CHINESE JOURNAL OF PARASITOLOGY AND PARASITIC DISEASES ›› 2024, Vol. 42 ›› Issue (3): 367-371.doi: 10.12140/j.issn.1000-7423.2024.03.013

• ORIGINAL ARTICLES • Previous Articles     Next Articles

Infection status and genotype identification of Toxoplasma gondii in pigs in Jinzhong City, Shanxi Province

LI Jing1(), YANG Shufeng1, GAO Wenwei1, LIU Qing1, ZHU Xingquan1,2, ZHENG Wenbin1,*()   

  1. 1 College of Veterinary Medicine, Shanxi Agricultural University, Taigu 030801, China
    2 Key Laboratory of Veterinary Public Health of Higher Education of Yunnan Province, College of Veterinary Medicine, Yunnan Agricultural University, Kunming 650201, China
  • Received:2023-11-24 Revised:2024-02-01 Online:2024-06-30 Published:2024-07-16
  • Supported by:
    Student Research and Innovation Training Program of the College of Veterinary Medicine, Shanxi Agricultural University(J202111315);College Students’ Innovative Entrepreneurial Training of Shanxi Higher Education Institution(20220147);National Key Research and Development Program of China(2021YFC2300800);National Key Research and Development Program of China(2021YFC2300802);Special Research Fund of Shanxi Agricultural University for High-level Talents(2021XG001)

Abstract:

Objective To understand the genotype characteristics of Toxoplasma gondii in Jinzhong City, Shanxi Province, and provide a basis for the prevention and control of toxoplasmosis in pigs. Methods In 2021, pig lymphatic and muscle tissues were collected from Taigu District, Pingyao County, and Xiyang County in Jinzhong City, Shanxi Province. The genomic DNA of the samples was extracted using an animal tissue extraction kit, and the B1 gene of T. gondii was amplified and sequenced using semi-nested PCR. Using the polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) method, 12 loci including SAG1, 5'-SAG2, 3'-SAG2, alter. SAG2, SAG3, BTUB, GRA6, c22-8, c29-2, L358, PK1, and Apico were amplified from positive samples and 8 reference strains of T. gondii. The amplified fragments were digested using restriction endonucleases, and the digested products were compared with 8 international reference strains of T. gondii. Genotypes were determined by band size. Results A total of 37 positive samples of T. gondii were detected in 130 pigs in Jinzhong City, Shanxi Province, with a positive rate of 28.5% (37/130). Among them, the positive rate in Taigu District is 32.7% (18/55), Pingyao County is 26.0% (13/50), and Xiyang County is 24.0% (6/25). The positive rate of T. gondii in pig lymphoid tissue is 33.0% (33/100), and the positive rate of T. gondii in muscle tissue is 13.3% (4/30). Out of 37 positive tissues for T. gondii, one sample was successfully amplified and all loci were cleaved, identified as ToxoDB#9; One sample successfully amplified and cleaved 8 sites, suspected to be ToxoDB#9, ToxoDB#20, or ToxoDB#137; Three samples were successfully amplified and enzyme cleaved to 6 sites, suspected to be ToxoDB#9, ToxoDB#20, or ToxoDB#137; One sample successfully amplified and cleaved 8 sites, suspected to be Type I or ToxoDB#27 or ToxoDB#35; One sample successfully amplified and cleaved 6 loci, suspected to be Type I or ToxoDB#24, ToxoDB#27, or ToxoDB#35. Conclusion This study conducted molecular detection and genotype identification of T. gondii infection in pigs in Jinzhong City, Shanxi Province. The positivity rate was high, and the positivity rate in lymphoid tissue was higher than in muscle tissue. ToxoDB#9 genotype and suspected ToxoDB#9 or Type Ⅰ genotype samples were identified by PCR-RFLP.

Key words: Shanxi Province, Pig, Toxoplasma gondii, Molecular detection, Genotyping

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