| Literature DB >> 25523128 |
Tsuyoshi Yamaguchi1, Shuji Kawakami1,2, Masashi Hatamoto1, Hiroyuki Imachi3, Masanobu Takahashi1,4, Nobuo Araki5, Takashi Yamaguchi1, Kengo Kubota4.
Abstract
In situ detection of microorganisms by fluorescence in situ hybridization (FISH) is a powerful tool for environmental microbiology, but analyses can be hampered by low rRNA content in target organisms, especially in oligotrophic environments. Here, we present a non-enzymatic, hybridization chain reaction (HCR)-based signal amplified in situ whole-cell detection technique (in situ DNA-HCR). The components of the amplification buffer were optimized to polymerize DNA amplifier probes for in situ DNA-HCR. In situ hybridization of initiator probes followed by signal amplification via HCR produced bright signals with high specificity and probe permeation into cells. The detection rates for Bacteria in a seawater sample and Archaea in anaerobic sludge samples were comparable with or greater than those obtained by catalyzed reporter deposition (CARD)-FISH or standard FISH. Detection of multiple organisms (Bacteria, Archaea and Methanosaetaceae) in an anaerobic sludge sample was achieved by simultaneous in situ DNA-HCR. In summary, in situ DNA-HCR is a simple and easy technique for detecting single microbial cells and enhancing understanding of the ecology and behaviour of environmental microorganisms in situ.Mesh:
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Year: 2015 PMID: 25523128 DOI: 10.1111/1462-2920.12745
Source DB: PubMed Journal: Environ Microbiol ISSN: 1462-2912 Impact factor: 5.491