Evidence map›Paper›PMID 41774704›Full record

ArticlePLoS neglected tropical diseases2026

Anthrax-causing bacteria form biofilms on a soil-inspired porous glass bead model.

Leonard Borst, Sabine Howaldt, Rocío Berdaguer, Christoph Schaudinn, Susann Dupke, Maren Stämmler, Peter Lasch, Holger C Scholz, Silke R Klee

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Leonard BorstCentre for Biological Threats and Special Pathogens, ZBS 2: Highly Pathogenic Microorganisms, Robert Koch Institute, Berlin, Germany.
Sabine HowaldtCentre for Biological Threats and Special Pathogens, ZBS 2: Highly Pathogenic Microorganisms, Robert Koch Institute, Berlin, Germany.
Rocío BerdaguerCentre for Biological Threats and Special Pathogens, ZBS 2: Highly Pathogenic Microorganisms, Robert Koch Institute, Berlin, Germany.
Christoph SchaudinnCentre for Biological Threats and Special Pathogens, ZBS 4: Advanced Light and Electron Microscopy, Robert Koch Institute, Berlin, Germany.
Susann DupkeCentre for Biological Threats and Special Pathogens, ZBS 2: Highly Pathogenic Microorganisms, Robert Koch Institute, Berlin, Germany.
Maren StämmlerCentre for Biological Threats and Special Pathogens, ZBS 6: Proteomics and Spectroscopy, Robert Koch Institute, Berlin, Germany.
Peter LaschCentre for Biological Threats and Special Pathogens, ZBS 6: Proteomics and Spectroscopy, Robert Koch Institute, Berlin, Germany.
Holger C ScholzCentre for Biological Threats and Special Pathogens, ZBS 2: Highly Pathogenic Microorganisms, Robert Koch Institute, Berlin, Germany.
Silke R KleeCentre for Biological Threats and Special Pathogens, ZBS 2: Highly Pathogenic Microorganisms, Robert Koch Institute, Berlin, Germany.ORCID https://orcid.org/0000-0002-2358-9642

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacillus anthracis and the emerging pathogen Bacillus cereus biovar anthracis (Bcbva) are causative agents of the lethal disease anthrax. Their ability to form highly resistant endospores enables them to persist in the environment, posing significant threats to wild herbivores, livestock, and also humans globally, especially considering their potential use as bioweapons. Despite the importance of these pathogens, the exact mechanisms underlying host infection remain poorly understood. Notably, both require relatively high infectious doses to cause disease. Proposed transmission routes include soil-based transmission and dissemination by carrion flies, which contaminate the area surrounding infected carcasses. However, considering the substantial dilution of bacteria and spores in these processes alongside the high infectious dose required, sustained transmission under natural conditions appears improbable. An alternative hypothesis is that B. anthracis and Bcbva can survive and proliferate in the environment by forming biofilms, structured bacterial communities attached to surfaces, which may serve as reservoirs for infection. While biofilm formation has been demonstrated for B. anthracis, data on Bcbva are lacking. To address this, we examined the biofilm-forming abilities of multiple B. anthracis and Bcbva strains using a three-dimensional, soil-inspired porous glass bead model (PGB) system. We applied confocal laser scanning microscopy, scanning electron microscopy, and quantitative cell counts to characterize biofilm development in detail. Our results confirm that both B. anthracis and Bcbva form biofilms under somewhat soil-like conditions. Furthermore, differences observed in biofilm structure and density between the above-mentioned species suggest that Bcbva may prefer additional environmental niches beyond soil, such as plant surfaces or small water bodies, potentially expanding our understanding of its environmental persistence and infection routes.

Indexed as

AnthraxBacillus anthracisBacillus cereusBiofilmsGlassPorositySoil Microbiology

Identifiers

PMID41774704
PMCPMC12956075

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Registered trials

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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.