Hughes P J, Evans D M, Minor P D, Schild G C, Almond J W, Stanway G
J Gen Virol. 1986 Oct;67 ( Pt 10):2093-102. doi: 10.1099/0022-1317-67-10-2093.
We have cloned and sequenced the complete genome of a strain of poliovirus type 3 (23127) isolated during an outbreak of poliomyelitis in Finland. The genome is 7435 nucleotides long excluding the 3' poly(A) stretch and is 95.5% homologous at the amino acid level to the previously sequenced type 3 strain, P3/Leon/37. The most striking feature of the presented sequence is the extent of amino acid substitutions relative to P3/Leon/37 and other type 3 strains in areas of known antigenic importance. The major antigenic determinant for virus neutralization (site 1), located at residues 89 to 100 of VP1, has three amino acid substitutions and there are six substitutions in site 3, a composite site made up of sequences from VP1 and VP3. The variation in these regions probably accounts for the observed unusual antigenicity and may explain why the virus was able to spread in a well-vaccinated community. Sequence comparisons imply that the virus is not derived from the currently used live attenuated vaccine.
我们克隆并测序了在芬兰脊髓灰质炎疫情期间分离出的一株3型脊髓灰质炎病毒(23127)的完整基因组。该基因组长度为7435个核苷酸,不包括3' 聚腺苷酸序列,在氨基酸水平上与先前测序的3型毒株P3/Leon/37有95.5%的同源性。所呈现序列最显著的特征是,在已知具有抗原重要性的区域,相对于P3/Leon/37和其他3型毒株,氨基酸替换的程度。病毒中和的主要抗原决定簇(位点1)位于VP1的第89至100位残基,有三个氨基酸替换,位点3有六个替换,位点3是由VP1和VP3的序列组成的复合位点。这些区域的变异可能解释了所观察到的异常抗原性,并可能解释了为什么该病毒能够在一个疫苗接种良好的社区中传播。序列比较表明,该病毒并非源自目前使用的减毒活疫苗。