Evidence map›Paper›PMID 31751365›Full record

ArticlePloS one2019

iTRAQ-based high-throughput proteomics analysis reveals alterations of plasma proteins in patients infected with human bocavirus.

Junmei Bian, Min Liang, Shuxian Ding, Liyan Wang, Wenchang Ni, Shisi Xiong, Wan Li, Xingxing Bao, Xue Gao, Rong Wang

Abstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

10 authors.

Junmei BianTongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, PR China.
Min LiangTongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, PR China.
Shuxian DingTongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, PR China.
Liyan WangTongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, PR China.
Wenchang NiTongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, PR China.
Shisi XiongTongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, PR China.
Wan LiTongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, PR China.
Xingxing BaoTongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, PR China.
Xue GaoTongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, PR China.
Rong WangTongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, PR China.ORCID 0000-0002-9595-8101

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human bocavirus (HBoV) is a member of the genus Bocavirus, family Parvoviridae, and subfamily Parvovirus and was first identified in nasopharyngeal aspirates of Swedish children with acute respiratory tract infection (ARTI) in 2005. It is the causative agent of nasopharyngeal aspirate disease and death in children. The HboV genomic structure is a linear single-stranded DNA (ssDNA). Its clinical pathogenic characteristics have been extensively studied, however, at present the molecular mechanism underlying the pathogenesis of HBoV infection is not completely clear. In this study, a total of 293 differentially expressed proteins (DEPs) between ARTI cases and healthy plasma samples were characterized using isobaric tags for relative and absolute quantitation (iTRAQ)-coupled bioinformatics analysis, among which 148 were up-regulated and 135 were down-regulated. Gene Ontology (GO) and Cluster of Orthologous Groups of proteins (COG) annotated an enrichment of DEPs in complement activation and biological processes like immunity, inflammation, signal transduction, substance synthesis, and metabolism. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis enriched DEPs mainly in the Wnt signaling pathway (ko04310), PPAR signaling pathway (ko03320), intestinal immune network for IgA production (ko04672), complement and coagulation cascades (ko04610), Toll-like receptor signaling pathway (ko04620) and B cell receptor signaling pathway (ko04662). Further, expression levels of three candidate proteins (upregulated PPP2R1A and CUL1, and downregulated CETP) were validated using western blotting. Our investigation is the first analysis of the proteomic profile of HBoV-infected ARTI cases using the iTRAQ approach, providing a foundation for a better molecular understanding of the pathogenesis of ARTI in children.

Indexed as

Host-Pathogen InteractionsHuman bocavirusProteomeProteomicsBlood ProteinsChromatography, LiquidComputational BiologyFemaleGene OntologyHumansMaleParvoviridae InfectionsReproducibility of ResultsTandem Mass SpectrometryBlood ProteinsProteome

Identifiers

PMID31751365
PMCPMC6872134

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