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pmid:35004354

Proteomics Investigations of Potential Protein Biomarkers in Sera of Rabbits Infected With Schistosoma japonicum.

Nian-Nian Bi · Song Zhao · Jian-Feng Zhang · Ying Cheng · Chen-Yang Zuo · Gang-Long Yang · Kun Yang

Frontiers in cellular and infection microbiology · 2021 doi:10.3389/fcimb.2021.784279

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

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Proteomics Investigations of Potential Protein Biomarkers in Sera of Rabbits Infected With Schistosoma japonicum.
doi
10.3389/fcimb.2021.784279
pmid
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Nian-Nian Bi
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Song Zhao
[2]
Jian-Feng Zhang
[3]
Ying Cheng
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Chen-Yang Zuo
[5]
Gang-Long Yang
[6]
Kun Yang
journal
Frontiers in cellular and infection microbiology
year
2021
abstract
Schistosomiasis is a chronic parasitic disease that continues to be a pressing public health problem in many developing countries. The primary pathological damage from the disease is granuloma and fibrosis caused by egg aggregation, and early treatment can effectively prevent the occurrence of liver fibrosis. Therefore, it is very important to identify biomarkers that can be used for early diagnosis of Schistosoma japonicum infection. In this study, a label-free proteomics method was performed to observe the alteration of proteins before infection, 1 and 6 weeks after infection, and 5 and 7 weeks after treatment. A total of 10 proteins derived from S. japonicum and 242 host-derived proteins were identified and quantified as significantly changed. Temporal analysis was carried out to further analyze potential biomarkers with coherent changes during infection and treatment. The results revealed biological process changes in serum proteins compared to infection and treatment groups, which implicated receptor-mediated endocytosis, inflammatory response, and acute-phase response such as mannan-binding lectin serine peptidase 1, immunoglobulin, and collagen. These findings offer guidance for the in-depth analysis of potential biomarkers of schistosomiasis, host protein, and early diagnosis of S. japonicum and its pathogenesis. Data are available via ProteomeXchange with identifier PXD029635.
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The proteins that were significantly up- or downregulated (two-sided, unpaired Student’s t-test with equal variance assumed, p-adjust< 0.05, n = 3, | log2FC | > | log21.5 |) in at least one infected sample compared with the corresponding Ctrl are shown.
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Proteomics investigations of potential protein biomarkers in sera of rabbits infected with Schistosoma japonicum
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