Laboratory of Hepatitis and Related Emerging Agents, DETTD-OBRR, Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, Maryland 20892, USA.
J Virol. 2010 Aug;84(16):8342-7. doi: 10.1128/JVI.01470-09. Epub 2010 Jun 9.
Hepatitis A virus (HAV), an atypical member of the Picornaviridae, grows poorly in cell culture. To define determinants of HAV growth, we introduced a blasticidin (Bsd) resistance gene into the virus genome and selected variants that grew at high concentrations of Bsd. The mutants grew fast and had increased rates of RNA replication and translation but did not produce significantly higher virus yields. Nucleotide sequence analysis and reverse genetic studies revealed that a T6069G change resulting in a F42L amino acid substitution in the viral polymerase (3D(pol)) was required for growth at high Bsd concentrations whereas a silent C7027T mutation enhanced the growth rate. Here, we identified a novel determinant(s) in 3D(pol) that controls the kinetics of HAV growth.
甲型肝炎病毒(HAV)是微小 RNA 病毒科的一个非典型成员,在细胞培养中生长不良。为了确定 HAV 生长的决定因素,我们将博来霉素(Bsd)抗性基因引入病毒基因组,并选择在高浓度 Bsd 下生长的变异体。突变体生长迅速,RNA 复制和翻译率增加,但病毒产量没有显著提高。核苷酸序列分析和反向遗传学研究表明,在病毒聚合酶(3D(pol))中导致 F42L 氨基酸取代的 T6069G 变化是在高 Bsd 浓度下生长所必需的,而沉默的 C7027T 突变则增强了生长速度。在这里,我们确定了 3D(pol)中控制 HAV 生长动力学的新决定因素。