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Molecular Characterization of Astroviruses by Reverse Transcriptase PCR and Sequence Analysis: Comparison of Clinical and Environmental Isolates from South Africa

机译:逆转录酶PCR和序列分析法鉴定星状病毒的分子特征:来自南非的临床和环境分离株的比较

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A comparative analysis was performed with 25 isolates of astroviruses (AstVs) detected in sewage sources and 22 concurrently identified clinical AstV isolates from the Tshwane (Pretoria) Metropolitan Area in South Africa. The samples and specimens were screened for AstVs by using an enzyme immunoassay and/or a reverse transcriptase PCR (RT-PCR) for the highly conserved untranslated region (3′ end) of the genome. The RT-PCR results were confirmed by oligonucleotide probe dot blot hybridization. Viable viruses were propagated in cell cultures for amplification when a minimal specimen was available or indeterminate sequences were obtained. AstV strains were characterized by RT-PCR and partial sequence analysis of the capsid region. The presence of multiple human AstV (HAstV) types in a single sewage sample complicated identification of individual strains, and additional type-specific RT-PCR and sequence analyses of the capsid region were required for characterization. Amplification and characterization of one genotype from a sample, therefore, did not preclude the possibility that a sample harbored additional different genotypes. Genotype and sequence information obtained from AstVs in wastewater samples were compared to information obtained from AstV strains from human stools. HAstV type 1 (HAstV-1), as well as HAstV-3, -5, -6, and -8, were identified among the clinical isolates, and HAstV-1, -2, -3, -4, -5, -7, and -8 were identified among the environmental samples. Phylogenetic analysis demonstrated that HAstV-1, -3, -5, and -8, which were present in human stool and sewage samples, clustered together, indicating that these viruses are closely related. The concurrent presence of identical HAstV strains in wastewater samples and in hospitalized patients suggests that AstVs present in the environment pose a potential risk to communities in which fecally contaminated water is used for recreational and domestic purposes.
机译:对在污水源中检测到的25种星状病毒(AstV)分离株和来自南非茨瓦内(比勒陀利亚)大都会地区的22种同时鉴定出的临床AstV分离株进行了比较分析。通过使用酶免疫测定和/或逆转录酶PCR(RT-PCR)筛选基因组中高度保守的非翻译区域(3'端)的样品和标本中的AstV。 RT-PCR结果通过寡核苷酸探针斑点印迹杂交证实。当可得到最少的标本或获得不确定的序列时,将活病毒在细胞培养物中繁殖以扩增。通过RT-PCR和衣壳区域的部分序列分析来表征AstV菌株。在单个污水样品中存在多种人类AstV(HAstV)类型使单个菌株的鉴定变得复杂,并且表征还需要其他类型特异性RT-PCR和衣壳区域的序列分析。因此,从样品中扩增和鉴定一种基因型并不排除样品包含其他不同基因型的可能性。从废水样品中的AstV获得的基因型和序列信息与从人类粪便中的AstV菌株获得的信息进行了比较。在临床分离物中鉴定出HAstV 1型(HAstV-1)以及HAstV-3,-5,-6和-8,HAstV-1,-2,-3,-4,-5,在环境样本中确定了-7和-8。系统发育分析表明,人类粪便和污水样品中存在的HAstV-1,-3,-5和-8聚集在一起,表明这些病毒密切相关。废水样品和住院患者中同时存在相同的HAstV菌株,这表明环境中存在的AstV对以粪便污染的水用于娱乐和家庭目的的社区构成潜在风险。

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