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| Status |
Public on Apr 01, 2015 |
| Title |
Porphyromonas gingivalis 33277 wild-type vs Fur orthologue Har isogenic mutant ECR455 |
| Platform organism |
Porphyromonas gingivalis W83 |
| Sample organism |
Porphyromonas gingivalis ATCC 33277 |
| Experiment type |
Expression profiling by array
|
| Summary |
Porphyromonas gingivalis is a major pathogen associated with the microbial biofilm-mediated disease chronic periodontitis. P. gingivalis has an obligate requirement for iron and protoporphyrin IX which it satisfies by transporting heme and iron liberated from the human host. The level of cellular iron in P. gingivalis affects the expression of a distinct iron-associated regulon of 64 genes and low iron invokes an iron sparing response. Iron homeostasis is usually mediated in Gram-negative bacteria at the transcriptional level by the Ferric Uptake Regulator (Fur). There is a single predicted P. gingivalis Fur superfamily orthologue named Har (heme associated regulator) that lacks the conserved metal binding residues found in other Fur orthologues. We show that Har binds both heme and ferrous iron resulting in a conformational change in the protein. Har was unable to complement the Escherichia coli H1780 fur mutant and there was no change in cellular metal content in a P. gingivalis Har mutant compared with the wild-type. The Har regulon of 44 genes is not predicted to play a role in iron homeostasis. Together these data indicated that Har does not regulate iron homeostasis in P. gingivalis. However, Har was required for heme-responsive biofilm development and its regulon overlapped P. gingivalis regulons previously identified after growth in heme limitation or as a homotypic biofilm. P. gingivalis is unique as an iron-dependent Gram-negative bacterium with a single heme-binding Fur superfamily orthologue, Har, that does not regulate iron homeostasis.
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| Overall design |
Paired samples were compared on the same microarray using a two-colour system. A total of 6 paired microarray hybridizations were performed representing 6 biological replicates, where a balanced dye design was used, with the overall analysis including three microarrays where P. gingivalis 33277 samples were labeled with Cy3 and the paired ECR455 samples were labeled with Cy5 and three other microarrays where samples were labeled with the opposite combination of fluorophores.
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| Contributor(s) |
Butler CA, Mitchell HL, Dashper SG, Reynolds EC |
| Citation(s) |
25375181, 26484248 |
| |
| Submission date |
Apr 09, 2012 |
| Last update date |
Jul 29, 2019 |
| Contact name |
Catherine Butler |
| E-mail(s) |
cbutler@unimelb.edu.au
|
| Phone |
61-3-93411565
|
| Organization name |
The University of Melbourne
|
| Department |
The Melbourne Dental School
|
| Lab |
The Reynolds Lab
|
| Street address |
720 Swanston St
|
| City |
Carlton |
| State/province |
VIC |
| ZIP/Postal code |
3053 |
| Country |
Australia |
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| Platforms (1) |
| GPL1438 |
PFGRC Porphyromonas gingivalis 70 mer oligo array. |
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| Samples (6)
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| Relations |
| BioProject |
PRJNA158399 |
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