Evidence map›Paper›PMID 37596603›Full record

ArticleBMC veterinary research2023

The role of AJB35136 and fdtA genes in biofilm formation by avian pathogenic Escherichia coli.

Muhammad Moman Khan, Aamir Ali, Rafał Kolenda, Olugbenga Adekunle Olowe, Jörg Weinreich, Ganwu Li, Peter Schierack

Open access · goldAbstract read
In one paragraph

Article in BMC veterinary research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
6.9field-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

5 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  3. Comparative Genomic and Phylogenetic Analysis ofTransboundary and emerging diseases · 2025
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  4. Isolation and Characterization of a NovelAntibiotics (Basel, Switzerland) · 2024
    Article
  5. 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

7 authors at 4 institutions in 7 countries.

Muhammad Moman KhanInstitute of Biotechnology, Brandenburg University of Technology, Cottbus-Senftenberg, Universitätsplatz 1, D-01968, Senftenberg, Germany.
Aamir AliInstitute of Biotechnology, Brandenburg University of Technology, Cottbus-Senftenberg, Universitätsplatz 1, D-01968, Senftenberg, Germany. myaamirali@yahoo.com.
Rafał KolendaDepartment of Biochemistry and Molecular Biology, Faculty of Veterinary Medicine, Wrocław University of Environmental and Life Sciences, Wrocław, Poland.
Olugbenga Adekunle OloweInstitute of Biotechnology, Brandenburg University of Technology, Cottbus-Senftenberg, Universitätsplatz 1, D-01968, Senftenberg, Germany.
Jörg WeinreichInstitute of Biotechnology, Brandenburg University of Technology, Cottbus-Senftenberg, Universitätsplatz 1, D-01968, Senftenberg, Germany.
Ganwu LiDepartment of Veterinary Diagnostic and Production Animal Medicine, College of Veterinary Medicine, Iowa State University, Ames, USA.
Peter SchierackInstitute of Biotechnology, Brandenburg University of Technology, Cottbus-Senftenberg, Universitätsplatz 1, D-01968, Senftenberg, Germany.
Brandenburg University of Technology Cottbus-Senftenberg · DEHarbin Veterinary Research Institute · CNNational Institute for Biotechnology and Genetic Engineering · PKWrocław University of Environmental and Life Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInfections caused by avian pathogenic Escherichia coli (APEC) result in significant economic losses in poultry industry. APEC strains are known to form biofilms in various conditions allowing them to thrive even under harsh and nutrient-deficient conditions on different surfaces, and this ability enables them to evade chemical and biological eradication methods. Despite knowing the whole genome sequences of various APEC isolates, little has been reported regarding their biofilm-associated genes. A random transposon mutant library of the wild-type APEC IMT 5155 comprising 1,300 mutants was analyzed for biofilm formation under nutrient deprived conditions using Videoscan technology coupled with fluorescence microscopy. Seven transposon mutants were found to have reproducibly and significantly altered biofilm formation and their mutated genes were identified by arbitrary PCR and DNA sequencing. The intact genes were acquired from the wild-type strain, cloned in pACYC177 plasmid and transformed into the respective altered biofilm forming transposon mutants, and the biofilm formation was checked in comparison to the wild type and mutant strains under the same conditions.

resultsIn this study, we report seven genes i.e., nhaA, fdeC, yjhB, lysU, ecpR, AJB35136 and fdtA of APEC with significant contribution to biofilm formation. Reintroduction of AJB35136 and fdtA, reversed the altered phenotype proving that a significant role being played by these two O-antigen related genes in APEC biofilm formation. Presence of these seven genes across nonpathogenic E. coli and APEC genomes was also analyzed showing that they are more prevalent in the latter.

conclusionsThe study has elucidated the role of these genes in APEC biofilm formation and compared them to adhesion expanding the knowledge and understanding of the economically significant pathogens.

Indexed as

BirdsEscherichia coliAnimalsBiofilmsMicroscopy, FluorescenceNutrientsNutrientsAPECBiofilmGene complementationTransposon mutantVideoScan

Identifiers

PMID37596603
PMCPMC10436575
OpenAlexW4385971209

What OpenQuestion holds

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LicenceCC BY
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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.