Evidence map›Paper›PMID 39791890›Full record

ArticlemSystems2025

Genomic re-sequencing reveals mutational divergence across genetically engineered strains of model archaea.

Andrew L Soborowski, Rylee K Hackley, Sungmin Hwang, Guangyin Zhou, Keely A Dulmage, Peter Schönheit, Charles Daniels, Alexandre W Bisson-Filho, Anita Marchfelder, Julie A Maupin-Furlow and 2 more

Abstract read
In one paragraph

Article in mSystems, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Exploring Genome-Wide Mutation Dynamics and Bacterial Cellulose Impairment inComputational and structural biotechnology journal · 2026
    Article
  2. Article
  3. Article
  4. Journal of bacteriology · 2025
    Review
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

12 authors.

Andrew L SoborowskiDepartment of Biology, Duke University, Durham, North Carolina, USA.
Rylee K HackleyDepartment of Biology, Duke University, Durham, North Carolina, USA.
Sungmin HwangDepartment of Biology, Duke University, Durham, North Carolina, USA.
Guangyin ZhouDepartment of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, Florida, USA.
Keely A DulmageDepartment of Biology, Duke University, Durham, North Carolina, USA.
Peter SchönheitInstitut für Allgemeine Mikrobiologie, Christian-Albrechts-Universität Kiel, Kiel, Germany.ORCID 0000-0003-0915-8608
Charles DanielsDepartment of Microbiology, The Ohio State University, Columbus, Ohio, USA.
Alexandre W Bisson-FilhoDepartment of Biology, Rosenstiel Basic Medical Science Research Center, Brandeis University, Waltham, Massachusetts, USA.
Anita MarchfelderBiology II, Ulm University, Ulm, Germany.ORCID 0000-0002-1382-1794
Julie A Maupin-FurlowDepartment of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, Florida, USA.ORCID 0000-0001-6105-0923
Thorsten AllersSchool of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, United Kingdom.
Amy K SchmidDepartment of Biology, Duke University, Durham, North Carolina, USA.ORCID 0000-0001-5821-8000

Funding

Archaea as a microbial model for developmental mechanoplasticityR35GM156992 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI Alexandre W Bisson Filho · 2025 to 2026
$793k
National Science Foundation (NSF) 1651117National Science Foundation (NSF) 1936024NIGMS NIH HHS R35 GM156992Pew Charitable Trusts (PCT)
6 · The paper itself

Abstract

Archaeal molecular biology has been a topic of intense research in recent decades as their role in global ecosystems, nutrient cycles, and eukaryotic evolution comes to light. The hypersaline-adapted archaeal species IMPORTANCE: Archaea are a domain of microbial life whose member species play a critical role in the global carbon cycle, climate regulation, the human microbiome, and persistence in extreme habitats. In particular, hypersaline-adapted archaea are important, genetically tractable model organisms for studying archaeal genetics, genomics, and biochemistry. As the archaeal research community grows, keeping track of the genetic integrity of strains of interest is necessary. In particular, routine genetic manipulations and the common practice of sharing strains between labs allow mutations to arise in lab stocks. If these mutations affect cellular processes, they may jeopardize the reproducibility of work between research groups and confound the results of future studies. In this work, we examine DNA sequences from 60 strains across two species of archaea. We identify shared and unique mutations occurring between and within strains. Independently, we trace the lineage of each strain, identifying which genetic manipulations lead to observed off-target mutations. While overall divergence across labs is minimal so far, our work highlights the need for labs to continue proper strain husbandry.

Indexed as

Genome, ArchaealHalobacterium salinarumHaloferax volcaniiMutationArchaeaGenetic EngineeringGenetic VariationGenomicsWhole Genome Sequencingarchaeagenomicsmutational analysiswhole genome re-sequencing

Identifiers

PMID39791890
PMCPMC11834397

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.