triazole used in the treatment of Candida, Aspergillus, and other opportunistic and dimorphic fungi encountered clinically (Gonzalez et al., 2007). Posaconazole is considered a more dominant inhibitor of 14-a-demethylase sterol and is essentially for prophylaxis of invasive forms of fungal infections (Owotade et al., 2016). In an experiment conducted by Owotade and colleagues (2016), C. albicans strains were collected from the oral cavities of 205 HIV patients, 49 cancer patients, and 20 healthy individuals to test for antifungal susceptibility. Their results showed that seven isolates (3.4%) of C. albicans were resistant to posaconazole. It was also stated in the same study that posaconazole increased its minimum inhibitory concentration from 1.1% in 2001 to 3.2% in 2009. Furthermore, Chen and colleagues (2013) demonstrated that posaconazole (0.03–16µg/mL) with caspofungin (0.25–16µg/mL) exhibited synergistic antifungal activity against C. albicans. These cases of increased resistance with posaconazole were presumably caused by a sixth mutation in ERG11, which functions to disrupt the binding segments of the drugs, elevating the level of posaconazole resistance (Li et al., 2015).

The present study identified that the serially grown biofilms were found to be resistant to miconazole. Miconazole was the first azole identified to be effective against systemic infections (Loeffler & Stevens, 2003). As was described for triazoles, miconazole also functions to affect membrane asymmetry and fluidity, and this altered plasma membrane composition may have contributed to the observed resistance to miconazole (Loeffler & Stevens, 2003). Miconazole is an exception to fungistatic azoles because of its fungicidal effect against yeast cells by accumulating reactive oxygen species (ROS). De Cremer and colleagues (2015) found that miconazole and artemisinins combination have the potential to treat infection caused by biofilm formation of one strain of C. albicans. Artemisinins are antimalarial drugs that were found to act synergistically with miconazole because of dihydroartemisinin, a structural homologue of artesunate, a semisynthetic derivative of artemisinin, and its ability to increase the capability of miconazole against biofilms of C. albicans (De Cremer et al., 2015). Furthermore, another study conducted by De Cremer and colleagues (2016) also showed that combination of miconazole (125µM) to antimycin A (25µM) exhibited high superoxide induction, which is significant to fungicidal compounds and their production of ROS to increase susceptibility of miconazole to biofilms.

In the present study, C. albicans biofilms exhibited a decreasing susceptibility pattern with the tested antifungal azoles. In particular, the susceptibility pattern of C. albicans biofilms with posaconazole has a kinetic profile described by a zero-order rate equation. Posaconazole is a new triazole antifungal drug which exhibits a similar mechanism of action as other azole derivatives. Moreover, C. albicans biofilms on the surface of silicone NGT remained susceptible to fluconazole and voriconazole, although a significant reduction in the zones of inhibition was noted as early as 48-h biofilm formation. Nett et al. (2014) established the tolerance to fluconazole of in vitro and in vivo C. albicans biofilms on silicone urinary catheter. Fluconazole was selected primarily for its clinical utility in the treatment of urinary candidiasis since the presence of a halogenated phenyl ring increases its antifungal activity (Dash & Elmquist, 2001). Fluconazole basically alters the cellular membranes which leads to increased membrane permeability, impaired uptake of precursor, and leakage of essential elements from the cell (Charlier et al., 2006). However, Nasrollahi et al. (2015) reported resistance of C. albicans to fluconazole since Pir1p, a protein responsible for cell wall maintenance, was found overexpressed in the fungal cell wall due to prolonged fluconazole treatment. Moreover, another triazole examined in the present study was voriconazole, a second-generation triazole and a synthetic derivative of fluconazole. Candida albicans biofilms when compared to planktonic cells exhibited a significantly different susceptibility pattern, but the fungal biofilm remained susceptible to voriconazole. This might be attributed to the stronger affinity of voriconazole with lanosterol 14-a-demethylase which results in complete disruption of ergosterol synthesis and eventual fungal cell death (Saralovatz et al., 2003). Interestingly, the present study identified the resistance of C. albicans biofilms on the surface of silicone NGT to miconazole. However, miconazole, as an imidazole, should have its cumulative effect on C. albicans consistent with its direct interaction with the fungal plasma membrane causing growth inhibition, and its contact with the intracellular membranes resulting in cellular disorganization, and eventual fungal death (Cope, 1980).

The planktonic C. albicans is different from C. albicans in the biofilms on the surfaces of medical devices. The fungal biofilm exhibited tolerance to some antifungal drugs and biofilms are becoming progressively resistant to the first-line and second-line antifungal drugs (Martin, 1999). Some of the major mechanisms which lead to azole resistance include reduced drug intracellular accumulation, decreased target affinity, and drug effect counteraction (Sanglard, 2016; Spampinato & Leonardi, 2013). Resistance of biofilms to antifungal drugs is found to be multifactorial, a combination of the b-1,3 glucan drug sequestration activity, upregulation of several efflux pump genes in the biofilms, and the presence of persister cells (Desai et al., 2014). Several documents alarmingly reported the developing resistance of C. albicans to azoles. Mutations in ERG11 have been observed to alter substitution of amino acids, which leads to the revision of mechanisms of azoles, preventing ERG11 inhibition resulting to resistance (Flowers et al., 2015). Another mechanism involved in drug-resistance property of C. albicans is the upregulation of several efflux pump genes, which specifically increases resistance of C. albicans cell membrane to azoles during early stages of biofilm development. CDR1 and CDR2 ATP binding cassette transporters, along with MDR1, a major facilitator transporter were found in low concentrations in clinical isolates without exposure to antifungal resistance (Silva et al., 2017). In increased levels, C. albicans cell membrane also exhibited increased drug resistance to azoles. Furthermore, Silva and colleagues (2017) reported that efflux pumps are time-specific, and higher expression are observed in 12-h biofilm formation, in comparison to a 48-h mature biofilm formation. A group of cells, called persister cells, may also contribute to biofilm drug resistance (Palkova & Vichova, 2016). In Candida biofilms, persister cells have the capacity to repopulate the biofilm even after they were eliminated by amphotericin B and chlorhexidine (Palkova & Vichova, 2016). The resistance of these cells can be attributed to the upregulated production of proteins involved in its virulence and stress responses (Li et al, 2015). Due to these emerging cases of antifungal drug resistance, there is an increase in the synthesis and manufacture of new drugs. However, some newer generation azoles have no significant activity against C. albicans biofilms (Katragkou et al., 2008).


Candida albicans biofilms on the surface of NGT revealed a complex structure with hyphal elements and yeast cells entrenched within a polysaccharide matrix. These biofilms were resistant to miconazole but remained susceptible to fluconazole and voriconazole, although significant reduction in the zone of inhibition was observed as the biofilm matures. The susceptibility kinetic profile of the fungal biofilm with posaconazole can be described using the zero-order rate kinetic model. In the present study, information on model biofilms with focus on structural organization and susceptibility pattern can possibly provide baseline information which can lead to further resistance mechanism elucidation and subsequent development of novel therapies.


The organism used in this study was kindly provided by the Department of Medical Microbiology, College of Public Health, University of the Philippines Manila. Fluorescence microscopy was performed in the Molecular Biology Unit Laboratory, De La Salle University, Manila, Philippines.

Conflict of Interest
The authors declare that there is no conflict of interest.

Authors’ Contribution
All authors listed have made a substantial, direct, and intellectual contribution to the work, and approved it for publication.


Data Availability
All datasets analyzed in the study are included in the manuscript and presented as tables and figures.

Ethics Statement
The study protocol was approved by the University of the Philippines Manila Research Ethics Board (UPMREB 2018-486-01). The biosafety clearance was granted by the University of the Philippines Manila Institutional Biosafety and Biosecurity Committee (UPMIBBC 2018-018).

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