Candida albicans triggers recurrent infections of the oropharyngeal mucosa that result from biofilm growth. Prior studies have indicated that the transcription factor Bcr1 regulates biofilm formation in a catheter model, both in vitro and in vivo. We thus hypothesized that Bcr1 plays similar roles in the formation of oral mucosal biofilms and tested this hypothesis in a mouse model of oral infection. We found that a bcr1/bcr1 mutant did not form significant biofilm on the tongues of immunocompromised mice, in contrast to reference and reconstituted strains that formed pseudomembranes covering most of the tongue dorsal surface. Overexpression of HWP1, which specifies an epithelial adhesin that is under the transcriptional control of Bcr1, partly but significantly rescued the bcr1/bcr1 biofilm phenotype in vivo. Since HWP1 overexpression only partly reversed the biofilm phenotype, we investigated whether additional mechanisms, besides adhesin down-regulation, were responsible for the reduced virulence of this mutant. We discovered that the bcr1/bcr1 mutant was more susceptible to damage by human leukocytes when grown on plastic or on the surface of a human oral mucosa tissue analogue. Overexpression of HYR1, but not HWP1, significantly rescued this phenotype. Furthermore a hyr1/hyr1 mutant had significantly attenuated virulence in the mouse oral biofilm model of infection. These discoveries show that Bcr1 is critical for mucosal biofilm infection via regulation of epithelial cell adhesin and neutrophil function.
Citation: Dwivedi P, Thompson A, Xie Z, Kashleva H, Ganguly S, Mitchell AP, et al. (2011) Role of Bcr1-Activated Genes Hwp1 and Hyr1 in Candida Albicans Oral Mucosal Biofilms and Neutrophil Evasion. PLoS ONE 6(1): e16218. https://doi.org/10.1371/journal.pone.0016218
Editor: Dana Davis, University of Minnesota, United States
Received: August 24, 2010; Accepted: December 10, 2010; Published: January 25, 2011
Copyright: © 2011 Dwivedi et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: These studies were supported by National Institutes of Health grants RO1DE013986, RO1DE013986-08S1 (ADB) and R01AI067703 (APM). The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Oral pseudomembranous candidiasis (thrush) is the most prevalent form of Candida infection in patients with weakened or immature immune systems, such as HIV+ children, neonates and patients with malignancies , , . A resurgence of oral thrush in children was recently reported due to the rising use of inhaled corticosteroids, affecting up to 40% of children after long term treatment . Surprisingly, up to 15% of children with no underlying immune abnormalities present with oral thrush lesions in the pediatric practice .
Pseudomembranous candidiasis is one of several clinical forms of Candida infection and has distinct clinical and histopathological characteristics. Clinically this infection presents as white plaques on the oral mucosa, which can be removed by gentle rubbing . These pseudomembranes were recently recognized as archetypal, complex tissue biofilms and were proposed to be responsible for the recalcitrant nature of this infection , . Using a mouse model of oral thrush we characterized these biofilms and discovered that they are complex, comprising of yeast, hyphae, commensal bacteria, and neutrophils that form nests within the biofilm mass . Both host and fungal-derived products fill the intercellular spaces, thus forming a supporting biofilm matrix . Although several C. albicans gene products have been implicated in biofilm development on abiotic surfaces , , , , , , information on genes that enable biofilm formation on mucous membranes has only recently begun to emerge .
The transcription factor Bcr1 governs biofilm formation in vivo in the catheter, denture and vaginal models , , . Although Bcr1 is not required for hyphal morphogenesis, it acts as a positive regulator of hyphal-specific adhesins , . Manipulation of Bcr1 downstream target genes through mutation and overexpression showed that the surface adhesins Als3 and Hwp1 significantly contribute to biofilm formation in the catheter model. Because biofilm formation on abiotic and biological surfaces may be regulated by similar processes we hypothesized that a bcr1/bcr1 mutant may also be defective in oral mucosal biofilm development. Using both in vivo and in vitro models we tested the ability of this mutant to form biofilms on the oral mucosa and dissected the specific contribution of Bcr1-regulated genes in this phenotype.
Results and Discussion
To study the contribution of Bcr1-regulated genes in mucosal biofilms, a mouse oral infection model was used where C. albicans forms white pseudomembranes (biofilms) on the dorsal surface of the tongue . Tongues from animals infected with genetically manipulated strains were excised and examined by macroscopic “clinical” evaluation, assessment of cultivable fungal burden, and histologic analysis to visualize the thickness of biofilms. Consistent with results in the mouse vaginal mucosa model , we found that the bcr1/bcr1 strain was deficient in forming a clinically visible mucosal biofilm on the tongues of immunocompromised mice in vivo (Fig. 1). At the histologic level this mutant formed a thin, interrupted biofilm on the dorsal surface of the tongue (Fig. 1, arrows). These results are in agreement with the recently reported attenuated biofilm phenotype of a bcr1/bcr1 mutant in the rat denture biofilm model .
Tongues of immunocomrpomised animals were excised after five days of infection and the dorsal aspect was digitally photographed. Four mice were infected with each strain and representative clinical pictures are shown from 1 mouse in each group on the left panel. On the right panel, representative PAS-stained thin sections of the tongue of one mouse per group are shown. Arrows indicate the biofilm thickness.
Surface area estimates of pseudomembranes, examined macroscopically during necropsy, showed approximately 80–100% coverage of the tongue dorsal surface with biofilm formed by the reference and reconstituted strains, while less than 10% of the tongue surface in mice infected with the bcr1/bcr1 mutant was covered by biofilm (Fig. 2A). In accordance with this we also found that the tongue fungal burden of mice infected with the bcr1/bcr1 mutant was significantly lower than that of mice infected with either the reference or complemented strains (Fig. 2B).
(A) Percent tongue surface area covered by biofilm. Results represent the average of 4 tongues in each group. Image J was used to calculate the area covered by white plaques as well as the total surface area of each tongue. Error bars represent standard deviations. *p = 0.0000 for bcr1/bcr1 mutant versus reconstituted strain, **p = 0.026 for bcr1/bcr1TEF-HWP1 versus bcr1/bcr1 mutant strain. (B) Tongue fungal burden. Results represent the average of four mice per group and error bars represent standard deviations. *p = 0.0004 for bcr1/bcr1 mutant versus reconstituted strain, **p = 0.0002 for bcr1/bcr1TEF-HWP1 versus bcr1/bcr1 mutant strain.
C. albicans also forms a biofilm when grown on a three-dimensional model of the human oral mucosa . When grown on this model, the bcr1/bcr1 mutant was slow in forming a mature biofilm, and after 24 hours of growth formed a biofilm comprised mainly of yeast cells, in contrast to its reference and complemented strains (Fig. 3). Moreover, this mutant was significantly less capable of triggering mucosal tissue damage (Fig. 4). This could be attributed to the dominant yeast morphotype in biofilm cells, which lacks expression of several hyphae-specific epithelial adhesins that may also be involved in oral epithelial cell damage , , .
Histologic pictures show 40× magnification after 6 and 24 hours of inoculation. Thin sections were stained with PAS. Arrows indicate biofilms forming on the (apical) epithelial surface of the cultures. Results are representative of one of three experiments.
Cell damage by the bcr1/bcr1 mutant and reference strains was quantified by the release of lactate dehydrogenase (LDH) in the media. Results are the mean ± SD of three experiments, each condition set up in triplicate. *bcr1/bcr1 mutant significantly different from DAY185 (reference) strain, p = 0.001–0.03.
Adhesion is a fundamental process under Bcr1 control that promotes biofilm formation on catheter surfaces . Therefore, we evaluated the contribution of the Bcr1-regulated adhesins Als1, Als3 and Hwp1 in the capacity of C. albicans to form a biofilm on the oral mucosa in vivo. Increased expression of ALS1 in the bcr1/bcr1 mutant background did not significantly affect the surface area covered by biofilm (Fig. 2A), increase the tongue fungal burden (Fig. 2B), or promote mucosal biofilm formation at the histologic or macroscopic level (Fig. 5). Similarly, expression of ALS3 under the TEF1 promoter did not significantly affect the surface area covered by biofilm (Fig. 2A), the tongue fungal burden (Fig. 2B), or the biofilm thickness (Fig. 5, arrows); the strain's intermediate phenotype is discussed further below. A clear example of phenotypic rescue from overexpression was observed with HWP1. Specifically, HWP1 overexpression in this genetic background improved biofilm formation and increased fungal burden in the animals significantly (Fig. 2A, 2B, 5). This finding agrees with observations in the catheter biofilm model where this construct partly but significantly reversed the bcr1/bcr1 phenotype . In addition to being important in biofilm development , , Hwp1 is also a well established oral epithelial cell adhesin , which plays a role in the pathogenesis of oral infection , . Our findings provide additional support for the role of Hwp1 in oral infection, and in addition argue that the reduced expression of HWP1 in the bcr1/bcr1 mutant is a major cause of the mutant's oral epithelial biofilm defect.
Tongues of immunocomrpomised animals were excised after five days of infection and the dorsal aspect was digitally photographed. Four mice were infected with each strain and representative clinical pictures are shown from 1 mouse in each group on the left panel. On the right panel, representative PAS-stained thin sections of the tongue of one mouse per group are shown. Arrows indicate the biofilm thickness.
ALS3 overexpression in the bcr1/bcr1 background partly reversed the bcr1/bcr1 phenotype, based upon visual inspection (Fig. 5). However, the mean percentage surface area covered by biofilm and the CFU counts from infected tissue with this strain did not reach statistical significance (Fig. 2A, 2B). These findings were thus somewhat in contrast with data in the venous catheter biofilm model showing that, although Als3 is not absolutely required for biofilm formation, ALS3 overexpression completely reverses the biofilm phenotype of the bcr1/bcr1 mutant . We note that these two biofilm experimental systems are quite different, and that C. albicans adhesins exhibit high substrate specificity, even when they have highly related sequences in their binding domains . In addition, innate host defense mechanisms in the oral cavity, coupled with salivary flow and mechanical cleansing by chewing, may modify the ability of these strains to establish a biofilm in vivo.
However, because regulation of biofilm-associated gene expression may vary significantly in different biofilm model systems , we wanted to rule out the possibility that Als3 expression is Bcr1-independent in the oral mucosa, which could explain the disparate results with these strains in different model systems. Therefore, we quantified Als3 gene expression in the bcr1/bcr1 mutant and adhesin-overexpressing strains, when grown on a three dimensional model of the human oral mucosa. As anticipated, when grown on an oral mucosa tissue analogue Als3 expression levels were lower in the bcr1/bcr1 deletion mutant as well as in the ALS1- and HWP1-overexpressing strains, compared to the reference strain (Fig. 6). In contrast, Als3 expression levels in the ALS3-overexpressing strain were three fold higher than the reference strain (Fig. 6). This finding argues against the possibility of differential regulation of Als adhesins in the oral mucosa, and further supports the idea that different experimental systems can reveal tissue-specific functions of adhesins. Thus our results establish that Hwp1, and not Als3, is a critical Brc1 adhesin target relevant to oral thrush. In agreement with our findings, it has been reported that biofilm formation in a subcutaneous rat model requires Bcr1 but not Als3 .
The indicated strains of C. albicans were grown for 24 h and C. albicans RNA was extracted. The relative transcript levels of Als3 were measured by real-time PCR. Results are the mean ±SD of three biological replicates, each tested in duplicate.
Due to the complexity of the structure of oral mucosal biofilms , transcriptional deregulation of a single C. albicans gene is unlikely to be responsible for mediating loss of the mucosal biofilm phenotype in the bcr1/bcr1 mutant. This explains the finding that HWP1 overexpression only partially reversed the bcr1/bcr1 phenotype. We thus sought to identify additional, adhesion-unrelated genes under the transcriptional control of Bcr1, contributing to its inability to form mucosal biofilms.
A prominent feature of infections characterized by soft tissue biofilms is infiltration of infected tissues by neutrophils, which confer innate immune protection , . We previously showed that neutrophils infiltrate the oral mucosal biofilm mass in this mouse oral infection model . We thus hypothesized that the bcr1/bcr1 mutant fails to develop a robust biofilm on the oral mucosa at least partly because it is more efficiently cleared by biofilm-infiltrating neutrophils. To begin to test this hypothesis we examined susceptibility of this mutant to killing on plastic by the HL-60 neutrophil-like cell line using a modification of the XTT assay . Indeed, we found that the bcr1/bcr1 mutant was more susceptible to killing than its reference and reconstituted strains, regardless of the effector to target ratio used in killing assays (Fig. 7). In fact the effector to target ratio of the bcr1/bcr1 strain corresponding to the MIC50 in this assay was five times lower than the reference and reconstituted strains (Fig. 7). These findings were confirmed when freshly isolated human neutrophils were used in killing assays (Fig. 8A–B). Finally, we extended these findings to the oral mucosa, by testing susceptibility of the bcr1/bcr1 mutant to leukocyte killing on a three-dimensional model of the human oral mucosa (Fig. 8C). As expected, this mutant was also more susceptible to leukocyte-inflicted damage when grown on a three dimensional model of the human oral mucosa (Fig. 8C), supporting our hypothesis that it may be more effectively cleared in the oral environment.
Strains were exposed to HL-60 cells that had been differentiated into neutrophil-like cells in vitro. HL-60 cells were added to C. albicans for 3 h at effector to target cell ratios (E∶T) ranging from 5∶1 to 1∶2. Results represent the mean ± SD of three experiments, each condition set up in triplicate.
Susceptibility was tested on 96 well plates (A,B) or on a three dimensional model of the human oral mucosa (C). Strains were exposed to differentiated HL-60 cells (A,C) or freshly isolated neutrophils from one human donor (B) at an effector to target cell ratio of 1∶1 (A,B) or 10∶1 (C). Results represent the mean ± SD of three experiments, each condition set up in triplicate. *p<0.03 and **p<0.05 for a comparison between the bcr1/bcr1 mutant and HYR1- overexpressing strain in the bcr1/bcr1 background.
Overexpression of HYR1, but not HWP1, in the bcr1/bcr1 background, significantly rescued the higher susceptibility phenotype of this mutant to killing by leukocytes both on plastic and on the oral tissue surface (Fig. 8A–C). These findings confirmed previous reports showing that Hyr1, but not Hwp1 is involved in susceptibility to neutrophil killing , . More importantly, these data, combined with the finding that the hyr1/hyr1 mutant was highly susceptible to killing in an oral mucosal tissue model (Fig. 8C), suggest that this gene is indirectly contributing to the observed mucosal biofilm phenotype by conferring resistance to neutrophil killing. Thus, this study now strongly implicates Hyr1 in innate immune cell evasion of C. albicans in the oral mucosa.
Hyr1 is a GPI-anchored cell wall protein, expressed during hyphal development  and repressed upon neutrophil encounter , , however, relatively little is known about its exact role in virulence. Because there is no severe biofilm defect on catheter surfaces in the hyr1/hyr1 mutant , we hypothesized that this mutant may have only a moderately attenuated biofilm phenotype on the tongue surface. As expected, this mutant formed biofilms covering part of the tongue surface, and overexpression of HYR1 in the bcr1/bcr1 background did not rescue the oral mucosal biofilm phenotype (Fig. 9, 10A). However, we also anticipated that due to increased susceptibility to neutrophil killing, preventing deep tissue invasion , the tissue fungal burden in mice infected with the hyr1/hyr1 mutant would be severely attenuated. Consistent with this hypothesis, histological assessment showed that, in contrast to the reference strain which reached the granular and prickle epithelial cell layers, the hyr/hyr1 mutant was confined within the keratin layer (Fig. 9 arrows). As a result, the tissue fungal burden was severely attenuated in mice infected with the hyr1/hyr1 mutant (Fig. 10B). However, overexpression of HYR1 in the bcr1/bcr1 background was not sufficient to reverse the tissue invasion or fungal burden phenotype of the bcr1/bcr1 mutant (Fig. 9 arrows, and 10B). This finding is consistent with the fact that, in addition to neutrophil clearance, other virulence mechanisms directly related to epithelial adhesion and invasion, as noted above, are contributing to the severely attenuated phenotype of this mutant.
Tongues of immunocomrpomised animals were excised after five days of infection and the dorsal aspect was digitally photographed. Four mice were infected with each strain and representative clinical pictures are shown from 1 mouse in each group on the left panel. On the right panel, representative PAS-stained thin sections of the tongue of one mouse per group are shown. Arrows indicate microorganisms invading the spinous cell layer of the epithelium (strain DAY286) or remaining superficially within biofilms (hyr1/hyr1 mutant and HYR1- overexpressing strains).
(A) Percent tongue surface area covered by biofilm. Results represent the average of 4 tongues in each group. Image J was used to calculate the area covered by white plaques as well as the total surface area of each tongue. Error bars represent standard deviations. *p = 0.015 for hyr1/hyr1 mutant versus reference strain; **p = 0.008 for hyr1/hyr1 mutant versus bcr1/bcr1TEF-HYR1 strain; ***p = 006 for bcr1/bcr1TEF-HYR1 versus reference strain. (B) Tongue fungal burden. Results represent the average of four mice per group and error bars represent standard deviations. *p = 0.000 for bcr1/bcr1TEF-HYR1 or hyr1/hyr1 compared to reference strain, **p = 0.23 for hyr1/hyr1 versus the bcr1/bcr1TEF-HYR1 strain.
In conclusion, our studies provide valuable new insights which promote the understanding of the pathogenesis of Candida mucosal biofilm infections. We have shown that the transcription factor Bcr1 is a critical regulator of oral mucosal biofilm formation and identified two genes, HWP1 and HYR1, under Bcr1 control that govern the inability of the bcr1/bcr1 strain to form robust oral mucosal biofilms. Although much is known about the function of Hwp1 and its role in oral mucosal infection, this is the first study implicating Hyr1 in the pathogenesis of oral biofilm infection.
The study was approved by the University of Connecticut Health Center Animal Care Committee (Protocol Number: 2009-541) and the Human Subjects Protection Office (IRB Number: 02-288-2). Animals were monitored daily for distress. Given that the oral cavity is readily accessible, lesions are detected relatively early in their onset and animals are euthanized after lesion formation before visible distress/behavior signs are observed. A written informed consent was signed by all healthy human blood donors.
C. albicans strains
The C. albicans deletion mutants and overexpressing strains and their construction are described in detail elsewhere , . Strain DAY185 is a His+ reference strain used to construct the His+ bcr1/bcr1 deletion mutant used in all experiments , . Strain DAY286  was used as a reference strain for the hyr1/hyr1 null mutant in some experiments. The two reference strains were phenotypically similar in all experimental systems described in this study. All strains exhibited similar growth characteristics when grown overnight in epithelial cell media (not shown).
Mouse model of mucosal biofilm
Different strains were tested for their ability to form an oral biofilm using our previously described mouse model . Briefly, 6–8 week old female C57BL/6 mice were immunosuppressed by subcutaneous injection with cortisone acetate (225 mg/kg, dissolved in 200 µl PBS containing 0.5% Tween-20) on days -1, 1 and 3 relative to infection. To deliver the C. albicans challenge mice were anaesthetized by an intramuscular injection of ketamine and xylazine (90–100 mg/kg and 10 mg/kg of body weight, respectively) and a small cotton pad soaked with 100 µl of C. albicans cell suspension (6×108 cells/ml) was used to swab the entire oral cavity. The swab was left for 2 h under the tongue and was removed before the animals awoke. This procedure was repeated 2 days later and mice were sacrificed after 5 days of total exposure to C. albicans. During the infection period animals were also given drinking water containing a daily-fresh suspension of each strain (6×106 yeast organisms/ml) to maintain high oral carriage loads throughout the experimental period. Tongues were removed aseptically at necropsy, photographed, and images were saved as jpg files. Images were subsequently analyzed using the NIH Image J software (http://rsb.info.nih.gov/ij) and data were expressed as percent surface area covered by biofilm (total surface area of white lesions/entire tongue dorsal surface area).
To determine the number of viable organisms in oral tissues, the tongue was longitudinally dissected in three equal pieces and the central portion was processed for colony forming unit (CFU) quantification at the time of sacrifice. The tissue was weighed, rinsed with phosphate buffered saline and then homogenized using a tissue homogenizer. Serial dilutions were plated onto Sabouraud dextrose agar plates containing 10 mg/ml chloramphenicol (Sigma, USA) and plates were incubated at 30°C for 48 h. Results were expressed as log CFU counts/g of tissue. One portion of the longitudinally dissected tongues was fixed with 10% buffered formalin and embedded in paraffin. Five µm thick sections were prepared and stained with hematoxylin and eosin (H&E) and Periodic Acid Schiff (PAS) stains.
Three-dimensional model of the oral mucosa
To investigate in vitro mucosal biofilm formation, tissue damage by C. albicans and leukocyte-mediated fungal killing in an oral-like environment we used a three-dimensional model of the oral mucosa as previously described . This system is composed of 3T3 fibroblasts embedded in a biomatrix of collagen type I, overlaid by a multilayer of well-differentiated oral epithelial cells (OKF6/TERT-1). C. albicans cells (1×106 yeast cells) were added to the cultures apically in 100 µl of airlift medium without FBS and antibiotics. In some experiments, after 6–44 hours of co-culture mucosal tissues were formalin-fixed, embedded in paraffin and sections were stained with PAS. The extent of mucosal tissue damage was quantified at different time points by measuring extracellular leakage of LDH in the medium, using the cytotox-96 assay (Promega) as previously described . Leukocyte-mediated fungal cell damage was assessed in this model as described below.
Assessment of susceptibility to neutrophil killing
The susceptibility of the different strains to a neutrophil-like cell line (HL-60 cells) or to human freshly isolated peripheral blood neutrophils was determined by the XTT assay, as previously described . Briefly, HL-60 cells were cultured in RPMI 1640 medium containing 10% fetal bovine serum and 25 mM HEPES and were induced to differentiate into neutrophil-like cells by exposure to 1.25% of dimethyl sulfoxide for 7–9 days. Neutrophils were isolated from anticoagulated blood of one healthy donor by dextran T-500 (Sigma-Aldrich, St. Louis, MO) sedimentation followed by Histopaque-1077 (Sigma-Aldrich) density gradient centrifugation. Granulocyte-erythrocyte pellet was collected, and erythrocytes were lysed by hypotonic shock. Neutrophils were washed with HBSS without Ca, Mg (Mediatech, Inc., Herndon, VA) and resuspended in RPMI1640 (Mediatech, Inc.) with 10 mM HEPES (Gibco Invitrogen, Grand Island, NY). The resulting cell preparations consisted of more than 95% of neutrophils by Wright-Giemsa stain and were more than 98% viable by trypan blue exclusion.
To perform Candida killing assays on plastic, overnight YPD broth cultures of C. albicans were resuspended in DMEM 10% fetal bovine serum and were added to 96 well plates (100 µl/well) at concentrations ranging from 105 to 2×104 cells/well. There was a linear relationship between viable cell number and colorimetric signal (XTT activity) in this concentration range with all strains (not shown). Immune cells were added to C. albicans at effector to target cell ratios (E∶T) ranging from 5∶1 to 1∶2. To perform Candida killing assays in an oral-like environment C. albicans cells were grown as above and added apically to the three-dimensional model of the oral mucosa (1×105 yeast cells/tissue), in 50 µl of airlift medium without FBS and antibiotics. After a 4 h incubation period, differentiated HL-60 cells were added apically at an effector to target ratio of 10∶1 and incubated for 3 more hours.
After incubation of Candida with effectors at 37°C, 5% CO2 for 3 hours, media were aspirated and mammalian cells were lysed with sterile H2O. 100 µl/well of XTT solution containing Coenzyme Q0 (0.25 mg/ml XTT and 40 µg/ml coenzymeQ0) was added to each well and plates were incubated at 37°C and 5%CO2 for 2 hrs. Supernatants were transferred into new plates, and optical densities (OD) were measured by an Opsys Microplate Reader (Thermo Labsystems, Franklin, MA) at 450–490 nm, with a 630 nm reference filter. Antifungal activity was calculated according to the following formula: %fungal damage = (1−x/n)*100, where x is the OD450 of experimental wells (C. albicans with effectors) and n is the OD450 of control wells (C. albicans only).
To test expression of the Bcr1-regulated gene ALS3 in an oral model of infection, we quantified expression by real-time RT-PCR after 24 h growth on the 3D model of the human oral mucosa. Briefly, media were aspirated and the collagen gel was transferred to a centrifuge tube, followed by a brief centrifugation at 4°C. Next, the transferred gel was dissolved in mammalian cell RNA extraction buffer (4 M guanidine thiocyanate, 25 mM sodium citrate, 0.5% Sarkosyl [N-lauroyl-sarcosine], and 0.1 M Beta-mercaptoethanol), and repeatedly passed through a 20½ gauge needle . The organisms were spun in a centrifuge at 14 000×g at 4°C, and then snap-frozen in liquid nitrogen. Fungal RNA was isolated using the RiboPure yeast kit (Ambion, Inc.), according to the manufacturer's instructions. RNA was reverse transcribed with oligo(dT) primers using Superscript reverse transcriptase II (Invitrogen).
Primers used for measurement of transcript levels were as follows. We used the sequences described by Green et al.  for measuring ALS3 RNA levels: ALS3 FOR: 5′-CCACTTCACAATCCCCATC-3′, and ALS3 REV: 5′-CAGCAGTAGTAGTAACAGTAGTAGTTTCATC-3′. We used sequences described by Blankenship et al.  for measuring control TDH3 RNA levels: TDH3 FOR: 5′-AAATCGGTGGAGACAACAGC-3′, and TDH3 REV: 5′-TGCTAAAGCCGTTGGTAAGG-3′.
RT-PCR reaction conditions were as follows: 2× iQ SYBR Green Supermix (Bio-Rad), 1 µl of first-strand cDNA reaction mixture, and 0.1 µM of primers were mixed in a total volume of 50 µl per reaction. Real-time PCR was carried out in duplicate for each sample using the iCycler iQ real-time PCR detection system (Bio-Rad). The program for amplification included an initial denaturation step at 95°C for 5 min, followed by 40 cycles of 95°C for 45 s and 58°C for 30 s. Product amplification was detected using SYBR Green fluorescence during the 58°C step. The reaction specificity was monitored by melt-curve analysis. TDH3 was used as a reference gene for normalization of gene expression, which was done using Bio-Rad iQ5 software (ΔΔCT method).
Conceived and designed the experiments: ADB APM. Performed the experiments: PD AT HK ZX SG. Analyzed the data: PD AT HK SG. Contributed reagents/materials/analysis tools: APM. Wrote the paper: ADB.
- 1. Brent N (2001) Thrush in the breastfeeding dyad: results of a survey on diagnosis and treatment. Clin Pediatr 40: 503–506.N. Brent2001Thrush in the breastfeeding dyad: results of a survey on diagnosis and treatment.Clin Pediatr40503506
- 2. Fonseca R, Cardoso AS, Pomarico I (2000) Frequency of oral manifestations in children infected with human immunodeficiency virus. Quintessence Int 31: 419–422.R. FonsecaAS CardosoI. Pomarico2000Frequency of oral manifestations in children infected with human immunodeficiency virus.Quintessence Int31419422
- 3. Nicolatou-Galitis O, Dardoufas K, Markoulatos PL, Sotiropoulou-Lontou A, Kyprianou K, et al. (2001) Oral pseudomembranous candidiasis, herpes simplex virus-1 infection, and oral mucositis in head and neck cancer patients receiving radiotherapy and granulocyte-macrophage colony-stimulating factor (GM-CSF) mouthwash. J Oral Pathol Med 30: 471–480.O. Nicolatou-GalitisK. DardoufasPL MarkoulatosA. Sotiropoulou-LontouK. Kyprianou2001Oral pseudomembranous candidiasis, herpes simplex virus-1 infection, and oral mucositis in head and neck cancer patients receiving radiotherapy and granulocyte-macrophage colony-stimulating factor (GM-CSF) mouthwash.J Oral Pathol Med30471480
- 4. Passalacqua G, Albano J, Canonica GW, Bachert C, Van Cauwenberge P, et al. (2000) Inhaled and nasal corticosteroids: safety aspects. Allergy 55: 16–33.G. PassalacquaJ. AlbanoGW CanonicaC. BachertP. Van Cauwenberge2000Inhaled and nasal corticosteroids: safety aspects.Allergy551633
- 5. Deconinck S, Boeke AJP, van der Waal I, van der Windt DAWM (2003) Incidence and management of oral conditions in general practice. Brit J Gen Pract 53: 130–132.S. DeconinckAJP BoekeI. van der WaalDAWM van der Windt2003Incidence and management of oral conditions in general practice.Brit J Gen Pract53130132
- 6. Holmstrup P, Axell T (1990) Classification and clinical manifestations of oral yeast infections. Acta Odontol Scand 48: 57–59.P. HolmstrupT. Axell1990Classification and clinical manifestations of oral yeast infections.Acta Odontol Scand485759
- 7. Coogan M, Fidel PL, Komesu MC, Maeda N, Samaranayake LP (2006) Candida and mycotic infections. Adv Dent Res 19: 130–138.M. CooganPL FidelMC KomesuN. MaedaLP Samaranayake2006Candida and mycotic infections.Adv Dent Res19130138
- 8. Jin Y, Yip HK, Samaranayake YH, Yau JY, Samaranayake LP (2003) Biofilm-forming ability of Candida albicans is unlikely to contribute to high levels of oral yeast carriage in cases of human immunodeficiency virus infection. J Clin Microbiol 41: 2961–2967.Y. JinHK YipYH SamaranayakeJY YauLP Samaranayake2003Biofilm-forming ability of Candida albicans is unlikely to contribute to high levels of oral yeast carriage in cases of human immunodeficiency virus infection.J Clin Microbiol4129612967
- 9. Dongari-Bagtzoglou A, Kashleva H, Dwivedi P, Diaz PI, Vasilakos JP (2009) Characterization of Mucosal biofilms by C. albicans. PLoS One 24 4: e7967.A. Dongari-BagtzoglouH. KashlevaP. DwivediPI DiazJP Vasilakos2009Characterization of Mucosal biofilms by C. albicans.PLoS One24 4e7967
- 10. Kumamoto C (2005) A contact-activated kinase signals Candida albicans invasive growth and biofilm development. PNAS 102: 5576–5581.C. Kumamoto2005A contact-activated kinase signals Candida albicans invasive growth and biofilm development.PNAS10255765581
- 11. Nobile C, Mitchell AP (2005) Regulation of cell-surface genes and biofilm formation by the C. albicans transcription factor Bcr1p. Curr Biol 15: 1150–1155.C. NobileAP Mitchell2005Regulation of cell-surface genes and biofilm formation by the C. albicans transcription factor Bcr1p.Curr Biol1511501155
- 12. Ramage G, VandeWalle K, Lopez-Ribot JL, Wickes BL (2002) The filamentation pathway controlled by the Efg1 regulator protein is required for normal biofilm formation and developmentj in Candida albicans. FEMS Microbiol Lett 214: 95–100.G. RamageK. VandeWalleJL Lopez-RibotBL Wickes2002The filamentation pathway controlled by the Efg1 regulator protein is required for normal biofilm formation and developmentj in Candida albicans.FEMS Microbiol Lett21495100
- 13. Richard M, Nobile CJ, Bruno VM, Mitchell AP (2005) Candida albicans Biofilm-Defective Mutants. Eukaryotic Cell 4: 1493–1502.M. RichardCJ NobileVM BrunoAP Mitchell2005Candida albicans Biofilm-Defective Mutants.Eukaryotic Cell414931502
- 14. Thomas D, Bachmann SP, Lopez-Ribot JL (2006) Proteomics for the analysis of the Candida albicans biofilm lifestyle. Proteomics 6: 1–10.D. ThomasSP BachmannJL Lopez-Ribot2006Proteomics for the analysis of the Candida albicans biofilm lifestyle.Proteomics6110
- 15. Zhao X, Daniels KJ, Oh S-H, Green CB, Yeater KM, et al. (2006) Candida albicans Als3p is required for wild-type biofilm formation on silicone elastomer surfaces. Microbiology 152: 2287–2299.X. ZhaoKJ DanielsS-H OhCB GreenKM Yeater2006Candida albicans Als3p is required for wild-type biofilm formation on silicone elastomer surfaces.Microbiology15222872299
- 16. Harriott M, Lilly EA, Rodriguez TE, Fidel PL Jr, Noverr MC (2010) Candida albicans forms biofilms on the vaginal mucosa. Microbiology 156: 3635–3644.M. HarriottEA LillyTE RodriguezPL Fidel JrMC Noverr2010Candida albicans forms biofilms on the vaginal mucosa.Microbiology15636353644
- 17. Nett J, Marchillo K, Spiegel CA, Andes DR (2010) Development and validation of an in vivo Candida albicans biofilm denture model. Infect Immun 78: 3650–3659.J. NettK. MarchilloCA SpiegelDR Andes2010Development and validation of an in vivo Candida albicans biofilm denture model.Infect Immun7836503659
- 18. Nobile C, Andes DR, Nett JE, Smith FJ, Yue F, et al. (2006a) Critical role of Bcr1-dependent adhesins in C. albicans biofilm formation in vitro and in vivo. PLoS Pathog 2: e63.C. NobileDR AndesJE NettFJ SmithF. Yue2006aCritical role of Bcr1-dependent adhesins in C. albicans biofilm formation in vitro and in vivo.PLoS Pathog2e63
- 19. Phan Q, Myers CL, Fu Y, Sheppard DC, Yeaman MR, et al. (2007) Als3 is a Candida albicans invasin that binds to cadherins and induces endocytosis by host cells. PLoS Biol 53: e64.Q. PhanCL MyersY. FuDC SheppardMR Yeaman2007Als3 is a Candida albicans invasin that binds to cadherins and induces endocytosis by host cells.PLoS Biol53e64
- 20. Staab J, Bradway SD, Fidel PL, Sundstrom P (1999) Adhesive and mammalian transglutaminase substrate properties of Candida albicans Hwp1. Science 283: 1535–1538.J. StaabSD BradwayPL FidelP. Sundstrom1999Adhesive and mammalian transglutaminase substrate properties of Candida albicans Hwp1.Science28315351538
- 21. Villar C, Kashleva H, Dongari-Bagtzoglou A (2004) Role of C. albicans Polymorphism in Interactions with Oral Epithelial Cells. Oral Microbiol Immunol 19: 262–269.C. VillarH. KashlevaA. Dongari-Bagtzoglou2004Role of C. albicans Polymorphism in Interactions with Oral Epithelial Cells.Oral Microbiol Immunol19262269
- 22. Nobile C, Nett JE, Andes DR, Mitchell AP (2006b) Function of Candida albicans adhesion Hwp1 in biofilm formation. Eukaryot Cell 5: 1604–1610.C. NobileJE NettDR AndesAP Mitchell2006bFunction of Candida albicans adhesion Hwp1 in biofilm formation.Eukaryot Cell516041610
- 23. Cheng S, Clancy CJ, Checkley MA, Handfield M, Hillman JD, et al. (2003) Identification of Candida albicans genes induced during thrush offers insight into pathogenesis. Mol Microbiol 48: 1275–1288.S. ChengCJ ClancyMA CheckleyM. HandfieldJD Hillman2003Identification of Candida albicans genes induced during thrush offers insight into pathogenesis.Mol Microbiol4812751288
- 24. Sundstrom P, Balish E, Allen CM (2002) Essential role of the Candida albicans transglutaminase substrate, hyphal wall protein 1, in lethal oroesophageal candidiasis in immunodeficient mice. J Infect Dis 185: 521–530.P. SundstromE. BalishCM Allen2002Essential role of the Candida albicans transglutaminase substrate, hyphal wall protein 1, in lethal oroesophageal candidiasis in immunodeficient mice.J Infect Dis185521530
- 25. Zhao X, Oh S-H, Cheng G, Green CB, Nuessen JA, et al. (2004) ALS3 and ALS8 represent a single locus that encodes a Candida albicans adhesin; functional comparisons between Als3p and Als1p. Microbiology 150: 2415–2428.X. ZhaoS-H OhG. ChengCB GreenJA Nuessen2004ALS3 and ALS8 represent a single locus that encodes a Candida albicans adhesin; functional comparisons between Als3p and Als1p.Microbiology15024152428
- 26. Ricicová M, Kucharíková S, Tournu H, Hendrix J, Bujdáková H, et al. (2010) Candida albicans biofilm formation in a new in vivo rat model. Microbiology 156: 909–919.M. RicicováS. KucharíkováH. TournuJ. HendrixH. Bujdáková2010Candida albicans biofilm formation in a new in vivo rat model.Microbiology156909919
- 27. Jesaitis A, Franklin MJ, Berglund D, Sasaki M, Lord CI, et al. (2003) Compromised host defense on Pseudomonas aeruginosa biofilms: Characterization of neutrophil and biofilm interactions. J Immunol 171: 4329–4339.A. JesaitisMJ FranklinD. BerglundM. SasakiCI Lord2003Compromised host defense on Pseudomonas aeruginosa biofilms: Characterization of neutrophil and biofilm interactions.J Immunol17143294339
- 28. Scaramuzzino D, McNiff JM, Bessen DE (2000) Humanized In Vivo Model for Streptococcal Impetigo. Infect Immun 68: 2880–2887.D. ScaramuzzinoJM McNiffDE Bessen2000Humanized In Vivo Model for Streptococcal Impetigo.Infect Immun6828802887
- 29. Dongari-Bagtzoglou A, Villar CC, Kashleva H (2005) Candida albicans-infected oral epithelial cells augment the anti-fungal activity of human neutrophils in vitro. Med Mycol 43: 545–549.A. Dongari-BagtzoglouCC VillarH. Kashleva2005Candida albicans-infected oral epithelial cells augment the anti-fungal activity of human neutrophils in vitro.Med Mycol43545549
- 30. Luo G, Ibrahim AS, Spellberg B, Nobile CJ, Mitchell AP, Fu Y (2010) Candida albicans Hyr1p confers resistance to neutrophil killing and is a potential vaccine target. J Infect Dis 11: 1718–1728.G. LuoAS IbrahimB. SpellbergCJ NobileAP MitchellY. Fu2010Candida albicans Hyr1p confers resistance to neutrophil killing and is a potential vaccine target.J Infect Dis1117181728
- 31. Tsuchimori N, Sharkey LL, Fonzi WA, French SW, Edwards JE, Filler SG (2000) Reduced virulence of HWP1-deficient mutants of Candida albicans and their interactions with host cells. Infect Immun 68: 1997–2002.N. TsuchimoriLL SharkeyWA FonziSW FrenchJE EdwardsSG Filler2000Reduced virulence of HWP1-deficient mutants of Candida albicans and their interactions with host cells.Infect Immun6819972002
- 32. Bailey D, Feldmann PJF, Boney M, Gow N, Brown AJP (1996) The Candida albicans HYR1 gene, which is activated in response to hyphal development, belongs to a gene family encoding yeast cell wall proteins. J Bacteriol 178: 5353–5360.D. BaileyPJF FeldmannM. BoneyN. GowAJP Brown1996The Candida albicans HYR1 gene, which is activated in response to hyphal development, belongs to a gene family encoding yeast cell wall proteins.J Bacteriol17853535360
- 33. Fradin C, De Groot P, MacCallum D, Schaller M, Klis F, et al. (2005) Granulocytes govern the transcriptional response, morphology and proliferation of Candida albicans in human blood. Mol Microbiol 56: 397–415.C. FradinP. De GrootD. MacCallumM. SchallerF. Klis2005Granulocytes govern the transcriptional response, morphology and proliferation of Candida albicans in human blood.Mol Microbiol56397415
- 34. Schaller M, Boeld U, Oberbauer S, Hamm G, Hube B, Korting H (2004) Polymorphonuclear leukocytes (PMNs) induce protective Th1-type cytokine epithelial responses in an in vitro model of oral candidosis. Microbiology 150: 2807–2813.M. SchallerU. BoeldS. OberbauerG. HammB. HubeH. Korting2004Polymorphonuclear leukocytes (PMNs) induce protective Th1-type cytokine epithelial responses in an in vitro model of oral candidosis.Microbiology15028072813
- 35. Davis D, Wilson RB, Mitchell AP (2000) RIM101-dependent and -independent pathways govern pH responses in Candida albicans. Mol Cell Biol 20: 971–978.D. DavisRB WilsonAP Mitchell2000RIM101-dependent and -independent pathways govern pH responses in Candida albicans.Mol Cell Biol20971978
- 36. Davis D, Bruno VM, Loza L, Filler SG, Mitchell AP (2002) Candida albicans Mds3p, a conserved regulator of pH responses and virulence identified through insertional mutagenesis. Genetics 162(4): 1573–1581.D. DavisVM BrunoL. LozaSG FillerAP Mitchell2002Candida albicans Mds3p, a conserved regulator of pH responses and virulence identified through insertional mutagenesis.Genetics162415731581
- 37. Dongari-Bagtzoglou A, Kashleva H (2006) Development of a highly reproducible 3D organotypic model of the oral mucosa. Nature Protocols 1: 2012–2018.A. Dongari-BagtzoglouH. Kashleva2006Development of a highly reproducible 3D organotypic model of the oral mucosa.Nature Protocols120122018
- 38. Chomczynski P, Sacchi N (1987) Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 162: 156–159.P. ChomczynskiN. Sacchi1987Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.Anal Biochem162156159
- 39. Green CB, Cheng G, Chandra J, Mukherjee P, Ghannoum MA, Hoyer LL (2004) RT-PCR detection of Candida albicans ALS gene expression in the reconstituted human epithelium (RHE) model of oral candidiasis and in model biofilms. Microbiology 150(2): 267–275.CB GreenG. ChengJ. ChandraP. MukherjeeMA GhannoumLL Hoyer2004RT-PCR detection of Candida albicans ALS gene expression in the reconstituted human epithelium (RHE) model of oral candidiasis and in model biofilms.Microbiology1502267275
- 40. Blankenship JR, Fanning S, Hamaker JJ, Mitchell AP (2010) An extensive circuitry for cell wall regulation in Candida albicans. PLoS Pathog Feb 5;6(2): e1000752.JR BlankenshipS. FanningJJ HamakerAP Mitchell2010An extensive circuitry for cell wall regulation in Candida albicans.PLoS Pathog Feb5;62e1000752