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从巴西疫苗相关病例中分离出的2型脊髓灰质炎病毒的基因组特征分析。

Genomic characterization of type 2 polioviruses isolated from vaccine-associated cases in Brazil.

作者信息

Friedrich F, Filippis A M, Ferreira F C, Schatzmayr H G, Da-Silva E E

机构信息

Departamento de Virologia, Instituto Oswaldo Cruz, Fiocruz, Rio de Janeiro, Brasil.

出版信息

Braz J Med Biol Res. 1995 Jul;28(7):733-42.

PMID:8580863
Abstract

Twenty strains of P2/Sabin-related polioviruses isolated in Brazil were analyzed; ten from persistent paralytic poliomyelitis cases, three from suspected polio cases with transient paralysis, and seven from healthy contacts. The serotypes of the viral isolates were identified by the neutralization test with hyperimmune equine sera. The relationship of the isolates to the P2/Sabin strain was demonstrated by molecular hybridization and polymerase chain reaction (PCR). Partial sequencing demonstrated mutations at nucleotide 481 in the 5' noncoding region and at amino acid 143 of the capsid protein VP1 in most of these isolates from vaccine-associated cases in Brazil. These data support previous studies on the importance of mutations at these attenuated determinants in the establishment of the disease. However, the existence of isolates without mutations at these positions suggests that they are not essential. The results also strengthen the possibility of the participation of a mutation at nucleotide 398 in the establishment of the disease, and suggest that a mutation at nucleotide 491 or 500 may also be involved in this process. The isolates from healthy contacts presented the same mutations as the isolates from vaccine-associated cases with which they were in contact. This strengthens the observation that, although mutations in the genome of the P2/Sabin strain are important for the establishment of the disease, host factors are also involved.

摘要

对在巴西分离出的20株P2/Sabin相关脊髓灰质炎病毒进行了分析;其中10株来自持续性麻痹性脊髓灰质炎病例,3株来自伴有短暂麻痹的疑似脊髓灰质炎病例,7株来自健康接触者。通过用超免疫马血清进行中和试验来鉴定病毒分离株的血清型。通过分子杂交和聚合酶链反应(PCR)证明了分离株与P2/Sabin株的关系。部分测序显示,在巴西这些与疫苗相关病例的大多数分离株中,5'非编码区的核苷酸481以及衣壳蛋白VP1的氨基酸143处存在突变。这些数据支持了先前关于这些减毒决定簇处的突变在疾病发生中的重要性的研究。然而,在这些位置没有突变的分离株的存在表明它们并非必不可少。结果还强化了核苷酸398处的突变参与疾病发生的可能性,并表明核苷酸491或500处的突变也可能参与这一过程。来自健康接触者的分离株与他们所接触的与疫苗相关病例的分离株具有相同的突变。这强化了以下观察结果,即尽管P2/Sabin株基因组中的突变对疾病发生很重要,但宿主因素也起作用。

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