Key result
The development of viral genome editing technologies, such as BAC and the CRISPR/Cas9 system, has significantly advanced the understanding of HSV-1 tegument protein functions and vaccine development.
Genome editing technologies such as CRISPR/Cas9 provide powerful new tools for elucidating the complex functions of HSV-1 tegument proteins and developing potential vaccines.
May guide HSV-1 vaccine research; leaves open clinical translation pending prospective trials.
Herpes simplex virus 1 (HSV-1) is composed of complex structures primarily characterized by four elements: the nucleus, capsid, tegument and envelope. The tegument is an important viral component mainly distributed in the spaces between the capsid and the envelope. The development of viral genome editing technologies, such as the identification of temperature-sensitive mutations, homologous recombination, bacterial artificial chromosome, and the CRISPR/Cas9 system, has been shown to largely contribute to the rapid promotion of studies on the HSV-1 tegument protein. Many researches have demonstrated that tegument proteins play crucial roles in viral gene regulatory transcription, viral replication and virulence, viral assembly and even the interaction of the virus with the host immune system. This article briefly reviews the recent research on the functions of tegument proteins and specifically elucidates the function of tegument proteins in viral infection, and then emphasizes the significance of using genome editing technology in studies of providing new techniques and insights into further studies of HSV-1 infection in the future.
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Xu et al. (2016) conducted a review in Herpes simplex virus 1 (HSV-1) infection. Genome editing technologies (BAC, CRISPR/Cas9) was evaluated. The development of viral genome editing technologies, such as BAC and the CRISPR/Cas9 system, has significantly advanced the understanding of HSV-1 tegument protein functions and vaccine development.
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