Rapid screening for freshwater bacterial groups by using reverse line blot hybridization

G. Zwart, E.J. Van Hannen, M.P. Kamst-van Agterveld, K. Van der Gucht, E.S. Lindström, J. Van Wichelen, T. Lauridsen, B.C. Crump, S.K. Han, S.A.J. Declerck

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    The identification of phylogenetic clusters of bacteria that are common in freshwater has provided a basis for probe design to target important freshwater groups. We present a set of 16S ribosomal RNA gene-based oligonucleotide probes specific for 15 of these freshwater clusters. The probes were applied in reverse line blot hybridization, a simple method that enables the rapid screening of PCR products from many samples against an array of probes. The optimized assay was made stringent to discriminate at approximately the single-mismatch level. This made 10 of the probes highly specific, with at least two mismatches to the closest noncluster member in the global database. Screening of PCR products from bacterioplankton of 81 diverse lakes from Belgium, The Netherlands, Denmark, Sweden, and Norway showed that the respective probes were reactive against 5 to 100% of the lake samples. Positive reactivity of six highly specific probes showed that bacteria from actinobacterial clusters ACK-M1 and Sta2-30 and from verrucomicrobial cluster CLO-14 occurred in at least 90% of the investigated lakes. Furthermore, bacteria from alpha-proteobacterial cluster LD12 (closely related to the marine SAR11 cluster), beta-proteobacterial cluster LD28 and cyanobacterial cluster Synechococcus 6b occurred in more than 70% of the lakes. Reverse line blot hybridization is a new tool in microbial ecology that will facilitate research on distribution and habitat specificity of target species at relatively low costs
    Originele taal-2Engels
    Pagina's (van-tot)5875-5883
    TijdschriftApplied and Environmental Microbiology
    Volume69
    Nummer van het tijdschrift10
    DOI's
    StatusGepubliceerd - 2003

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