Evidence map›Paper›PMID 35630474›Full record

ArticleMicroorganisms2022

Heterologous Expression, Purification, and Immunomodulatory Effects of Recombinant Lipoprotein GUDIV-103 Isolated from

Manoel Neres Santos-Junior, Wanderson Souza Neves, Ronaldo Silva Santos, Palloma Porto Almeida, Janaina Marinho Fernandes, Bruna Carolina de Brito Guimarães, Maysa Santos Barbosa, Lucas Santana Coelho da Silva, Camila Pacheco Gomes, Beatriz Almeida Sampaio and 7 more

Open access · goldAbstract read
In one paragraph

Article in Microorganisms, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 54% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

17 authors at 4 institutions in 1 country.

Manoel Neres Santos-JuniorDepartment of Biointeraction, Multidisciplinary Institute of Health, Federal University of Bahia, Vitória da Conquista 40170-110, Brazil.ORCID 0000-0001-8181-4556
Wanderson Souza NevesDepartment of Biointeraction, Multidisciplinary Institute of Health, Federal University of Bahia, Vitória da Conquista 40170-110, Brazil.
Ronaldo Silva SantosDepartment of Biointeraction, Multidisciplinary Institute of Health, Federal University of Bahia, Vitória da Conquista 40170-110, Brazil.ORCID 0000-0002-5460-3822
Palloma Porto AlmeidaBioinformatics and Computational Biology Lab, Division of Experimental and Translational Research, Brazilian National Cancer Institute (INCA), Rio de Janeiro 20231-050, Brazil.ORCID 0000-0002-1588-8722
Janaina Marinho FernandesDepartment of Biointeraction, Multidisciplinary Institute of Health, Federal University of Bahia, Vitória da Conquista 40170-110, Brazil.
Bruna Carolina de Brito GuimarãesDepartment of Biology, and Biotechnology of Microorganisms, State University of Santa Cruz (UESC), Ilhéus 45662-900, Brazil.
Maysa Santos BarbosaDepartment of Microbiology, Institute of Biomedical Science, University of São Paulo, São Paulo 05508-000, Brazil.ORCID 0000-0003-2126-1202
Lucas Santana Coelho da SilvaDepartment of Biology, and Biotechnology of Microorganisms, State University of Santa Cruz (UESC), Ilhéus 45662-900, Brazil.
Camila Pacheco GomesDepartment of Biology, and Biotechnology of Microorganisms, State University of Santa Cruz (UESC), Ilhéus 45662-900, Brazil.
Beatriz Almeida SampaioDepartment of Biology, and Biotechnology of Microorganisms, State University of Santa Cruz (UESC), Ilhéus 45662-900, Brazil.
Izadora de Souza RezendeDepartment of Microbiology, Institute of Biomedical Science, University of São Paulo, São Paulo 05508-000, Brazil.
Thiago Macedo Lopes CorreiaDepartment of Biointeraction, Multidisciplinary Institute of Health, Federal University of Bahia, Vitória da Conquista 40170-110, Brazil.ORCID 0000-0003-1654-614X
Nayara Silva de Macedo NeresDepartment of Biointeraction, Multidisciplinary Institute of Health, Federal University of Bahia, Vitória da Conquista 40170-110, Brazil.
Guilherme Barreto CamposDepartment of Biology, and Biotechnology of Microorganisms, State University of Santa Cruz (UESC), Ilhéus 45662-900, Brazil.
Bruno Lopes BastosDepartment of Biology, and Biotechnology of Microorganisms, State University of Santa Cruz (UESC), Ilhéus 45662-900, Brazil.
Jorge TimenetskyDepartment of Microbiology, Institute of Biomedical Science, University of São Paulo, São Paulo 05508-000, Brazil.
Lucas Miranda MarquesDepartment of Biointeraction, Multidisciplinary Institute of Health, Federal University of Bahia, Vitória da Conquista 40170-110, Brazil.
Universidade Federal da Bahia · BRUniversidade Estadual de Santa Cruz · BRUniversidade de São Paulo · BRInstituto Nacional de Câncer - INCA · BR

Funding

Coordenação de Aperfeicoamento de Pessoal de Nível Superior Code 001National Council for Scientific and Technological Development 409758/2018-3
6 · The paper itself

Abstract

Ureaplasma diversum is a bacterial pathogen that infects cattle and can cause severe inflammation of the genital and reproductive systems. Lipid-associated membrane proteins (LAMPs), including GUDIV-103, are the main virulence factors in this bacterium. In this study, we heterologously expressed recombinant GUDIV-103 (rGUDIV-103) in Escherichia coli, purified it, and evaluated its immunological reactivity and immunomodulatory effects in bovine peripheral blood mononuclear cells (PBMCs). Samples from rabbits inoculated with purified rGUDIV-103 were analysed using indirect enzyme-linked immunosorbent assay and dot blotting to confirm polyclonal antibody production and assess kinetics, respectively. The expression of this lipoprotein in field isolates was confirmed via Western blotting with anti-rGUDIV-103 serum and hydrophobic or hydrophilic proteins from 42 U. diversum strains. Moreover, the antibodies produced against the U. diversum ATCC 49783 strain recognised rGUDIV-103. The mitogenic potential of rGUDIV-103 was evaluated using a lymphoproliferation assay in 5(6)-carboxyfluorescein diacetate succinimidyl ester−labelled bovine PBMCs, where it induced lymphocyte proliferation. Quantitative polymerase chain reaction analysis revealed that the expression of interleukin-1β, toll-like receptor (TLR)-α, TLR2, TLR4, inducible nitric oxide synthase, and caspase-3−encoding genes increased more in rGUDIV-103−treated PBMCs than in untreated cells (p < 0.05). Treating PBMCs with rGUDIV-103 increased nitric oxide and hydrogen peroxide levels. The antigenic and immunogenic properties of rGUDIV-103 suggested its suitability for immunobiological application.

Indexed as

immunomodulationlipoproteinslymphoproliferationUreaplasma diversum

Identifiers

PMID35630474
PMCPMC9147684
OpenAlexW4280552500

What OpenQuestion holds

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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.