Verma Shiv K, Minicucci Larissa, Murphy Darby, Carstensen Michelle, Humpal Carolin, Wolf Paul, Calero-Bernal Rafael, Cerqueira-Cézar Camila K, Kwok Oliver C H, Su Chunlei, Hill Dolores, Dubey Jitender P
United States Department of Agriculture, Agricultural Research Service, Beltsville Agricultural Research Center, Animal Parasitic Diseases Laboratory, Building 1001, Beltsville, Maryland, 20705-2350.
Department of Veterinary Population Medicine, College of Veterinary Medicine, University of Minnesota, 1988 Fitch Avenue, St. Paul, Minnesota, 55108.
J Eukaryot Microbiol. 2016 Sep;63(5):567-71. doi: 10.1111/jeu.12301. Epub 2016 Mar 2.
Little is known of the epidemiology of toxoplasmosis in Minnesota. Here, we evaluated Toxoplasma gondii infection in 50 wild bobcats (Lynx rufus) and 75 other animals on/near 10 cattle farms. Antibodies to T. gondii were assayed in serum samples or tissue fluids by the modified agglutination test (MAT, cut-off 1:25). Twenty nine of 50 bobcats and 15 of 41 wildlife trapped on the vicinity of 10 farms and nine of 16 adult domestic cats (Felis catus) and six of 14 domestic dogs resident on farms were seropositive. Toxoplasma gondii oocysts were not found in feces of any felid. Tissues of all seropositive wild animals trapped on the farm were bioassayed in mice and viable T. gondii was isolated from two badgers (Taxidea taxus), two raccoons (Procyon lotor), one coyote (Canis latrans), and one opossum (Didelphis virginiana). All six T. gondii isolates were further propagated in cell culture. Multi-locus PCR-RFLP genotyping using 10 markers (SAG1, SAG2 (5'-3'SAG2, and alt.SAG2), SAG3, BTUB, GRA6, c22-8, c29-2, L358, PK1, and Apico), and DNA from cell culture derived tachyzoites revealed three genotypes; #5 ToxoDataBase (1 coyote, 1 raccoon), #1 (1 badger, 1 raccoon, 1 opossum), and #2 (1 badger). This is the first report of T. gondii prevalence in domestic cats and in bobcats from Minnesota, and the first isolation of viable T. gondii from badger.
关于明尼苏达州弓形虫病的流行病学,人们所知甚少。在此,我们评估了50只野生短尾猫(猞猁)和10个奶牛场及其附近的75只其他动物的弓形虫感染情况。通过改良凝集试验(MAT,临界值1:25)检测血清样本或组织液中的弓形虫抗体。50只短尾猫中有29只、10个农场附近捕获的41只野生动物中有15只、16只成年家猫(家猫)中有9只以及农场中14只家犬中有6只血清呈阳性。在任何猫科动物的粪便中均未发现弓形虫卵囊。对农场捕获的所有血清阳性野生动物的组织进行小鼠生物测定,并从两只獾(美洲獾)、两只浣熊(浣熊)、一只郊狼(郊狼)和一只负鼠(弗吉尼亚负鼠)中分离出活的弓形虫。所有6株弓形虫分离株均在细胞培养中进一步繁殖。使用10个标记(SAG1、SAG2(5'-3'SAG2和alt.SAG2)、SAG3、BTUB、GRA6、c22-8、c29-2、L358、PK1和Apico)以及细胞培养衍生速殖子的DNA进行多位点PCR-RFLP基因分型,结果显示有三种基因型;#5 Toxo数据库(1只郊狼、1只浣熊)、#1(1只獾、1只浣熊、1只负鼠)和#2(1只獾)。这是明尼苏达州家猫和短尾猫中弓形虫流行率的首次报告,也是从獾中首次分离出活的弓形虫。