Iwaisako Yuki, Shimizu Karin, Suzuki Youichi, Nakano Takashi, Fujimuro Masahiro
Department of Cell Biology, Kyoto Pharmaceutical University, Kyoto, Japan.
Department of Microbiology and Infection Control, Faculty of Medicine, Osaka Medical and Pharmaceutical University, Osaka, Japan.
Microbiol Spectr. 2025 Sep 9:e0330824. doi: 10.1128/spectrum.03308-24.
Kaposi's sarcoma-associated herpesvirus (KSHV) belongs to the Gammaherpesvirinae subfamily. During the lytic phase of herpesviruses, viral capsids form in the host cell nucleus, and the replicated viral genome is packaged into these capsids. The herpesviral genome is replicated as a precursor head-to-tail concatemer consisting of tandemly repeated genomic units, each flanked by terminal repeats (TRs). The herpesvirus terminase complex packages a single genomic unit into a capsid by cleaving the TRs in the precursor genome. Although the terminase complexes of alpha- and beta-herpesviruses are well characterized, the KSHV terminase complex is poorly understood. KSHV ORF7, ORF67.5, and ORF29 are thought to be components of this complex. We previously reported that KSHV deficient in either ORF7 or ORF67.5 formed immature, soccer ball-like capsids and failed to cleave the TRs, resulting in decreased virion production. Moreover, ORF7 interacted with both ORF29 and ORF67.5; however, ORF29 and ORF67.5 did not interact with each other. Thus, although ORF7 and ORF67.5 are important for KSHV terminase function, the function of ORF29 remains largely unknown. In this study, we constructed an ORF29-deficient KSHV and analyzed its virological properties. ORF29 was found to be essential for virion production and TR cleavage. Numerous immature, soccer ball-like capsids were observed in cells harboring ORF29-deficient KSHV. The N-terminal region of ORF29 was important for its interaction with ORF7, although the full-length ORF29 was required for effective assembly of the KSHV terminase complex. Furthermore, ORF29 preferentially interacted with itself rather than with ORF7. Thus, our data show that ORF29 functions as a fundamental component of the terminase complex.IMPORTANCEBecause the role of ORF29 in the Kaposi's sarcoma-associated herpesvirus (KSHV) terminase complex remains unknown, we constructed ORF29-deficient KSHV. Our results demonstrated that ORF29 functions as a component of the KSHV terminase and is essential for mature capsid formation, terminal repeat (TR) cleavage, and terminase complex assembly. Moreover, ORF29 strongly interacted with itself. In herpes simplex virus 1 (HSV-1), the terminase complex (comprising UL15, UL28, and UL33) forms a trimer, and six such trimers assemble into a hexameric ring. The HSV-1 genome passes through this ring and undergoes TR cleavage and genome packaging into a capsid. The self-interaction of ORF29 may be involved in the multimerization of the terminase complex or in the formation of the KSHV terminase ring.
卡波西肉瘤相关疱疹病毒(KSHV)属于γ疱疹病毒亚科。在疱疹病毒的裂解期,病毒衣壳在宿主细胞核中形成,复制的病毒基因组被包装到这些衣壳中。疱疹病毒基因组以前体头对头串联体的形式进行复制,该串联体由串联重复的基因组单元组成,每个单元两侧都有末端重复序列(TRs)。疱疹病毒末端酶复合物通过切割前体基因组中的TRs将单个基因组单元包装到衣壳中。尽管α和β疱疹病毒的末端酶复合物已得到充分表征,但对KSHV末端酶复合物的了解却很少。KSHV的ORF7、ORF67.5和ORF29被认为是该复合物的组成成分。我们之前报道过,缺乏ORF7或ORF67.5的KSHV会形成不成熟的、足球状的衣壳,并且无法切割TRs,导致病毒粒子产量下降。此外,ORF7与ORF29和ORF67.5都相互作用;然而,ORF29和ORF67.5彼此之间不相互作用。因此,尽管ORF7和ORF67.5对KSHV末端酶功能很重要,但ORF29的功能在很大程度上仍然未知。在本研究中,我们构建了缺失ORF29的KSHV,并分析了其病毒学特性。结果发现ORF29对病毒粒子的产生和TR切割至关重要。在含有缺失ORF29的KSHV的细胞中观察到大量不成熟的、足球状的衣壳。ORF29的N端区域对其与ORF7的相互作用很重要,尽管KSHV末端酶复合物的有效组装需要全长的ORF29。此外,ORF29优先与自身相互作用,而不是与ORF7相互作用。因此,我们的数据表明ORF29作为末端酶复合物的基本组成成分发挥作用。
重要性
由于ORF29在卡波西肉瘤相关疱疹病毒(KSHV)末端酶复合物中的作用仍然未知,我们构建了缺失ORF29的KSHV。我们的结果表明,ORF29作为KSHV末端酶的一个组成成分发挥作用,对成熟衣壳的形成、末端重复序列(TR)的切割以及末端酶复合物的组装至关重要。此外,ORF29与自身强烈相互作用。在单纯疱疹病毒1(HSV - 1)中,末端酶复合物(由UL15、UL28和UL33组成)形成三聚体,六个这样的三聚体组装成一个六聚体环。HSV - 1基因组穿过这个环,进行TR切割并将基因组包装到衣壳中。ORF29的自我相互作用可能参与末端酶复合物的多聚化或KSHV末端酶环的形成。