Larva migrans in BALB/c mice experimentally infected with Toxocara cati ensured by PCR assay

被引:2
|
作者
Naderbandi, Majid [1 ]
Zibaei, Mohammad [2 ]
Haniloo, Ali [1 ]
Firoozeh, Farzaneh [3 ]
Hatami, Zahra [2 ]
Shokri, Elham [1 ]
Taira, Kensuke [4 ]
机构
[1] Zanjan Univ Med Sci, Dept Parasitol & Mycol, Sch Med, Zanjan, Iran
[2] Alborz Univ Med Sci, Sch Med, Dept Parasitol & Mycol, POB 3149779453, Karaj, Iran
[3] Alborz Univ Med Sci, Sch Med, Dept Microbiol, Karaj, Iran
[4] Azabu Univ, Sch Vet Med, Lab Parasitol, Sagamihara, Kanagawa, Japan
关键词
Toxocara cati; Larva Migrans; BALB; c mice; Microscopic larvae count; PCR; HIGH INFECTIVITY; CANIS LARVAE; MIGRATION; BEHAVIOR; HISTORY; MUSCLES; MODEL;
D O I
10.1186/s12917-022-03366-6
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Background Toxocara cati, the cat roundworm, is a parasitic nematode that known to cause toxocariasis in intermediate hosts and humans. In this study, we characterized the dynamics of T. cati larvae migration in BALB/c mice after inoculation with eggs and ensured the migration detecting the larval DNA by a PCR. To evaluate the dynamics of larval migration and distribution, twenty-four BALB/c mice were orally inoculated with 2500 T. cati infective eggs and the visceral organs of the infected animals were examined by pepsin digestion and microscopic parasite counts, followed by PCR at day 1 to 28 post-inoculation. Results The PCR assays were successfully used for detection of T. cati larvae in tissue samples and T. cati larvae and the DNAs were found in the liver, lungs, heart, kidneys and the brain. We detected T. cati in 92.2% of tissue samples by PCR, 30% higher than the conventional pepsin digestion technique. Conclusion Our findings demonstrated that the PCR assay is a sensitive and specific for the detection of T. cati larvae. Therefore, it could become a useful tool for the investigation of the dynamics of larval migration and Toxocara infection in murine model.
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页数:8
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