A quantitative real-time RT-PCR assay for mature C. albicans biofilms
© Xie et al; licensee BioMed Central Ltd. 2011
Received: 30 June 2010
Accepted: 6 May 2011
Published: 6 May 2011
Fungal biofilms are more resistant to anti-fungal drugs than organisms in planktonic form. Traditionally, susceptibility of biofilms to anti-fungal agents has been measured using the 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxyanilide (XTT) assay, which measures the ability of metabolically active cells to convert tetrazolium dyes into colored formazan derivatives. However, this assay has limitations when applied to high C. albicans cell densities because substrate concentration and solubility are limiting factors in the reaction. Because mature biofilms are composed of high cell density populations we sought to develop a quantitative real-time RT-PCR assay (qRT-PCR) that could accurately assess mature biofilm changes in response to a wide variety of anti-fungal agents, including host immune cells.
The XTT and qRT-PCR assays were in good agreement when biofilm changes were measured in planktonic cultures or in early biofilms which contain lower cell densities. However, the real-time qRT-PCR assay could also accurately quantify small-medium size changes in mature biofilms caused by mechanical biomass reduction, antifungal drugs or immune effector cells, that were not accurately quantifiable with the XTT assay.
We conclude that the qRT-PCR assay is more accurate than the XTT assay when measuring small-medium size effects of anti-fungal agents against mature biofilms. This assay is also more appropriate when mature biofilm susceptibility to anti-fungal agents is tested on complex biological surfaces, such as organotypic cultures.
Microbial biofilms have an innate resistance to antimicrobials and immune attack and have been recently linked to many recalcitrant or recurrent infections [1–3]. The ability of C. albicans to form biofilms on prosthetic devices and mucosal surfaces is believed to be intimately associated with its ability to trigger systemic or mucosal infection [4–6]. Therefore the development of novel anti-biofilm agents is of paramount importance in the treatment or prevention of these infections.
Susceptibility of Candida biofilms to anti-fungal agents is frequently measured using colorimetric assays that estimate metabolic activity of viable cells residing in biofilms [2, 6, 7]. Such assays have also been widely used to assess viable cell numbers [8–16]. In these assays metabolically active cells convert tetrazolium dyes into colored formazan derivatives that can be measured by a multi-well scanning spectrophotometer [9, 14, 16–21]. A key component of one of the formazan assays is sodium salt of 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxyanilide, or XTT. Mitochondrial dehydrogenases of viable cells cleave the tetrazolium ring of XTT yielding water-soluble orange formazan. The bioreduction of XTT is inefficient and can be potentiated by addition of an electron-coupling agent such as phenazine methosulfate [9, 13, 16, 17, 19, 22], menadione [2, 13, 16, 19, 22] or coenzyme Q0 (CoQ) [15, 20, 23].
The XTT assay has been used under various conditions for viability assessment of different organisms including mammalian cells, bacteria and fungi [19, 24]. Its wide-spread use is due to the fact that it is simple, fast, and does not require highly specialized equipment other than a spectrophotometer. However, it is accurate only if there is a linear relationship between cell metabolic activity (or cell number) and colorimetric signal. Thus, for the assay to be quantitative, it is important to optimize several key experimental parameters (such as cell number, concentration of XTT, type and concentration of electron-coupling agent) for every organism and every experimental condition [5, 12, 13, 15]. Assay optimization can be more challenging in mature biofilms since metabolic activity and viable cell number may not be linearly related [12, 13]. In addition, colony counting methods of viability assessment are not appropriate for mature biofilms since they consist of multicellular hyphal organisms encased in a polysaccharide matrix, which hinders single cell colony growth. Given these facts we sought to critically examine the limitations of the XTT assay in measuring metabolic changes in mature biofilms and develop a molecular assay based on PCR for biofilm viability estimates that would overcome these limitations.
Increasing the concentration of XTT up to 2 mg/ml (since XTT maximum solubility in water is 2.5 mg/ml) did not result in a change in OD450 when the seeding yeast cell number was equal to or lower than 1 × 105 cells per well (Figure 1A). With yeast cell numbers higher than 1 × 105 cells per well, increasing the concentration of XTT resulted in higher OD450 values, which extended the linearity range only up to 2 × 105 cells per well. This suggests that XTT solubility and final concentration are limiting factors in this reaction, especially when large numbers of yeast cells are used to start biofilms.
We also investigated if varying the concentration of the electron-coupling agent CoQ (8-350 μM) would allow us to extend the linearity range of the XTT signal. XTT conversion rates were slower at lower concentrations of CoQ, generating flat slopes (Figure 1B). However, we found that increasing the concentration of CoQ would not increase the linearity range (Figure 1B). Reading the plates at 490 nm as opposed to 450 nm or increasing the XTT reaction time to 3 hours still did not improve the linearity range (data not shown), since reaction time in higher cell densities (>106 cells/well) was typically very fast (less than 10 min). Collectively, these data suggest that the XTT assay cannot be adequately optimized to accommodate the cell numbers present in mature biofilms.
To further address this issue we developed a molecular assay for biofilm assessment based on quantitation of EFB1 gene transcripts in Candida cells, since the EF-1β protein is critical in regulating cell protein translation rates and growth . The EFB1 primer pairs specifically amplified PCR products of the predicted size (136 bp) from C. albicans cDNA and gave no PCR product when tested with HL-60 cell cDNA (data not shown). To generate standard curves amplification of serially diluted plasmid pEFB was monitored by fluorescence versus cycle number curves. The assay could detect 1 fg of pEFB, which is equivalent to 224.37 copies of pEFB.
Neutrophils exhibit potent candidacidal activities in vitro [26, 27] and interact with Candida biofilms forming on mucosal tissues in vivo . However there is a paucity of information regarding the outcome of the interactions of neutrophils with biofilm organisms . One of the difficulties in studying these interactions in vitro is the shortage of quantitative assays to accurately assess neutrophil-inflicted damage in mature biofilms. Therefore, we compared the ability of the two assays to detect and quantify damage inflicted to early and mature biofilms by HL-60 cells, a human neutrophil-like cell line.
Real-Time PCR technologies combine the sensitivity of conventional PCR with the generation of a quantifiable fluorescent signal and have been increasingly used to assess viability of microorganisms [11, 29–31]. Quantitative real-time PCR allows for the detection of PCR products produced at each step of the reaction, since an increase in reporter fluorescent signal is directly proportional to the number of amplicons generated. As we have done in this work, PCR products can be quantitated by generating a standard curve, in which the absolute concentration of the plasmid standard is known.
In this study we measured the effect of anti-fungal agents against mature biofilms with a real-time RT-PCR assay based on the quantification of EFB1 transcript copy numbers in biofilm cells. The EFB1 gene is constitutively expressed under most growth conditions and is frequently used as a normalization gene in real-time RT-PCR quantification of other Candida genes [32–37]. By designing sense primers that span an intron splice site in the EFB1 sequence, we expected that only intact mRNA molecules would serve as a template in the RT-PCR assay and that these molecules would be degraded following the death of the organisms in the biofilm. Our results with this molecular assay are consistent with our expectations and show that it is highly quantitative in a wider range of seeding fungal cell densities and that it more accurately measures small-moderate mature biofilm changes in response to stressors, compared to the traditional XTT assay. We have also shown that this assay is particularly well suited for fungal biofilm viability estimates in complex biological systems containing immune effectors or mucosal cell cultures. This may be partly due to the fact that mammalian cells also metabolize XTT, which further limits substrate availability .
Compared to the XTT assay, the real-time assay is more technically demanding, more prone to experimental errors due to the multiple additional steps required in sample preparation, more costly, and significantly more time consuming. Thus it should be reserved for susceptibility testing of mature biofilms growing in complex biological model systems containing immune effectors or mucosal cells or used as a confirmatory assay when small changes in mature biofilms are detected with the XTT assay.
In conclusion, our results indicate that the XTT assay has to be applied with caution to biological systems containing large numbers of organisms alone or in combination with mammalian cells. We also conclude that molecular assessment of biofilms based on quantitation of EFB1 transcripts is a sensitive, reproducible and quantitative method to measure the damaging effect of anti-fungal agents against mature biofilms. The new quantitative assay will aid in further investigations of the mechanisms of Candida biofilm resistance to immune effector cells, which are presently unknown. In addition the new assay can be applied in quantitative assessment of mature biofilm susceptibility to novel anti-biofilm therapeutic agents that are applied topically on mucosal surfaces.
Strain C. albicans SC5314 was used in this study . Yeast from frozen stocks were maintained on YPD agar plates. For experimentation, yeast were inoculated into YPD broth supplemented with 2% dextrose and grown overnight at 24°C with shaking. Biofilms were grown by seeding C. albicans blastoconidia in flat bottom well plates (Becton Dickinson, Franklin Lakes, N.J.) and incubating at 37°C from 3 h to 48 h. In preliminary work, five different seeding media (YNB-0.5% glucose, DMEM, DMEM-5%FBS, DMEM-10%FBS and RPMI-10%FBS) were tested. Microscopic observations showed that the best attachment of biofilms to plastic was achieved in DMEM-10%FBS. Thus we used DMEM-10%FBS (Biowest/USA Scientific) in all experiments that followed.
To grow biofilms under conditions resembling in vivo mucosal biofilm development a three dimensional model of the human oral mucosa, developed in our laboratory, was used which faithfully mimics the oral mucosal tissue architecture in vivo . Briefly, this model 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 and incubated for 24 h. To assess mucosal tissue damage and invasion tissues were formalin-fixed, embedded in paraffin and 5 μm sections were stained with the Periodic Acid Schiff (PAS) stain.
The XTT assay was performed as we described earlier . Briefly, media were aspirated from biofilms and were replaced with 100 μl/well of XTT solution (Sigma Chemical Co., St. Louis, MO) containing Coenzyme Q0 (CoQ, Sigma Chemical Co., St. Louis, MO). Fresh mixtures of XTT and CoQ [1 mg/ml and 40 μg/ml (or 220 μM), respectively, unless otherwise indicated] were prepared for each experiment. Plates were incubated at 37°C for up to 3 hours, after which 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. When optical densities were higher than the limits of the microplate reader, dilutions of the supernatants in water were made.
Quantitative Real-Time RT-PCR Assay
To quantify changes in viable biofilms using an alternative approach, we measured mRNA expression of the translation elongation factor-1β (EF-1β), encoded by the EFB1 gene in C. albicans, by real-time quantitative RT-PCR. The choice of this gene was based on these facts: a) fungal cells transcriptionally regulate components of their translational machinery according to external stresses that affect protein synthesis [25, 36]; b) the number of EFB1 gene transcripts did not change significantly during biofilm or planktonic growth between 3 h and 48 h (not shown); and c) EFB1 is frequently used as a housekeeping gene in real-time RT-PCR quantification of other Candida genes [29, 32, 33, 36]. Total RNA from biofilms was isolated using the RiboPure yeast kit (Ambion, Inc.), according to the manufacturer's instructions. RNA concentrations and purity were determined by measuring the absorbance at 260 nm and 280 nm (ND-1000 spectrophotometer, NanoDrop Technologies). Equal amounts of RNA (3 μg in 20 μl reactions) were reverse transcribed with oligo(dT) primers using Superscript reverse transcriptase II (Invitrogen).
Primers were based on the published sequence of the EFB1 gene of C. albicans. Primer sequences used were as follows: Forward: 5'- CAT TGA TGG TAC TAC TGC CAC -3'; Reverse: 5'- TTT ACC GGC TGG CAA GTC TT -3'. The forward primer spanned the sole exon-exon boundary of EFB1, thus excluding amplification of genomic C. albicans DNA. The uniqueness of the primers for C. albicans EFB1 was determined using the BLAST database http://www.tigr.org.
To generate standard curves for quantitative analyses a pEFB plasmid was prepared as follows. A 136-bp C. albicans EFB exon fragment, containing the target sequence, was amplified with the above mentioned primers. PCR was performed in a DNA thermal cycler with 1 cycle of 5 min at 95°C; 40 cycles of 1 min at 95°C, 30 s at 62°C, 30 s at 72°C; and a final extension at 72°C for 5 min. This fragment was ligated into the pCR 2.1 plasmid vector (3.931 kb) and transformed into One Shot cells (Top10F') using a TA cloning kit (Invitrogen). Plasmids were digested with xhoI to generate a linear template and purified with the PureYield™ Plasmid Miniprep System (Promega). Plasmid concentrations were determined spectrophotometrically and copy numbers calculated based on linear plasmid mass. Serial plasmid dilutions (500 pg, 50 pg, 5 pg, 500 fg, 50 fg, 5 fg, 1 fg of DNA/μl) were then used to generate standard curves for detection and quantification of EFB1 mRNA by the iCycler iQ RT-PCR assay.
Real-time PCR was performed with an iCycler iQ real-time PCR detection system (Bio-Rad). All PCR reaction mixtures contained the following: 10 μl 2 × iQ™ SYBR® Green Supermix (BioRad, Hercules, CA), 1 μl of first-strand cDNA reaction mixture or linear plasmid DNA, 0.1 μM of primers and H2O to bring the final volume to 20 μl. The program for amplification had an incubation step at 50°C for 2 min, and 95°C incubation for 5 min, followed by 40 cycles of 95°C for 10 s and 62°C for 30 s. Reactions to estimate transcript copy number were run in duplicate from two biologic RNA replicates. Data were analyzed using the iCycle iQ system software (BioRad).
Testing of planktonic cells
Candida cells were grown overnight in YPD broth as described above. Cultures were adjusted to a cellular density equivalent to 1.0 × 106 cells/ml and subjected to caspofungin (CAS, Merck Research Laboratories, Rahway, N.J.) or fluconazole (FLU, Pfizer Inc., Sandwich, United Kingdom) treatment for 24 h, at doses ranging from 0.0625-1024 μg/ml [40, 41]. Untreated cells served as negative controls. Four replicates were included in each experiment. The effects of the anti-fungals on planktonic cells were measured by colony counts on Sabouraud agar plates (CFU), or by the XTT and qRT-PCR assays as described above.
To compare the ability of the two assays to quantify changes in mature biofilms stemming from biomass reduction, organisms were grown in 12 well plates for 48 h and their biomass was physically reduced by removing 50%, 33% or 25% of the biofilm from the well surface. To perform this, the round surface area of each well was divided into two, three or four equal parts, and removal of the biofilm from 1/2, 1/3 or 1/4 of the surface area was accomplished with the help of a modified rubber policeman, with a sweeping edge cut to the size of the well radius. Remaining biofilm cells observed microscopically were removed using a sterile glass suction tip. XTT and real-time RT-PCR measurements in residual biofilms in these wells were subsequently compared to intact biofilms.
To compare the ability of the two assays to quantify changes in viable biofilms in response to different stressors, biofilms grown on plastic were exposed to pharmacologic [amphotericin B (AMB), 4 μg/ml, 4 h], environmental (100°C, 1 h) or immune cell stressors and viability was measured by the XTT or qRT-PCR assays. To quantify susceptibility to immune cell-inflicted damage we used a neutrophil-like cell line (HL-60, ATCC), as previously described . Briefly, pre-activated HL-60 cells (1.25% DMSO for 7-9 days) were added to biofilms at varying effector to target cell ratios, based on seeding cell densities. After incubation at 37°C, 5% CO2 for 2 hours, media were aspirated, HL-60 cells were lysed with sterile H2O, and fungal viability was assessed with the XTT or qRT-PCR assays. Biofilms grown on mucosal tissues were exposed to anti-fungal drugs (4 μg/ml amphotericin B, 70 μg/ml fluconazole or 8 μg/ml caspofungin [40, 41]) or HL-60 cells for 24 hours, followed by mammalian cell lysis with sterile water. This was followed by the XTT or qRT-PCR assays. Anti-biofilm activity was calculated according to the following formula: % fungal damage = (1-x/n)*100, where × is the OD450 or EFB1 transcript copy number of experimental wells (C. albicans with stressors/effectors) and n is the OD450 or EFB1 transcript copy number of control wells (C. albicans only). All experiments were performed in triplicate.
This study was supported by NIH/NIDCR grant R01 DE13986 to ADB and in part by a General Clinical Research Center grant from NIH (M01RR06192) awarded to the University of Connecticut Health Center, Farmington, CT.
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