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使用矿物糊剂对历史建筑进行盐分缓解处理期间微生物群落的变化:对盐分及相关生物膜的长期监测

Microbial community shifts during salt mitigation treatments of historic buildings using mineral poultices: a long-term monitoring of salt and associated biofilms.

作者信息

Tichy Johannes, Sipek Beate, Ortbauer Martin, Fürnwein Lukas, Waldherr Monika, Graf Alexandra, Sterflinger Katja, Piñar Guadalupe

机构信息

Institute for Natural Sciences and Technology in the Art, Academy of Fine Arts Vienna, Vienna, Austria.

Institute for Conservation - Restoration, Academy of Fine Arts Vienna, Vienna, Austria.

出版信息

Front Microbiol. 2025 May 22;16:1603289. doi: 10.3389/fmicb.2025.1603289. eCollection 2025.

DOI:10.3389/fmicb.2025.1603289
PMID:40475385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12137350/
Abstract

Increased heavy rainfall followed by periods of drought due to climate change is leading to more frequent salt-crystallization cycles. This not only leads to increased salt-weathering on architectural surfaces of cultural heritage monuments, but also creates an ideal ecological niche for the formation of biofilms by salt-loving microorganisms. These biofilms, characterized by a distinctive pink coloration, cause additional esthetic alterations to affected surfaces. In this study, mineral poultices prepared with different clay minerals (sepiolite, kaolinite and vermiculite) were developed and tested for a long-term (1 year) application on salt-weathered surfaces, thus contributing to their preservation. The poultices were tested on the surfaces of two historic buildings: the St. Virgil's Chapel in Vienna and the Mauerbach Charterhouse in Lower Austria, both showing salt efflorescence and a uniform pink biofilm. First, the poultices were tested to evaluate their salt retention capacity, salt-weathering resistance and processability. The retention properties of the poultices were examined by measuring their salt content throughout the treatment using high performance liquid chromatography (HPLC) and continuous flow analysis (CFA). Salt content was also measured on the wall surfaces before and after treatment. Second, the effect of the desalination treatments on salt-associated pink biofilms was also evaluated. The shifts within the biofilm communities during and after the treatment were monitored by qPCR and long-read archaeal- and bacterial-16S rRNA amplicon analysis using the Nanopore sequencing technology. The results demonstrate that both the selected clay minerals and the salt composition in the treated areas significantly influenced the salt storage capacity of the poultices and their resistance to salt weathering. Fluctuations in salt load and ionic composition during and after treatment affected biofilm composition, with bacterial communities proving more sensitive than archaea to these changes. Both qPCR and metataxonomic results show that the effects of the poultices on the colonizing biofilms depend not only on the composition of their microbial members, but also on external abiotic factors such as the chemical composition and concentration of the salt mixtures on the surfaces. In addition, the biodiversity within the biofilms shows to be affected differently depending on the mineral clay used.

摘要

气候变化导致暴雨增多,随后出现干旱期,这使得盐结晶循环更加频繁。这不仅导致文化遗产古迹建筑表面的盐风化加剧,还为嗜盐微生物形成生物膜创造了理想的生态位。这些以独特粉色为特征的生物膜,会对受影响的表面造成额外的美学改变。在本研究中,开发了用不同粘土矿物(海泡石、高岭土和蛭石)制备的矿物糊剂,并在盐风化表面进行了长期(1年)应用测试,从而有助于对其进行保护。这些糊剂在两座历史建筑的表面进行了测试:维也纳的圣维吉尔教堂和下奥地利州的毛尔巴赫卡尔特修道院,二者均出现了盐析出现象和均匀的粉色生物膜。首先,对糊剂进行测试以评估其盐分保留能力、抗盐风化能力和可加工性。通过使用高效液相色谱法(HPLC)和连续流动分析法(CFA)在整个处理过程中测量糊剂的盐分含量,来检查糊剂的保留特性。还在处理前后测量了墙面的盐分含量。其次,还评估了脱盐处理对与盐相关的粉色生物膜的影响。使用纳米孔测序技术,通过定量聚合酶链反应(qPCR)以及长读长古菌和细菌16S rRNA扩增子分析,监测处理期间和处理后生物膜群落的变化。结果表明,所选的粘土矿物和处理区域中的盐分组成均显著影响糊剂的盐分储存能力及其抗盐风化能力。处理期间和处理后的盐负荷和离子组成波动影响了生物膜组成,事实证明细菌群落比古菌对这些变化更敏感。qPCR和宏分类学结果均表明,糊剂对定殖生物膜的影响不仅取决于其微生物成员的组成,还取决于外部非生物因素,例如表面盐混合物的化学成分和浓度。此外,生物膜内的生物多样性显示出受所用矿物粘土的影响各不相同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c84/12137350/e28accf799d1/fmicb-16-1603289-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c84/12137350/63cdc9990b4a/fmicb-16-1603289-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c84/12137350/e5523745e891/fmicb-16-1603289-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c84/12137350/f4e94e528c10/fmicb-16-1603289-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c84/12137350/561f17ac64c9/fmicb-16-1603289-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c84/12137350/0c9269b7554a/fmicb-16-1603289-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c84/12137350/e28accf799d1/fmicb-16-1603289-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c84/12137350/63cdc9990b4a/fmicb-16-1603289-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c84/12137350/e5523745e891/fmicb-16-1603289-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c84/12137350/f4e94e528c10/fmicb-16-1603289-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c84/12137350/561f17ac64c9/fmicb-16-1603289-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c84/12137350/0c9269b7554a/fmicb-16-1603289-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c84/12137350/e28accf799d1/fmicb-16-1603289-g006.jpg

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