Evidence map›Paper›PMID 23857904›Full record

ArticleDNA research : an international journal for rapid publication of reports on genes and genomes2013

The genome sequence of Leishmania (Leishmania) amazonensis: functional annotation and extended analysis of gene models.

Fernando Real, Ramon Oliveira Vidal, Marcelo Falsarella Carazzolle, Jorge Maurício Costa Mondego, Gustavo Gilson Lacerda Costa, Roberto Hirochi Herai, Martin Würtele, Lucas Miguel de Carvalho, Renata Carmona e Ferreira, Renato Arruda Mortara and 6 more

Open access · goldAbstract read
In one paragraph

Article in DNA research : an international journal for rapid publication of reports on genes and genomes, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 1 pooled it
10.1field-weighted citation impact, top 2% 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

70 citing papers in PubMed, 1 synthesis or guideline pooled it, 120 citations in OpenAlex.

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  12. A New Strategy for Mapping Epitopes of LACK and PEPCK Proteins ofInternational journal of molecular sciences · 2023
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10 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

16 authors at 8 institutions in 2 countries.

Fernando Real1Departamento de Microbiologia, Imunologia e Parasitologia, Escola Paulista de Medicina, Universidade Federal de São Paulo - EPM/UNIFESP, Rua Botucatu 862, 6 andar, 04023-062 São Paulo, Brazil.
Ramon Oliveira Vidal
Marcelo Falsarella Carazzolle
Jorge Maurício Costa Mondego
Gustavo Gilson Lacerda Costa
Roberto Hirochi Herai
Martin Würtele
Lucas Miguel de Carvalho
Renata Carmona e Ferreira
Renato Arruda Mortara
Clara Lucia Barbiéri
Piotr Mieczkowski
José Franco da Silveira
Marcelo Ribeiro da Silva Briones
Gonçalo Amarante Guimarães Pereira
Diana Bahia
Universidade Federal de São Paulo · BRBrazilian Center for Research in Energy and Materials · BRBrazilian Biosciences National Laboratory · BRUniversidade Estadual de Campinas (UNICAMP) · BRUniversidade Federal de Minas Gerais · BRAgronomical Institute of Campinas · BRDepartamento de Ciência e Tecnologia · BRUniversity of California San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present the sequencing and annotation of the Leishmania (Leishmania) amazonensis genome, an etiological agent of human cutaneous leishmaniasis in the Amazon region of Brazil. L. (L.) amazonensis shares features with Leishmania (L.) mexicana but also exhibits unique characteristics regarding geographical distribution and clinical manifestations of cutaneous lesions (e.g. borderline disseminated cutaneous leishmaniasis). Predicted genes were scored for orthologous gene families and conserved domains in comparison with other human pathogenic Leishmania spp. Carboxypeptidase, aminotransferase, and 3'-nucleotidase genes and ATPase, thioredoxin, and chaperone-related domains were represented more abundantly in L. (L.) amazonensis and L. (L.) mexicana species. Phylogenetic analysis revealed that these two species share groups of amastin surface proteins unique to the genus that could be related to specific features of disease outcomes and host cell interactions. Additionally, we describe a hypothetical hybrid interactome of potentially secreted L. (L.) amazonensis proteins and host proteins under the assumption that parasite factors mimic their mammalian counterparts. The model predicts an interaction between an L. (L.) amazonensis heat-shock protein and mammalian Toll-like receptor 9, which is implicated in important immune responses such as cytokine and nitric oxide production. The analysis presented here represents valuable information for future studies of leishmaniasis pathogenicity and treatment.

Indexed as

Genome, ProtozoanHost-Parasite InteractionsHumansLeishmaniaLeishmaniasis, CutaneousModels, GeneticMolecular Sequence AnnotationMolecular Sequence DataPhylogenyamastingenomeheat-shock proteininteractomeLeishmania amazonensis

Identifiers

PMID23857904
PMCPMC3859324
OpenAlexW1994226299

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.