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Journal of Bacteriology, June 2000, p. 3508-3516, Vol. 182, No. 12
Department of Genetics, Harvard Medical
School, and Department of Molecular Biology, Massachusetts General
Hospital, Boston, Massachusetts 02114
Received 4 November 1999/Accepted 10 March 2000
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
The Alternative Sigma Factor RpoN Is Required for hrp
Activity in Pseudomonas syringae pv. Maculicola and Acts
at the Level of hrpL Transcription

-Glucuronidase (uidA) reporter gene fusions were
constructed for the hrpZ, hrpL, and
hrpS genes from the phytopathogen Pseudomonas syringae pv. maculicola strain ES4326. These reporters, as well as an avrRpt2-uidA fusion, were used to measure
transcriptional activity in ES4326 and a ES4326 rpoN
mutant. rpoN was required for the expression of
avrRpt2, hrpZ, and hrpL in vitro in
minimal media and in vivo when infiltrated into Arabidopsis
thaliana leaves. In contrast, the expression of hrpS
was essentially the same in wild-type and rpoN mutant
strains. Constitutive expression of hrpL in an
rpoN mutant restored hrpZ transcription to
wild-type levels, restored the hypersensitive response when infiltrated into tobacco (Nicotiana tobacum), and partially restored
the elicitation of virulence-related symptoms but not growth when
infiltrated into Arabidopsis leaves. These data indicate
that rpoN-mediated control of hrp gene
expression acts at the level of hrpL and that in planta
growth of P. syringae is not required for the elicitation of disease symptoms.
*
Corresponding author. Mailing address: Massachusetts
General Hospital, Department of Molecular Biology, Wellman 10, Boston, MA 02114. Phone: (617) 726-5969. Fax: (617) 726-5949. E-mail: ausubel{at}frodo.mgh.harvard.edu.
Present address: Department of Microbiology, University of
Washington, Seattle, WA 98195.
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