Evidence map›Paper›PMID 42374590›Full record

ArticleMicrobiome2026

Uncovering transcriptional processes in microbial communities adapted to differing saline conditions in salt-weathered historic buildings.

Lukas Fürnwein, Johannes Tichy, Monika Waldherr, Elias Lehner, Martin Ortbauer, Ylenia Vassallo, Beate Sipek, Katja Sterflinger, Guadalupe Piñar, Alexandra B Graf

Abstract read
In one paragraph

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

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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Lukas Fürnwein *Department of Applied Life Sciences/Bioengineering/Bioinformatics, Hochschule Campus Wien, Favoritenstrasse 222, Vienna, 1100, Austria.
Johannes Tichy *Institute for Natural Sciences and Technology in the Art, Academy of Fine Arts Vienna, Schillerplatz 3, Vienna, 1010, Austria.
Monika WaldherrDepartment of Applied Life Sciences/Bioengineering/Bioinformatics, Hochschule Campus Wien, Favoritenstrasse 222, Vienna, 1100, Austria.
Elias LehnerDepartment of Applied Life Sciences/Bioengineering/Bioinformatics, Hochschule Campus Wien, Favoritenstrasse 222, Vienna, 1100, Austria.
Martin OrtbauerInstitute for Conservation - Restoration, Academy of Fine Arts Vienna, Schillerplatz 3, Vienna, 1010, Austria.
Ylenia VassalloDepartment of Medical Biotechnology, University of Siena, Siena, Italy.
Beate SipekInstitute for Conservation - Restoration, Academy of Fine Arts Vienna, Schillerplatz 3, Vienna, 1010, Austria.
Katja SterflingerInstitute for Natural Sciences and Technology in the Art, Academy of Fine Arts Vienna, Schillerplatz 3, Vienna, 1010, Austria.
Guadalupe PiñarInstitute for Natural Sciences and Technology in the Art, Academy of Fine Arts Vienna, Schillerplatz 3, Vienna, 1010, Austria.
Alexandra B GrafDepartment of Applied Life Sciences/Bioengineering/Bioinformatics, Hochschule Campus Wien, Favoritenstrasse 222, Vienna, 1100, Austria. alexandra.graf@hcw.ac.at.

Funding

Österreichischen Akademie der Wissenschaften Heritage_2020-005_RESTOROMIC
6 · The paper itself

Abstract

backgroundMicrobial colonization of architectural surfaces in historic buildings can cause not only aesthetic damage but also biodeterioration. One example is the colonizing microbiome on salt-weathered architectural surfaces. Halotolerant and halophilic communities on such surfaces produce colored pigments that visually alter cultural heritage sites and could potentially degrade organic binders used for mural paintings. Although the microorganisms involved in these deterioration processes have already been described, detailed information about the molecular processes that allow these communities to succeed, survive, and thrive under such extreme conditions is still lacking.

resultsA combined metagenome and metatranscriptome approach were employed to investigate three sampling sites located in two Austrian historic buildings displaying different environmental and saline compositions. The chapel of St. Virgil (Vienna) is a subsurface, climate-controlled environment. In contrast, the Charterhouse Mauerbach (Lower Austria) is exposed to natural fluctuations in temperature and humidity. DNA and total RNA were extracted from each sampling site simultaneously and sequenced. Two methods for gene assembly were compared and functionally evaluated. Results showed a minor bias in both methods, with improved results when they were combined. Comparison between DNA and RNA showed interesting variations in the taxonomic composition between the DNA- and RNA-based dataset, distinguishing the dormant from the active microbiome. The annotated halotolerance mechanisms in the metatranscriptomes indicated genome and proteome adaptations, showing high GC content, proteome acidification, with elevated aspartate and glutamate levels, and low isoelectric point profiles. Furthermore, the communities used both "salt-in" and "salt-out" osmoregulatory mechanisms. Pigment production was confirmed in all sampling points, revealing diverse pathways for carotenoid biosynthesis. Various protective mechanisms against oxidative stress were detected, such as those against reactive oxygen species (ROS), but also detoxification, protein folding, protein and DNA repair, and RNA chaperones. Key metabolic pathways revealed diverse pathways related to carbon, nitrogen, and sulfur cycling, linked to varying oxygen concentrations within biofilms. The results also highlighted the need for an in-depth analysis of the capabilities of the involved microorganisms.

conclusionsThe study shows highly specialized and cooperative adaptations, using both "salt-in" and "salt-out" strategies, diverse phototrophic and redox metabolisms that tightly couple C-N-S cycling.

Indexed as

BacteriaMicrobiotaAdaptation, PhysiologicalAustriaMetagenomeSalinitySodium ChlorideTranscriptomeSodium ChlorideCultural heritageHypersaline environmentsMetagenomicsMetatranscriptomicsOsmoregulationStress-prevention mechanisms

Identifiers

PMID42374590
PMCPMC13326497

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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.