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: UMLS:C0022568 (
keratitis
)
5,133
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Acanthamoeba
is free-living protist pathogen capable of causing a blinding
keratitis
and granulomatous encephalitis. However, the mechanisms of
Acanthamoeba
pathogenesis are still not clear. Here, our results show that cells co-cultured with pathogenic
Acanthamoeba
would be spherical and floated, even without contacting the protists. Then, the
Acanthamoeba
protists would contact and engulf these cells. In order to clarify the contact-independent pathogenesis mechanism in
Acanthamoeba
, we collected the
Acanthamoeba
-secreted proteins (Asp) to incubate with cells for identifying the extracellular virulent factors and investigating the cytotoxicity process. The Asps of pathogenic
Acanthamoeba
express protease activity to reactive Leu amino acid in ECM and induce cell-losing adhesion ability. The M20/M25/
M40
superfamily aminopeptidase protein (ACA1_264610), an aminopeptidase be found in Asp, is upregulated after
Acanthamoeba
and C6 cell co-culturing for 6 h. Pre-treating the Asp with leucine aminopeptidase inhibitor and the specific antibodies of
Acanthamoeba
M20/M25/
M40
superfamily aminopeptidase could reduce the cell damage during Asp and cell co-incubation. These results suggest an important functional role of the
Acanthamoeba
secreted extracellular aminopeptidases in the
Acanthamoeba
pathogenesis process. This study provides information regarding clinically pathogenic isolates to target specific molecules and design combined drugs.
...
PMID:Pathogenic Acanthamoeba castellanii Secretes the Extracellular Aminopeptidase M20/M25/M40 Family Protein to Target Cells for Phagocytosis by Disruption. 2925 52