United States Department of Agriculture, Agricultural Research Service, Beltsville Agricultural Research Center, Animal Parasitic Diseases Laboratory, Building 1001, Beltsville, MD 20705-2350, USA.
United States Department of Agriculture, Animal Plant Health Inspection Service, Wildlife Services, Harrisburg, PA 17106-0827, USA.
Vet Parasitol. 2014 Feb 24;200(1-2):74-84. doi: 10.1016/j.vetpar.2013.11.001. Epub 2013 Nov 14.
Recent studies indicated the predominance of Toxoplasma gondii haplogroup 12 in wildlife in the USA. However, still little is known of the genetic diversity of this parasite circulating in wildlife. In the present study, we tested coyotes (Canis latrans), red foxes (Vulpes vulpes), white-tailed deer (Odocoileus virginianus), and geese (Branta canadensis) from the state of Pennsylvania for T. gondii infection. Antibodies to T. gondii were found in 160 of 367 animals, including 92 (34.5%) of 266 coyotes, 49 (62.0%) of 79 white-tailed deer, 17 (85.0%) of 20 red fox, and two of two Canada geese tested by the modified agglutination test (cut off titer 1:25). Tissues from 105 seropositive animals were bioassayed in mice, and viable T. gondii was isolated from 29 animals, including 10 of 53 coyotes, 11 of 16 foxes, 7 of 49 deer, and one of one goose. DNA isolated from culture-derived tachyzoites of these isolates was characterized initially using multilocus PCR-RFLP markers. Nine genotypes were revealed, including ToxoDB PCR-RFLP #1 (4 isolates), #2 (2 isolates), #3 (4 isolates), #4 (6 isolates), #5 (4 isolates), #54 (1 isolate), #141 (1 isolate), #143 (1 isolate), and #216 (6 isolates), indicating high genetic diversity of T. gondii in wildlife in Pennsylvania. Pathogenicity of six T. gondii isolates (5 of #216 and #141) was determined in outbred Swiss Webster mice. Three of #216 and the #141 isolates were acute virulent to mice, and the other 2 #216 isolates were intermediate virulent. To determine the extent of genetic variation of these as well as a few recently reported virulent isolates from wildlife in North America, intron sequences were generated. Analysis of intron sequences and PCR-RFLP genotyping results indicated that the #216 isolates are likely derived from recombination of the clonal type I and III lineages. To determine if T. gondii virulence can be predicted by typing, we genotyped a collection of strains using PCR-RFLP markers for polymorphic genes ROP5, ROP16, ROP18 and GRA15, which are known to interact with host immune response. The results showed that there is an association of genotypes of ROP5 and ROP18 with mouse-virulence, however, additional gene(s) may also contribute to virulence in distinct T. gondii genotypes.
最近的研究表明,在美国野生动物中,弓形虫单倍群 12 占据优势。然而,目前对于在野生动物中循环的这种寄生虫的遗传多样性仍知之甚少。在本研究中,我们检测了宾夕法尼亚州的郊狼(Canis latrans)、红狐(Vulpes vulpes)、白尾鹿(Odocoileus virginianus)和鹅(Branta canadensis)是否感染了弓形虫。改良凝集试验检测到 367 只动物中有 160 只(92 只郊狼,34.5%;49 只白尾鹿,62.0%;17 只红狐,85.0%;2 只加拿大鹅,检测滴度为 1:25)抗体呈阳性。对 105 只血清阳性动物的组织进行了生物检测,在 29 只动物中分离出活的弓形虫,包括 53 只郊狼中的 10 只、16 只狐狸中的 11 只、49 只白尾鹿中的 7 只和 1 只鹅。从这些分离株的培养速殖子中提取的 DNA 最初使用多位点 PCR-RFLP 标记进行了特征描述。揭示了 9 种基因型,包括 ToxoDB PCR-RFLP #1(4 株)、#2(2 株)、#3(4 株)、#4(6 株)、#5(4 株)、#54(1 株)、#141(1 株)、#143(1 株)和#216(6 株),表明宾夕法尼亚州野生动物中的弓形虫具有很高的遗传多样性。用杂交瑞士韦伯斯特小鼠测定了六种弓形虫分离株(#216 的 5 株和#141)的致病性。#216 的 3 株和#141 株对小鼠急性毒力,而其他 2 株#216 株中度毒力。为了确定这些以及最近报道的一些来自北美的野生动物的毒力分离株的遗传变异程度,我们生成了内含子序列。对内含子序列和 PCR-RFLP 基因分型结果的分析表明,#216 分离株可能是由克隆型 I 和 III 谱系的重组产生的。为了确定通过分型是否可以预测弓形虫的毒力,我们使用 PCR-RFLP 标记对一组菌株进行了基因分型,这些标记针对与宿主免疫反应相互作用的多态性基因 ROP5、ROP16、ROP18 和 GRA15。结果表明,ROP5 和 ROP18 的基因型与小鼠毒力有关,然而,在不同的弓形虫基因型中,其他基因也可能对毒力有贡献。