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首页> 外文期刊>Veterinary Parasitology >Molecular characterization of Cryptosporidium spp. in pre-weaned dairy calves in the Czech Republic: Absence of C. ryanae and management-associated distribution of C. andersoni, C. bovis and C. parvum subtypes
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Molecular characterization of Cryptosporidium spp. in pre-weaned dairy calves in the Czech Republic: Absence of C. ryanae and management-associated distribution of C. andersoni, C. bovis and C. parvum subtypes

机译:隐孢子虫的分子表征。捷克共和国断奶的奶牛犊中的黑麦草:黑麦草假单胞菌的缺乏和与管理相关的C. andersoni,C。bovis和C. parvum亚型的分布

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A total of 750 faecal samples of dairy calves at up to 2 months of age kept in various housing systems were screened for Cryptosporidium spp. infection using the aniline-carbol-methyl violet staining method. DNA was extracted from Cryptosporidium positive samples and from 150 randomly selected microscopically negative samples. Nested PCR was performed to amplify the partial SSU rRNA gene of Cryptosporidium that was subsequently digested by SspI, VspI and MboII restriction enzymes to determine the present Cryptosporidium species and genotype. In addition, the samples characterized as Cryptosporidium parvum were subsequently analyzed at the GP60 gene to determine the distribution of zoonotic subtypes. Sequence analyses and RFLP identified C. parvum in 137. Cryptosporidium andersoni in 21 and Cryptosporidium bovis in 3 samples. Neither mixed infections nor Cryptosporidium ryanae was detected. Sequencing of the GP60 gene from C. parvum-positive samples revealed all five subtypes of family IIa (A15G2R1, A16G1R1, A22G1R1, A18G1R1, and A15G1R1). The obvious management-associated distribution of Cryptosporidium spp. was demonstrated. Direct contact with adult animals was found to be a risky factor for C. andersoni and C bovis infection. IIaA15G2R1 and IIaA16G1R1 were detected as major subtypes, whereas only the IIaA16G1R1 subtype was found in animals kept in boxes. Three of the five detected subtypes were previously associated with human cryptosporidiosis, and moreover, the IIaA15G1R1 subtype, previously reported in humans only, was detected in calves for the first time
机译:筛选了在各种住房系统中保存的最多2个月龄的750头小牛粪便样本,以检测隐孢子虫属。感染使用苯胺-甲醇-甲基紫染色方法。从隐孢子虫阳性样品和150个随机选择的显微镜阴性样品中提取DNA。进行巢式PCR以扩增隐孢子虫的部分SSU rRNA基因,其随后被SspI,VspI和MboII限制性酶消化,以确定当前的隐孢子虫种类和基因型。此外,随后在GP60基因上分析了特征为小隐孢子虫的样品,以确定人畜共患病亚型的分布。序列分析和RFLP在137个样品中鉴定了小隐孢子虫。在21个样品中鉴定了安德森隐孢子虫,在3个样品中鉴定了牛隐孢子虫。既没有检测到混合感染,也没有检测到隐孢子虫。从小球藻阳性样本的GP60基因测序揭示了IIa家族的所有五个亚型(A15G2R1,A16G1R1,A22G1R1,A18G1R1和A15G1R1)。隐孢子虫的明显与管理相关的分布。被证明。发现与成年动物直接接触是C. andersoni和C. bovis感染的危险因素。 IIaA15G2R1和IIaA16G1R1被检测为主要亚型,而仅IIaA16G1R1亚型在保存在盒子中的动物中被发现。在五个检测到的亚型中,有三个先前与人类隐孢子虫病有关,此外,以前仅在人类中报告的IIaA15G1R1亚型是首次在犊牛中检测到

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