Interpain A, a Cysteine Proteinase from Prevotella intermedia, Inhibits Complement by Degrading Complement Factor C3.
Potempa, Michal LU ; Potempa, Jan ; Kantyka, Tomasz ; Nguyen, Ky-Anh ; Wawrzonek, Katarzyna ; Manandhar, Surya P ; Popadiak, Katarzyna ; Riesbeck, Kristian LU
; Eick, Sigrun
and Blom, Anna
LU
(2009)
In PLoS Pathogens
5(2).
- Abstract
- Periodontitis is an inflammatory disease of the supporting structures of the teeth caused by, among other pathogens, Prevotella intermedia. Many strains of P. intermedia are resistant to killing by the human complement system, which is present at up to 70% of serum concentration in gingival crevicular fluid. Incubation of human serum with recombinant cysteine protease of P. intermedia (interpain A) resulted in a drastic decrease in bactericidal activity of the serum. Furthermore, a clinical strain 59 expressing interpain A was more serum-resistant than another clinical strain 57, which did not express interpain A, as determined by Western blotting. Moreover, in the presence of the cysteine protease inhibitor E64, the killing of strain 59... (More)
- Periodontitis is an inflammatory disease of the supporting structures of the teeth caused by, among other pathogens, Prevotella intermedia. Many strains of P. intermedia are resistant to killing by the human complement system, which is present at up to 70% of serum concentration in gingival crevicular fluid. Incubation of human serum with recombinant cysteine protease of P. intermedia (interpain A) resulted in a drastic decrease in bactericidal activity of the serum. Furthermore, a clinical strain 59 expressing interpain A was more serum-resistant than another clinical strain 57, which did not express interpain A, as determined by Western blotting. Moreover, in the presence of the cysteine protease inhibitor E64, the killing of strain 59 by human serum was enhanced. Importantly, we found that the majority of P. intermedia strains isolated from chronic and aggressive periodontitis carry and express the interpain A gene. The protective effect of interpain A against serum bactericidal activity was found to be attributable to its ability to inhibit all three complement pathways through the efficient degradation of the alpha-chain of C3-the major complement factor common to all three pathways. P. intermedia has been known to co-aggregate with P. gingivalis, which produce gingipains to efficiently degrade complement factors. Here, interpain A was found to have a synergistic effect with gingipains on complement degradation. In addition, interpain A was able to activate the C1 complex in serum, causing deposition of C1q on inert and bacterial surfaces, which may be important at initial stages of infection when local inflammatory reaction may be beneficial for a pathogen. Taken together, the newly characterized interpain A proteinase appears to be an important virulence factor of P. intermedia. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1302061
- author
- Potempa, Michal
LU
; Potempa, Jan
; Kantyka, Tomasz
; Nguyen, Ky-Anh
; Wawrzonek, Katarzyna
; Manandhar, Surya P
; Popadiak, Katarzyna
; Riesbeck, Kristian
LU
; Eick, Sigrun
and Blom, Anna
LU
- organization
- publishing date
- 2009
- type
- Contribution to journal
- publication status
- published
- subject
- in
- PLoS Pathogens
- volume
- 5
- issue
- 2
- article number
- e1000316
- publisher
- Public Library of Science (PLoS)
- external identifiers
-
- wos:000263928000007
- pmid:19247445
- scopus:61449091498
- ISSN
- 1553-7366
- DOI
- 10.1371/journal.ppat.1000316
- language
- English
- LU publication?
- yes
- id
- 0b3ef73c-3784-4b66-bde7-4fd4227fe81e (old id 1302061)
- alternative location
- http://www.ncbi.nlm.nih.gov/pubmed/19247445?dopt=Abstract
- date added to LUP
- 2016-04-04 07:38:04
- date last changed
- 2022-05-09 00:43:31
@article{0b3ef73c-3784-4b66-bde7-4fd4227fe81e,
abstract = {{Periodontitis is an inflammatory disease of the supporting structures of the teeth caused by, among other pathogens, Prevotella intermedia. Many strains of P. intermedia are resistant to killing by the human complement system, which is present at up to 70% of serum concentration in gingival crevicular fluid. Incubation of human serum with recombinant cysteine protease of P. intermedia (interpain A) resulted in a drastic decrease in bactericidal activity of the serum. Furthermore, a clinical strain 59 expressing interpain A was more serum-resistant than another clinical strain 57, which did not express interpain A, as determined by Western blotting. Moreover, in the presence of the cysteine protease inhibitor E64, the killing of strain 59 by human serum was enhanced. Importantly, we found that the majority of P. intermedia strains isolated from chronic and aggressive periodontitis carry and express the interpain A gene. The protective effect of interpain A against serum bactericidal activity was found to be attributable to its ability to inhibit all three complement pathways through the efficient degradation of the alpha-chain of C3-the major complement factor common to all three pathways. P. intermedia has been known to co-aggregate with P. gingivalis, which produce gingipains to efficiently degrade complement factors. Here, interpain A was found to have a synergistic effect with gingipains on complement degradation. In addition, interpain A was able to activate the C1 complex in serum, causing deposition of C1q on inert and bacterial surfaces, which may be important at initial stages of infection when local inflammatory reaction may be beneficial for a pathogen. Taken together, the newly characterized interpain A proteinase appears to be an important virulence factor of P. intermedia.}},
author = {{Potempa, Michal and Potempa, Jan and Kantyka, Tomasz and Nguyen, Ky-Anh and Wawrzonek, Katarzyna and Manandhar, Surya P and Popadiak, Katarzyna and Riesbeck, Kristian and Eick, Sigrun and Blom, Anna}},
issn = {{1553-7366}},
language = {{eng}},
number = {{2}},
publisher = {{Public Library of Science (PLoS)}},
series = {{PLoS Pathogens}},
title = {{Interpain A, a Cysteine Proteinase from Prevotella intermedia, Inhibits Complement by Degrading Complement Factor C3.}},
url = {{https://lup.lub.lu.se/search/files/5146243/1389738.pdf}},
doi = {{10.1371/journal.ppat.1000316}},
volume = {{5}},
year = {{2009}},
}