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Putative transcription antiterminator RfaH contributes to Erwinia amylovora virulence
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Abstract
The gram‐negative bacterium
Erwinia amylovora
causes fire blight disease of apple and pear trees. The exopolysaccharide amylovoran and lipopolysaccharides are essential
E. amylovora
virulence factors. Production of amylovoran and lipopolysaccharide is specified in part by genes that are members of long operons. Here, we show that full virulence of
E. amylovora
in apple fruitlets and tree shoots depends on the predicted transcription antiterminator RfaH. RfaH reduces pausing in the production of long transcripts having an operon polarity suppressor regulatory element within their promoter region. In
E. amylovora
, only the amylovoran operon and a lipopolysaccharide operon have such regulatory elements within their promoter regions and in the correct orientation. These operons showed dramatically increased polarity in the Δ
rfaH
mutant compared to the wild type as determined by RNA sequencing. Amylovoran and lipopolysaccharide production in vitro was reduced in
rfaH
mutants compared to the wild type, which probably contributes to the
rfaH
mutant virulence phenotype. Furthermore, type VI secretion cluster 1, which contributes to
E. amylovora
virulence, showed reduced expression in Δ
rfaH
compared to the wild type, although without an increase in polarity. The data suggest that
E. amylovora
RfaH directly, specifically, and exclusively suppresses operon polarity in the amylovoran operon and a lipopolysaccharide operon.
Title: Putative transcription antiterminator RfaH contributes to
Erwinia amylovora
virulence
Description:
Abstract
The gram‐negative bacterium
Erwinia amylovora
causes fire blight disease of apple and pear trees.
The exopolysaccharide amylovoran and lipopolysaccharides are essential
E.
amylovora
virulence factors.
Production of amylovoran and lipopolysaccharide is specified in part by genes that are members of long operons.
Here, we show that full virulence of
E.
amylovora
in apple fruitlets and tree shoots depends on the predicted transcription antiterminator RfaH.
RfaH reduces pausing in the production of long transcripts having an operon polarity suppressor regulatory element within their promoter region.
In
E.
amylovora
, only the amylovoran operon and a lipopolysaccharide operon have such regulatory elements within their promoter regions and in the correct orientation.
These operons showed dramatically increased polarity in the Δ
rfaH
mutant compared to the wild type as determined by RNA sequencing.
Amylovoran and lipopolysaccharide production in vitro was reduced in
rfaH
mutants compared to the wild type, which probably contributes to the
rfaH
mutant virulence phenotype.
Furthermore, type VI secretion cluster 1, which contributes to
E.
amylovora
virulence, showed reduced expression in Δ
rfaH
compared to the wild type, although without an increase in polarity.
The data suggest that
E.
amylovora
RfaH directly, specifically, and exclusively suppresses operon polarity in the amylovoran operon and a lipopolysaccharide operon.
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