Identification and profiling of Trichinella spiralis circulating antigens and proteins in sera of mice with trichinellosis
0301 basic medicine
Science
Trichinella
Immunology
Antibodies, Helminth
Muscle Proteins
Enzyme-Linked Immunosorbent Assay
FOS: Health sciences
Global Impact of Helminth Infections and Control Strategies
Mice
Ecological Interactions of Parasites in Ecosystems
03 medical and health sciences
Virology
Helminths
Health Sciences
Animals
Biology
Parasitic Diseases and Treatment Strategies
Antibody
Trichinella spiralis
Immunology and Microbiology
0303 health sciences
Ecology
FOS: Clinical medicine
Q
R
Life Sciences
Trichinosis
Trichinellosis
Helminth Proteins
3. Good health
Infectious Diseases
Immune system
Antigens, Helminth
Larva
FOS: Biological sciences
Antigen
Environmental Science
Physical Sciences
Medicine
Parasitology
Research Article
DOI:
10.1371/journal.pone.0265013
Publication Date:
2022-03-10T18:36:25Z
AUTHORS (5)
ABSTRACT
Trichinellosis is a zoonotic disease caused by the ingestion of the Trichinella nematode. With a worldwide incidence of approximately 10,000 cases per year, Trichinella spiralis is responsible for most human infections. There are no specific signs or symptoms of this parasitic infection. Muscle biopsy is the gold diagnostic standard for trichinellosis, but the technique is invasive and unable to detect the early stage of infection. Although immunodiagnostics are also available, antibody detection usually occurs after 3 weeks and prolonged up to 19 years after the acute phase. Therefore, additional diagnostic biomarkers must be identified to improve trichinellosis diagnosis. This study aimed to measure concentration changes in mouse serum proteins prior to T. spiralis infection and 2, 4 and 8 weeks after infection, and to identify T. spiralis circulating proteins and antigens using mass spectrometry-based proteomics. Mouse muscle-related proteins including inter-alpha-trypsin inhibitor heavy chain H2, a protein involved in the response to muscle tissue damage, were up-regulated in mouse sera during the T. spiralis larvae invasion. Additionally, 33 circulatory parasite proteins were identified in infected mouse sera. Notably, T. spiralis long-chain fatty acid transport protein 1 could be detected in the early stage of infection and peroxidasin-like protein was identified 2, 4 and 8 weeks after infection. Seventeen T. spiralis circulating antigens were detected in mouse immune complexes, with PX domain protein being found 2, 4 and 8 weeks after infection. Because peroxidasin-like protein and PX domain protein were detected at all post-infection time points, sequence alignments of these proteins were performed, which showed they are conserved among Trichinella spp. and have less similarity to the human and murine sequences. Integrative analysis of T. spiralis biomarkers throughout the course of infection may reveal additional diagnostic targets to improve early diagnosis of trichinellosis.
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