Evidence map›Paper›PMID 34173722›Full record

ArticleMicrobial biotechnology2021

emPAI-assisted strategy enhances screening and assessment of Mycobacterium tuberculosis infection serological markers.

Guorong Ma, Pei Wang, Yanhui Yang, Wei Wang, Jinhua Ma, Lin Zhou, Junlin Ouyang, Rongxiu Li, Shulin Zhang

Open access · goldAbstract read
In one paragraph

Article in Microbial biotechnology, 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
1.0field-weighted citation impact, top 21% 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, 7 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Guorong MaSchool of Basic Medical Sciences, Ningxia Medical University, Yinchuan, 750004, China.ORCID 0000-0003-3308-8021
Pei WangSchool of Basic Medical Sciences, Ningxia Medical University, Yinchuan, 750004, China.
Yanhui YangSchool of Basic Medical Sciences, Ningxia Medical University, Yinchuan, 750004, China.
Wei WangCollege of Biological Science and Engineering, Northern University for Nationalities, Yinchuan, 750021, China.
Jinhua MaSchool of Basic Medical Sciences, Ningxia Medical University, Yinchuan, 750004, China.
Lin ZhouSchool of Basic Medical Sciences, Ningxia Medical University, Yinchuan, 750004, China.
Junlin OuyangSchool of Basic Medical Sciences, Ningxia Medical University, Yinchuan, 750004, China.
Rongxiu LiState Key Laboratory of Microbial Metabolism, School of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai, 200240, China.
Shulin ZhangDepartment of Immunology and Microbiology, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200025, China.
Ningxia Medical University · CNShanghai Jiao Tong University · CNNorth Minzu University · CN

Funding

Ningxia hui autonomous region education department outstanding young teachers training fund project NGY2018-79Ningxia hui autonomous region key research and development 2018BEB04033Superior discipline group (Orthopedics) construction research project in 2019 of Ningxia medical university, The third batch of special talents launched in 2017 of Ningxia medical university XT2017028The National Science & Technology Major Projects of China 2017ZX10201301-003-004The Ningxia hui autonomous region key R&D 2019BEG03065Undergraduate innovation and entrepreneurship project of Ningxia Hui Autonomous Region S201910752013
6 · The paper itself

Abstract

Discovering new serological markers of Mycobacterium tuberculosis (MTB) infection and establishing a rapid and efficient detection technology is of great significance for the prevention and control of tuberculosis. In this study, we established an exponentially modified protein abundance index (emPAI) value-assisted strategy to investigate and improve the screening efficiency of serological biomarkers of tuberculosis. First, we used LC-MS/MS to analyse MTB culture filtrate proteins (MTB-CFPs), and 632 MTB proteins were identified. Then, the characteristic values of MTB-CFPs - including emPAI value, molecular weight (Mw), isoelectric point (pI), grand average of hydropathy (GRAVY), transmembrane domain (TMD) and functional groups were calculated. Next, we successfully prepared 10 MTB proteins with emPAI value > 1.0 and recombinantly expressed these proteins in Escherichia coli. At the same time, 3 MTB proteins with emPAI between 0.1 and 0.5 were randomly selected as the control groups, and the immunogenicity of the recombinant MTB proteins was detected using ELISA. The sensitivity and receiver operating characteristic (ROC) curves were calculated for each recombinant MTB protein. The results showed that the areas under the curve (AUC) value of Rv2031c, Rv0577, Rv0831c, Rv0934 and Rv3248c were all higher than those of Rv3875 (AUC, 0.6643). Further analysis of the relationship between emPAI value and antibody sensitivity, AUC value and antibody affinity in mice immunized with recombinant MTB protein showed that emPAI values were positively correlated with them, and R-squared value ranged from 0.64 to 0.79. The only exception was ESAT-6 (encoded by the Rv3875 gene), which AUC value was relatively low owing to its strong immunosuppressive properties. This study provides a rationale for the serological marker screening of emPAI-assisted tuberculosis clinical test. The results also provide new technical support for the screening of candidate serological markers of infectious diseases in the future.

Indexed as

Mycobacterium tuberculosisTuberculosisAnimalsAntigens, BacterialBacterial ProteinsBiomarkersChromatography, LiquidMiceTandem Mass SpectrometryAntigens, BacterialBacterial ProteinsBiomarkers

Identifiers

PMID34173722
PMCPMC8313264
OpenAlexW3174572474

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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.