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对减毒的、适应小鼠的2型脊髓灰质炎病毒W-2株具有特异性的基因组区域的定位

Localization of genomic regions specific for the attenuated, mouse-adapted poliovirus type 2 strain W-2.

作者信息

Pevear D C, Oh C K, Cunningham L L, Calenoff M, Jubelt B

机构信息

Les Turner ALS Research Laboratory, Department of Neurology, Northwestern University Medical School, Chicago, Illinois 60611.

出版信息

J Gen Virol. 1990 Jan;71 ( Pt 1):43-52. doi: 10.1099/0022-1317-71-1-43.

Abstract

In order to begin to elucidate the genomic basis of the attenuation of mouse-adapted, poliovirus type 2 strain W-2 (PV2/W-2), we have cloned and sequenced the virus and compared it with the virulent, mouse-adapted PV2/Lansing strain. In addition, we have performed computer-generated comparisons of PV2/W-2 to the non-mouse-adapted, attenuated PV2/Sabin strain to determine whether mutational patterns occur that result in attenuation. The PV2/W-2 genome is 7434 nucleotides in length, which is three bases shorter than PV2/Lansing. The 5' non-coding region of PV2/W-2 is 747 nucleotides in length (compared to 744 in PV2/Lansing) and shares 98.8% identity with PV2/Lansing and 82.3% identity with PV2/Sabin. Overall, the PV2/W-2 polyprotein (2205 amino acids) is two amino acids shorter than that of either PV2/Lansing or PV2/Sabin (2207 amino acids). These contiguous deletions fall within the P3-D region (polymerase). Within these 2205 amino acid residues only 26 differences were observed between PV2/W-2 and PV2/Lansing (98.8% identity), whereas 92 occurred between PV2/W-2 and PV2/Sabin (95.8% identity). The 3' non-coding region of PV2/W-2 is 72 nucleotides in length and shares 100% identity with PV2/Lansing and 98.6% identity with PV2/Sabin. Amino acid changes in the capsid protein region occurred in neutralization sites 1 and 3, areas previously shown to be important for pathogenicity. The cleavage site between non-structural proteins P2-C/P3-A consisted of a glutamine-serine pair, in contrast to other sequenced polioviruses which have a glutamine-glycine dipeptide.

摘要

为了开始阐明适应小鼠的2型脊髓灰质炎病毒W-2株(PV2/W-2)减毒的基因组基础,我们对该病毒进行了克隆和测序,并将其与强毒的、适应小鼠的PV2/Lansing株进行比较。此外,我们利用计算机对PV2/W-2与未适应小鼠的减毒PV2/Sabin株进行了比较,以确定是否存在导致减毒的突变模式。PV2/W-2基因组长度为7434个核苷酸,比PV2/Lansing短3个碱基。PV2/W-2的5'非编码区长度为747个核苷酸(PV2/Lansing为744个核苷酸),与PV2/Lansing的同源性为98.8%,与PV2/Sabin的同源性为82.3%。总体而言,PV2/W-2多聚蛋白(2205个氨基酸)比PV2/Lansing或PV2/Sabin(均为2207个氨基酸)短两个氨基酸。这些连续缺失位于P3-D区域(聚合酶)。在这2205个氨基酸残基中,PV2/W-2与PV2/Lansing之间仅观察到26个差异(同源性98.8%),而PV2/W-2与PV2/Sabin之间有92个差异(同源性95.8%)。PV2/W-2的3'非编码区长度为72个核苷酸,与PV2/Lansing的同源性为100%,与PV2/Sabin的同源性为98.6%。衣壳蛋白区域的氨基酸变化发生在中和位点1和3,这些区域先前已被证明对致病性很重要。非结构蛋白P2-C/P3-A之间的切割位点由谷氨酰胺-丝氨酸对组成,这与其他已测序的脊髓灰质炎病毒的谷氨酰胺-甘氨酸二肽不同。

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