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猴痘病毒反向末端重复区域中的独特串联重复序列

Unique Tandem Repeats in the Inverted Terminal Repeat Regions of Monkeypox Viruses.

作者信息

Desingu Perumal Arumugam, Nagarajan K, Sundaresan Nagalingam R

机构信息

Department of Microbiology and Cell Biology, Indian Institute of Science, Bengaluru, India.

Department of Veterinary Pathology, Madras Veterinary College, Tamil Nadu Veterinary and Animal Sciences University (TANUVAS), Vepery, Chennai, Tamil Nadu, India.

出版信息

Microbiol Spectr. 2023 Mar 28;11(2):e0319922. doi: 10.1128/spectrum.03199-22.

Abstract

The genetic diversity, especially in noncoding regions between clade I, clade IIa, and clade IIb monkeypox viruses (MPXVs), is still not fully understood. Here, we report that unique 16-nucleotide-length tandem repeats in MPXVs viruses are located in the noncoding regions of inverted terminal repeats (ITR), and the copy number of this repeat is different among clade I, clade IIa, and clade IIb viruses. It is noteworthy that tandem repeats containing these specific sequences (AACTAACTTATGACTT) are only present in MPXVs and are not found in other poxviruses. Also, the tandem repeats containing these specific sequences (AACTAACTTATGACTT) do not correspond to the tandem repeats present in the human and rodent (mice and rat) genomes. On the other hand, some of the reported tandem repeats in the human and rodent (mice and rat) genomes are present in the clade IIb-B.1 lineage of MPXV. In addition, it is noteworthy that the genes flanking these tandem repeats are lost and gained compared between clade I, clade IIa, and clade IIb MPXV. The different groups of MPXVs contain unique tandem repeats with different copy numbers in the ITR regions, and these repeats may be likely to play a role in the genetic diversity of the virus. Clade IIb (B) MPXV contains 38 and 32 repeats similar to the Tandem repeats reported in the human and rodent genome, respectively. However, none of these 38 (human) and 32 (rodent) tandem repeats matched the tandem repeats (AACTAACTTATGACTT) found in the present study. Finally, when developing attenuated or modified MPXV vaccine strains, these repeats in noncoding genomic regions can be exploited to incorporate foreign proteins (adjuvants/other virus proteins/racking fluorescent proteins such as green fluorescent protein) to carry out studies such as vaccine production and virus pathogenesis.

摘要

猴痘病毒(MPXV)I 分支、IIa 分支和 IIb 分支之间的遗传多样性,尤其是非编码区的遗传多样性,目前仍未完全明确。在此,我们报告称,MPXV 病毒中独特的 16 个核苷酸长度的串联重复序列位于反向末端重复序列(ITR)的非编码区,且该重复序列的拷贝数在 I 分支、IIa 分支和 IIb 分支病毒中有所不同。值得注意的是,包含这些特定序列(AACTAACTTATGACTT)的串联重复序列仅存在于 MPXV 中,在其他痘病毒中未被发现。此外,包含这些特定序列(AACTAACTTATGACTT)的串联重复序列与人类和啮齿动物(小鼠和大鼠)基因组中的串联重复序列并不对应。另一方面,人类和啮齿动物(小鼠和大鼠)基因组中一些已报道的串联重复序列存在于 MPXV 的 IIb - B.1 分支中。此外,值得注意的是,与 I 分支、IIa 分支和 IIb 分支 MPXV 相比,这些串联重复序列两侧的基因存在丢失和获得的情况。不同组的 MPXV 在 ITR 区域包含具有不同拷贝数的独特串联重复序列,这些重复序列可能在病毒的遗传多样性中发挥作用。IIb(B)分支 MPXV 分别包含 38 个和 32 个与人类和啮齿动物基因组中报道的串联重复序列相似的重复序列。然而,这 38 个(人类)和 32 个(啮齿动物)串联重复序列均与本研究中发现的串联重复序列(AACTAACTTATGACTT)不匹配。最后,在开发减毒或改造的 MPXV 疫苗株时,可以利用基因组非编码区的这些重复序列来掺入外源蛋白(佐剂/其他病毒蛋白/追踪荧光蛋白,如绿色荧光蛋白),以开展疫苗生产和病毒致病机制等研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa19/10101126/1298159997e2/spectrum.03199-22-f001.jpg

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