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Photobacterium damselae subsp. damselae Major Virulence Factors Dly, Plasmid-Encoded HlyA, and Chromosome-Encoded HlyA Are Secreted via the Type II Secretion System
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ABSTRACT
Photobacterium damselae
subsp.
damselae
is a marine bacterium that causes septicemia in marine animals and in humans. Previously, we had determined a major role of pPHDD1 plasmid-encoded Dly (damselysin) and HlyA (HlyA
pl
) and the chromosome-encoded HlyA (HlyA
ch
) hemolysins in virulence. However, the mechanisms by which these toxins are secreted remain unknown. In this study, we found that a mini-Tn
10
transposon mutant in a plasmidless strain showing an impaired hemolytic phenotype contained an insertion in
epsL
, a component of a type II secretion system (T2SS). Reconstruction of the mutant by allelic exchange confirmed the specific involvement of
epsL
in HlyA
ch
secretion. In addition, mutation of
epsL
in a pPHDD1-harboring strain caused an almost complete abolition of hemolytic activity against sheep erythrocytes, indicating that
epsL
plays a major role in secretion of the plasmid-encoded HlyA
pl
and Dly. This was further demonstrated by analysis of different combinations of hemolysin gene mutants and by strain-strain complementation assays. We also found that mutation of the putative prepilin peptidase gene
pilD
severely affected hemolysis, which dropped at levels inferior to those of
epsL
mutants. Promoter expression analyses suggested that impairment of hemolysin secretion in
epsL
and
pilD
mutants might constitute a signal that affects hemolysin and T2SS gene expression at the transcriptional level. In addition, single
epsL
and
pilD
mutations caused a drastic decrease in virulence for mice, demonstrating a major role of T2SS and
pilD
in
P. damselae
subsp.
damselae
virulence.
American Society for Microbiology
Title: Photobacterium damselae subsp. damselae Major Virulence Factors Dly, Plasmid-Encoded HlyA, and Chromosome-Encoded HlyA Are Secreted via the Type II Secretion System
Description:
ABSTRACT
Photobacterium damselae
subsp.
damselae
is a marine bacterium that causes septicemia in marine animals and in humans.
Previously, we had determined a major role of pPHDD1 plasmid-encoded Dly (damselysin) and HlyA (HlyA
pl
) and the chromosome-encoded HlyA (HlyA
ch
) hemolysins in virulence.
However, the mechanisms by which these toxins are secreted remain unknown.
In this study, we found that a mini-Tn
10
transposon mutant in a plasmidless strain showing an impaired hemolytic phenotype contained an insertion in
epsL
, a component of a type II secretion system (T2SS).
Reconstruction of the mutant by allelic exchange confirmed the specific involvement of
epsL
in HlyA
ch
secretion.
In addition, mutation of
epsL
in a pPHDD1-harboring strain caused an almost complete abolition of hemolytic activity against sheep erythrocytes, indicating that
epsL
plays a major role in secretion of the plasmid-encoded HlyA
pl
and Dly.
This was further demonstrated by analysis of different combinations of hemolysin gene mutants and by strain-strain complementation assays.
We also found that mutation of the putative prepilin peptidase gene
pilD
severely affected hemolysis, which dropped at levels inferior to those of
epsL
mutants.
Promoter expression analyses suggested that impairment of hemolysin secretion in
epsL
and
pilD
mutants might constitute a signal that affects hemolysin and T2SS gene expression at the transcriptional level.
In addition, single
epsL
and
pilD
mutations caused a drastic decrease in virulence for mice, demonstrating a major role of T2SS and
pilD
in
P.
damselae
subsp.
damselae
virulence.
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