ORIGINAL ARTICLES

Immunoproteomic analysis on the soluble antigens of Trichinella spiralis newborn larvae

  • HAO Huinan ,
  • CHENG Yongkang ,
  • ZHANG Ru ,
  • HAN Lulu ,
  • SONG Yanyan ,
  • LONG Shaorong ,
  • LIU Ruodan ,
  • ZHANG Xi ,
  • WANG Zhongquan ,
  • CUI Jing
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  • Department of Pathogens, Basic Medical College, Zhengzhou University, Zhengzhou 450001, Henan, China

Received date: 2022-07-01

  Revised date: 2022-10-04

  Online published: 2023-04-26

Supported by

National Natural Science Foundation of China(82172300);National Natural Science Foundation of China(82272367)

Abstract

Objective To identify the soluble antigens of Trichinella spiralis newborn larvae recognizable by the serum of mice infected with T. spiralis for screening candidate antigens of anti-newborn larvae vaccines. Methods The adult worms were collected from the intestine of T. spiralis-infected BALB/c mice and cultured to collect the newborn larvae, of which the soluble antigens were extracted for screening out the antigen band recognized by sera from T. spiralis-infected mice using Western blotting. The recognized antigen on the blotting band was identified by liquid chromatograph tandem mass spectrometer (LC-MS/MS), and aligned with data of T. spiralis in the Uniprot database. The physicochemical properties of identified proteins were analyzed using the bioinformatics online website. The InterProscan software was used to perform proteins sequences searches against InterPro member databases to identify signatures, and the matched terms were further subjected to gene ontology (GO) categorizing using WEGO online software. The worms at different developmental stages including muscle larvae, infectious intestinal larvae (6 h post-infection), adult worms (2 d post-infection) and newborn larvae were collected to extract total RNA,which was then reversely transcribed into cDNA. The relactive transcription levels of the C-type lectin (CTL), calreticulin (CRT), zinc finger protein (ZFP) and pyruvate kinase (PK) at four developmental stages were analyzed by qPCR using glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene as the internal reference and compared with their transcription level at muscle larval stage using one-way ANOVA. Results Western blotting showed that among the 11 protein bands of the soluble antigens of newborn larvae, 4 bands [the relative molecular mass (Mr) were 99 700, 79 600, 68 900 and 46 000] were recognized by T. spiralis-infected mice sera. A total of 353 T. spiralis proteins were identified by LC-MS/MS, of which 166 proteins (47.0%) had Mr 40 000-70 000, 182 proteins (51.8%) had isoelectric point of 5-6, 31 proteins had signal peptides and 58 proteins had transmembrane domains. Out of the 353 proteins, 285 proteins had the GO annotations, of which 177 proteins (62.1%) had catalytic activity, 192 proteins (67.4%) had binding activity, 158 proteins (55.4%) were involved in the metabolic process and 149 proteins (52.3%) were involved in the cellular process. The qPCR results showed that compared to those at the muscle larvae stage, the relative transcript level of CTL at infectious intestinal larvae, adult worm and newborn larvae stages were 140.99%, 90.99% and 65.71%, respectively (F = 1 875.105, P ˂ 0.01); the CRT were 79.33%, 41.59% and 58.58%, respectively (F = 2 192.665, P ˂ 0.01); the ZFP were 64.93%, 105.36% and 126.74%, respectively (F = 475.836, P ˂ 0.01); the PK were 73.93%, 98.09% and 43.19%, respectively (F = 1 373.743, P ˂ 0.01). Conclusion A total of 353 soluble proteins of T. spiralis newborn larvae recognized by T. spiralis-infected mice sera were identified, and these proteins may involve in the processes of growth and development, immune evasion, and invasion of the host etc, and might be the candidate target molecules for anti-newborn larvae vaccines.

Cite this article

HAO Huinan , CHENG Yongkang , ZHANG Ru , HAN Lulu , SONG Yanyan , LONG Shaorong , LIU Ruodan , ZHANG Xi , WANG Zhongquan , CUI Jing . Immunoproteomic analysis on the soluble antigens of Trichinella spiralis newborn larvae[J]. CHINESE JOURNAL OF PARASITOLOGY AND PARASITIC DISEASES, 2023 , 41(2) : 176 -182 . DOI: 10.12140/j.issn.1000-7423.2023.02.008

References

[1] Food and Agriculture Organization of the United Nations FAO/World Health Organization WHO. Multicriteria-based ranking for risk management of food-borne parasites[M]//Microbiological Risk Assessment. Rome: FAO/WHO. 2014.
[2] European Food Safety Authority, European Centre for Disease Prevention and Control. The European Union one health 2019 zoonoses report[J]. EFSA J, 2021, 19(2): e06406.
[3] Zhang XZ, Wang ZQ, Cui J. Epidemiology of trichinellosis in the People’s Republic of China during 2009—2020[J]. Acta Trop, 2022, 229: 106388.
[4] Zhang XZ, Yue WW, Bai SJ, et al. Oral immunization with attenuated Salmonella encoding an elastase elicits protective immunity against Trichinella spiralis infection[J]. Acta Trop, 2022, 226: 106263.
[5] Liu RD, Cui J, Liu XL, et al. Comparative proteomic analysis of surface proteins of Trichinella spiralis muscle larvae and intestinal infective larvae[J]. Acta Trop, 2015, 150: 79-86.
[6] Lei JJ, Hu YY, Liu F, et al. Molecular cloning and characterization of a novel peptidase from Trichinella spiralis and protective immunity elicited by the peptidase in BALB/c mice[J]. Vet Res, 2020, 51(1): 111.
[7] Tang B, Li J, Li TT, et al. Vaccines as a strategy to control trichinellosis[J]. Front Microbiol, 2022; 13: 857786.
[8] Liu RD, Jiang P, Wen H, et al. Screening and characterization of early diagnostic antigens in excretory-secretory proteins from Trichinella spiralis intestinal infective larvae by immunoproteomics[J]. Parasitol Res, 2016, 115(2): 615-622.
[9] Sun GG, Wang ZQ, Liu CY, et al. Early serodiagnosis of trichinellosis by ELISA using excretory-secretory antigens of Trichinella spiralis adult worms[J]. Parasit Vectors, 2015, 8(1): 484.
[10] Sun GG, Song YY, Jiang P, et al. Characterization of a Trichinella spiralis putative serine protease. Study of its potential as sero-diagnostic tool[J]. PloS Negl Trop Dis, 2018, 12(5): e0006485.
[11] Hu CX, Jiang P, Yue X, et al. Molecular characterization of a Trichinella spiralis elastase-1 and its potential as a diagnostic antigen for trichinellosis[J]. Parasit Vectors, 2020, 13(1): 97.
[12] Wang ZQ, Liu RD, Sun GG, et al. Proteomic analysis of Trichinella spiralis adult worm excretory-secretory proteins recognized by sera of patients with early trichinellosis[J]. Front Microbiol, 2017, 8: 986.
[13] Ren HN, Liu RD, Song YY, et al. Label-free quantitative proteomic analysis of molting-related proteins of Trichinella spiralis intestinal infective larvae[J]. Vet Res, 2019, 50(1): 70.
[14] Liu RD, Qi X, Sun GG, et al. Proteomic analysis of Trichinella spiralis adult worm excretory-secretory proteins recognized by early infection sera[J]. Vet Parasitol, 2016, 231: 43-46.
[15] Ren HN, Zhuo TX, Bai SJ, et al. Proteomic analysis of hydrolytic proteases in excretory/secretory proteins from Trichinella spiralis intestinal infective larvae using zymography combined with shotgun LC-MS/MS approach[J]. Acta Trop, 2021, 216: 105825.
[16] Xu J, Liu RD, Bai SJ, et al. Molecular characterization of a Trichinella spiralis aspartic protease and its facilitation role in larval invasion of host intestinal epithelial cells[J]. PloS Negl Trop Dis, 2020, 14(4): e0008269.
[17] Hu YY, Zhang R, Yan SW, et al. Characterization of a novel cysteine protease in Trichinella spiralis and its role in larval intrusion, development and fecundity[J]. Vet Res, 2021, 52: 113.
[18] Liu JY, Zhang NZ, Li WH, et al. Proteomic analysis of differentially expressed proteins in the three developmental stages of Trichinella spiralis[J]. Vet Parasitol, 2016, 231: 32-38.
[19] Bruschi F, Solfanelli S, Binaghi RA. Trichinella spiralis: modifications of the cuticle of the newborn larva during passage through the lung[J]. Exp Parasitol, 1992, 75(1): 1-9.
[20] Wang ZQ, Wang L, Cui J. Proteomic analysis of Trichinella spiralis proteins in intestinal epithelial cells after culture with their larvae by shotgun LC-MS/MS approach[J]. J Proteomics, 2012, 75(8): 2375-2383.
[21] Yang J, Pan W, Sun XM, et al. Immunoproteomic profile of Trichinella spiralis adult worm proteins recognized by early infection sera[J]. Parasit Vectors, 2015, 8: 20.
[22] Bruschi F, Gómez-Morales MA, Hill DE. International commission on trichinellosis: recommendations on the use of serological tests for the detection of Trichinella infection in animals and humans[J]. Food Waterborne Parasitol, 2019, 14: e00032.
[23] Robinson MW, Hutchinson AT, Dalton JP, et al. Peroxiredoxin: a central player in immune modulation[J]. Parasite Immunol, 2010, 32(5): 305-313.
[24] Zhong W, Li K, Cai Q, et al. Pyruvate kinase from Plasmodium falciparum: structural and kinetic insights into the allosteric mechanism[J]. Biochem Biophys Res Commun, 2020, 532(3): 370-376.
[25] Yue WW, Yan SW, Zhang R, et al. Characterization of a novel pyruvate kinase from Trichinella spiralis and its participation in sugar metabolism, larval molting and development[J]. PLoS Negl Trop Dis, 2022, 16(10): e0010881.
[26] Ngwa CJ, Farrukh A, Pradel G. Zinc finger proteins of Plasmodium falciparum[J]. Cell Microbiol, 2021, 23(12): e13387.
[27] Shi W, Xue C, Su XZ, et al. The roles of galectins in parasitic infections[J]. Acta Trop, 2018, 177: 97-104.
[28] Zhao L, Shao S, Chen Y, et al. Trichinella spiralis calreticulin binds human complement C1q as an immune evasion strategy[J]. Front Immunol, 2017, 8: 636.
[29] Bai SJ, Han LL, Liu RD, et al. Oral vaccination of mice with attenuated Salmonella encoding Trichinella spiralis calreticulin and serine protease 1.1 confers protective immunity in BALB/c mice[J]. PLoS Negl Trop Dis, 2022, 16(11): e0010929.
[30] Hao HN, Song YY, Ma KN, et al. A novel C-type lectin from Trichinella spiralis mediates larval invasion of host intestinal epithelial cells[J]. Vet Res, 2022, 53(1): 85.
[31] Das B, Ramnath, Dutta AK, Tandon V. Differential kinetics at PK/PEPCK branch point in the cestode, Raillietina echinobothrida[J]. Exp Parasitol, 2015, 153: 151-599.
[32] Zhang YL, Wang Y, Bai X, et al. iTRAQ-based proteomics of excretory-secretory products of Trichinella spiralis and Trichinella pseudospiralis at the muscle larva stage[J]. Chin J Parasitol Parasit Dis, 2020, 38(1): 47-53. (in Chinese)
  (张雨璐, 王洋, 白雪, 等. 旋毛虫和伪旋毛虫肌幼虫时期排泄分泌产物iTRAQ法蛋白质组学分析[J]. 中国寄生虫学与寄生虫病杂志, 2020, 38(1): 47-53.)
[33] Fu BQ, Liu MY, Kapel CM, et al. Cloning and analysis of a novel cDNA from Trichinella spiralis encoding a protein with an FYVE zinc finger domain[J]. Vet Parasitol, 2005, 132(1/2): 27-30.
[34] Li LG, Wang ZQ, Liu RD, et al. Trichinella spiralis: low vaccine potential of glutathione S-transferase against infections in mice[J]. Acta Trop, 2015, 146: 25-32.
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