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一种新型H基因型野生型腮腺炎病毒株的鉴定及其与其他强毒株和减毒株的分子亲缘关系。

Identification of a new genotype H wild-type mumps virus strain and its molecular relatedness to other virulent and attenuated strains.

作者信息

Amexis Georgios, Rubin Steven, Chatterjee Nando, Carbone Kathryn, Chumakov Kostantin

机构信息

Center for Biologics Evaluation and Research, FDA, Rockville, Maryland, USA.

出版信息

J Med Virol. 2003 Jun;70(2):284-6. doi: 10.1002/jmv.10392.

Abstract

A single clinical isolate of mumps virus designated 88-1961 was obtained from a patient hospitalized with a clinical history of upper respiratory tract infection, parotitis, severe headache, fever and lymphadenopathy. We have sequenced the full-length genome of 88-1961 and compared it against all available full-length sequences of mumps virus. Based upon its nucleotide sequence of the SH gene 88-1961 was identified as a genotype H mumps strain. The overall extent of nucleotide and amino acid differences between each individual gene and protein of 88-1961 and the full-length mumps samples showed that the missense to silent ratios were unevenly distributed. Upon evaluation of the consensus sequence of 88-1961, four positions were found to be clearly heterogeneous at the nucleotide level (NP 315C/T, NP 318C/T, F 271A/C, and HN 855C/T). Sequence analysis revealed that the amino acid sequences for the NP, M, and the L protein were the most conserved, whereas the SH protein exhibited the highest variability among the compared mumps genotypes A, B, and G. No identifying molecular patterns in the non-coding (intergenic) or coding regions of 88-1961 were found when we compared it against relatively virulent (Urabe AM9 B, Glouc1/UK96, 87-1004 and 87-1005) and non-virulent mumps strains (Jeryl Lynn and all Urabe Am9 A substrains).

摘要

一株名为88 - 1961的腮腺炎病毒临床分离株,取自一名因上呼吸道感染、腮腺炎、严重头痛、发热及淋巴结病病史而住院的患者。我们已对88 - 1961的全长基因组进行测序,并将其与所有现有的腮腺炎病毒全长序列进行比较。根据其SH基因的核苷酸序列,88 - 1961被鉴定为H基因型腮腺炎毒株。88 - 1961的每个基因和蛋白质与全长腮腺炎病毒样本之间核苷酸和氨基酸差异的总体程度表明,错义与沉默比率分布不均。在评估88 - 1961的共有序列时,发现有四个位置在核苷酸水平上明显异质(NP 315C/T、NP 318C/T、F 271A/C和HN 855C/T)。序列分析显示,NP、M和L蛋白的氨基酸序列最为保守,而SH蛋白在比较的腮腺炎A、B和G基因型中表现出最高的变异性。当我们将88 - 1961与相对强毒的(Urabe AM9 B、Glouc1/UK96、87 - 1004和87 - 1005)和无毒的腮腺炎毒株(Jeryl Lynn和所有Urabe Am9 A亚毒株)进行比较时,在88 - 1961的非编码(基因间)或编码区域未发现识别分子模式。

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