Evidence map›Paper›PMID 33165807›Full record

ArticleFolia microbiologica2021

iTRAQ®-based quantitative proteomics reveals the proteomic profiling of methicillin-resistant Staphylococcus aureus-derived extracellular vesicles after exposure to imipenem.

Jichun Wang, Junrui Wang, Yanyan Wang, Peng Sun, Xiaohui Zou, Luo Ren, Chunxia Zhang, Enmei Liu

Abstract read
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In one paragraph

Article in Folia microbiologica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
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  4. Review
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

8 authors at 3 institutions in 2 countries.

Jichun WangDepartment of Respiratory Medicine, Children's Hospital of Chongqing Medical University, No.136, Zhong Shan 2nd Road, Chongqing, 400014, Yuzhong District, China.
Junrui WangDepartment of Clinical Laboratory, Affiliated Hospital of Inner Mongolia Medical University, No.1, Tongdao North Street, Huimin District, Hohhot, 010110, Inner Mongolia, China. wangjunrui123@yeah.net.
Yanyan WangDepartment of Clinical Laboratory, Affiliated Hospital of Inner Mongolia Medical University, No.1, Tongdao North Street, Huimin District, Hohhot, 010110, Inner Mongolia, China.
Peng SunPathogen and Immunity Research Centre, College of Basic Medicine, Inner Mongolia Medical University, Jinshan Development Zone, Hohhot, 010110, Inner Mongolia, China.
Xiaohui ZouChinese National Influenza Center, National Institute for Viral Disease Control and Prevention; China CDC, Key Laboratory for Medical Virology, Ministry of Health, Beijing, 102206, China.
Luo RenPediatrics Institute, Children's Hospital Chongqing Medical University, Chongqing, 400014, China.
Chunxia ZhangDepartment of Pediatrics, Affiliated hospital of Inner Mongolia Medical University, Hohhot, 010110, Inner Mongolia, China.
Enmei LiuDepartment of Respiratory Medicine, Children's Hospital of Chongqing Medical University, No.136, Zhong Shan 2nd Road, Chongqing, 400014, Yuzhong District, China. nmgwangjunrui123@163.com.ORCID http://orcid.org/0000-0003-2897-8169
Children's Hospital of Chongqing Medical University · CNInner Mongolia Medical University · CNNational Influenza Center · MN

Funding

National Natural Science Foundation of China 81660352
6 · The paper itself

Abstract

This study sought to reveal the proteomic profiling of methicillin-resistant Staphylococcus aureus (MRSA)-derived extracellular vesicles (EVs) after exposure to imipenem. The advanced isobaric tags for relative and absolute quantitation (iTRAQ®) proteomic approach were used to analyze the alterations in MRSA-derived EV protein patterns upon exposure to imipenem. A total of 1260 EV proteins were identified and quantified. Among these, 861 differentially expressed exosome proteins (P < 0.05) were found. Multivariate analysis, Gene Ontology (GO) annotation, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were used to analyze the identified proteins. Enrichment analysis of GO annotations indicated that imipenem primarily regulated the metabolic processes in MRSA. The metabolism of differentially expressed proteins was found to be the most significant in the combined analysis of the KEGG pathway analysis. Based on the results from the STRING analysis, 50S ribosomal protein L16 (RplP) and 30S ribosomal protein S8 (RpsH) were involved in the imipenem-induced MRSA-derived EVs. These results provide vital information on MRSA-derived EVs, increasing our knowledge of the proteome level changes in EVs upon exposure to imipenem. Moreover, these results pave the way for developing novel MRSA treatments.

Indexed as

Extracellular VesiclesMethicillin-Resistant Staphylococcus aureusGene Expression ProfilingImipenemProteomicsImipenem

Identifiers

PMID33165807
OpenAlexW3103990526

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.