Evidence map›Paper›PMID 24023660›Full record

ArticlePloS one2013

Whole transcriptome analysis of Acinetobacter baumannii assessed by RNA-sequencing reveals different mRNA expression profiles in biofilm compared to planktonic cells.

Soraya Rumbo-Feal, Manuel J Gómez, Carmen Gayoso, Laura Álvarez-Fraga, María P Cabral, Ana M Aransay, Naiara Rodríguez-Ezpeleta, Ane Fullaondo, Jaione Valle, María Tomás and 2 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

88 citing papers in PubMed, 147 citations in OpenAlex.

  1. Virulence · 2026
    Review
  2. Redefining Antimicrobial Resistance inInternational journal of molecular sciences · 2026
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  3. Article
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  6. The glutathione pathway is required for biofilm formation inCurrent research in microbial sciences · 2026
    Article
  7. Article
  8. InvasiveMicrobiology (Reading, England) · 2025
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  9. Article
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  11. Iron-dependent mechanisms inJAC-antimicrobial resistance · 2025
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  12. Omp34-MediatedAnalytical cellular pathology (Amsterdam) · 2025
    Article
  13. Article
  14. The intricacies ofFrontiers in microbiology · 2025
    Review
  15. Review
  16. Article
  17. Article
  18. Extensive Drug Resistance of Strong Biofilm-ProducingPathogens (Basel, Switzerland) · 2023
    Article
  19. Article
  20. Review

28 more citing papers are in PubMed but not listed here.

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 at 4 institutions in 1 country.

Soraya Rumbo-FealDepartment of Microbiology, Biomedical Research Institute, University Hospital, A Coruña, Spain.
Manuel J Gómez
Carmen Gayoso
Laura Álvarez-Fraga
María P Cabral
Ana M Aransay
Naiara Rodríguez-Ezpeleta
Ane Fullaondo
Jaione Valle
María Tomás
Germán Bou
Margarita Poza
Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas · ESAgrobiotechnology Institute · ESCentro de Astrobiología · ESCIC bioGUNE · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acinetobacterbaumannii has emerged as a dangerous opportunistic pathogen, with many strains able to form biofilms and thus cause persistent infections. The aim of the present study was to use high-throughput sequencing techniques to establish complete transcriptome profiles of planktonic (free-living) and sessile (biofilm) forms of A. baumannii ATCC 17978 and thereby identify differences in their gene expression patterns. Collections of mRNA from planktonic (both exponential and stationary phase cultures) and sessile (biofilm) cells were sequenced. Six mRNA libraries were prepared following the mRNA-Seq protocols from Illumina. Reads were obtained in a HiScanSQ platform and mapped against the complete genome to describe the complete mRNA transcriptomes of planktonic and sessile cells. The results showed that the gene expression pattern of A. baumannii biofilm cells was distinct from that of planktonic cells, including 1621 genes over-expressed in biofilms relative to stationary phase cells and 55 genes expressed only in biofilms. These differences suggested important changes in amino acid and fatty acid metabolism, motility, active transport, DNA-methylation, iron acquisition, transcriptional regulation, and quorum sensing, among other processes. Disruption or deletion of five of these genes caused a significant decrease in biofilm formation ability in the corresponding mutant strains. Among the genes over-expressed in biofilm cells were those in an operon involved in quorum sensing. One of them, encoding an acyl carrier protein, was shown to be involved in biofilm formation as demonstrated by the significant decrease in biofilm formation by the corresponding knockout strain. The present work serves as a basis for future studies examining the complex network systems that regulate bacterial biofilm formation and maintenance.

Indexed as

BiofilmsGene Expression ProfilingGene Expression Regulation, Bacterial4-ButyrolactoneAcinetobacter baumanniiGene Knockout TechniquesGenes, BacterialMutationPlanktonRNA, MessengerSequence Analysis, RNATranscriptomeUp-Regulation4-Butyrolactonehomoserine lactoneRNA, Messenger

Identifiers

PMID24023660
PMCPMC3758355
OpenAlexW2042407594

What OpenQuestion 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 OpenQuestion graph.