a Archaea Center, Department of Biology , University of Copenhagen, Copenhagen Biocenter , Copenhagen N , Denmark.
b State Key Laboratory of Agricultural Microbiology and College of Life Science and Technology , Huazhong Agricultural University , Wuhan , China.
RNA Biol. 2019 Apr;16(4):549-556. doi: 10.1080/15476286.2018.1460993. Epub 2018 Jul 9.
Sulfolobus islandicus Rey15A encodes one Type I-A and two Type III-B systems, all of which are active in mediating nucleic acids interference. However, the effectiveness of each CRISPR system against virus infection was not tested in this archaeon. Here we constructed S. islandicus strains that constitutively express the antiviral immunity from either I-A, or III-B, or I-A plus III-B systems against SMV1 and tested the response of each host to SMV1 infection. We found that, although both CRISPR immunities showed a strong inhibition to viral DNA replication at an early stage of incubation, the host I-A CRISPR immunity gradually lost the control on virus proliferation, allowing accumulation of cellular viral DNA and release of a large number of viral particles. In contrast, the III-B CRISPR immunity showed a tight control on both viral DNA replication and virus particle formation. Furthermore, the SMV1 tolerance to the I-A CRISPR immunity did not result from the occurrence of escape mutations, suggesting the virus probably encodes an anti-CRISPR protein (Acr) to compromise the host I-A CRISPR immunity. Together, this suggests that the interplay between viral Acrs and CRISPR-Cas systems in thermophilic archaea could have shaped the stable virus-host relationship that is observed for many archaeal viruses.
嗜酸热硫化叶菌 Rey15A 编码一个 I-A 型和两个 III-B 型系统,它们都能积极介导核酸干扰。然而,在这种古菌中,每个 CRISPR 系统对病毒感染的有效性尚未得到测试。在这里,我们构建了持续表达 I-A、III-B 或 I-A 和 III-B 系统抗病毒免疫的嗜酸热硫化叶菌菌株,以测试每个宿主对 SMV1 感染的反应。我们发现,尽管两种 CRISPR 免疫都在孵育的早期对病毒 DNA 复制表现出强烈的抑制作用,但宿主的 I-A CRISPR 免疫逐渐失去了对病毒增殖的控制,导致细胞内病毒 DNA 的积累和大量病毒颗粒的释放。相比之下,III-B CRISPR 免疫对病毒 DNA 复制和病毒颗粒形成都有严格的控制。此外,SMV1 对 I-A CRISPR 免疫的耐受性不是由于逃逸突变的发生,这表明病毒可能编码一种抗 CRISPR 蛋白(Acr)来破坏宿主的 I-A CRISPR 免疫。总的来说,这表明在嗜热古菌中,病毒 Acrs 和 CRISPR-Cas 系统之间的相互作用可能塑造了许多古菌病毒所观察到的稳定的病毒-宿主关系。