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8 - Whole Cell Identification of Microorganisms in Their Natural Environment with Fluorescence in situ Hybridization (FISH)

from Part III - Imaging Techniques

Published online by Cambridge University Press:  06 July 2019

Janice P. L. Kenney
Affiliation:
MacEwan University, Edmonton
Harish Veeramani
Affiliation:
Carleton University, Ottawa
Daniel S. Alessi
Affiliation:
University of Alberta
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Summary

One of the main goals in biogeochemistry is to explore the global relationships between organisms and chemical elements in different ecosystems. A diversity of analytical techniques based on chemical-physical or molecular biological procedures are available to explore different organisms and their abiotic and biotic interactions in a variety of ecosystems. Even though many of these modern analytical techniques are irreplaceable in today´s research, most of them can only provide indirect results because they are built on a “black-box” approach, where the biological species in an ecosystem or a geological environment are disrupted for extraction of nucleic acids, proteins, etc. Essential biological information, such as the morphology of specific species, their location, distribution, association with other organisms in their natural environment, and individual activities and functions, is therefore lost. Fluorescence in situ hybridization (FISH) helps retrieve this information without either cultivation or extraction of cell components, and can therefore provide a quick and useful complement to different “black-box”-based approaches. FISH is based on fluorescently labeled gene probes with a unique nucleotide composition designed to match specific genes in different cellular species. Thus, different biological species can be identified simultaneously with different gene probes labeled with different fluorochromes in their natural environment. The technique has undergone extensive development with around 30 variations for different applications. FISH is evaluated either by microscopy (e.g., fluorescence microscopy, Raman micro spectroscopy, Nano-SIMS), or by nonmicroscope-based methods, such as flow cytometry, microarray technology, or molecular biological methods such as proteomics. This chapter will serve as a guide for sample preparation, selection of appropriate FISH protocols, evaluation and design of gene probes, and evaluation of FISH experiments.

Type
Chapter
Information
Analytical Geomicrobiology
A Handbook of Instrumental Techniques
, pp. 187 - 212
Publisher: Cambridge University Press
Print publication year: 2019

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References

8.10 References

Alm, E, Oerther, D, Larsen, N, Stahl, D, Raskin, L (1996). The Oligonucleotide Probe Database. Appl. Environ. Microbiol. 62: 35573559.Google Scholar
Amann, RI (1995). In situ identification of microorganisms by whole cell hybridization with rRNA targeted nucleic acid probes, pp. 331345. In Molecular Microbial Ecology Manual.Google Scholar
Amann, RI, Fuchs, BM (2008). Single-cell identification in microbial communities by improved fluorescence in situ hybridization techniques. Nat Rev Microbiol. 6(5): 339348. doi:10.1038/nrmicro1888.Google Scholar
Amann, R, Schleifer, KH (2001). Nucleic acid probes and their application in environmental microbiology, pp. 6782. In Garrity, GM (ed.), Bergey’s Manual of Systematic Bacteriology, 2nd Edition.Google Scholar
Antón, JLlobet-Brossa, ERodríguez-Valera, FAmann, R (1999) Fluorescence in situ hybridization analysis of the prokaryotic community inhabiting crystallizer ponds. Environ Microbiol1(6): 517523.CrossRefGoogle ScholarPubMed
Asheldford, KE, Weightman, AJ, Fry, JC (2002). PRIMROSE: a computer program for generating and estimating the phylogenetic range of 16 rRNA oligonucleotide probes and primers in conjunction with the RDP-II database. Nucleic Acids Res. 30: 34813489.Google Scholar
Becking, LB (2015). Baas Becking’s Geobiology. Canfield, DE (ed.). Wiley-Blackwell. 152 pp. ISBN: 978–0-470–67381-2, http://eu.wiley.com/WileyCDA/WileyTitle/productCd-0470673818,subjectCd-EN64.html#CrossRefGoogle Scholar
Behnam, F, Vilcinskas, A, Wagner, M, Stoecker, K (2012). A straightforward DOPE-FISH method for simultaneous multicolor detection of six microbial populations. Appl. Environ. Microbiol. 78: 51385142.Google Scholar
Boas, V, Almeida, C, Sillankorva, S, et al. (2016). Discrimination of bacteriophage infected cells using locked nucleic acid fluorescent in situ hybridization (LNA-FISH). Biofouling. 32(2): 179190. doi:10.1080/08927014.2015.1131821.Google Scholar
Caracciolo, AB, Grenni, P, Cupo, C, Rossetti, S (2005). In situ analysis of native microbial communities in complex samples with high particulate loads. FEMS Microbiol. Lett. 253: 5558.CrossRefGoogle Scholar
Chou, YY, Heaton, NS, Gao, Q, et al. (2013). Colocalization of different influenza viral RNA segments in the cytoplasm before viral budding as shown by single-molecule sensitivity FISH analysis. PLoS Pathog. 9(5): e1003358. doi:10.1371/journal.ppat.1003358.Google Scholar
Cole, JR, Wang, Q, Fish, JA, et al. (2014). Ribosomal Database Project: data and tools for high throughput rRNA analysis. Nucleic Acids Res. 42(Database issue): D633D642.Google Scholar
Cutler, NA, Oliver, AO, Viles, HA, Whiteley, AS (2012). Non-destructive sampling of rock-dwelling microbial communities using sterile adhesive tape. J. Microbiol Methods. 91: 391398.CrossRefGoogle ScholarPubMed
Daims, H (2009). Use of fluorescence in situ hybridization and the daime image analysis program for the cultivation-independent quantification of microorganisms in environmental and medical samples. Cold Spring Harbor Protocols website, http://cshprotocols.cshlp.org/content/2009/7/pdb.prot5253.full.Google Scholar
Dang, VT, Sullivan, MB (2014). Emerging methods to study bacteriophage infection at the single-cell level. Front. Microbiol. 2014; 5: 724.Google Scholar
Dekas, AE, Connon, SA, Chadwick, GL, Trembath-Reichert, E, Orphan, VJ (2016). Activity and interactions of methane seep microorganisms assessed by parallel transcription and FISH-NanoSIMS analyses. ISME J. 10(3): 678692.Google Scholar
Eichorst, SA, Strasser, F, Woyke, T, et al. (2015). Advancements in the application of NanoSIMS and Raman microspectroscopy to investigate the activity of microbial cells in soils. FEMS Microbiol. Ecol. 91(10) pii: fiv106.Google Scholar
Foissner, W (1992). Preparation of samples for scanning electron microscopy. In Lee, JJ and Soldo, AT (eds), Protocols for Protozoology. Society of Protozoologists, Lawrence, Kansas, USA. Section C. Fixation, staining, light and electron microscopical techniques, chapter 20.Google Scholar
Fuchs, BM, Glöckner, FO, Wulf, J, Amann, R (2000). Unlabelled helper oligonucleotides increase the in situ accessibility to 16S rRNA of fluorescently labelled oligonucleotide probes. Appl. Environ. Microbiol. 66: 36033607.CrossRefGoogle Scholar
Gérard, E, Guyot, F, Philippot, P, López-García, P (2005). Fluorescence in situ hybridisation coupled to ultra small immunogold detection to identify prokaryotic cells using transmission and scanning electron microscopy. J. Microbiol. Methods. 63(1): 2028.CrossRefGoogle ScholarPubMed
Giovannoni, SJ, Delong, E, Olsen, GJ, Pace, NR (1988). Phylogenetic group-specific oligodeoxynucleotide probes for in situ microbial identification. J. Bacteriol. 170: 720.Google Scholar
Glöckner, FO, Yilmaz, P, Quast, C, et al. (2017). 25 years of serving the community with ribosomal RNA gene reference databases and tools. J. Biotechnol. 261: 169176.CrossRefGoogle ScholarPubMed
Greuter, D, Loy, A, Horn, M, Rattei, T. (2016). probeBase – an online resource for rRNA-targeted oligonucleotide probes and primers: new features 2016. Nucleic Acids Res. 44(D1): D586589.Google Scholar
Juretschko, S, Loy, A, Lehner, A, Wagner, M (2002). The microbial community composition of a nitrifying-denitrifying activated sludge from an industrial sewage treatment plant analyzed by the full-cycle rRNA approach. Syst. Appl. Microbiol. 25(1): 8499.Google Scholar
Kubota, K (2013). CARD-FISH for environmental microorganisms: technical advancement and future applications. Microbes Environ. 28: 312.Google Scholar
Lee, NM, Meisinger, DB, Schmid, M, Rothballer, M, Löffler, FE (2011). Fluorescence in situ hybridization in geomicrobiology, pp. 854880. In Reitner, HJ and Thiel, V (eds), Encyclopedia in Geobiology. Springer Verlag.Google Scholar
Ludwig, L, Strunk, OWestram, R, et al. (2004). ARB: a software environment for sequence data. Nucleic Acids Res. 32: 13631371.Google Scholar
Manz, W, Amann, R, Ludwig, W, Wagner, M, Schleifer, KH (1992). Phylogenetic oligodeoxynucleotide probes for the major subclasses of proteobacteria: problems and solutions. Syst. Appl. Microbiol. 15: 593600.Google Scholar
Meier, H, Amann, R, Ludwig, W, Schleifer, KH (1999). Specific oligonucleotide probes for in situ detection of a major group of gram-positive bacteria with low DNA G+C content. Syst. Appl. Microbiol. 22: 186196.Google Scholar
Moraru, C, Lam, P, Fuchs, BM, Kuypers, MM, Amann, R (2010). GeneFISH – an in situ technique for linking gene presence and cell identity in environmental microorganisms. Environ. Microbiol. 12(11): 30573073. doi:10.1111/j.1462-2920.2010.02281.x.Google Scholar
Nakamura, K, Terada, T, Sekiguchi, Y, et al. (2006). Application of pseudomurein endoisopeptidase to fluorescence in situ hybridization of methanogens within the family Methanobacteriaceae. Appl. Environ. Microbiol. 72: 69076913.CrossRefGoogle ScholarPubMed
Neuenschwander, SM, Salcher, MM, Pernthaler, J (2015). Fluorescence in situ hybridization and sequential catalyzed reporter deposition (2C-FISH) for the flow cytometric sorting of freshwater ultramicrobacteria. Front. Microbiol. 6(247): 18.Google Scholar
Nikolaki, S, Tsiamis, G (2013). Microbial diversity in the era of omic technologies. Biomed. Res. Int. 2013; 2013: 958719. doi:10.1155/2013/958719. Epub October 24, 2013.Google Scholar
Pavlekovic, M, Schmid, MC, Schmider-Poignee, N, et al. (2009). Optimization of three FISH procedures for in situ detection of anaerobic ammonium oxidizing bacteria in biological wastewater treatment. J. Microbiol. Methods. 78: 119126.CrossRefGoogle ScholarPubMed
Pernthaler, A, Amann, R (2004). Simultaneous fluorescence in situ hybridization of mRNA and rRNA in environmental bacteria. Appl. Environ. Microbiol. 70: 54265433.Google Scholar
Richter, H, Lanthier, M, Nevin, KP, Lovley, DR (2007). Lack of electricity production by Pelobacter carbinolicus indicates that the capacity for Fe(III) oxide reduction does not necessarily confer electron transfer ability to fuel cell anodes. Appl. Environ. Microbiol. 73: 53475353.CrossRefGoogle Scholar
Rossetti, S, Tomei, MC, Blackall, LL, Tandoi, V (2007). Bacterial growth kinetics estimation by fluorescence in situ hybridization and spectrofluorometric quantification. Lett. Appl. Microbiol. 44: 643648.Google Scholar
Schimak, MP, Kleiner, M, Wetzel, S, et al. (2016). MiL-FISH: multilabelled oligonucleotides for fluorescence in situ hybridization improve visualization of bacterial cells. Appl. Environ. Microbiol. 82: 6270.Google Scholar
Schmidt, S, Eickhorst, T, Tippkötter, R (2012). Evaluation of tyramide solutions for an improved detection and enumeration of single microbial cells in soil by CARD-FISH. J. Microbiol. Methods. 91: 399.Google Scholar
Schönhuber, W, Fuchs, B, Juretschko, S, Amann, R (1997). Improved sensitivity of whole-cell hybridization by the combination of horseradish peroxidase-labelled oligonucleotides and tyramide signal amplification. Appl. Environ Microbiol. 63: 3268.CrossRefGoogle Scholar
Shiraishi, F, Zippel, B, Neu, TR, Arp, G (2008). In situ detection of bacteria in calcified biofilms using FISH and CARD-FISH. J. Microbiol Methods. 75:103108.Google Scholar
Stoecker, K, Dorninger, C, Daims, H, Wagner, M (2010). Double labelling of oligonucleotide probes for fluorescence in situ hybridization (DOPE-FISH) improves signal intensity and increases rRNA accessibility. Appl. Environ Microbiol. 76(3): 922.CrossRefGoogle ScholarPubMed
Teira, E, Reinthaler, T, Pernthaler, A, Pernthaler, J, Herndl, GJ (2004). Combining catalyzed reporter deposition-fluorescence in situ hybridization and microautoradiography to detect substrate utilization by bacteria and Archaea in the deep ocean. Appl. Environ. Microbiol. 70(7): 4411.Google Scholar
Valm, AM, Welch, JLM, Borisy, GG (2013). CLASI-FISH: principles of combinatorial labeling and spectral imaging. Syst. Appl. Microbiol. 35: 496502.CrossRefGoogle Scholar
Volpi, EV, Bridger, JM (2008). FISH glossary: an overview of the fluorescence in situ hybridization technique. BioTechniques 45: 385409.CrossRefGoogle ScholarPubMed
Wagner, M, Haider, S (2012). New trends in fluorescence in situ hybridization for identification and functional analyses of microbes. Curr. Opin. Biotechnol. 23: 96102.Google Scholar
Wagner, M, Rath, G, Amann, R, Koops, H-P, Schleifer, KH (1995). In situ identification of ammonia-oxidizing bacteria. Syst. Appl. Microbiol. 18: 251264.Google Scholar
Wang, YY, Huang, WE, Cui, L, Wagner, M (2016). Single cell stable isotope probing in microbiology using Raman microspectroscopy. Curr. Opin. Biotechnol. 41: 3442.CrossRefGoogle ScholarPubMed
Weerasekara, ML, Ryuda, N, Miyamoto, H, et al. (2013). Double-color fluorescence in situ hybridization (FISH) for the detection of Bacillus anthracis spores in environmental samples with a novel permeabilization protocol. J. Microbiol Methods. 93(3): 177184. doi:10.1016/j.mimet.2013.03.007.Google Scholar
Wendeberg, A (2010). Fluorescence in situ hybridization for the identification of environmental microbes. Cold Spring Harbor Protocols, http://cshprotocols.cshlp.org/content/2010/1/pdb.prot5366.fullGoogle Scholar
Yilmaz, LS, Okten, HE, Noguera, DR (2006). Making all parts of the 16S rRNA of Escherichia coli accessible in situ to single DNA oligonucleotides. Appl. Environ. Microbiol. 72: 733744.Google Scholar
Yilmaz, LS, Parnekar, S, Noguera, DR (2010). mathFISH, a web tool that uses thermodynamics-based mathematical models for in silico evaluation of oligonucleotide probes for fluorescence in situ hybridization. Appl. Environ. Microbiol. 77: 11181122.CrossRefGoogle ScholarPubMed
Yilmaz, S, Haroon, M, Rabkin, B, Tyson, G, Hugenholtz, P (2010) Fixation-free fluorescence in situ hybridization for targeted enrichment of microbial populations. ISME J. 4(10): 13521356.CrossRefGoogle Scholar
Zwirglmaier, K (2005). Fluorescence in situ hybridisation (FISH) – the next generation. FEMS Microbiol. Lett. 246(2): 151.CrossRefGoogle ScholarPubMed

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