Veterinary Pathology, Henan Agricultural University, Zhengzhou, PR China.
Zhengzhou Zoo, Zhengzhou, PR China.
Parasitol Int. 2023 Feb;92:102687. doi: 10.1016/j.parint.2022.102687. Epub 2022 Oct 7.
Wallabies and kangaroos are susceptible to Toxoplasma gondii. However, little information concerning T. gondii infection in captive macropods is available. Three dead macropods collected from a zoo exhibited no clinical symptoms associated with toxoplasmosis. Heart fluids were tested for T. gondii antibodies using a modified agglutination test. T. gondii DNA samples derived from macropod tissues were tested by Polymerase Chain Reaction. Viable T. gondii were isolated from myocardium of macropods via mouse bioassay. Tissues (brain, lungs, or mesenteric lymph nodes) from T. gondii-positive mice were seeded into Vero cell culture flasks. The virulence of the isolated T. gondii strains was evaluated in Swiss mice. The DNA from T. gondii tachyzoites obtained from cell cultures was characterized by 10 PCR-RFLP markers and the virulence genes, ROP18 and ROP5. T. gondii antibodies were identified in two of the three macropods (Macropod5 and 7). T. gondii DNA was obtained from the heart and lungs of Macropod7. Two viable T. gondii strains were isolated from the myocardium of Macropus rufogriseus (Macropod5) and M. rufus (Macropod7) via mouse bioassay and designated as TgRooCHn2 and TgRooCHn3, respectively. TgRooCHn2 was ToxoDB genotype3, and TgRooCHn3 was ToxoDB genotyp2. Both 10 TgRooCHn2 and TgRooCHn3 tachyzoites had intermediate virulence in mice. M. rufogriseus (Macropod5) and M. rufus (Macropod7) may have been in the initial stages of toxoplasmosis, due to a recent T. gondii infection with oocysts. This study is the first to document the T. gondii ToxoDB3 isolate in macropods. T. gondii infection in captive macropods indicates the urgent need to control the transmission of this parasite in the environment, food and water of zoo animals.
袋熊和袋鼠容易感染刚地弓形虫。然而,有关圈养有袋类动物感染刚地弓形虫的信息却很少。从一家动物园收集的三只死亡的有袋类动物没有表现出与弓形虫病相关的临床症状。使用改良的凝集试验检测心脏液中的刚地弓形虫抗体。从有袋类动物组织中提取的刚地弓形虫 DNA 样本通过聚合酶链反应进行检测。通过小鼠生物测定法从有袋动物的心肌中分离出活的刚地弓形虫。将来自刚地弓形虫阳性小鼠的组织(脑、肺或肠系膜淋巴结)接种到 Vero 细胞培养瓶中。在瑞士小鼠中评估分离的刚地弓形虫株的毒力。从细胞培养物中获得的刚地弓形虫速殖子的 DNA 通过 10 个 PCR-RFLP 标记和毒力基因 ROP18 和 ROP5 进行特征分析。在三只有袋动物中的两只(Macropod5 和 7)中检测到刚地弓形虫抗体。从 Macropod7 的心脏和肺部获得刚地弓形虫 DNA。通过小鼠生物测定法从 Macropus rufogriseus(Macropod5)和 M. rufus(Macropod7)的心肌中分离出两种活的刚地弓形虫株,并分别命名为 TgRooCHn2 和 TgRooCHn3。TgRooCHn2 是 ToxoDB 基因型 3,TgRooCHn3 是 ToxoDB 基因型 2。10 个 TgRooCHn2 和 TgRooCHn3 速殖子在小鼠中的毒力均为中等。由于近期感染了卵囊,Macropus rufogriseus(Macropod5)和 M. rufus(Macropod7)可能处于弓形虫病的初始阶段。本研究首次记录了刚地弓形虫 ToxoDB3 分离株在有袋类动物中的存在。圈养有袋类动物感染刚地弓形虫表明迫切需要控制该寄生虫在动物园动物的环境、食物和水中的传播。