JoVE Journal > Immunology and Infection
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Immunology and Infection

एक filamentous फफूंद कालोनियों पर बैक्टीरियल biofilms के गुणात्मक बहु पैमाने विश्लेषण के लिए नई विधि का उपयोग Confocal और इलेक्ट्रॉन माइक्रोस्कोपी

Published: January 25, 2017
doi:
10.3791/54771
, , , , ,
1Interactions Arbres – Microorganismes, UMR1136,INRA Université de Lorraine, 2Ecologie et Ecophysiologie Forestières – PTEF, UMR 1137,INRA Université de Lorraine, 3Biosciences Division,Oak Ridge National Laboratory

Summary

This protocol describes a new method to grow and qualitatively analyze bacterial biofilms on fungal hyphae by confocal and electron microscopy.

Abstract

बैक्टीरियल biofilms अक्सर फंगल सतहों पर फार्म और इस तरह के चयापचय सहयोग, प्रतियोगिता, या शिकार के रूप में कई बैक्टीरियल फंगल बातचीत प्रक्रियाओं में शामिल किया जा सकता है। biofilms के अध्ययन पर्यावरण विज्ञान, खाद्य उत्पादन, और चिकित्सा सहित कई जैविक क्षेत्रों में महत्वपूर्ण है। हालांकि, कुछ अध्ययनों से आंशिक रूप से उन्हें जांच की कठिनाई के कारण, इस तरह के जीवाणु biofilms पर ध्यान केंद्रित किया है। गुणात्मक और मात्रात्मक biofilm के लिए तरीके साहित्य में वर्णित विश्लेषण के अधिकांश अजैव सतहों पर या इस तरह के उपकला कोशिकाओं की एक monolayer के रूप में सजातीय और पतली जैविक सतहों पर बनाने biofilms के लिए ही उपयुक्त हैं।

जबकि लेजर स्कैनिंग confocal माइक्रोस्कोपी (एल एस सी एम) अक्सर सीटू और इन विवो biofilms में विश्लेषण करने के लिए प्रयोग किया जाता है, इस तकनीक बहुत ही चुनौतीपूर्ण जब फंगल hyphae पर बैक्टीरियल biofilms के लिए आवेदन किया, मोटाई और hyphal netw के तीन आयाम के कारण हो जाता हैorks। इस कमी को दूर करने के लिए, हम फंगल कालोनियों में hyphal परतों के संचय को सीमित करने की एक विधि के साथ माइक्रोस्कोपी के संयोजन एक प्रोटोकॉल विकसित की है। इस पद्धति का उपयोग करके, हम दोनों एल एस सी एम और स्कैनिंग इलेक्ट्रॉन माइक्रोस्कोपी (SEM) का उपयोग कर कई पैमानों पर फंगल hyphae पर बैक्टीरियल biofilms के विकास की जांच करने में सक्षम थे। इस रिपोर्ट में सूक्ष्मजीव संस्कृतियों, जीवाणु biofilm गठन की स्थिति, biofilm धुंधला हो जाना, और एल एस सी एम और SEM दृश्यावलोकन सहित प्रोटोकॉल का वर्णन है।

Introduction

कवक और बैक्टीरिया एक दूसरे के साथ बातचीत करने के लिए है क्योंकि वे सबसे स्थलीय वातावरण में रहना कई अवसर हैं। उनकी विविधता और उनकी सर्वव्यापकता के कारण, इन मुलाकातों जैव प्रौद्योगिकी, कृषि, खाद्य प्रसंस्करण, और दवा के 1, 2 सहित कई जैविक क्षेत्रों में महत्वपूर्ण हैं। आणविक बातचीत भागीदारों के बीच आदान-प्रदान को अनुमति देने के लिए निकटता की एक निश्चित डिग्री की आवश्यकता होती है, और कुछ मामलों में, भागीदारों के एक भौतिक एसोसिएशन एक कार्यात्मक बातचीत 3 के लिए आवश्यक है। बैक्टीरिया और कवक के बीच एक आम शारीरिक एसोसिएशन फंगल सतहों 4 पर बैक्टीरियल biofilms के गठन है। बैक्टीरियल कोशिकाओं और कवक hyphae के बीच यह सीधा संपर्क अंतरंग बातचीत है कि विभिन्न जैविक प्रक्रियाओं में शामिल रहे हैं अनुमति देता है। उदाहरण के लिए, चिकित्सा, oppor पर Pseudomonas aeruginosa की biofilm गठन के अध्ययन मेंtunistic कवक रोगज़नक़ कैंडिडा सफेद biofilm गठन और डाह 5 के बीच की कड़ी में अंतर्दृष्टि प्रदान कर सकता है। कृषि में, अध्ययनों से संकेत मिलता है कि संयंत्र से विकास को बढ़ावा देने के rhizobacteria और जैव नियंत्रण बैक्टीरिया एक वृद्धि की दक्षता जब एक मिश्रित biofilm में एक कवक के साथ जुड़े है। उदाहरण के लिए, Bradyrhizobium elkanii जब एक मिश्रित biofilm 6 में Pleurotus ostreatus के साथ जुड़े एन 2 -fixing गतिविधि में वृद्धि की है। अंत में, जैविक उपचार में, बैक्टीरियल कवक मिश्रित biofilms प्रदूषित साइटों 7 के remediation, 8 के लिए इस्तेमाल किया गया है।

एल एस सी एम विशेष रूप से biofilms का अध्ययन करने के बाद से यह न्यूनतम pretreatments साथ हाइड्रेटेड biofilms रहने वाले जिससे biofilm संरचना और संगठन बनाए रखने का एक तीन आयामी अवलोकन के लिए अनुमति देता है उपयुक्त है। इस प्रकार, एल एस सी एम द्वारा biofilm विश्लेषण बहुत जानकारीपूर्ण है, विशेष रूप से करने के लिए detएक परिपक्व biofilm के विकास के लिए आसंजन कदम से, biofilm गठन के समय पाठ्यक्रम और विशेषता चरणों 9, 10 का पता लगाने के एमिन। यह भी विशेष रूप से biofilm संरचना और मैट्रिक्स 11, 12 कल्पना करने के लिए या biofilm आकार 13, 14 यों के लिए अनुकूल है। हालांकि इस पद्धति अजैव या पतली जैविक सतहों पर biofilms अध्ययन करने के लिए, एक कवक filamentous कॉलोनी पर जीवाणु biofilm का अध्ययन उपयुक्त है अभी भी बहुत चुनौतीपूर्ण है। वास्तव में, सबसे filamentous कवक संस्कृति में मोटी, जटिल, tridimensional नेटवर्क का निर्माण। मोटी वस्तुओं confocal माइक्रोस्कोपी द्वारा imaged किया जा सकता है, भले ही लेजर प्रवेश की क्षीणन और प्रतिदीप्ति उत्सर्जन अक्सर 50 माइक्रोन 15 की गहराई पर अंतिम छवियों की गुणवत्ता में कमी। इसके अलावा, क्योंकि कवक कालोनियों कठोर नहीं हैं, मैंटी biofilms परेशान बिना सूक्ष्मजीवों को संभालने के लिए मुश्किल है। नमूनों की मोटाई के कारण, फंगल hyphae पर बैक्टीरियल biofilms के कुछ सूक्ष्म विश्लेषण आमतौर पर केवल फंगल कॉलोनी के एक छोटे से हिस्से पर इसलिए केवल कुछ hyphae 16, 17, 18 से युक्त प्रदर्शन कर रहे हैं। यह सब फंगल कॉलोनी पर biofilm वितरण का वर्णन करने की हमारी क्षमता को सीमित करता है और इस तरह फंगल कॉलोनी के भीतर biofilm की heterogenic वितरण के मामले में विश्लेषण में पूर्वाग्रहों को ला सकते हैं।

ऐसी कठिनाइयों को दूर करने के लिए, हम विकास और फंगल hyphae पर जीवाणु biofilm के विश्लेषण के लिए एक विधि की रिपोर्ट। इस विधि biofilm गठन का अध्ययन करने के स्यूडोमोनास ectomycorrhizal basidiomycete Laccaria bicolor S238N की hyphae पर BBc6 fluorescens में लागू किया गया था। इन दो वन-मिट्टी सूक्ष्मजीवों पहले से मिश्रित रूप को वर्णित किया गयाbiofilm संरचनाओं की तरह 19, 20। इस विधि को आसानी से आगे अन्य filamentous कवक / बैक्टीरिया का प्रणालियों के लिए अनुकूलित किया जा सकता है। यहाँ प्रस्तुत विधि एक कवक संस्कृति विधि के संयोजन पर आधारित है, बहुत पतली फंगल कालोनियों के विकास, एल एस सी एम और SEM इमेजिंग के साथ के लिए अनुमति देता है। यह सूक्ष्म (माइक्रोन रेंज) को प्राप्त करने और meso- (मिमी रेंज) के लिए दो सूक्ष्मजीवों के बीच बातचीत के विचारों के पैमाने पर अमेरिकी अनुमति दी, biofilm के गुणात्मक लक्षण वर्णन के लिए अनुमति देता है। हम यह भी पता चला है कि नमूने नैनो पैमाने स्तर (एनएम रेंज) पर biofilm की संरचनात्मक विश्लेषण की अनुमति देने SEM के साथ मनाया जा सकता है।

Protocol

1. Preparation of Bacterial and Fungal Cultures Preparation of fungal cultures Prepare cellophane membranes with the same diameter as the Petri dishes and boil them in EDTA (1 g/L in deionized water) for 30 min. Rinse the sheets with deionized water and autoclave them twice. Prepare a fungal pre-culture by inoculating fungal agar plugs on the appropriate agar medium covered with an EDTA pre-treated cellophane membrane. Incubate it at the optimal growth temperature to obtain colonies approximately 1 cm in diameter. For L. bicolor S238N, incubate at 25 °C for 5 days on Pachlewski P5 agar medium, made of 0.5 g of diNH4 tartrate, 1 g of KH2PO4, 0.5 g of MgSO4.7H2O, 5 g of Maltose D+, 20 g of Glucose D+, 1 ml of 10% Thiamine-HCl, 1 ml of 1/10 diluted micronutrient solution (6 g/L ferrous sulfate; 0.27 g/L molybdenum trioxyde; 8.45 g/L boric acid; 5 g/L manganese sulfate; 5 g/L cupric sulfate; 2.27 g/L zinc sulfate) made up to 1 L with deionized water; and 20 g of agar; pH 5.5. From the fungal pre-culture, inoculate a new agar plate covered with the EDTA pre-treated cellophane membrane containing a low-carbon agar medium to promote the radial expansion of the colonies . To inoculate the Petri dish, gently scratch the external area (where cells have the same physiological state) of a fungal colony from the pre-culture with a scalpel and transfer the hyphae to the new agar plate. Incubate at the optimal growth temperature until the new colonies are approximately 1 cm in diameter. For L. bicolor S238N, incubate them at 25 °C for 5 days on P20 agar medium (0.25 g of diNH4 tartrate; 0.5 g of KH2PO4; 0.25 g of MgSO4.7H2O; 1 g of Glucose D+; 0.5 ml of 10% Thiamine-HCl; 0.5 ml of 1/10 diluted micronutrient solution (cf 1.1.2.1), made up to 1 L with deionized water; and 20 g of agar; pH 5.5). Note: Due to the pre-culture on cellophane, the second culture will not contain agar media in the central plugs. The agar plugs should be removed for further analysis of the biofilms, since these plugs introduce agar and nutrients that can create biases in the analysis. This step concerns only fungal species that are kept and propagated on agar plates, and it is not necessary for fungi that are propagated from spores or frozen stocks. Preparation of bacterial cultures Use a sterile loop to collect 2 to 3 individual bacterial colonies from a culture on the appropriate agar medium and inoculate 25 ml of liquid Luria-Bertani (LB) medium (or any other appropriate medium, depending on the strain used). For P. fluorescens BBc6, incubate an overnight culture at 28 °C with gentle shaking (~150 rpm). Note: Using a strain tagged with fluorescent protein, such as GFP, is preferable, because this avoids performing a double-staining (fungus and bacteria) prior to microscopic observations. The timing, the stirring speed, and the temperature of the incubation depend on the strain used, the goal being to obtain a culture in late exponential growth. 2. Preparation of N In Vitro Biofilm of Bacteria on the Fungal Colony Centrifuge the bacterial culture at 5,000 x g for 3 min and suspend the pellet in 25 ml of sterile 0.1 M potassium phosphate buffer (25 g/L KH2PO4 and 2.78 g/L K2HPO4 , pH 5.8). Repeat this step once and adjust the final bacterial concentration to 109 cells/ml with the same buffer. Fill a 6-well microplate with 5 ml of the bacterial suspension (or sterile 0.1 M potassium phosphate buffer for the negative control). Cut the cellophane membrane of the fungal culture with a sterile razor blade to obtain squares of cellophane with a single fungal colony on each membrane. Carefully remove the cellophane squares containing hyphae from the solid medium using forceps and transfer the square of cellophane containing hyphae to a well of the microplate containing the bacterial suspension. Gently shake the microplate while the fungal colonies are still attached to the cellophane; then, remove the cellophane sheets, leaving the fungal colonies in the plate. Incubate the microplate with gentle agitation (~60 rpm) at a temperature adapted to the studied microorganisms. Note: The time of incubation depends on the speed of establishment of the biofilm and the stage to be analyzed. For P. fluorescens BBc6/L. bicolor, incubate at 20 °C for 30 min to get early-stage biofilms and up to 16 hr to get mature biofilms. 3. Laser Scanning Confocal Microscopy Analysis of the Biofilm Formation Sample preparation To remove planktonic bacteria and bacteria electrostatically-attached to the hyphae, rinse the fungus by transferring it to a new 6-well microplate filled with 5 ml of a strong salt solution (NaCl, 17 g/L) 17 ; gently shake for 1 min. Transfer the fungus to a new 6-well microplate containing 5 ml of sterile 0.1 M potassium phosphate buffer, gently shake for 2 min, and transfer the fungus to fresh potassium phosphate buffer. Cut the part of the fungal colony to be imaged with a scalpel while keeping it in the potassium phosphate buffer, such that the obtained section contains about half of the fungal colony. To stain the sample, transfer it to a Petri dish filled with sterile water containing an appropriate fluorescent dye (depending on the aim of the analysis), and incubate it in the dark. To visualize the fungal network, use, for example, Congo Red (0.1% final concentration, 5 min of incubation), wheat germ agglutin (WGA) lectin conjugated to Alexa Fluor 633 (10 µg/ml final concentration, 10 min of incubation) or FUN1 (10 µM final concentration, 10 min of incubation). If using a non-fluorescent-tagged bacterium, counterstain the bacterial cells with a DNA-specific fluorescent probe among the numerous cell-permeant DNA dyes commercially available. For example, use DAPI (0.25 µg/ml final concentration, 10 min of incubation). To visualize the matrix proteins, use a protein stain21. After staining, rinse the sample by transferring it to a Petri dish lid containing 10 ml of sterile 0.1 M potassium phosphate and gently shake for 1 min. Half submerge a slide in the Petri dish lid and delicately bring the cut section to float above the slide. Then, slowly remove the slide from the buffer solution, allowing the sample to gently settle on the slide. Note: For this step, it is very important to proceed gently to avoid biofilm disturbance. Finally, add 10 μl of anti-fading mounting medium to the sample and cover it with a glass coverslip. Note: Once the slide is prepared, the microscopic analysis must be performed as soon as possible (within at most 30 min) to avoid modification in the biofilm structure. Confocal microscopic analysis Examine the slides under a confocal laser microscope with a 10X or 40X objective lens coupled to imaging software. Note: Here, a multi-beam scanning confocal microscope equipped with 405, 488, and 561 nm excitation lasers, a GaAsp PMT detector, and 10X 0.3 NA and 40X 1.2 NA objectives was used. Perform imaging using parameters adapted to the type of data requested and to the time constrains. Use laser excitation/emission wavelengths according to the stain used and to the manufacturer's recommendations. Use a combination of tile scan and the Z-stack functions to obtain global 3D views of the fungal colony and the biofilms. Note: Images on Figure 3 were acquired using the following parameters: 8-bit/pixel, averaging = 2, pixel dwell = 1.58 µsec, tiles scan of 5×5 images with online stitching (10% coverage, threshold = 0.7); Z-step = 2 µm. For 3D data visualization, use one of the many free or commercial softwares (these offer many options for 3D rendering). For example, to display Z-stack data as 2D maximum intensity projections, subtract the bright-field channel, adjust the brightness and contrast, and merge channels to create a composite image. If they are present, eliminate slices without signal at the Z-stack extremities. Then, perform a 2D maximum-intensity projection and convert the result into RGB color. Use the "Z project" function in the ImageJ software22 to obtain the images presented here by 2D maximum intensity projections. 4. Electron Microscopy Analysis Prepare the samples as described for LSCM, except in step 3.1.2, transfer the biofilms to sterile water instead of potassium phosphate buffer after the rinse steps. This avoids the formation of salt crystals during the dehydration step, which would perturb SEM imaging. Transfer the biofilms to a sample holder and remove excess water; only allow a small pellicle of water to cover the sample. Transfer the sample to the chamber of a variable-pressure scanning electron microscope (VP-SEM); freeze it to -50 °C on a Peltier cooling stage; and allow it to slowly freeze-dry, directly in the SEM chamber, with 100 Pa of variable pressure set for 15 hr. After completion of the freeze-drying, retrieve the sample and transfer it into a high-vacuum film deposition system. Coat the sample with 2 nm of platinum (quartz measurement) under argon plasma (2.5 x 10-2 mbar, 35 mA). Observe the coated sample with an SEM equipped with a field emission gun (FEG) using the high resolution "in lens" detector and an electronic high tension of 1 kV.

Representative Results

The overall schematic procedure of fungal culture and biofilm preparation are given in Figure 1. The culture method allowed us to obtain fungal colonies 20  to 50 µm thick containing a few layers of hyphae, allowing micro- and meso-scale analyses of hydrated living biofilm using LSCM. The application of the method permitted the acquisition of high-quality images of P. fluorescens BBc6 biofilms on L. bicolor hyphae along the formation of the biofilm (Figures 2-4). The meso-scale analysis of the biofilms demonstrated the heterogenic distribution of the biofilm of P. fluorescens BBc6 on the hyphae of L. bicolor S238N (Figures 2 and 3). Meso-scale analysis also allowed for the tracking of the biofilm formation over time (Figure 3) from the early steps, in which only some bacteria were attached to hyphae (Figure 3a), to the formation of a thick, mature biofilm (Figure 3b). The high resolution of the meso-scale images allowed us to perform micro-scale analysis on the same images in order to obtain the colony architectures (Figure 3c-d). The micro-scale analysis combined with the specific labeling enabled us to go a step further in biofilm characterization. Here, SYPRO Ruby23, which labels most classes of proteins, was applied to the samples (Figure 4) and shows the presence of proteins in the matrix. Finally, further details of the biofilm structure were obtained by SEM imaging of the same sample after dehydration and coating (Figure 5). SEM imaging provided access to the nanoscale level, thus giving access to the matrix structure. Figure 1: Overall schematic procedure of fungal culture and biofilm preparation. This figure describes the main steps of the method, from microorganism cultures to sample analyses. More details are given in the protocol. Please click here to view a larger version of this figure. Figure 2: BBc6 biofilm repartition on the fungal colony. The sample was imaged after 18 hr of interaction at 10X magnification. The image was obtained via 2D maximum intensity projection of 3D confocal microscopy images. The grey grid on the figure depicts the mosaic positions. L. bicolor hyphae are stained with Congo Red (red) and bacteria are GFP-tagged (green). Please click here to view a larger version of this figure. Figure 3: Early and late stages of BBc6 biofilm formation on L. bicolor hyphae. This image was obtained via 2D maximum intensity projection of 3D confocal microscopy images. Imaging was performed at 40X magnification. (a) Biofilms repartition after 2 hr of interaction. (b) Biofilm repartition after 14 hr of interaction. (c) Enlargement of the white rectangle in (a). (d) Enlargement of the white rectangle in (b). Fungal hyphae are stained with Congo Red (red) and bacteria are GFP-tagged (green). Please click here to view a larger version of this figure. Figure 4: Matrix staining of BBc6 biofilm on L. bicolor hyphae. (a) Biofilms after 16 hr of interaction. (b) Enlargement of the white rectangle in (a). Imaging was performed at 40X magnification, and these images were obtained via 2D maximum intensity projection of 3D confocal microscopy images. Bacteria are GFP-tagged (green), fungus is stained with Fun1 (dark green), and proteins are stained with S. Ruby (red). Please click here to view a larger version of this figure. Figure 5: SEM imaging of BBc6 biofilms on L. bicolor hyphae. SEM Imaging was performed at 2360X, EHT: 1kV. Before imaging, the sample was slowly freeze-dried in the SEM chamber and coated with platinum. Green arrows point to bacterial biofilms and yellow arrows point to fungal hyphae. Please click here to view a larger version of this figure.

Discussion

Bacterial biofilms are retrieved in many environments and have been studied since the 1950s, leading to the development of a number of methods to analyze them24. Classical methods to quantify and monitor biofilms include micro-titer assays and, the most widely-used method, crystal violet (CV) staining. These methods are fast, low cost, and easy to handle25 and are particularly useful to quantify total biofilm biomass or to perform viability and matrix quantification assays. On an other hand, "omics" methods are also useful in biofilm studies, allowing for quantitative and functional analyses of biofilms26,27. Despite the advantages of micro-titer plate and "omics" methods, several essential features of biofilms cannot be captured with these techniques, hindering a complete understanding of this process. Such features include matrix structures, bacterial colony architectures, cell/cell interactions, and colonization patterns, which are key data for understanding both the functioning of biofilms and the dynamics of their formation. Despite the capacity of microscopy to capture these features, microscopy analysis of bacterial biofilms on filamentous fungi are still scarce. This is mainly due to the growth of filamentous fungi, which often forms colonies of thick, complex, tridimensional networks. Formation of bacterial biofilms on fungi is common in diverse environments and is significantly involved in various fields4 (e.g., medicine, agriculture, and environment); hence, it is critical to develop new methods to facilitate their investigation. To this end, we combined a method to generate very thin fungal colonies with microscopic imaging of the bacterial biofilms. In addition, we proposed a set of microscopy tools to qualitatively analyze those biofilms. The success of the method relies upon the ability to produce very thin hyphal colonies and to apply the appropriate dyes. These points are discussed below.

Due to the complex structures of the biofilms, understanding their function requires a multi-scale approach28,29. Distribution patterns of the biofilms, bacterial colony architecture, and matrix structure and composition are analyzed at different scales (i.e., meso-scale and micro-scale). Moreover, nanoscale resolution allows access to the cell/cell physical interactions and the nano-structure of the matrix. Thus, the developed method easily enables a multi-scale analysis of the bacterial biofilms formed on the fungal colony.

In most studies, LSCM analyses of biofilms are limited to the micro-scale, the meso-scale usually being performed by optical coherence tomography30,31,32. The method presented here enables both micro- and meso-scale analyses by LSCM. It demonstrates the utility of combining both analyses in the same region of the sample and even on the same image using new-generation confocal microscopes with high resolution (Figure 3). Thus, issues linked to compiled data gathered at different scales with different methods are here avoided.

This combination of analyses gave access concomitantly to the biofilm repartition on the fungal colony, the bacterial colony architecture along the developing biofilm, and the matrix structure. The meso-scale analysis showed a heterogenic distribution of the bacterial biofilms on the fungal colonies (Figures 2 and 3). This observation would not have been possible with protocols that only permit imaging of a small portion of the fungal colony, which is not necessarily representative of the entire colony. Thus, while often neglected, the meso-scale analysis can give precious information about biofilm distribution patterns.

Finally, the developed method can be used to analyze samples with different microscopy techniques, including scanning electron microscopy. Here, SEM was used to reach the nano-scale and to obtain the bacterial spatial organization within the biofilm. It performed very well with the thin fungal colonies, while SEM only permitted surface imaging. In contrast to LSCM, SEM, however, required sample dehydration and, most often, coating with a conductive metal. This dehydration process might alter biological structures when it is not properly executed and may require optimization. Here, sample dehydration using slow lyophilization was used33. Nevertheless, applying both LSCM and SEM to the samples will allow the performance of correlative microscopy at the same location of the sample.

Despite the advantages described above, some limitations exist. Firstly, it may not be applicable to all kind of fungi. Indeed, this culturing method is developed for fungi spreading radially on the surface of solid media. This method may not be suitable for fungi forming mainly aerial hyphae (e.g., Fusarium sp.) or for micro-aerobic fungi spreading mainly inside agar. Moreover, fungi degrading cellophane may be problematic as well (e.g., Trichoderma sp.). Secondly, it is important to note that the staining strategy is a critical point and the choice of the stain must be made carefully, as the stain must not disturb the biofilm. For example, we noticed that Calcofluor White caused partial biofilm disruption (data not shown), likely due to the high pH of this stain. Also, some dyes produced heterogeneous staining (e.g., Congo Red), while others produced homogeneous staining (e.g., cell wall staining with WGA lectin), giving a heterogeneous image quality. Moreover, it is important to be aware that some dyes might not be fully specific. For example, WGA stains not only fungal cell walls but also N-acetylneuraminic acid in gram-positive bacterial cell walls and adhesins produced by gram-positive and -negative bacteria during biofilm formation34,35. Therefore, using fluorescent protein-tagged bacteria and/or fungi is recommended to avoid multiple staining. If multiple dyes are used, they must not chemically interfere, and their emission spectra should not overlap.

Meso-scale analyses require a large scanned area, and therefore, LSCM may be time-consuming (40 min to 1 hr, depending on the sample thickness) and bottleneck the analysis of a large number of samples. Nonetheless, adjustments can be made depending on the type of data required. It is possible to decrease acquisition time and image size by altering the image quality. For example, high resolution is not necessary to analyze the biofilm general repartition.

Finally, some limitations need to be considered when choosing to display Z- stack data as 2D or 3D projections. Two-dimensional projections are a good way to summarize data, but depth information is lost, and overlapped structures become hidden. On the other hand, 3D projections allow the visualization from different points of view, but they often render poorly in case of spatial complexity.

In conclusion, we have reported a method for the characterization of bacterial biofilms on hyphae at the structural level. The methodology can be extended to other applications. Indeed, this method allows the performance of functional or chemical characterization of bacterial biofilms forming on fungal hyphae. Due to the great variety of existing fluorescent reporter systems, LSCM analysis can be used for multiple purposes29. For example, the fluorescence microscopy could be used to monitor pH gradient36 or molecule diffusion in biofilms37. Additionally, the method allows for community analysis in multispecies biofilms. For example, fluorescence in situ hybridization targeting specific bacterial groups is particularly useful to study specific bacterial repartition in multispecies biofilms38,39. Last, numerous fluorescent dyes can be used to characterize the matrix composition of the biofilms21. Here, proteins were targeted using Sypro, which stains a large range of proteins, among them matrix proteins (Figure 4), but other dyes allow for the visualization of other important matrix constituents, such as exopolysaccharides or extracellular DNA. Interestingly, all these analyses could be performed at the meso-scale using the described method. Since LSCM can be performed on living samples, it is also possible to achieve time-lapse imaging using, for example, coverwell chambers, particularly suitable for thin fungal colonies. This option is particularly interesting, as biofilm formation is a complex, dynamic process. Finally, for a quantitative purpose, the reported method may improve the accuracy of automatic quantitative analysis by making this quantification possible on meso-scale images. This may overcome biofilm heterogeneity and statistical issues29.

Disclosures

The authors have nothing to disclose.

Acknowledgements

This work was supported by the French National Research Agency through the Laboratory of Excellence ARBRE (ANR-11-LABX-0002-01), the Plant-Microbe Interfaces Scientific Focus Area in the Genomic Science Program, and the Office of Biological and Environmental Research in the DOE Office of Science. Oak Ridge National Laboratory is managed by UT-Battelle, LLC, for the United States Department of Energy under contract DE-AC05-00OR22725.

Materials

6 well Falcon Tissue Culture Plates Fisher Scientific 08-772-33 Used in 2.2 & 3.1
Congo Red Fisher Scientific C580-25 Used in 3.1.4.1
FUN 1 Cell Stain Thermo Fisher Scientific F7030 Used in 3.1.4.1
Wheat Germ Agglutinin, Alexa Fluor 633 Conjugate Thermo Fisher Scientific W21404 Used in 3.1.4.1
DAPI solution Thermo Fisher Scientific 62248 Used in 3.1.4.2
Propidium iodide Thermo Fisher Scientific P3566 Used in 3.1.4.3
FilmTracer SYPRO Ruby Biofilm Matrix protein Stain Thermo Fisher Scientific F10318 Used in 3.1.4.4
Fluoromount-G Slide Mounting Medium Fisher Scientific OB100-01 Used in 3.1.7
LSM780 Axio Observer Z1 Zeiss Used in 3.2.1
ZEN 2.1 lite black software  Zeiss Used in 3.2.1
High Vacuum Coater Leica EM ACE600 Leica Used in 4
GeminiSEM-FEG Zeiss Used in 4
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References

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Tags

Bacterial BiofilmFilamentous Fungal ColoniesConfocal MicroscopyElectron MicroscopyMulti-scale AnalysisCellophane MembraneEDTAFungal Pre-cultureP. FluorescensPotassium Phosphate Buffer
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Miquel Guennoc, C., Rose, C., Guinnet, F., Miquel, I., Labbé, J., Deveau, A. A New Method for Qualitative Multi-scale Analysis of Bacterial Biofilms on Filamentous Fungal Colonies Using Confocal and Electron Microscopy. J. Vis. Exp. (119), e54771, doi:10.3791/54771 (2017).
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