Evidence map›Paper›PMID 40034390›Full record

ArticleFrontiers in cellular and infection microbiology2025

Assessing mutation accumulation in DNA repair-deficient

Astrid Füszl, Ariane Pietzka, Patrick Hyden, Tobias Mösenbacher, Anna Stöger, Marion Blaschitz, Silke Stadlbauer, Petra Hasenberger, Stefanie Schindler, Florian Heger and 2 more

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2025. 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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0cells of the map it votes in
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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Astrid FüszlNational Reference Centre/Laboratory for Listeriosis, Austrian Agency for Health and Food Safety (AGES), Vienna/Graz, Austria.
Ariane PietzkaNational Reference Centre/Laboratory for Listeriosis, Austrian Agency for Health and Food Safety (AGES), Vienna/Graz, Austria.
Patrick HydenDepartment of Statistics and Analytical Epidemiology, Austrian Agency for Health and Food Safety (AGES), Vienna, Austria.
Tobias MösenbacherDepartment of Statistics and Analytical Epidemiology, Austrian Agency for Health and Food Safety (AGES), Vienna, Austria.
Anna StögerDepartment of Clinical Molecular Biology, Austrian Agency for Health and Food Safety (AGES), Vienna, Austria.
Marion BlaschitzDepartment of Clinical Molecular Biology, Austrian Agency for Health and Food Safety (AGES), Vienna, Austria.
Silke StadlbauerNational Reference Centre/Laboratory for Listeriosis, Austrian Agency for Health and Food Safety (AGES), Vienna/Graz, Austria.
Petra HasenbergerNational Reference Centre/Laboratory for Listeriosis, Austrian Agency for Health and Food Safety (AGES), Vienna/Graz, Austria.
Stefanie SchindlerNational Reference Centre/Laboratory for Listeriosis, Austrian Agency for Health and Food Safety (AGES), Vienna/Graz, Austria.
Florian HegerNational Reference Centre/Laboratory for Listeriosis, Austrian Agency for Health and Food Safety (AGES), Vienna/Graz, Austria.
Sonja PleiningerNational Reference Centre/Laboratory for Listeriosis, Austrian Agency for Health and Food Safety (AGES), Vienna/Graz, Austria.
Alexander IndraNational Reference Centre/Laboratory for Listeriosis, Austrian Agency for Health and Food Safety (AGES), Vienna/Graz, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Methods: This study investigated mutation rates in Results: Mutation rates were significantly higher in repair-deficient isolates, exceeding typical cgMLST thresholds currently used in Conclusions: The standard 7-allele cgMLST threshold effectively identifies related strains in most cases, but may require adjustments for hypermutator strains. Incorporating DNA repair data could improve the accuracy of outbreak investigations, ensuring reliable public health responses.

Indexed as

Disease OutbreaksDNA RepairListeria monocytogenesListeriosisMultilocus Sequence TypingMutationMutation RateAllelesGenetic VariationGenome, BacterialHumansWhole Genome Sequencingallele thresholdcore genome multilocus sequence typingListeria monocytogeneslisteriosismutation rateoutbreak detection

Identifiers

PMID40034390
PMCPMC11872914

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Registered trials

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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.