Generation of Infectious Recombinant Human Rotaviruses from Just 11 Cloned cDNAs Encoding the Rotavirus Genome
| Autor: | Takayuki Murata, Kazuhiko Katayama, Chitose Koyama, Masanori Kugita, Satoshi Komoto, Riona Hatazawa, Koki Taniguchi, Saori Fukuda |
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| Rok vydání: | 2018 |
| Předmět: |
Rotavirus
DNA Complementary viruses Immunology Genome Viral Biology Viral Nonstructural Proteins medicine.disease_cause Microbiology Genome Virus law.invention Cell Line Plasmid law Virology Complementary DNA Cricetinae medicine Animals Humans Cloning Molecular Gene Genetics Reverse genetics Genome Replication and Regulation of Viral Gene Expression Insect Science Recombinant DNA Plasmids |
| Zdroj: | Journal of virology. 93(8) |
| ISSN: | 1098-5514 |
| Popis: | The generation of recombinant group A rotaviruses (RVAs) entirely from cloned cDNAs has been described only for a single animal RVA strain, simian SA11-L2. We recently developed an optimized RVA reverse genetics system based on only RVA cDNAs (11-plasmid system), in which the concentration of cDNA plasmids containing the NSP2 and NSP5 genes is 3- or 5-fold increased in relation to that of the other plasmids. Based on this approach, we generated a recombinant human RVA (HuRVA)-based monoreassortant virus containing the VP4 gene of the simian SA11-L2 virus using the 11-plasmid system. In addition to this monoreassortant virus, authentic HuRVA (strain KU) was also generated with the 11-plasmid system with some modifications. Our results demonstrate that the 11-plasmid system involving just RVA cDNAs can be used for the generation of recombinant HuRVA and recombinant HuRVA-based reassortant viruses. IMPORTANCE Human group A rotavirus (HuRVA) is a leading pathogen causing severe diarrhea in young children worldwide. In this paper, we describe the generation of recombinant HuRVA (strain KU) from only 11 cloned cDNAs encoding the HuRVA genome by reverse genetics. The growth properties of the recombinant HuRVA were similar to those of the parental RVA, providing a powerful tool for better understanding of HuRVA replication and pathogenesis. Furthermore, the ability to manipulate the genome of HuRVAs “to order” will be useful for next-generation vaccine production for this medically important virus and for the engineering of clinical vectors expressing any foreign genes. |
| Databáze: | OpenAIRE |
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