Evidence map›Paper›PMID 42001010›Full record

ArticleBMC genomics2026

Staphylococcus aureus sequence type 71 is a chimera that emerged twice.

Stefan Monecke, Sascha D Braun, Celia Diezel, Elke Müller, Martin Reinicke, David C Coleman, Hosny El-Adawy, Orla M Keane, Amira A Moawad, Renata Piccinini and 1 more

Abstract read
In one paragraph

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

0numbers the graph read from it
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

11 authors.

Stefan MoneckeLeibniz Institute of Photonic Technology (IPHT), Leibniz Center for Photonics in Infection Research (LPI), Jena, Germany. stefan.monecke@leibniz-ipht.de.
Sascha D BraunLeibniz Institute of Photonic Technology (IPHT), Leibniz Center for Photonics in Infection Research (LPI), Jena, Germany.
Celia DiezelLeibniz Institute of Photonic Technology (IPHT), Leibniz Center for Photonics in Infection Research (LPI), Jena, Germany.
Elke MüllerLeibniz Institute of Photonic Technology (IPHT), Leibniz Center for Photonics in Infection Research (LPI), Jena, Germany.
Martin ReinickeLeibniz Institute of Photonic Technology (IPHT), Leibniz Center for Photonics in Infection Research (LPI), Jena, Germany.
David C ColemanMicrobiology Research Unit, Division of Oral Biosciences, Dublin Dental University Hospital, University of Dublin, Trinity College Dublin, Dublin, Ireland.
Hosny El-AdawyInstitute of Bacterial Infections and Zoonoses, Friedrich-Loeffler-Institut (Federal Research Institute for Animal Health), Jena, Germany.
Orla M KeaneAnimal and Bioscience Department, Teagasc, Grange, Dunsany, Co. Meath, Ireland.
Amira A MoawadInstitute of Bacterial Infections and Zoonoses, Friedrich-Loeffler-Institut (Federal Research Institute for Animal Health), Jena, Germany.
Renata PiccininiDepartment of Veterinary Medicine and Animal Science - DIVAS, University of Milan, Lodi, Italy.
Ralf EhrichtLeibniz Institute of Photonic Technology (IPHT), Leibniz Center for Photonics in Infection Research (LPI), Jena, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStaphylococcus aureus is a Gram-positive coccus that colonises or infects humans and a wide range of domestic and wild animals. Various lineages of S. aureus are adapted to ruminants, including cattle, where they commonly cause mastitis. This is of significant animal welfare and economic relevance. Clonal complex (CC) 97 is one of the S. aureus lineages found predominantly in bovines, but also in other animals and humans. Sequence Type (ST) 71 is a related bovine-associated lineage with part of its genome identical to CC97. Thus, it has been assumed that ST71 was a chimera consisting of a fragment of DNA from an unknown donor strain inserted into a CC97 backbone genome.

resultsIn this study, S. aureus ST3042 was identified as a putative donor of this fragment based on core genome multilocus sequence typing and alignment of core and genomic island markers. We also identified a second ST71 lineage from Sardinia that differs from previously known ST71 from Ireland, the United Kingdom and continental Europe, both in size and demarcations of the ST3042-derived insert. Sardinian ST71 sequences also differed from other ST71 in the orientation of a large part of the genome. As the inversion affected the ST3042-derived region, this event must have taken place later in time than the recombination of CC97 and ST3042.

conclusionsThe observation that ST71 emerged twice adds to the body of evidence that recombination involving large segments of the genome is another, highly effective, mode of horizontal gene transfer in S. aureus and likely contributes to the extraordinary success of this pathogen.

Indexed as

Staphylococcus aureusAnimalsCattleEvolution, MolecularGenome, BacterialGenomic IslandsMultilocus Sequence TypingPhylogenyBacterial evolutionChimerismHorizontal gene transferNext-generation sequencingStaphylococcus aureus

Identifiers

PMID42001010
PMCPMC13093988

What Socratic holds

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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 Socratic graph.