Comparison of techniques for counting prokaryotes in marine planktonic and biofilm samples

Though a large number of techniques are available for the study of aquatic bacteria, the aim of this study was to establish a technique for analysing free-living and biofilm prokaryotic cells through laboratory assays. In particular, we wished to analyse the efficiency of ultrasound to detach and disrupt biofilm, to obtain an efficient stain treatment for quantifying free-living and biofilm prokaryotes in flow cytometry (FC), and to compare epifluorescence microscopy (EFM), scanning electron microscopy (SEM) and FC for quantifying free-living and biofilm prokaryotes#. Marine-grade plywood substrates were immersed in natural marine water that was conditioned for 12 days. At 6 and 12 days, water aliquots and substrates were removed to estimate free-living and biofilm prokaryote density. Ultrasound efficiently removed marine biofilm from substrates (up to 94%) without cell damage. FC analysis (unstained) reliably quantified marine plankton and young or mature biofilm prokaryotes compared with other staining (acridine orange, 4′,6-diamidino-2-phenylindole, propidium iodide and green fluorescent nucleic acid), EFM or SEM techniques. FC and SEM achieved similar results, while a high variability was observed in the EFM technique. FC was faster and more precise than SEM because the count is not dependent on the observer.

[1]  Andrew T. McKenzie Glutaraldehyde: A review of its fixative effects on nucleic acids, proteins, lipids, and carbohydrates , 2019 .

[2]  A. Macêdo,et al.  Effect of antimicrobials, salinity, and contamination by air on bacterial and fungal growth in cyprid cultures of Amphibalanus improvisus , 2018, Marine Ecology.

[3]  V. O. Agostini,et al.  Evaluation of the effect of antimicrobials in marine cultures, using the copepod Acartia tonsa as a bioindicator , 2018, Chemistry and Ecology.

[4]  R. Parthasarathy Monitoring microbial communities using light sheet fluorescence microscopy. , 2018, Current opinion in microbiology.

[5]  A. Macêdo,et al.  Inhibition of biofilm bacteria and adherent fungi from marine plankton cultures using an antimicrobial combination , 2018, International Aquatic Research.

[6]  A. Macêdo,et al.  Sneaker Store Air 1 Av3735 Max 002 By Nike Day 43einhalb zq8Cxpdw , 2017 .

[7]  Fernando Erthal,et al.  What determines sclerobiont colonization on marine mollusk shells? , 2017, PloS one.

[8]  J. Pinhassi,et al.  Marine Bacterioplankton Seasonal Succession Dynamics. , 2017, Trends in microbiology.

[9]  Sergey Dobretsov,et al.  Evaluating the Reliability of Counting Bacteria Using Epifluorescence Microscopy , 2017 .

[10]  Alexandra Kroll,et al.  Flow cytometry combined with viSNE for the analysis of microbial biofilms and detection of microplastics , 2016, Nature Communications.

[11]  Joon-Hee Lee,et al.  Biofilm dispersion in Pseudomonas aeruginosa , 2016, Journal of Microbiology.

[12]  A. Macêdo,et al.  Evaluation of antibiotics as a methodological procedure to inhibit free-living and biofilm bacteria in marine zooplankton culture. , 2016, Anais da Academia Brasileira de Ciencias.

[13]  Qian Li,et al.  Erratum to: Visualization and analysis of EPS glycoconjugates of the thermoacidophilic archaeon Sulfolobus metallicus , 2015, Applied Microbiology and Biotechnology.

[14]  L. Maes,et al.  A flow cytometric approach to quantify biofilms , 2015, Folia Microbiologica.

[15]  D. Beniac,et al.  A mobile biosafety microanalysis system for infectious agents , 2015, Scientific Reports.

[16]  Xiaomei Yan,et al.  Rapid detection and enumeration of total bacteria in drinking water and tea beverages using a laboratory-built high-sensitivity flow cytometer , 2015 .

[17]  Verónica Ambriz-Aviña,et al.  Applications of Flow Cytometry to Characterize Bacterial Physiological Responses , 2014, BioMed research international.

[18]  Mari Ophus Bacterial Community Dynamics in a Biofilter exposed to a Micropollutant , 2014 .

[19]  A. Nerland,et al.  Characterization of extracellular polymeric matrix, and treatment of Fusobacterium nucleatum and Porphyromonas gingivalis biofilms with DNase I and proteinase K , 2013, Journal of oral microbiology.

[20]  T. Bigelow,et al.  Mechanical destruction of pseudomonas aeruginosa biofilms by ultrasound exposure , 2012 .

[21]  E. Fischer,et al.  Scanning Electron Microscopy , 2012, Current protocols in microbiology.

[22]  R. Franklin,et al.  Enumerating bacterial cells on bioadhesive coated slides. , 2011, Journal of microbiological methods.

[23]  H. Flemming,et al.  The biofilm matrix , 2010, Nature Reviews Microbiology.

[24]  F. Azam,et al.  New Method for Counting Bacteria Associated with Coral Mucus , 2010, Applied and Environmental Microbiology.

[25]  K Toté,et al.  Biofilms: an extra hurdle for effective antimicrobial therapy. , 2010, Current pharmaceutical design.

[26]  C. Combs,et al.  Fluorescence Microscopy: A Concise Guide to Current Imaging Methods , 2010, Current protocols in neuroscience.

[27]  W. Knol,et al.  Forming of a functional biofilm on wood surfaces , 2010 .

[28]  S. Fazi,et al.  Recovery and quantification of bacterial cells associated with streambed sediments. , 2008, Journal of microbiological methods.

[29]  J. Gasol,et al.  Evaluating the Flow-Cytometric Nucleic Acid Double-Staining Protocol in Realistic Situations of Planktonic Bacterial Death , 2008, Applied and Environmental Microbiology.

[30]  R. Martinuzzi,et al.  The use of microscopy and three-dimensional visualization to evaluate the structure of microbial biofilms cultivated in the Calgary Biofilm Device , 2006, Biological Procedures Online.

[31]  S. Günther,et al.  Limits of propidium iodide as a cell viability indicator for environmental bacteria , 2007, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

[32]  Jordi Catalan,et al.  Suitability of Flow Cytometry for Estimating Bacterial Biovolume in Natural Plankton Samples: Comparison with Microscopy Data , 2007, Applied and Environmental Microbiology.

[33]  Frederik Hammes,et al.  Assessment and Interpretation of Bacterial Viability by Using the LIVE/DEAD BacLight Kit in Combination with Flow Cytometry , 2007, Applied and Environmental Microbiology.

[34]  W. W. Junior,et al.  Caracterização da assembléia de bactérias nitrificantes pelo método "fluorescent in situ hybridization" (fish) no biofilme e água de larvicultura do camarão-Rosa farfantepenaeus paulensis , 2006 .

[35]  L. Samaranayake,et al.  The use of new probes and stains for improved assessment of cell viability and extracellular polymeric substances in Candida albicans biofilms , 2005, Mycopathologia.

[36]  L. Blum,et al.  Combined effect of chelating agents and ultrasound on biofilm removal from stainless steel surfaces. Application to “ Escherichia coli milk” and “ Staphylococcus aureus milk” biofilms , 2004 .

[37]  H. Shapiro,et al.  Multiparameter flow cytometry of bacteria. , 2004, Methods in molecular biology.

[38]  John R. Lawrence,et al.  Assessment of Fluorochromes for Two-Photon Laser Scanning Microscopy of Biofilms , 2002, Applied and Environmental Microbiology.

[39]  C. R. Lovell,et al.  Numerical Dominance and Phylotype Diversity of Marine Rhodobacter Species during Early Colonization of Submerged Surfaces in Coastal Marine Waters as Determined by 16S Ribosomal DNA Sequence Analysis and Fluorescence In Situ Hybridization , 2002, Applied and Environmental Microbiology.

[40]  F. Jochem Morphology and DNA content of bacterioplankton in the northern Gulf of Mexico: analysis by epifluorescence microscopy and flow cytometry , 2001 .

[41]  J. Pernthaler,et al.  Precision of bacterioplankton biomass determination: a comparison of two fluorescent dyes, and of allometric and linear volume-to-carbon conversion factors , 2001 .

[42]  P. Servais,et al.  Using light scatter signal to estimate bacterial biovolume by flow cytometry. , 2001, Cytometry.

[43]  G. Rutter,et al.  Simultaneous evanescent wave imaging of insulin vesicle membrane and cargo during a single exocytotic event , 2000, Current Biology.

[44]  C. Hewitt,et al.  Analysis of bacterial function by multi-colour fluorescence flow cytometry and single cell sorting. , 2000, Journal of microbiological methods.

[45]  Josep M. Gasol,et al.  Using flow cytometry for counting natural planktonic bacteria and understanding the structure of planktonic bacterial communities , 2000 .

[46]  P. Servais,et al.  Flow cytometric discrimination of bacterial populations in seawater based on SYTO 13 staining of nucleic acids , 1999 .

[47]  R. Desjardins,et al.  LIVE/DEAD BacLight : application of a new rapid staining method for direct enumeration of viable and total bacteria in drinking water. , 1999, Journal of microbiological methods.

[48]  D. Kell,et al.  Fluorescent brighteners: novel stains for the flow cytometric analysis of microorganisms. , 1997, Cytometry.

[49]  D. Kell,et al.  Flow cytometry and cell sorting of heterogeneous microbial populations: the importance of single-cell analyses , 1996 .

[50]  H. Steen,et al.  Rapid flow cytometric assessment of mecillinam and ampicillin bacterial susceptibility. , 1996, The Journal of antimicrobial chemotherapy.

[51]  J. Pratt,et al.  Use of fluorochromes for direct enumeration of total bacteria in environmental samples: past and present , 1994 .

[52]  J. Pratt,et al.  Use of fluorochromes for direct enumeration of total bacteria in environmental samples: past and present. , 1994, Microbiological reviews.

[53]  E. Sherr,et al.  DAPI direct counting underestimates bacterial abundances and average cell size compared to AO direct counting , 1993 .

[54]  V. Gant,et al.  The application of flow cytometry to the study of bacterial responses to antibiotics. , 1993, Journal of medical microbiology.

[55]  P Monfort,et al.  Comparison of flow cytometry and epifluorescence microscopy for counting bacteria in aquatic ecosystems. , 1992, Cytometry.

[56]  R. Sinsabaugh,et al.  Biofilm development on leaf and wood surfaces in a boreal river , 1991 .

[57]  K. Porter,et al.  The use of DAPI for identifying and counting aquatic microflora1 , 1980 .

[58]  J. Hobbie,et al.  Use of nuclepore filters for counting bacteria by fluorescence microscopy , 1977, Applied and environmental microbiology.

[59]  R. Barer,et al.  The Action of Formaldehyde on Living Cells as Studied by Phase-contrast Microscopy , 1951 .