Cargando…

regT can modulate gingipain activity and response to oxidative stress in Porphyromonas gingivalis

Recombinant VimA protein can interact with the gingipains and several other proteins that may play a role in its biogenesis in Porphyromonas gingivalis. In silico analysis of PG2096, a hypothetical protein that was shown to interact with VimA, suggests that it may have environmental stress resistanc...

Descripción completa

Detalles Bibliográficos
Autores principales: Vanterpool, E., Aruni, A. Wilson, Roy, F., Fletcher, H. M.
Formato: Texto
Lenguaje:English
Publicado: Microbiology Society 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068696/
https://www.ncbi.nlm.nih.gov/pubmed/20595264
http://dx.doi.org/10.1099/mic.0.038315-0
_version_ 1782201276408266752
author Vanterpool, E.
Aruni, A. Wilson
Roy, F.
Fletcher, H. M.
author_facet Vanterpool, E.
Aruni, A. Wilson
Roy, F.
Fletcher, H. M.
author_sort Vanterpool, E.
collection PubMed
description Recombinant VimA protein can interact with the gingipains and several other proteins that may play a role in its biogenesis in Porphyromonas gingivalis. In silico analysis of PG2096, a hypothetical protein that was shown to interact with VimA, suggests that it may have environmental stress resistance properties. To further evaluate the role(s) of PG2096, the predicted open reading frame was PCR amplified from P. gingivalis W83 and insertionally inactivated using the ermF-ermAM antibiotic-resistance cassette. One randomly chosen PG2096-defective mutant created by allelic exchange and designated FLL205 was further characterized. Under normal growth conditions at 37 °C, Arg-X and Lys-X gingipain activities in FLL205 were reduced by approximately 35 % and 21 %, respectively, compared to the wild-type strain. However, during prolonged growth at an elevated temperature of 42 °C, Arg-X activity was increased by more than 40 % in FLL205 in comparison to the wild-type strain. In addition, the PG2096-defective mutant was more resistant to oxidative stress when treated with 0.25 mM hydrogen peroxide. Taken together these results suggest that the PG2096 gene, designated regT (regulator of gingipain activity at elevated temperatures), may be involved in regulating gingipain activity at elevated temperatures and be important in oxidative stress resistance in P. gingivalis.
format Text
id pubmed-3068696
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Microbiology Society
record_format MEDLINE/PubMed
spelling pubmed-30686962011-10-01 regT can modulate gingipain activity and response to oxidative stress in Porphyromonas gingivalis Vanterpool, E. Aruni, A. Wilson Roy, F. Fletcher, H. M. Microbiology (Reading) Microbial Pathogenicity Recombinant VimA protein can interact with the gingipains and several other proteins that may play a role in its biogenesis in Porphyromonas gingivalis. In silico analysis of PG2096, a hypothetical protein that was shown to interact with VimA, suggests that it may have environmental stress resistance properties. To further evaluate the role(s) of PG2096, the predicted open reading frame was PCR amplified from P. gingivalis W83 and insertionally inactivated using the ermF-ermAM antibiotic-resistance cassette. One randomly chosen PG2096-defective mutant created by allelic exchange and designated FLL205 was further characterized. Under normal growth conditions at 37 °C, Arg-X and Lys-X gingipain activities in FLL205 were reduced by approximately 35 % and 21 %, respectively, compared to the wild-type strain. However, during prolonged growth at an elevated temperature of 42 °C, Arg-X activity was increased by more than 40 % in FLL205 in comparison to the wild-type strain. In addition, the PG2096-defective mutant was more resistant to oxidative stress when treated with 0.25 mM hydrogen peroxide. Taken together these results suggest that the PG2096 gene, designated regT (regulator of gingipain activity at elevated temperatures), may be involved in regulating gingipain activity at elevated temperatures and be important in oxidative stress resistance in P. gingivalis. Microbiology Society 2010-10 /pmc/articles/PMC3068696/ /pubmed/20595264 http://dx.doi.org/10.1099/mic.0.038315-0 Text en Copyright © 2010, SGM
spellingShingle Microbial Pathogenicity
Vanterpool, E.
Aruni, A. Wilson
Roy, F.
Fletcher, H. M.
regT can modulate gingipain activity and response to oxidative stress in Porphyromonas gingivalis
title regT can modulate gingipain activity and response to oxidative stress in Porphyromonas gingivalis
title_full regT can modulate gingipain activity and response to oxidative stress in Porphyromonas gingivalis
title_fullStr regT can modulate gingipain activity and response to oxidative stress in Porphyromonas gingivalis
title_full_unstemmed regT can modulate gingipain activity and response to oxidative stress in Porphyromonas gingivalis
title_short regT can modulate gingipain activity and response to oxidative stress in Porphyromonas gingivalis
title_sort regt can modulate gingipain activity and response to oxidative stress in porphyromonas gingivalis
topic Microbial Pathogenicity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068696/
https://www.ncbi.nlm.nih.gov/pubmed/20595264
http://dx.doi.org/10.1099/mic.0.038315-0
work_keys_str_mv AT vanterpoole regtcanmodulategingipainactivityandresponsetooxidativestressinporphyromonasgingivalis
AT aruniawilson regtcanmodulategingipainactivityandresponsetooxidativestressinporphyromonasgingivalis
AT royf regtcanmodulategingipainactivityandresponsetooxidativestressinporphyromonasgingivalis
AT fletcherhm regtcanmodulategingipainactivityandresponsetooxidativestressinporphyromonasgingivalis