4.4 Article

Codon pair bias deoptimization of essential genes in infectious laryngotracheitis virus reduces protein expression

Journal

JOURNAL OF GENERAL VIROLOGY
Volume 104, Issue 4, Pages -

Publisher

MICROBIOLOGY SOC
DOI: 10.1099/jgv.0.001836

Keywords

codon deoptimization; ICP8; ILTV; recombination; UL12

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Infectious laryngotracheitis virus (ILTV) is a respiratory pathogen of chickens that causes significant economic losses in the poultry industry and poses health and welfare concerns. This study explored two different codon deoptimization techniques to disrupt and downregulate the expression of essential ILTV genes, ICP8 and UL12. Viruses deoptimized through codon pair bias deoptimization (CPBD) showed decreased protein expression, while viruses deoptimized through codon usage deoptimization (CUD) had inconsistent results. This study demonstrates the potential of CPBD as a tool for studying essential genes in ILTV.
Infectious laryngotracheitis virus (ILTV; an alphaherpesvirus) is a respiratory pathogen of chickens and causes significant eco-nomic losses in the poultry industry globally, in addition to severe animal health and welfare concerns. To date, studying the role of ILTV genes in viral infection, replication or pathogenesis has largely been limited to genes that can be deleted from the ILTV genome and the resultant deletion mutants characterized in vitro or in vivo. However, this approach is not suitable for the study of essential genes. This study trialled two different codon deoptimization techniques that aimed to separately disrupt and downregulate the expression of two ILTV genes, ICP8 and UL12, which are essential or very important in viral replication. The target genes were partially recoded using codon usage deoptimization (CUD) and codon pair bias deoptimization (CPBD) approaches and characterized in vitro. Viruses deoptimized via CPBD showed decreased protein expression as assessed by Western blotting and/or fluorescence microscopy to measure the intensity of the fluorescent marker fused to the target protein. Viruses deoptimized by CUD showed less consistent results, with some mutants that could not be generated or isolated. The results indicate that CPBD is an attractive and viable tool for the study of essential or critically important genes in ILTV. This is the first study, to our knowledge, that utilizes CPBD and CUD techniques for the study of ILTV genes.

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