Evidence map›Paper›PMID 41422198›Full record

ArticleBMC infectious diseases2025

Development and evaluation of novel Brucella diagnostic antigen protein ST.

Juan Shi, Tingting Tian, Xinxin Qi, Huidong Shi, Kaiyu Shang, Zhengwei Yin, Jianbing Ding, Ruixue Xu, Fuling Pu, Mingzhe Li and 3 more

Abstract readEvaluation Study
In one paragraph

Article in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Juan Shi *State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, 830011, PR China.
Tingting Tian *State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, 830011, PR China.
Xinxin QiState Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, 830011, PR China.
Huidong ShiState Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, 830011, PR China.
Kaiyu ShangState Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, 830011, PR China.
Zhengwei YinState Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, 830011, PR China.
Jianbing DingState Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, 830011, PR China.
Ruixue XuXinjiang Medical University, Urumqi, Xinjiang, 830011, PR China.
Fuling PuXinjiang Medical University, Urumqi, Xinjiang, 830011, PR China.
Mingzhe LiXinjiang Medical University, Urumqi, Xinjiang, 830011, PR China.
Junyu KuangXinjiang Medical University, Urumqi, Xinjiang, 830011, PR China.
Yuejie ZhuReproductive Medicine Center, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, 830011, PR China. zhuyuejie_1216@163.com.
Fengbo ZhangState Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, 830011, PR China. zfb131@163.com.

Funding

the Central Government Guides Local Science and Technology Development Fund Project ZYYD2025ZY19the Natural Science Foundation of China No. 82360394,82460399the Outstanding Youth Project of the Autonomous Region No.2023D01E12the Youth Science and Technology Top Talent Project No.2022TSYCCX0112
6 · The paper itself

Abstract

backgroundBrucellosis continues to pose a significant zoonotic challenge, necessitating the development of improved diagnostic solutions. This study innovatively integrates bioinformatics predictions with prokaryotic expression techniques to create novel diagnostic antigens for the detection of Brucella melitensis.

methodsOur study systematically analyzed four outer membrane proteins (OMP10, OMP25, VirB8, and VirB10). B-cell epitope prediction was conducted using the IEDB and ABCpred algorithms. A chimeric antigen was designed by fusing these four proteins in the sequence OMP10-OMP25-VirB8-VirB10. The recombinant protein was expressed in E. coli BL21(DE3) and purified using nickel-affinity chromatography. The diagnostic performance of the purified chimeric antigen was evaluated through indirect ELISA, utilizing 180 brucellosis sera, 20 healthy control sera, and 88 sera from other infections.

resultsIn our study, we successfully predicted and designed a novel recombinant Brucella diagnostic antigen protein, named OMP10-OMP25-VirB8-VirB10, referred to as the ST protein. We assessed its performance as a serological diagnostic biomarker for brucellosis using the indirect enzyme-linked immunosorbent assay. The results demonstrated that the ST protein exhibited a detection sensitivity of 98.33% and a specificity of 85.22%, with an AUC value of 0.9802.

conclusionThe ST protein, a fusion of four proteins derived from Brucella, demonstrates significant diagnostic potential in ELISA, offering a novel approach for the accurate diagnosis of brucellosis. This discovery provides an innovative perspective for enhancing early brucellosis screening in endemic regions. CLINICAL TRIAL: Not applicable.

Indexed as

Antigens, BacterialBacterial Outer Membrane ProteinsBrucella melitensisBrucellosisAntibodies, BacterialEnzyme-Linked Immunosorbent AssayEpitopes, B-LymphocyteEscherichia coliHumansRecombinant ProteinsSensitivity and SpecificityAntibodies, BacterialAntigens, BacterialBacterial Outer Membrane ProteinsEpitopes, B-LymphocyteRecombinant ProteinsBioinformaticsBrucellosisDiagnosticsELISAProkaryotic expression

Identifiers

PMID41422198
PMCPMC12836974

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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.