In situ detection of bacteria in calcified biofilms using FISH and CARD–FISH

• Published in: Journal of microbiological methods Vol. 75; no. 1; pp. 103 - 108
• Main Authors: Shiraishi, Fumito, Zippel, Barbara, Neu, Thomas R., Arp, Gernot
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 01.09.2008; Elsevier
• Subjects: Bacteria - genetics; Bacteria - isolation & purification; Bacteriological methods and techniques used in bacteriology; Bacteriological Techniques; Bacteriology; Biofilms; Biological and medical sciences; CARD–FISH; FISH; Fresh Water - microbiology; Fundamental and applied biological sciences. Psychology; Geologic Sediments - microbiology; In Situ Hybridization, Fluorescence - methods; Microbiology; Mineralized biofilm; Nucleic Acid Hybridization - methods; Oligonucleotide Probes - genetics; Stromatolite; Tyramide signal amplification (TSA); FISH; Tyramide signal amplification (TSA); CARD–FISH; Mineralized biofilm; Stromatolite; Fluorescence in situ hybridization; Biofilm; Bacteria; Method; Detection; CARD-FISH
• DOI: 10.1016/j.mimet.2008.05.015
• ISSN: 0167-7012

Modified protocols of fluorescence in situ hybridization (FISH) and catalyze reporter deposition fluorescence in situ hybridization (CARD–FISH) were developed in order to detect bacteria in situ in calcified stromatolite biofilms. Smooth, well-preserved thin sections of calcified biofilms (~ 5 µm thin, vertical sectioning of ~ 1 cm deep) were obtained by cryo-sectioning using the adhesive tape-stabilization technique. A modified hybridization buffer was applied during hybridization to prevent calcite dissolution as well as false binding of oligonucleotide probes to the charged mineral surfaces. Particularly, bright and specific CARD–FISH signals allowed the detection of bacteria in intensively calcified biofilms even at low magnification, which is suitable for investigating millimeter- to centimeter-scale vertical distribution patterns of bacteria.