Immunoproteomic and mass spectrometric analysis of Eimeria acervulina antigens recognized by antisera from chickens infected with E. acervulina, E. tenella or E. necatrix

• Published in: Parasites & vectors Vol. 13; no. 1; p. 93
• Main Authors: Liu, Jin, Tuo, Wenbin, Wu, Xiangdong, Xiong, Jiaming, Yu, Enchao, Yin, Chao, Ma, Zhiwu, Liu, Liheng
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 21.02.2020; BioMed Central; BMC
• Subjects: AIDS vaccines; Antigen-antibody reactions; Antigens; Antisera; Apicomplexa; Biosynthesis; Chickens; Common immunoreactive antigens; Diseases; Dressed poultry; Drug dosages; Drug resistance; Eimeria; Eimeria acervulina; Electrophoresis; Enzymes; Gel electrophoresis; Genetic aspects; Glycerol; Immunoproteomics; Infections; Mass spectrometry; Medical research; Membranes; Observations; Parasites; Peptides; Poultry; Poultry industry; Proteins; Shock; Spectrometry; Spectroscopy; Sporozoite; Testing; Two-dimensional gel electrophoresis (2-DE); Vaccines; China; United States > US; Sporozoite; Eimeria; Common immunoreactive antigens; Mass spectrometry; Immunoproteomics; Two-dimensional gel electrophoresis (2-DE)
• ISSN: 1756-3305; 1756-3305
• DOI: 10.1186/s13071-020-3965-y

Coccidiosis is caused by Eimeria spp. and can result in severe economic losses to the global poultry industry. Due to anticoccidial drug resistance rapidly developing in the parasites and drug residues in poultry products, efficacious and safe alternative coccidia control measures are needed. The objective of the present study was to identify common protective antigens which may be used as vaccine candidates in the development of subunit, multivalent, cross-protective vaccines against most of the economically important Eimeria species. Whole sporozoite proteins of Eimeria acervulina were prepared and analyzed by 2-dimensional gel electrophoresis (2-DE) followed by western blotting using immune sera specific to E. tenella, E. acervulina, or E. necatrix. The protein spots detected by all three immune sera were then excised from the preparative gel and protein ID was performed by MALDI-TOF-MS/MS. Approximately 620 E. acervulina sporozoite protein spots were demonstrated by 2-DE with silver staining, among which 23 protein spots were recognized by immune sera specific to all three Eimeria species. The results showed that 21 putative E. acervulina proteins were identified, which include proteins with known enzymatic properties, and those which are involved in protein translation, transport and trafficking, and ribosomal biogenesis and functions. There is one protein which may be involved in transcription and one heat-shock protein. Two proteins contain predicted domains, but with no apparent functions known. There were 2 protein spots which had no detectable proteins. None of the proteins has a predicted signal peptide or a transmembrane domain; however, 6 of the 21 putative proteins were predicted to be potentially secretory through the non-classical pathway. Our study identified a diverse group of antigens immunologically common to all three Eimeria species, none of which was previously characterized and tested as a vaccine candidate. Further research on immunogenicity and cross-protective potential of these individual proteins as vaccine candidates will aid the development of vaccines against the most common and pathogenic Eimeria spp.