An Introduction to Fluorescence in situ Hybridization in Microorganisms.
Detection
FISH
Hybridization
Microorganism
Probes
Single-cell microbiology
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2021
2021
Historique:
entrez:
12
2
2021
pubmed:
13
2
2021
medline:
31
3
2021
Statut:
ppublish
Résumé
Fluorescence in situ hybridization (FISH) is a molecular biology technique that enables the localization, quantification, and identification of microorganisms in a sample. This technique has found applications in several areas, most notably the environmental, for quantification and diversity assessment of microorganisms and, the clinical, for the rapid diagnostics of infectious agents. The FISH method is based on the hybridization of a fluorescently labeled nucleic acid probe with a complementary sequence that is present inside the microbial cell, typically in the form of ribosomal RNA (rRNA). In fact, an hybridized cell is typically only detectable because a large number of multiple fluorescent particles (as many as the number of target sequences available) are present inside the cell. Here, we will review the major steps involved in a standard FISH protocol, namely, fixation/permeabilization, hybridization, washing, and visualization/detection. For each step, the major variables/parameters are identified and, subsequently, their impact on the overall hybridization performance is assessed in detail.
Identifiants
pubmed: 33576979
doi: 10.1007/978-1-0716-1115-9_1
doi:
Substances chimiques
Nucleic Acid Probes
0
Oligonucleotide Probes
0
RNA, Bacterial
0
RNA, Ribosomal
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1-15Références
Chargaff E (1950) Chemical specificity of nucleic acids and mechanism of their enzymatic degradation. Experientia 6(6):201–209
pubmed: 15421335
doi: 10.1007/BF02173653
Amann R, Fuchs BM (2008) Single-cell identification in microbial communities by improved fluorescence in situ hybridization techniques. Nat Rev Microbiol 6(5):339–348
pubmed: 18414500
doi: 10.1038/nrmicro1888
Forrest GN (2007) PNA FISH: present and future impact on patient management. Expert Rev Mol Diagn 7(3):231–236
pubmed: 17489730
doi: 10.1586/14737159.7.3.231
Diaz M et al (2010) Application of flow cytometry to industrial microbial bioprocesses. Biochem Eng J 48(3):385–407
doi: 10.1016/j.bej.2009.07.013
Delong EF, Wickham GS, Pace NR (1989) Phylogenetic stains - ribosomal RNA-based probes for the identification of single cells. Science 243(4896):1360–1363
pubmed: 2466341
doi: 10.1126/science.2466341
Giovannoni SJ et al (1988) Phylogenetic group-specific oligodeoxynucleotide probes for identification of single microbial-cells. J Bacteriol 170(2):720–726
pubmed: 2448289
pmcid: 210714
doi: 10.1128/JB.170.2.720-726.1988
Rocha R, Almeida C, Azevedo NF (2018) Influence of the fixation/permeabilization step on peptide nucleic acid fluorescence in situ hybridization (PNA-FISH) for the detection of bacteria. PLoS One 13(5):e0196522
pubmed: 29851961
pmcid: 5979007
doi: 10.1371/journal.pone.0196522
Thurnheer T, Gmur R, Guggenheim B (2004) Multiplex FISH analysis of a six-species bacterial biofilm. J Microbiol Methods 56(1):37–47
pubmed: 14706749
doi: 10.1016/j.mimet.2003.09.003
pmcid: 14706749
Perry-O’Keefe H et al (2001) Identification of indicator microorganisms using a standardized PNA FISH method. J Microbiol Methods 47(3):281–292
pubmed: 11714518
doi: 10.1016/S0167-7012(01)00303-7
Guimaraes N et al (2007) Development and application of a novel peptide nucleic acid probe for the specific detection of Helicobacter pylori in gastric biopsy specimens. J Clin Microbiol 45(9):3089–3094
pubmed: 17609326
pmcid: 2045269
doi: 10.1128/JCM.00858-07
Wu S et al (2009) Direct viable count combined with fluorescence in situ hybridization (DVC-FISH) for specific enumeration of viable Escherichia coli in cow manure. Microbes Environ 24(1):33–38
pubmed: 21566351
doi: 10.1264/jsme2.ME08543
pmcid: 21566351
Carr EL et al (2005) Improved permeabilization protocols for fluorescence in situ hybridization (FISH) of mycolic-acid-containing bacteria found in foams. J Microbiol Methods 61(1):47–54
pubmed: 15676195
doi: 10.1016/j.mimet.2004.10.023
pmcid: 15676195
Macnaughton SJ, O’Donnell AG, Embley TM (1994) Permeabilization of mycolic-acid-containing actinomycetes for in situ hybridization with fluorescently labelled oligonucleotide probes. Microbiology 140(Pt 10):2859–2865
pubmed: 8000549
doi: 10.1099/00221287-140-10-2859
pmcid: 8000549
Frickmann H et al (2017) Fluorescence in situ hybridization (FISH) in the microbiological diagnostic routine laboratory: a review. Crit Rev Microbiol 43(3):263–293
pubmed: 28129707
doi: 10.3109/1040841X.2016.1169990
pmcid: 28129707
Lawson TS et al (2011) Optimization of a two-step permeabilization fluorescence in situ hybridization (FISH) assay for the detection of Staphylococcus aureus. J Clin Lab Anal 25(5):359–365
pubmed: 21919072
pmcid: 6647555
doi: 10.1002/jcla.20486
Kubota K (2013) CARD-FISH for environmental microorganisms: technical advancement and future applications. Microbes Environ 28(1):3–12
pubmed: 23124765
doi: 10.1264/jsme2.ME12107
pmcid: 23124765
Fontenete S et al (2015) Towards fluorescence in vivo hybridization (FIVH) detection of H. pylori in gastric mucosa using advanced LNA probes. PLoS One 10(4):e0125494
pubmed: 25915865
pmcid: 4410960
doi: 10.1371/journal.pone.0125494
Hartmann H et al (2005) Rapid identification of Staphylococcus aureus in blood cultures by a combination of fluorescence in situ hybridization using peptide nucleic acid probes and flow cytometry. J Clin Microbiol 43(9):4855–4857
pubmed: 16145158
pmcid: 1234125
doi: 10.1128/JCM.43.9.4855-4857.2005
Batani G et al (2019) Fluorescence in situ hybridization (FISH) and cell sorting of living bacteria. Sci Rep 9(1):18618
pubmed: 31819112
pmcid: 6901588
doi: 10.1038/s41598-019-55049-2
Sikorav JL, Orland H, Braslau A (2009) Mechanism of thermal renaturation and hybridization of nucleic acids: Kramers’ process and universality in Watson-Crick base pairing. J Phys Chem B 113(12):3715–3725
pubmed: 19673131
doi: 10.1021/jp807096z
pmcid: 19673131
Yilmaz LS, Noguera DR (2004) Mechanistic approach to the problem of hybridization efficiency in fluorescent in situ hybridization. Appl Environ Microbiol 70(12):7126–7139
pubmed: 15574909
pmcid: 535158
doi: 10.1128/AEM.70.12.7126-7139.2004
Bremer H, Dennis PP (1996) Modulation of chemical composition and other parameters of the cell by growth rate. In: Neidhardt FC et al (eds) Escherichia coli and Salmonella: cellular and molecular biology, 2nd edn. ASM Press, Washington, DC, pp 1553–1569
Ortiz JO et al (2006) Mapping 70S ribosomes in intact cells by cryoelectron tomography and pattern recognition. J Struct Biol 156(2):334–341
pubmed: 16857386
doi: 10.1016/j.jsb.2006.04.014
pmcid: 16857386
Pang H, Winkler HH (1994) The concentrations of stable RNA and ribosomes in Rickettsia prowazekii. Mol Microbiol 12(1):115–120
pubmed: 7520114
doi: 10.1111/j.1365-2958.1994.tb01000.x
pmcid: 7520114
Yus E et al (2009) Impact of genome reduction on bacterial metabolism and its regulation. Science 326(5957):1263–1268
pubmed: 19965476
doi: 10.1126/science.1177263
pmcid: 19965476
Hoshino T et al (2008) Quantification of target molecules needed to detect microorganisms by fluorescence in situ hybridization (FISH) and catalyzed reporter deposition-FISH. Appl Environ Microbiol 74(16):5068–5077
pubmed: 18552182
pmcid: 2519275
doi: 10.1128/AEM.00208-08
Fuchs BM et al (2000) Unlabeled helper oligonucleotides increase the in situ accessibility to 16S rRNA of fluorescently labeled oligonucleotide probes. Appl Environ Microbiol 66(8):3603–3607
pubmed: 10919826
pmcid: 92190
doi: 10.1128/AEM.66.8.3603-3607.2000
Fuchs BM et al (1998) Flow cytometric analysis of the in situ accessibility of Escherichia coli 16S rRNA for fluorescently labeled oligonucleotide probes. Appl Environ Microbiol 64(12):4973–4982
pubmed: 9835591
pmcid: 90951
doi: 10.1128/AEM.64.12.4973-4982.1998
Fontenete S et al (2016) Prediction of melting temperatures in fluorescence in situ hybridization (FISH) procedures using thermodynamic models. Crit Rev Biotechnol 36(3):566–577
pubmed: 25586037
pmcid: 25586037
Cerqueira L et al (2008) DNA mimics for the rapid identification of microorganisms by fluorescence in situ hybridization (FISH). Int J Mol Sci 9(10):1944–1960
pubmed: 19325728
pmcid: 2635612
doi: 10.3390/ijms9101944
Fontenete S et al (2015) Mismatch discrimination in fluorescent in situ hybridization using different types of nucleic acids. Appl Microbiol Biotechnol 99(9):3961–3969
pubmed: 25840566
doi: 10.1007/s00253-015-6568-3
Petersen M, Wengel J (2003) LNA: a versatile tool for therapeutics and genomics. Trends Biotechnol 21(2):74–81
pubmed: 12573856
doi: 10.1016/S0167-7799(02)00038-0
Thomsen R, Nielsen PS, Jensen TH (2005) Dramatically improved RNA in situ hybridization signals using LNA-modified probes. RNA 11(11):1745–1748
pubmed: 16177135
pmcid: 1370861
doi: 10.1261/rna.2139705
Braasch DA, Corey DR (2001) Locked nucleic acid (LNA): fine-tuning the recognition of DNA and RNA. Chem Biol 8(1):1–7
pubmed: 11182314
doi: 10.1016/S1074-5521(00)00058-2
pmcid: 11182314
Kierzek E et al (2005) The influence of locked nucleic acid residues on the thermodynamic properties of 2’-O-methyl RNA/RNA heteroduplexes. Nucleic Acids Res 33(16):5082–5093
pubmed: 16155181
pmcid: 1201327
doi: 10.1093/nar/gki789
Majlessi M, Nelson NC, Becker MM (1998) Advantages of 2’-O-methyl oligoribonucleotide probes for detecting RNA targets. Nucleic Acids Res 26(9):2224–2229
pubmed: 9547284
pmcid: 147516
doi: 10.1093/nar/26.9.2224
Silverman AP, Kool ET (2007) Oligonucleotide probes for RNA-targeted fluorescence in situ hybridization. Adv Clin Chem 43:79–115
pubmed: 17249381
doi: 10.1016/S0065-2423(06)43003-1
pmcid: 17249381
Kurupati P et al (2007) Inhibition of gene expression and growth by antisense peptide nucleic acids in a multiresistant beta-lactamase-producing Klebsiella pneumoniae strain. Antimicrob Agents Chemother 51(3):805–811
pubmed: 17158940
doi: 10.1128/AAC.00709-06
Lima JF et al (2018) Targeting miR-9 in gastric cancer cells using locked nucleic acid oligonucleotides. BMC Mol Biol 19(1):6
pubmed: 29879907
pmcid: 5992815
doi: 10.1186/s12867-018-0107-6
Vieregg JR (2010) Encyclopedia of analytical chemistry: applications, theory and instrumentation. Wiley, New York
Hermanson GT (2013) Bioconjugate techniques, 3rd edn. Academic Press, London, pp 395–463
doi: 10.1016/B978-0-12-382239-0.00010-8
Santos RS et al (2014) Optimization of a peptide nucleic acid fluorescence in situ hybridization (PNA-FISH) method for the detection of bacteria and disclosure of a formamide effect. J Biotechnol 187:16–24
pubmed: 25034435
doi: 10.1016/j.jbiotec.2014.06.023
Farrell R (2010) Laboratory guide for isolation and characterization. In: RNA methodologies, 4th edn. Elsevier, Boston
Fontenete S et al (2016) Fluorescence in vivo hybridization (FIVH) for detection of Helicobacter pylori infection in a C57BL/6 mouse model. PLoS One 11(2):e0148353
pubmed: 26848853
pmcid: 4743915
doi: 10.1371/journal.pone.0148353
Matthiesen SH, Hansen CM (2012) Fast and non-toxic in situ hybridization without blocking of repetitive sequences. PLoS One 7(7):e40675
pubmed: 22911704
pmcid: 3404051
doi: 10.1371/journal.pone.0040675
Azevedo AS et al (2019) Optimizing locked nucleic acid/2’-O-methyl-RNA fluorescence in situ hybridization (LNA/2’OMe-FISH) procedure for bacterial detection. PLoS One 14(5):e0217689
pubmed: 31150460
pmcid: 6544301
doi: 10.1371/journal.pone.0217689
Rocha R et al (2016) Optimization of peptide nucleic acid fluorescence in situ hybridization (PNA-FISH) for the detection of bacteria: the effect of pH, dextran sulfate and probe concentration. J Biotechnol 226:1–7
pubmed: 27021959
doi: 10.1016/j.jbiotec.2016.03.047
pmcid: 27021959
Zustiak SP, Nossal R, Sackett DL (2011) Hindered diffusion in polymeric solutions studied by fluorescence correlation spectroscopy. Biophys J 101(1):255–264
pubmed: 21723836
pmcid: 3127197
doi: 10.1016/j.bpj.2011.05.035
Kalyuzhnaya MG et al (2006) Fluorescence in situ hybridization-flow cytometry-cell sorting-based method for separation and enrichment of type I and type II methanotroph populations. Appl Environ Microbiol 72(6):4293–4301
pubmed: 16751544
pmcid: 1489643
doi: 10.1128/AEM.00161-06
Musat N et al (2012) Detecting metabolic activities in single cells, with emphasis on nanoSIMS. FEMS Microbiol Rev 36(2):486–511
pubmed: 22092433
doi: 10.1111/j.1574-6976.2011.00303.x
Gahlmann A, Moerner WE (2014) Exploring bacterial cell biology with single-molecule tracking and super-resolution imaging. Nat Rev Microbiol 12(1):9–22
pubmed: 24336182
pmcid: 3934628
doi: 10.1038/nrmicro3154