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Appl. Environ. Microbiol., Feb 1997, 644-651, Vol 63, No. 2
PL Siering and WC Ghiorse
Comparative sequence analysis of the 16S rRNA genes from several Leptothrix
and Sphaerotilus strains led to the design of an oligonucleotide probe
(PS-1) based on a sequence within the hypervariable region 1 specific for
four Leptothrix strains and for one of the four Sphaerotilus natans strains
examined. Another probe (PSP-6) was based on a sequence within the
hypervariable region 2. PSP-6 was specific for one of the two evolutionary
lineages previously described for Leptothrix spp. (P. L. Siering and W. C.
Ghiorse, Int. J. Syst. Bacteriol. 46:173-182, 1996). Fluorescein-labeled
oligonucleotide probes were synthesized, and their specificity for
fluorescence in situ hybridization identification was confirmed by a laser
scanning microscopy technique (W. C. Ghiorse, D. N. Miller, R. L. Sandoli,
and P. L. Siering, Microsc. Res. Tech. 33:73-86, 1996) to compare whole-
cell hybridizations of closely related bacteria. Probe specificity was also
tested in dot blot against total RNA isolated from four Leptothrix strains,
four Sphaerotilus strains, and 15 other members of the class
Proteobacteria. When the probes were tested on samples from the Sapsucker
Woods wetland habitat where Leptothrix spp. are thought to play a role in
manganese and iron oxidation, positive signals were obtained from several
sheathed filamentous bacteria including some that were morphologically
similar to previously isolated strains of "Leptothrix discophora." Other
unknown filamentous sheathed bacteria also gave strong positive signals.
This work provides a foundation for future studies correlating the presence
of members of the Leptothrix- Sphaerotilus group of sheathed bacteria with
manganese and iron oxidation activity in habitats where biological iron and
manganese oxidation are important environmental processes.
Copyright © 1997, American Society for Microbiology
Development and application of 16S rRNA-targeted probes for detection of iron- and manganese-oxidizing sheathed bacteria in environmental samples
Section of Microbiology, Cornell University, Ithaca, New York 14853- 8101, USA.
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