Cell surface protease PRT1 identified in the fungal pathogen Pneumocystis carinii

1999 ◽  
Vol 31 (6) ◽  
pp. 1723-1733 ◽  
Author(s):  
Elena B. Lugli ◽  
Edward T. W. Bampton ◽  
David J. P. Ferguson ◽  
Ann E. Wakefield
2006 ◽  
Vol 5 (6) ◽  
pp. 916-923 ◽  
Author(s):  
Crystal R. Icenhour ◽  
Theodore J. Kottom ◽  
Andrew H. Limper

ABSTRACT Pneumocystis continues to represent an important opportunistic fungal pathogen of those with compromised immunity. Thus, it is crucial to identify factors that affect its viability and pathogenicity. We previously reported the first identification of melanins in Pneumocystis. In the present study, we sought to further characterize these components and define the function for these melanins. Melanins extracted from Pneumocystis and melanized Pneumocystis cells were analyzed by electron spin resonance spectroscopy, revealing spectra consistent with melanins from other fungi. Immunofluorescence assays using anti-melanin monoclonal antibodies showed that melanins are widely present across Pneumocystis host species, including mouse-, ferret-, and human-derived Pneumocystis organisms, as well as Pneumocystis carinii derived from rat. Using immunoelectron microscopy, melanins were found to localize to the cell wall and cytoplasm of P. carinii cysts, as well as to intracystic bodies within mature cysts. Next, the role of melanins on the maintenance of Pneumocystis viability was determined by using quantitative reverse transcription-PCR measurement of the heat shock protein mRNA under adverse environmental conditions. Using a new method to promote the melanization of Pneumocystis, we observed that strongly melanized Pneumocystis retained viability to a greater degree when exposed to UV irradiation or desiccation compared to less-pigmented organisms. These studies support our previous identification of Pneumocystis melanins across the genus, further characterize these Pneumocystis components, and demonstrate that melanins protect Pneumocystis from environmental stressors.


Author(s):  
Terrence J. Piva ◽  
Kari G. Francis ◽  
Darren R. Krause ◽  
Grace M. Chojnowski ◽  
Kay A.O. Ellem

2000 ◽  
Vol 279 (4) ◽  
pp. G726-G732 ◽  
Author(s):  
John Maa ◽  
Eileen F. Grady ◽  
Ed H. Kim ◽  
Shandra K. Yoshimi ◽  
Matthew M. Hutter ◽  
...  

Substance P (SP) induces plasma extravasation and neutrophil infiltration by activating the neurokinin-1 receptor (NK1-R). We characterized the mechanisms regulating this response in the rat pancreas. Anesthetized rats were continuously infused with SP, and plasma extravasation was quantified using Evans blue (EB) dye. Continuous infusion of SP (8 nmol · kg−1 · h−1) resulted in a threshold increase in EB at 15 min, a peak effect at 30 min (150% increase), and a return to baseline by 60 min. The NK1-R antagonist CP-96,345 blocked SP-induced plasma extravasation. After 60 min, the NK1-R was desensitized to agonist challenge. Resensitization was first detected at 20 min and increased until full recovery was seen at 30 min. Inhibition of the cell-surface protease neutral endopeptidase (NEP) by phosphoramidon potentiated the effect of exogenous SP; therefore endogenous NEP attenuates SP-induced plasma extravasation. Thus the continuous infusion of SP stimulates plasma extravasation in the rat pancreas via activation of the NK1-R, and these effects are terminated by both desensitization of the NK1-R and the cell-surface protease NEP.


2001 ◽  
Vol 183 (6) ◽  
pp. 2111-2116 ◽  
Author(s):  
Jeremy Mogridge ◽  
Michael Mourez ◽  
R. John Collier

ABSTRACT Protective antigen (PA), a component of anthrax toxin, binds receptors on mammalian cells and is activated by a cell surface protease. The resulting active fragment, PA63, forms ring-shaped heptamers, binds the enzymic moieties of the toxin, and translocates them to the cytosol. Of the four crystallographic domains of PA, domain 1 has been implicated in binding the enzymic moieties; domain 2 is involved in membrane insertion and oligomerization; and domain 4 binds receptor. To determine the function of domain 3, we developed a screen that allowed us to isolate random mutations that cause defects in the activity of PA. We identified several mutations in domain 3 that affect monomer-monomer interactions in the PA63 heptamer, indicating that this may be the primary function of this domain.


Diabetes ◽  
1984 ◽  
Vol 33 (1) ◽  
pp. 64-72 ◽  
Author(s):  
I. D. Goldfine ◽  
J. A. Williams ◽  
A. C. Bailey ◽  
K. Y. Wong ◽  
Y. Iwamoto ◽  
...  

1992 ◽  
Vol 167 (1) ◽  
pp. 19-24 ◽  
Author(s):  
Frank S. Steven ◽  
Margaret M. Griffin ◽  
Ian C. Talbot

2015 ◽  
Vol 1853 (10) ◽  
pp. 2515-2525 ◽  
Author(s):  
Julia D. Knopf ◽  
Stefan Tholen ◽  
Maria M. Koczorowska ◽  
Olivier De Wever ◽  
Martin L. Biniossek ◽  
...  

1986 ◽  
Vol 1 (2) ◽  
pp. 127-137 ◽  
Author(s):  
F. S. Steven ◽  
M. M. Griffin ◽  
T. L. H. Wong ◽  
S. Itzhaki

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