Khetawat D, Dutta P, Gupta S, Chakrabarti S
National Institute of Cholera and Enteric Diseases, Calcutta, India.
Intervirology. 2001;44(5):306-10. doi: 10.1159/000050062.
Rotavirus RNAs from the fecal samples were hybridized with cDNAs specific for G1 and G2 genotypes. 59 out of 138 samples (42.7%) did not hybridize with either probe. The cDNAs coding for VP7 and VP4 from one such sample, SC134, were synthesized by combined reverse transcriptase/polymerase chain reaction (PCR) using specific oligonucleotide primers and were used as probes to screen those local isolates which did not hybridize with either G1 or G2. 26/59 (44%) of fecal RNA hybridized with these cDNAs indicating a possible emergence of this strain in this part of India. The VP7 and VP4 genotype specificity of SC134 was found to be G4P8 by multiplex PCR. The VP7 gene of SC134 was cloned and characterized in detail by restriction enzyme digestion and DNA sequence analysis. Comparison of nucleotide and predicted amino acid sequence of the VP7 gene of SC134 with other serotypes revealed that the VP7 gene of SC134 was closely related to G4. However, amio acids within the VP7 sequence differed in seven positions with that of both the subtype 'A' and 'B' of the G4 serotype. To establish the relation of this emerging strain with the other reported G4 strains, a phylogenetic tree was constructed and SC134 was found to be more closely related to the ST3 strain isolated in England and included in the tetravalent vaccine formulation along with two Japanese strains, although all four were distinct and did not form any cluster as was evident by the horizontal distance separating them. The VP7 gene sequence of SC134 was submitted to EMBL and was assigned the accession number AJ278217.
将粪便样本中的轮状病毒RNA与G1和G2基因型特异性的cDNA进行杂交。138个样本中有59个(42.7%)未与任何一种探针杂交。使用特异性寡核苷酸引物通过逆转录酶/聚合酶链反应(PCR)组合合成了来自一个此类样本SC134的编码VP7和VP4的cDNA,并将其用作探针来筛选那些未与G1或G2杂交的本地分离株。59份粪便RNA中的26份(44%)与这些cDNA杂交,表明该毒株可能在印度的这一地区出现。通过多重PCR发现SC134的VP7和VP4基因型特异性为G4P8。对SC134的VP7基因进行克隆,并通过限制性酶切和DNA序列分析进行详细表征。将SC134的VP7基因的核苷酸序列和预测的氨基酸序列与其他血清型进行比较,发现SC134的VP7基因与G4密切相关。然而,VP7序列中的氨基酸在7个位置上与G4血清型的“A”和“B”亚型均不同。为了确定这种新出现的毒株与其他已报道的G4毒株的关系,构建了系统发育树,发现SC134与在英国分离的ST3毒株关系更密切,ST3毒株与两个日本毒株一起被纳入四价疫苗配方中,尽管这四个毒株各不相同,且未形成任何聚类,这一点从它们之间的水平距离可以明显看出。SC134的VP7基因序列已提交至EMBL,登录号为AJ278217。