Abstract
We investigated the spatial pattern of expression of ipdC, a plant inducible gene involved in indoleacetic acid biosynthesis in Erwinia herbicola, among individual cells on plants to gain a better understanding of the role of this phenotype in the epiphytic ecology of bacteria and the factors involved in the regulation of ipdC. Nonpathogenic E. herbicola strain 299R harboring a transcriptional fusion of ipdC to gfp was inoculated onto bean plants, recovered from individual leaves 48 h after inoculation, and subjected to fluorescence in situ hybridization using a 16S rRNA oligonucleotide probe specific to strain 299R. Epifluorescence images captured through a rhodamine filter were used to distinguish the 5carboxytetramethylrhodamine-labeled cells of strain 299R from other leaf microflora. Quantification of the green fluorescence intensity of individual cells by analysis of digital images revealed that about 65% of the 299R cells recovered from bean leaves had higher ipdC expression than in culture. Additionally, 10% of the cells exhibited much higher levels of green fluorescence than the median fluorescence intensity, indicating that they are more heterogeneous with respect to ipdC expression on plants than in culture. Examination of 299R cells in situ on leaf surfaces by confocal laser scanning microscopy after fluorescence in situ hybridization of cells on leaf samples showed that even cells that were in close proximity exhibited dramatically different green fluorescence intensities, and thus, were in a physical or chemical microenvironment that induced differential expression of ipdC.
MeSH Terms
Carboxy-Lyases/genetics
Erwinia/enzymology,genetics
Fabaceae/metabolism
Genes, Bacterial
Indoleacetic Acids/metabolism
Plant Leaves
Recombinant Fusion Proteins/genetics
Transcription, Genetic
Chemicals
Indoleacetic Acids
Recombinant Fusion Proteins
indoleacetic acid
indolepyruvate decarboxylase
Carboxy-Lyases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Brandl M T
Department of Plant and Microbial Biology, 111 Koshland Hall, University of California, Berkeley, CA 94720, USA.
Quiñones B
Lindow S E
References (21)
21 references, click to expand
-
Quantitative immunofluorescence of regulated eps gene expression in single cells of Ralstonia solanacearum.
Appl Environ Microbiol. 1999 Jun;65(6):2356-62
PMID: 10347013
-
Broad host range DNA cloning system for gram-negative bacteria: construction of a gene bank of Rhizobium meliloti.
Proc Natl Acad Sci U S A. 1980 Dec;77(12):7347-51
PMID: 7012838
-
Occurrence of indole-3-acetic Acid-producing bacteria on pear trees and their association with fruit russet.
Phytopathology. 1998 Nov;88(11):1149-57
PMID: 18944847
-
A mutation in the indole-3-acetic acid biosynthesis pathway of Pseudomonas syringae pv. syringae affects growth in Phaseolus vulgaris and syringomycin production.
J Bacteriol. 1994 Mar;176(5):1374-82
PMID: 8113177
-
Biological sensor for sucrose availability: relative sensitivities of various reporter genes.
Appl Environ Microbiol. 2001 Mar;67(3):1308-17
PMID: 11229926
-
In situ gene expression in mixed-culture biofilms: evidence of metabolic interactions between community members.
Appl Environ Microbiol. 1998 Feb;64(2):721-32
PMID: 9464414
-
Green fluorescent protein as a marker for gene expression.
Science. 1994 Feb 11;263(5148):802-5
PMID: 8303295
-
Appetite of an epiphyte: quantitative monitoring of bacterial sugar consumption in the phyllosphere.
Proc Natl Acad Sci U S A. 2001 Mar 13;98(6):3446-53
PMID: 11248098
-
Improved gfp and inaZ broad-host-range promoter-probe vectors.
Mol Plant Microbe Interact. 2000 Nov;13(11):1243-50
PMID: 11059491
-
Gene organization and primary structure of a ribosomal RNA operon from Escherichia coli.
J Mol Biol. 1981 May 15;148(2):107-27
PMID: 7028991
-
A biological sensor for iron available to bacteria in their habitats on plant surfaces.
Appl Environ Microbiol. 1994 Jun;60(6):1934-41
PMID: 16349283
-
Differential involvement of indole-3-acetic acid biosynthetic pathways in pathogenicity and epiphytic fitness of Erwinia herbicola pv. gypsophilae.
Mol Plant Microbe Interact. 1998 Jul;11(7):634-42
PMID: 9650296
-
Detection of induced beta-galactosidase activity in individual non-culturable cells of pathogenic bacteria by quantitative cytological assay.
Mol Microbiol. 1995 Aug;17(3):545-54
PMID: 8559073
-
Toxicity of an overproduced foreign gene product in Escherichia coli and its use in plasmid vectors for the selection of transcription terminators.
Gene. 1984 Feb;27(2):161-72
PMID: 6202587
-
Heterogeneity of iron bioavailability on plants assessed with a whole-cell GFP-based bacterial biosensor.
Microbiology. 2000 Oct;146 ( Pt 10):2435-45
PMID: 11021920
-
Distribution of bacterial growth activity in flow-chamber biofilms.
Appl Environ Microbiol. 1999 Sep;65(9):4108-17
PMID: 10473423
-
A new version of the RDP (Ribosomal Database Project).
Nucleic Acids Res. 1999 Jan 1;27(1):171-3
PMID: 9847171
-
Contribution of indole-3-acetic acid production to the epiphytic fitness of erwinia herbicola
Appl Environ Microbiol. 1998 Sep;64(9):3256-63
PMID: 9726868
-
Bacterial biosynthesis of indole-3-acetic acid.
Can J Microbiol. 1996 Mar;42(3):207-20
PMID: 8868227
-
Cloning and characterization of a locus encoding an indolepyruvate decarboxylase involved in indole-3-acetic acid synthesis in Erwinia herbicola.
Appl Environ Microbiol. 1996 Nov;62(11):4121-8
PMID: 8900003
-
An improved GFP cloning cassette designed for prokaryotic transcriptional fusions.
Gene. 1997 Jun 3;191(2):149-53
PMID: 9218713