Evidence map›Paper›PMID 29291715›Full record

ArticleBMC genomics2018

Comparative genome and phenotypic analysis of three Clostridioides difficile strains isolated from a single patient provide insight into multiple infection of C. difficile.

Uwe Groß, Elzbieta Brzuszkiewicz, Katrin Gunka, Jessica Starke, Thomas Riedel, Boyke Bunk, Cathrin Spröer, Daniela Wetzel, Anja Poehlein, Cynthia Chibani and 5 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
49.3field-weighted citation impact, top 1% of its field
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

8 citing papers in PubMed, 733 citations in OpenAlex.

  1. Article
  2. Article
  3. Detection and Genomic Characterisation ofPathogens (Basel, Switzerland) · 2022
    Article
  4. Review
  5. Genomics of the Pathogenic Clostridia.Microbiology spectrum · 2019
    Review
  6. Article
  7. Article
  8. 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

15 authors at 4 institutions in 1 country.

Uwe GroßInstitute for Medical Microbiology, University Medical Center Göttingen, Göttingen, Germany.
Elzbieta BrzuszkiewiczDepartment of Genomic and Applied Microbiology & Göttingen Genomics Laboratory, Institute of Microbiology and Genetics, Georg-August-University, Göttingen, Germany.
Katrin GunkaInstitute for Medical Microbiology, University Medical Center Göttingen, Göttingen, Germany.
Jessica StarkeDepartment of Genomic and Applied Microbiology & Göttingen Genomics Laboratory, Institute of Microbiology and Genetics, Georg-August-University, Göttingen, Germany.
Thomas RiedelLeibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Boyke BunkLeibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Cathrin SpröerLeibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Daniela WetzelInstitute for Medical Microbiology, University Medical Center Göttingen, Göttingen, Germany.
Anja PoehleinDepartment of Genomic and Applied Microbiology & Göttingen Genomics Laboratory, Institute of Microbiology and Genetics, Georg-August-University, Göttingen, Germany.
Cynthia ChibaniDepartment of Genomic and Applied Microbiology & Göttingen Genomics Laboratory, Institute of Microbiology and Genetics, Georg-August-University, Göttingen, Germany.
Wolfgang BohneInstitute for Medical Microbiology, University Medical Center Göttingen, Göttingen, Germany.
Jörg OvermannLeibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Ortrud ZimmermannInstitute for Medical Microbiology, University Medical Center Göttingen, Göttingen, Germany.
Rolf DanielDepartment of Genomic and Applied Microbiology & Göttingen Genomics Laboratory, Institute of Microbiology and Genetics, Georg-August-University, Göttingen, Germany.
Heiko LiesegangDepartment of Genomic and Applied Microbiology & Göttingen Genomics Laboratory, Institute of Microbiology and Genetics, Georg-August-University, Göttingen, Germany. hlieseg@gwdg.de.ORCID 0000-0003-1792-2047
University of Göttingen · DEUniversitätsmedizin Göttingen · DEGerman Center for Infection Research · DELeibniz Institute DSMZ – German Collection of Microorganisms and Cell Cultures · DE

Funding

Niedersächsisches Vorab VWZN2889/3215
6 · The paper itself

Abstract

backgroundClostridioides difficile infections (CDI) have emerged over the past decade causing symptoms that range from mild, antibiotic-associated diarrhea (AAD) to life-threatening toxic megacolon. In this study, we describe a multiple and isochronal (mixed) CDI caused by the isolates DSM 27638, DSM 27639 and DSM 27640 that already initially showed different morphotypes on solid media.

resultsThe three isolates belonging to the ribotypes (RT) 012 (DSM 27639) and 027 (DSM 27638 and DSM 27640) were phenotypically characterized and high quality closed genome sequences were generated. The genomes were compared with seven reference strains including three strains of the RT 027, two of the RT 017, and one of the RT 078 as well as a multi-resistant RT 012 strain. The analysis of horizontal gene transfer events revealed gene acquisition incidents that sort the strains within the time line of the spread of their RTs within Germany. We could show as well that horizontal gene transfer between the members of different RTs occurred within this multiple infection. In addition, acquisition and exchange of virulence-related features including antibiotic resistance genes were observed. Analysis of the two genomes assigned to RT 027 revealed three single nucleotide polymorphisms (SNPs) and apparently a regional genome modification within the flagellar switch that regulates the fli operon.

conclusionOur findings show that (i) evolutionary events based on horizontal gene transfer occur within an ongoing CDI and contribute to the adaptation of the species by the introduction of new genes into the genomes, (ii) within a multiple infection of a single patient the exchange of genetic material was responsible for a much higher genome variation than the observed SNPs.

Indexed as

Genome, BacterialEubacterialesFlagellaGene Transfer, HorizontalGenomicsGram-Positive Bacterial InfectionsHumansPhenotypePhylogenyClostridioides difficileClostridium difficileGenetic switchGenomic adaptationHorizontal gene transferMultiple infection

Identifiers

PMID29291715
PMCPMC5749029
OpenAlexW2781865485

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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 OpenQuestion graph.