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Tolerance of Sulfolobus SMV1 virus to the immunity of I-A and III-B CRISPR-Cas systems in Sulfolobus islandicus

机译:Sulfolobus smv1病毒对苏尔菲罗氏虫岛I-A和III-B CRISPR-CAS系统的耐受性

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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.
机译:Sulfolobus Islandicus Rey15a编码一种I-A和两种III-B系统,所有型在介导核酸干扰方面都是活性的。然而,在这古古朗没有测试每个CRISPR系统对病毒感染的有效性。在这里,我们构建了S.Isollsicus菌株,其构成来自I-A,或III-B或I-A加III-B系统的抗病毒免疫,对SMV1进行了测试,并测试了每个宿主对SMV1感染的响应。我们发现,虽然累积急剧患者的患者患者的患者患者对病毒DNA复制的强烈抑制效果很大,但炎症IA克切者免疫力逐渐失去对病毒增殖的对照,允许积聚细胞病毒DNA并释放大量病毒粒子。相比之下,III-B CrispRPRPREMS对病毒DNA复制和病毒颗粒形成的紧密控制。此外,对I-A CRISPRPRE的SMV1耐受性不会因发生逃生突变而导致的,表​​明病毒可能会编码抗CRISPR蛋白(ACR)来损害宿主I-A CRISPRPREM抗扰度。这表明,嗜热古物学中病毒ACRS和CRISPR-CAS系统之间的相互作用可以成形为许多古藻病毒观察到的稳定病毒宿主关系。

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