Evidence map›Paper›PMID 32410574›Full record

ArticleBMC microbiology2020

The exopolysaccharide-eDNA interaction modulates 3D architecture of Bacillus subtilis biofilm.

Na Peng, Peng Cai, Monika Mortimer, Yichao Wu, Chunhui Gao, Qiaoyun Huang

Abstract read
In one paragraph

Article in BMC microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 citing papers in PubMed.

  1. Review
  2. Article
  3. Bacillus cereus PelAThe Journal of biological chemistry · 2026
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  8. Review
  9. The Resistance Abilities of SomeFood science & nutrition · 2025
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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

6 authors.

Na PengState Key Laboratory of Agricultural Microbiology, College of Resources of Environment, Huazhong Agricultural University, Wuhan, 430070, China.
Peng CaiState Key Laboratory of Agricultural Microbiology, College of Resources of Environment, Huazhong Agricultural University, Wuhan, 430070, China. cp@mail.hzau.edu.cn.
Monika MortimerBren School of Environmental Science and Management and Earth Research Institute, University of California, Santa Barbara, California, 93106, USA.
Yichao WuState Key Laboratory of Agricultural Microbiology, College of Resources of Environment, Huazhong Agricultural University, Wuhan, 430070, China.
Chunhui GaoState Key Laboratory of Agricultural Microbiology, College of Resources of Environment, Huazhong Agricultural University, Wuhan, 430070, China.
Qiaoyun HuangState Key Laboratory of Agricultural Microbiology, College of Resources of Environment, Huazhong Agricultural University, Wuhan, 430070, China.

Funding

National Basic Research Program of China (973 Program) 2016YFD0800206National Key Research Program of China 2016YFD0800206National Natural Science Foundation of China 41877029Royal Society-Newton Advanced Fellowship NAF\R1\191017Wuhan Science and Technology Bureau 2019020701011469
6 · The paper itself

Abstract

backgroundBacterial biofilms are surface-adherent microbial communities in which individual cells are surrounded by a self-produced extracellular matrix of polysaccharides, extracellular DNA (eDNA) and proteins. Interactions among matrix components within biofilms are responsible for creating an adaptable structure during biofilm development. However, it is unclear how the interactions among matrix components contribute to the construction of the three-dimensional (3D) biofilm architecture.

resultsDNase I treatment significantly inhibited Bacillus subtilis biofilm formation in the early phases of biofilm development. Confocal laser scanning microscopy (CLSM) and image analysis revealed that eDNA was cooperative with exopolysaccharide (EPS) in the early stages of B. subtilis biofilm development, while EPS played a major structural role in the later stages. In addition, deletion of the EPS production gene epsG in B. subtilis SBE1 resulted in loss of the interaction between EPS and eDNA and reduced the biofilm biomass in pellicles at the air-liquid interface. The physical interaction between these two essential biofilm matrix components was confirmed by isothermal titration calorimetry (ITC).

conclusionsBiofilm 3D structures become interconnected through surrounding eDNA and EPS. eDNA interacts with EPS in the early phases of biofilm development, while EPS mainly participates in the maturation of biofilms. The findings of this study provide a better understanding of the role of the interaction between eDNA and EPS in shaping the biofilm 3D matrix structure and biofilm formation.

Indexed as

Bacillus subtilisBacterial ProteinsBiofilmsDeoxyribonuclease IDNA, BacterialMicroscopy, Atomic ForceMicroscopy, ConfocalPolysaccharides, BacterialBacterial ProteinsDeoxyribonuclease IDNA, BacterialPolysaccharides, BacterialBacillus subtilisBiofilm formationExopolysaccharide (EPS)Extracellular DNA (eDNA)

Identifiers

PMID32410574
PMCPMC7227074

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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.