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在实验性中间宿主和终末宿主中从负鼠(弗吉尼亚负鼠)建立达林贝斯诺孢子虫,在细胞培养中的增殖,以及超微结构和遗传特征的描述。

Establishment of Besnoitia darlingi from opossums (Didelphis virginiana) in experimental intermediate and definitive hosts, propagation in cell culture, and description of ultrastructural and genetic characteristics.

作者信息

Dubey J P, Lindsay D S, Rosenthal B M, Sreekumar C, Hill D E, Shen S K, Kwok O C H, Rickard L G, Black S S, Rashmir-Raven A

机构信息

Parasite Biology Laboratory, Beltsville Agricultural Research Center, Animal and Natural Resources Institute, United States Department of Agriculture, Building 1001, BARC-East, Beltsville, MD 20705-2350, USA.

出版信息

Int J Parasitol. 2002 Jul;32(8):1053-64. doi: 10.1016/s0020-7519(02)00060-7.

Abstract

Besnoitia darlingi from naturally infected opossums (Didelphis virginiana) from Mississippi, USA, was propagated experimentally in mice, cats, and cell culture and was characterised according to ultrastructural, genetic, and life-history characteristics. Cats fed tissue cysts from opossums shed oocysts with a prepatent period of nine or 11 days. Oocysts, bradyzoites, or tachyzoites were infective to outbred and interferon-gamma gene knockout mice. Tachyzoites were successfully cultivated and maintained in vitro in bovine monocytes and African green monkey cells and revived after an 18-month storage in liquid nitrogen. Schizonts were seen in the small intestinal lamina propria of cats fed experimentally-infected mouse tissues. These schizonts measured up to 45 x 25 microm and contained many merozoites. A few schizonts were present in mesenteric lymph nodes and livers of cats fed tissue cysts. Ultrastructurally, tachyzoites and bradyzoites of B. darlingi were similar to other species of Besnoitia. A close relationship to B. besnoiti and an even closer relationship to B. jellisoni was indicated for B. darlingi on the basis of the small subunit and ITS-1 portions of nuclear ribosomal DNA.

摘要

从美国密西西比州自然感染的负鼠(弗吉尼亚负鼠)中分离出的达林贝斯诺球虫,在小鼠、猫和细胞培养中进行了实验性繁殖,并根据超微结构、遗传学和生活史特征进行了鉴定。喂食来自负鼠组织包囊的猫排出卵囊,潜隐期为9天或11天。卵囊、缓殖子或速殖子对远交系和干扰素-γ基因敲除小鼠具有感染性。速殖子在牛单核细胞和非洲绿猴细胞中成功地进行了体外培养和维持,并在液氮中保存18个月后复苏。在喂食实验感染小鼠组织的猫的小肠固有层中可见裂殖体。这些裂殖体大小可达45×25微米,含有许多裂殖子。在喂食组织包囊的猫的肠系膜淋巴结和肝脏中存在少量裂殖体。在超微结构上,达林贝斯诺球虫的速殖子和缓殖子与贝斯诺球虫的其他物种相似。根据核糖体DNA的小亚基和ITS-1部分,达林贝斯诺球虫与贝斯诺球虫关系密切,与杰利森贝斯诺球虫关系更为密切。

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