Evidence map›Paper›PMID 41760687›Full record

ArticleNPJ biofilms and microbiomes2026

Colouring dysbiosis: FetB-dependent Mn-PPIX produced by Porphyromonas gingivalis shapes the oral microbiota.

Yupaporn Phonok, Alysha Pyne, Siyuan Liu, Sandro F Ataide, Haijing Gu, Xiaoyan Zhou, Jinlong Gao, Ann H Kwan

Abstract read
In one paragraph

Article in NPJ biofilms and microbiomes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. The survival status ofJournal of oral microbiology · 2026
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Yupaporn PhonokSchool of Dentistry, University of Phayao, Phayao, Thailand.
Alysha PyneSchool of Life and Environmental Sciences, University of Sydney, Sydney, NSW, Australia.
Siyuan LiuSydney Dental School and Westmead Centre for Oral Health, University of Sydney, Sydney, NSW, Australia.
Sandro F AtaideSchool of Life and Environmental Sciences, University of Sydney, Sydney, NSW, Australia.
Haijing GuSydney Dental School and Westmead Centre for Oral Health, University of Sydney, Sydney, NSW, Australia.
Xiaoyan ZhouSydney Dental School and Westmead Centre for Oral Health, University of Sydney, Sydney, NSW, Australia.
Jinlong GaoSydney Dental School and Westmead Centre for Oral Health, University of Sydney, Sydney, NSW, Australia. jinlong.gao@sydney.edu.au.
Ann H KwanSchool of Life and Environmental Sciences, University of Sydney, Sydney, NSW, Australia. ann.kwan@sydney.edu.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polymicrobial diseases, such as periodontitis, are shaped by microbial interactions and nutrient‑responsive metabolic adaptations. Here, we identify novel porphyrin pigments produced by Porphyromonas gingivalis in response to haemoglobin concentrations resembling those found in the gingival sulcus and periodontal pocket. Under these conditions, P. gingivalis develops a distinctive pink, highly fluorescent phenotype. Spectroscopic and mass‑spectrometric analyses revealed the accumulation of protoporphyrin IX (PPIX), manganese‑substituted PPIX (Mn‑PPIX), and haem. Deletion of the haemin‑binding protein gene fetB greatly reduced Mn‑PPIX production and fluorescence, whereas complementation restored both. Structural and biochemical characterisation demonstrated that FetB shares homology with bacterial metal chelatases and catalyses the insertion of metal ions into tetrapyrrole rings. Mn‑PPIX exhibited selective antimicrobial activity against several oral bacteria, including Streptococcus mitis, Streptococcus salivarius, Enterococcus faecalis, and oral Lactobacillus species, while other streptococci were resistant. These findings indicate that P. gingivalis modulates porphyrin metabolism in response to host‑derived haemoglobin, producing extracellular pigments with selective antimicrobial properties that may shape the oral community and promote dysbiosis. Targeting Mn‑PPIX production or limiting haemoglobin availability may offer new strategies to restore microbial balance and mitigate disease progression.

Indexed as

DysbiosisManganeseMicrobiotaMouthPorphyromonas gingivalisProtoporphyrinsBacterial ProteinsHemeHeme-Binding ProteinsHemoglobinsHumansBacterial ProteinsHemeHeme-Binding ProteinsHemoglobinsManganeseprotoporphyrin IXProtoporphyrins

Identifiers

PMID41760687
PMCPMC13065792

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.