首页> 外文期刊>Progress in Biophysics and Molecular Biology: An International Review Journal >Molecular characterization of Sarcocystis spp. in intestine mucosal scrapings and fecal samples of Pampas fox (Lycalopex gymnocercus)
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Molecular characterization of Sarcocystis spp. in intestine mucosal scrapings and fecal samples of Pampas fox (Lycalopex gymnocercus)

机译:Sarcocystis SPP的分子表征。 在肠粘菌粘膜刮膜刮渣和粪便样本中(Lycalopex Gymnocercus)

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Sarcocystis spp. are obligatory intracellular protozoan parasites which can infect humans and animals. Most of Sarcocystis species were identified based on the detection of muscle cysts in different intermediate hosts (IH). Regarding to natural infection in definitive host, there are few reports which have reached to determining species of Sarcocystis. The present work was aimed to studying the occurrence of Sarcocystis spp. (oocysts and sporocysts) in mucosal scrapings of small intestine and fecal samples of one the most abundant wild canids from South America, Lycalopex gymnocercus (Pampas fox), and to identify the Sarcocystis spp. using molecular tools. A total of 131 free-living L. gymnocercus were sampled in rural areas located in several departments from Buenos Aires province, Argentina. Fecal samples from all the animals and 33 small intestines were analyzed. Fecal and mucosal scrapings samples were analyzed by sugar flotation method and once oocysts or sporocysts were detected, sedimentation was performed and DNA extracted with a commercial kit. A PCR was conducted using primers targeting a fragment of the 18S rRNA gene and the amplicons were purified and sequenced. Of the total Pampas foxes analyzed, 23 (17.6%) had Sarcocystis spp. oocysts/sporocysts in fecal and/or mucosal samples. Sarcocystis spp. sporocysts were detected in 13.0% (17/131) of fecal samples and in 39.4% (13/33) of mucosal samples by the initial sugar flotation. Twenty one L. gymnocercus samples were processed by DNA extraction and PCR. Molecular identification of Sarcocystis spp. infection was successfully achieved in 14 foxes and was distributed as follows: 4.6% S. cruzi (6/131), 3.8% Sarcocystis spp. using birds as IH (S. albifronsi and S. anasi among others, 5/131), 0.8% S. tenella (1/131) and 1.5% (2/131) with low homology (97%) with S. miescheriana. In one fecal sample with spherical oocysts, the sequencing results showed a 100% sequence identity with Hammondia heydorni. The results show that the mucosal scrapings are the eligible sample to identify prevalence and to proceed with species identification. Lycalopex gyinnocercus is suggested as definitive host for S. cruzi, S. tenella and probably various Sarcocystis spp. using birds as intermediate hosts as well as for H. heydomi.
机译:sarcocystis spp。是可能感染人类和动物的强制性细胞内原生动物寄生虫。基于在不同中间宿主(IH)中的肌肉囊肿的检测来鉴定大多数SARCOCYSTIS物种。关于最终宿主的自然感染,少数报告涉及确定Sarcocystis的种类。目前的工作旨在研究Sarcocystis SPP的发生。 (卵囊和孢子囊)在南美洲南美洲最丰富的野生羊肉的小肠和粪便样本中的粘膜刮膜,并鉴定Sarcocystis SPP。使用分子工具。在阿根廷布宜诺斯艾利斯省的几个部门,共有131名自由生活L. Gymnocercus。分析了来自所有动物和33个小肠的粪便样本。通过糖浮选方法分析粪便和粘膜刮浆样品,一旦检测到卵囊或孢子囊,就进行沉降,用商业试剂盒提取DNA。使用靶向18S rRNA基因的片段的引物进行PCR,并纯化并测序扩增子。分析的总潘帕斯狐狸中,23例(17.6%)有Sarcocystis SPP。粪便和/或粘膜样品中的卵囊/孢子囊。 sarcocystis spp。通过初始糖浮选在13.0%(17/131)次粪便样品中检测到孢子囊肿和39.4%(13/33)粘膜样品。通过DNA提取和PCR加工二十一升Gymnocercus样品。 SARCOCYSTIS SPP的分子鉴定。在14个狐狸中成功地实现了感染,分布如下:4.6%S.Cruzi(6/131),3.8%Sarcocystis SPP。使用鸟类作为IH(albifronsi和S. Anasi等,5/131),0.8%的S. Tenella(1/131)和1.5%(2/131),具有低同源性(97%),S. miescheriana。在一个具有球形卵囊的粪便样品中,测序结果显示了哈蒙迪亚Heydorni的100%序列同一性。结果表明,粘膜刮擦是符合条件的样本,以鉴定患病率并进行物种鉴定。 Lycalopex Gyinnocercus被建议为S.Cruzi,S. Tenella和可能各种Sarcocystis SPP的最终宿主。使用鸟类作为中间宿主以及H. heydomi。

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