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通过将产生细菌纤维素的菌株与PAO1共培养来评估用于结构成分的多微生物生物膜模型。

Evaluating a polymicrobial biofilm model for structural components by co-culturing produced bacterial cellulose with PAO1.

作者信息

Mahadevaswamy Usha Rani, Mugunthan Sudarsan, Seviour Thomas, Kjelleberg Staffan, Lim Sierin

机构信息

School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, Singapore.

Singapore Centre for Environmental Life Sciences Engineering, Nanyang Technological University, Singapore.

出版信息

Biofilm. 2024 Jan 6;7:100176. doi: 10.1016/j.bioflm.2024.100176. eCollection 2024 Jun.

DOI:10.1016/j.bioflm.2024.100176
PMID:38322579
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10845243/
Abstract

A polymicrobial biofilm model of and was developed to understand whether a pre-existing matrix affects the ability of another species to build a biofilm. was inoculated onto the preformed biofilm consisting of a cellulose matrix. PAO1 colonized and infiltrated the bacterial cellulose biofilm (BC), as indicated by the presence of cells at 19 μm depth in the translucent hydrogel matrix. Bacterial cell density increased along the imaged depth of the biofilm (17-19 μm). On day 5, the average bacterial count across sections was 67 ± 4 % . PAO1 and 33 ± 6 % . Biophysical characterization of the biofilm indicated that colonization by modified the biophysical properties of the BC matrix, which inlcuded increased density, heterogeneity, degradation temperature and thermal stability, and reduced crystallinity, swelling ability and moisture content. This further indicates colonization of the biofilm by While eDNA fibres - a key viscoelastic component of biofilm - were present on the surface of the co-cultured biofilm on day 1, their abundance decreased over time, and by day 5, no eDNA was observed, either on the surface or within the matrix. -colonized biofilm devoid of eDNA retained its mechanical properties. The observations demonstrate that a pre-existing biofilm scaffold of inhibits PAO1 eDNA production and suggest that eDNA production is a response by to the viscoelastic properties of its environment.

摘要

构建了一个由[具体菌种1]和[具体菌种2]组成的多微生物生物膜模型,以了解预先存在的基质是否会影响另一种物种形成生物膜的能力。将[具体菌种2]接种到由纤维素基质组成的预先形成的[具体菌种1]生物膜上。PAO1定殖并渗透到[具体菌种1]细菌纤维素生物膜(BC)中,半透明水凝胶基质中19μm深度处存在细胞即表明了这一点。细菌细胞密度沿生物膜的成像深度(17 - 19μm)增加。在第5天,各切片的平均细菌计数为67±4% [具体菌种2]和33±6% PAO1。生物膜的生物物理表征表明,[具体菌种2]的定殖改变了BC基质的生物物理特性,包括密度增加、异质性增加、降解温度和热稳定性增加,以及结晶度降低、膨胀能力和水分含量降低。这进一步表明[具体菌种2]在生物膜中的定殖。虽然eDNA纤维——[具体菌种1]生物膜的关键粘弹性成分——在共培养生物膜表面在第1天就存在,但其丰度随时间下降,到第5天,在表面或基质内均未观察到eDNA。缺乏eDNA的[具体菌种2]定殖生物膜保留了其机械性能。这些观察结果表明,预先存在的[具体菌种1]生物膜支架抑制了PAO1的eDNA产生,并表明eDNA的产生是[具体菌种1]对其环境粘弹性特性的一种反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/4851900b086c/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/240398d88b92/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/fea90c9c1b4e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/7b56dc6542f9/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/4802f1fd016d/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/a695cc77403a/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/04643f26effa/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/afc2d2a05291/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/4851900b086c/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/240398d88b92/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/fea90c9c1b4e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/7b56dc6542f9/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/4802f1fd016d/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/a695cc77403a/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/04643f26effa/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/afc2d2a05291/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d21/10845243/4851900b086c/gr8.jpg

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