Evidence map›Paper›PMID 33070782›Full record

ArticleParasitology2021

The efficacy of recombinant protein lbk39 for the diagnosis of leishmaniosis in dogs.

Joyce Carvalho Pereira, Pedro Dos Santos Sousa, Ligia Moraes Barizon De Souza, Aline Kuhn Sbruzzi Pasquali, Michelle Bates, Paul Bates, Vanete Thomaz Soccol

Open access · greenAbstract read
In one paragraph

Article in Parasitology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Epidemic Preparedness-Frontiers in microbiology · 2021
    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 2 institutions in 2 countries.

Joyce Carvalho PereiraFederal University of Paraná, Post-graduate Course in Bioprocess Engineering and Biotechnology, Polytechnic Centre, Jardim das Américas, CEP 81530-980, Curitiba, Paraná, Brazil.
Pedro Dos Santos SousaFederal University of Paraná, Post-graduate Course in Bioprocess Engineering and Biotechnology, Polytechnic Centre, Jardim das Américas, CEP 81530-980, Curitiba, Paraná, Brazil.
Ligia Moraes Barizon De SouzaFederal University of Paraná, Post-graduate Course in Bioprocess Engineering and Biotechnology, Polytechnic Centre, Jardim das Américas, CEP 81530-980, Curitiba, Paraná, Brazil.
Aline Kuhn Sbruzzi PasqualiFederal University of Paraná, Post-graduate Course in Bioprocess Engineering and Biotechnology, Polytechnic Centre, Jardim das Américas, CEP 81530-980, Curitiba, Paraná, Brazil.
Michelle BatesDivision of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster, LA1 4YQ, UK.
Paul BatesDivision of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster, LA1 4YQ, UK.
Vanete Thomaz SoccolFederal University of Paraná, Post-graduate Course in Bioprocess Engineering and Biotechnology, Polytechnic Centre, Jardim das Américas, CEP 81530-980, Curitiba, Paraná, Brazil.ORCID 0000-0001-9301-541X
Universidade Federal do Paraná · BRLancaster University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Visceral leishmaniosis is one of the most important zoonotic diseases on the planet and dogs are the main reservoir of canine visceral leishmaniosis (CVL) in endemic areas. They play an important role in human infection because in dogs the disease appears long time after infection, and they can move uncontrollably, contributing to disperse the parasite. To take the decision to treat the animals or for euthanasia, in an elimination programme, in order to reduce the parasitic load, it is necessary to diagnose correctly, having more effective tools. Our group has developed a new recombinant antigen-based kinesin-related gene of Leishmania braziliensis (Lbk39), which shows 59% amino acid identity to the L. infantum homologue. The Lbk39 gene was synthesized, inserted into the pLEXSY-sat2 vector and transfected into L. tarentolae cells by electroporation. The recombinant protein was secreted in the culture with a C-terminal histidine marker, purified, generating a product at 337.68 μg mL-1. A total of 152 sera from dog's endemic and non-endemic areas were used, being 78 positives and 75 negatives. The antigen Lbk39 showed 100% sensitivity and 96.1% specificity. We compared this antigen with other antigens such as total extract of the parasite, TRDPP, and our data indicate that Lbk39 has potential application in the diagnosis of CVL through antibody detection.

Indexed as

AnimalsDog DiseasesDogsLeishmaniaLeishmania braziliensisLeishmaniasis, VisceralMicroorganisms, Genetically-ModifiedProtozoan ProteinsRecombinant ProteinsProtozoan ProteinsRecombinant ProteinsCanis familiarisdogsELISArecombinant antigenvisceral leishmaniosis

Identifiers

PMID33070782
PMCPMC11010170
OpenAlexW3093136033

What OpenQuestion holds

Textmetadata
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.