Evidence map›Paper›PMID 41474721›Full record

ArticlePloS one2025

Systematic analysis of spontaneous tandem genome amplification events in Yersinia pestis.

Dmitry N Konanov, Olga N Liubimova, Alexander V Kovrizhnikov, Ignat V Sonets, Alina N Balykova, Alexandra V Lukina-Gronskaya, Anna S Speranskaya, Danil V Krivonos, Galina A Eroshenko, Elena N Ilina and 2 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Dmitry N KonanovResearch Institute for System Biology and Medicine of Rospotrebnadzor, Moscow, Russia.ORCID https://orcid.org/0000-0002-1217-9234
Olga N LiubimovaMoscow Center for Advanced Studies, Moscow, Russia.
Alexander V KovrizhnikovRussian Research Anti-Plague Institute "Microbe", Saratov, Russia.ORCID https://orcid.org/0000-0002-7752-6321
Ignat V SonetsResearch Institute for System Biology and Medicine of Rospotrebnadzor, Moscow, Russia.ORCID https://orcid.org/0009-0009-7266-6657
Alina N BalykovaRussian Research Anti-Plague Institute "Microbe", Saratov, Russia.
Alexandra V Lukina-GronskayaResearch Institute for System Biology and Medicine of Rospotrebnadzor, Moscow, Russia.ORCID https://orcid.org/0009-0005-9452-0406
Anna S SperanskayaResearch Institute for System Biology and Medicine of Rospotrebnadzor, Moscow, Russia.
Danil V KrivonosResearch Institute for System Biology and Medicine of Rospotrebnadzor, Moscow, Russia.
Galina A EroshenkoRussian Research Anti-Plague Institute "Microbe", Saratov, Russia.
Elena N IlinaResearch Institute for System Biology and Medicine of Rospotrebnadzor, Moscow, Russia.ORCID https://orcid.org/0000-0003-0130-5079
Vadim M GovorunResearch Institute for System Biology and Medicine of Rospotrebnadzor, Moscow, Russia.
Vladimir V KutyrevRussian Research Anti-Plague Institute "Microbe", Saratov, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tandem amplification of genomic fragments is quite common in bacteria growing under stress conditions, while spontaneous genome amplification events are rare, unstable and generally poorly described. Plague pathogen Yersinia pestis is a unique microorganism that contains an enormous number of short repeat sequences in its genome and as a result is very prone to spontaneous genome rearrangements including large tandem genome amplification events. Eleven Y. pestis strains sequenced during this study and more than thousand read archives from SRA were analyzed in this study. It was shown that genomes of more than half of Y. pestis laboratory isolates contain tandem repeats. They are mainly caused by the presence of multicopy IS-elements but a few of them are associated with multicopy rRNA clusters, so the rearrangement mechanism is most likely RecA-dependent recombination. Four regions with unstable copy number reproduced between different bioprojects were found. One of them was identified as an integrative mobilizable element carrying a probably incomplete Type 4 secretion system. More interesting, two other reproducible regions were not identified as mobile elements but had the length and GC-content almost identical to the length and GC-content of pMT1 and pCD1 plasmids.

Indexed as

Genome, BacterialTandem Repeat SequencesYersinia pestisBase CompositionPlasmids

Identifiers

PMID41474721
PMCPMC12755819

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.