GeneFISH – an in situ technique for linking gene presence and cell identity in environmental microorganisms
Article first published online: 3 NOV 2010
© 2010 Society for Applied Microbiology and Blackwell Publishing Ltd
Volume 12, Issue 11, pages 3057–3073, November 2010
How to Cite
Moraru, C., Lam, P., Fuchs, B. M., Kuypers, M. M. M. and Amann, R. (2010), GeneFISH – an in situ technique for linking gene presence and cell identity in environmental microorganisms. Environmental Microbiology, 12: 3057–3073. doi: 10.1111/j.1462-2920.2010.02281.x
- Issue published online: 3 NOV 2010
- Article first published online: 3 NOV 2010
- Received 1 February, 2010; accepted 7 May, 2010.
Our knowledge concerning the metabolic potentials of as yet to be cultured microorganisms has increased tremendously with the advance of sequencing technologies and the consequent discoveries of novel genes. On the other hand, it is often difficult to reliably assign a particular gene to a phylogenetic clade, because these sequences are usually found on genomic fragments that carry no direct marker of cell identity, such as rRNA genes. Therefore, the aim of the present study was to develop geneFISH – a protocol for linking gene presence with cell identity in environmental samples, the signals of which can be visualized at a single cell level. This protocol combines rRNA-targeted catalysed reporter deposition – fluorescence in situ hybridization and in situ gene detection. To test the protocol, it was applied to seawater samples from the Benguela upwelling system. For gene detection, a polynucleotide probe mix was used, which was designed based on crenarchaeotal amoA clone libraries prepared from each seawater sample. Each probe in the mix was selected to bind to targets with up to 5% mismatches. To determine the hybridization parameters, the Tm of probes, targets and hybrids was estimated based on theoretical calculations and in vitro measurements. It was shown that at least 30%, but potentially the majority of the Crenarchaeota present in these samples harboured the amoA gene and were therefore likely to be catalysing the oxidation of ammonia.