Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:3.4.22.36 (
caspase-1
)
6,285
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Two
Shigella
species,
Shigella flexneri
and
Shigella sonnei
, cause approximately 90% of
bacterial dysentery
worldwide. While
S. flexneri
is the dominant species in low-income countries,
S. sonnei
causes the majority of infections in middle- and high-income countries.
S. flexneri
is a prototypic cytosolic bacterium; once intracellular, it rapidly escapes the phagocytic vacuole and causes pyroptosis of macrophages, which is important for pathogenesis and bacterial spread. In contrast, little is known about the invasion, vacuole escape, and induction of pyroptosis during
S. sonnei
infection of macrophages. We demonstrate here that
S. sonnei
causes substantially less pyroptosis in human primary monocyte-derived macrophages and THP1 cells. This is due to reduced bacterial uptake and lower relative vacuole escape, which results in fewer cytosolic
S. sonnei
and hence reduced activation of
caspase-1
inflammasomes. Mechanistically, the O-antigen (O-Ag), which in
S. sonnei
is contained in both the lipopolysaccharide and the capsule, was responsible for reduced uptake and the type 3 secretion system (T3SS) was required for vacuole escape. Our findings suggest that
S. sonnei
has adapted to an extracellular lifestyle by incorporating multiple layers of O-Ag onto its surface compared to other
Shigella
species.
IMPORTANCE
Diarrheal disease remains the second leading cause of death in children under five.
Shigella
remains a significant cause of diarrheal disease with two species,
S. flexneri
and
S. sonnei
, causing the majority of infections.
S. flexneri
are well known to cause cell death in macrophages, which contributes to the inflammatory nature of
Shigella
diarrhea. Here, we demonstrate that
S. sonnei
causes less cell death than
S. flexneri
due to a reduced number of bacteria present in the cell cytosol. We identify the O-Ag polysaccharide which, uniquely among
Shigella
spp., is present in two forms on the bacterial cell surface as the bacterial factor responsible. Our data indicate that
S. sonnei
differs from
S. flexneri
in key aspects of infection and that more attention should be given to characterization of
S. sonnei
infection.
...
PMID:
Shigella sonnei
O-Antigen Inhibits Internalization, Vacuole Escape, and Inflammasome Activation. 3184 80