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鉴定负鼠(弗吉尼亚负鼠)为肉孢子虫的假定终末宿主。

Identification of opossums (Didelphis virginiana) as the putative definitive host of Sarcocystis neurona.

作者信息

Fenger C K, Granstrom D E, Langemeier J L, Stamper S, Donahue J M, Patterson J S, Gajadhar A A, Marteniuk J V, Xiaomin Z, Dubey J P

机构信息

Department of Veterinary Sciences, University of Kentucky, Lexington 40546, USA.

出版信息

J Parasitol. 1995 Dec;81(6):916-9.

PMID:8544064
Abstract

Sarcocystis neurona is an apicomplexan that causes equine protozoal myeloencephalitis (EPM) in North and South America. Horses appear to be an aberrant host, because the merozoites continually divide in the central nervous system, without encysting. The natural host species has not previously been identified. The small subunit ribosomal RNA (SSURNA) gene of S. neurona was compared to those of Sarcocystis muris, Sarcocystis cruzi, Toxoplasma gondii, and Cryptosporidium parvum to identify a unique region suitable for a species-specific amplification primer. The S. neurona SSURNA primer was used in a polymerase chain reaction (PCR) assay for the purpose of identifying this organism in feces and intestinal digest of wildlife specimens. Sporocysts were isolated from 4 raccoons (Procyon lotor), 2 opossums (Didelphis virginiana), 7 skunks (Mephitis mephitis), 6 cats (Felis catus), 1 hawk (Accipiter sp.), and 1 coyote (Canis latrans). The S. neurona SSURNA PCR assay and a control PCR assay using protist-specific primers were applied to all sporocyst DNA samples. All sporocyst DNA samples tested positive on the control assay. The SSURNA PCR assay yielded a 484-bp product only when applied to opossum samples. The SSURNA gene of both opossum sporocyst samples was sequenced to determine its relationship to the S. neurona SSURNA gene. The sequence had 99.89% similarity with S. neurona. This suggests that opossums are the definitive host of S. neurona.

摘要

肉孢子虫是一种顶复门原虫,在北美洲和南美洲可引起马的原生动物脑脊髓炎(EPM)。马似乎是异常宿主,因为裂殖子在中枢神经系统中持续分裂,并不形成包囊。此前尚未确定其天然宿主物种。将肉孢子虫的小亚基核糖体RNA(SSURNA)基因与鼠肉孢子虫、克鲁兹肉孢子虫、刚地弓形虫和微小隐孢子虫的相应基因进行比较,以确定适合物种特异性扩增引物的独特区域。肉孢子虫SSURNA引物用于聚合酶链反应(PCR)检测,目的是在野生动物标本的粪便和肠道消化物中鉴定该病原体。从4只浣熊(北美浣熊)、2只负鼠(北美负鼠)、7只臭鼬(北美臭鼬)、6只猫(家猫)、1只鹰(鹰属)和1只郊狼(犬属)中分离出孢子囊。将肉孢子虫SSURNA PCR检测和使用原生生物特异性引物的对照PCR检测应用于所有孢子囊DNA样本。所有孢子囊DNA样本在对照检测中均呈阳性。仅将SSURNA PCR检测应用于负鼠样本时,产生了一个484碱基对的产物。对两个负鼠孢子囊样本的SSURNA基因进行测序,以确定其与肉孢子虫SSURNA基因的关系。该序列与肉孢子虫的相似性为99.89%。这表明负鼠是肉孢子虫的终末宿主。

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