Evidence map›Paper›PMID 27325348›Full record

ArticleAMB Express2016

The Burkholderia cenocepacia OmpA-like protein BCAL2958: identification, characterization, and detection of anti-BCAL2958 antibodies in serum from B. cepacia complex-infected Cystic Fibrosis patients.

Sílvia A Sousa, Mostafa Morad, Joana R Feliciano, Tiago Pita, Soad Nady, Rehab E El-Hennamy, Mona Abdel-Rahman, José Cavaco, Luísa Pereira, Celeste Barreto and 1 more

Open access · goldAbstract read
In one paragraph

Article in AMB Express, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

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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 at 6 institutions in 2 countries.

Sílvia A SousaiBB-Institute for Bioengineering and Biosciences, Department of Bioengineering, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, Torre Sul, Piso 6, 1049-001, Lisbon, Portugal. sousasilvia@tecnico.ulisboa.pt.
Mostafa MoradiBB-Institute for Bioengineering and Biosciences, Department of Bioengineering, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, Torre Sul, Piso 6, 1049-001, Lisbon, Portugal.
Joana R FelicianoiBB-Institute for Bioengineering and Biosciences, Department of Bioengineering, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, Torre Sul, Piso 6, 1049-001, Lisbon, Portugal.
Tiago PitaiBB-Institute for Bioengineering and Biosciences, Department of Bioengineering, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, Torre Sul, Piso 6, 1049-001, Lisbon, Portugal.
Soad NadyZoology Department, Faculty of Science, Helwan University, Cairo, Egypt.
Rehab E El-HennamyZoology Department, Faculty of Science, Helwan University, Cairo, Egypt.
Mona Abdel-RahmanZoology Department, Faculty of Science, Helwan University, Cairo, Egypt.
José CavacoCystic Fibrosis Center, Department of Paediatrics, Hospital de D. Estefânia, Centro Hospitalar de Lisboa Central, Rua Jacinta Marto, 1169-045, Lisbon, Portugal.
Luísa PereiraCystic Fibrosis Center, Department of Paediatrics, Hospital de Santa Maria, Centro Hospitalar Lisboa Norte, Av. Prof. Egas Moniz, 1649-028, Lisbon, Portugal.
Celeste BarretoCystic Fibrosis Center, Department of Paediatrics, Hospital de Santa Maria, Centro Hospitalar Lisboa Norte, Av. Prof. Egas Moniz, 1649-028, Lisbon, Portugal.
Jorge H LeitãoiBB-Institute for Bioengineering and Biosciences, Department of Bioengineering, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, Torre Sul, Piso 6, 1049-001, Lisbon, Portugal. jorgeleitao@tecnico.ulisboa.pt.
Helwan University · EGInstitute for Biotechnology and Bioengineering · PTUniversity of Lisbon · PTCentro Hospitalar Lisboa Norte · PTHospital de Dona Estefânia · PTHospital de Santa Maria · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Respiratory infections by bacteria of the Burkholderia cepacia complex (Bcc) remain an important cause of morbidity and mortality among cystic fibrosis patients, highlighting the need for novel therapeutic strategies. In the present work we have studied the B. cenocepacia protein BCAL2958, a member of the OmpA-like family of proteins, demonstrated as highly immunogenic in other pathogens and capable of eliciting strong host immune responses. The encoding gene was cloned and the protein, produced as a 6× His-tagged derivative, was used to produce polyclonal antibodies. Bioinformatics analyses led to the identification of sequences encoding proteins with a similarity higher than 96 % to BCAL2958 in all the publicly available Bcc genomes. Furthermore, using the antibody it was experimentally demonstrated that this protein is produced by all the 12 analyzed strains from 7 Bcc species. In addition, results are also presented showing the presence of anti-BCAL2958 antibodies in sera from cystic fibrosis patients with a clinical record of respiratory infection by Bcc, and the ability of the purified protein to in vitro stimulate neutrophils. The widespread production of the protein by Bcc members, together with its ability to stimulate the immune system and the detection of circulating antibodies in patients with a documented record of Bcc infection strongly suggest that the protein is a potential candidate for usage in preventive therapies of infections by Bcc.

Indexed as

Bcc positive CF serum samplesBurkholderia cepacia complex (Bcc)Cystic fibrosis (CF)Neutrophil activationOmpA-like proteins

Identifiers

PMID27325348
PMCPMC4916078
OpenAlexW2468479054

What OpenQuestion holds

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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.