Institute for Molecular Virology, University of Minnesota, Minneapolis, Minneapolis, MN 55455, USA.
Viruses. 2011 Jun;3(6):770-93. doi: 10.3390/v3060770. Epub 2011 Jun 14.
Human T-cell leukemia virus type 1 (HTLV-1) has a reputation for being extremely difficult to study in cell culture. The challenges in propagating HTLV-1 has prevented a rigorous analysis of how these viruses replicate in cells, including the detailed steps involved in virus assembly. The details for how retrovirus particle assembly occurs are poorly understood, even for other more tractable retroviral systems. Recent studies on HTLV-1 using state-of-the-art cryo-electron microscopy and fluorescence-based biophysical approaches explored questions related to HTLV-1 particle size, Gag stoichiometry in virions, and Gag-Gag interactions in living cells. These results provided new and exciting insights into fundamental aspects of HTLV-1 particle assembly-which are distinct from those of other retroviruses, including HIV-1. The application of these and other novel biophysical approaches promise to provide exciting new insights into HTLV-1 replication.
人类 T 细胞白血病病毒 1 型(HTLV-1)在细胞培养中极难研究是出了名的。在培养 HTLV-1 方面的挑战,阻碍了对这些病毒在细胞内复制的严格分析,包括病毒组装所涉及的详细步骤。即使对于其他更易于研究的逆转录病毒系统,逆转录病毒颗粒组装发生的细节也知之甚少。最近使用最先进的冷冻电子显微镜和基于荧光的生物物理方法对 HTLV-1 进行的研究,探讨了与 HTLV-1 颗粒大小、病毒粒子中 Gag 的化学计量以及活细胞中 Gag-Gag 相互作用有关的问题。这些结果为 HTLV-1 颗粒组装的基本方面提供了新的、令人兴奋的见解,这些方面与其他逆转录病毒(包括 HIV-1)不同。这些和其他新型生物物理方法的应用有望为 HTLV-1 的复制提供令人兴奋的新见解。