Packaging capacity and stability of human adenovirus type 5 vectors - PubMed (original) (raw)
Packaging capacity and stability of human adenovirus type 5 vectors
A J Bett et al. J Virol. 1993 Oct.
Abstract
Adenovirus vectors are extensively used for high-level expression of proteins in mammalian cells and are receiving increasing attention for their potential use as live recombinant vaccines and as transducing viruses for use in gene therapy. Although it is commonly argued that one of the chief advantages of adenovirus vectors is their relative stability, this has not been thoroughly investigated. To examine the genetic stability of adenovirus type 5 vectors and in particular to examine the relationship between genetic stability and genome size, adenovirus vectors were constructed with inserts of 4.88 (herpes simplex virus type 1 gB), 4.10 (herpes simplex virus type 1 gB), or 3.82 (LacZ) kb combined with a 1.88-kb E3 deletion or with a newly generated 2.69-kb E3 deletion. The net excess of DNA over the wild-type (wt) genome size ranged from 1.13 to 3.00 kb or 3.1 to 8.3%. Analysis of these vectors during serial passage in tissue culture revealed that when the size exceeded 105% of the wt genome length by approximately 1.2 kb (4.88-kb insert combined with a 1.88-kb deletion), the resulting vector grew very poorly and underwent rapid rearrangement, resulting in loss of the insert after only a few passages. In contrast, vectors with inserts resulting in viral DNA close to or less than a net genome size of 105% of that of the wt grew well and were relatively stable. In general, viruses with genomes only slightly above 105% of that of the wt were unstable and the rapidity with which rearrangement occurred correlated with the size of the insert. These findings suggest that there is a relatively tight constraint on the amount of DNA which can be packaged into virions and that exceeding the limit results in a sharply decreased rate of virus growth. The resultant strong selection for variants which have undergone rearrangement, generating smaller genomes, is manifested as genetic instability of the virus population.
Similar articles
- A helper-dependent system for adenovirus vector production helps define a lower limit for efficient DNA packaging.
Parks RJ, Graham FL. Parks RJ, et al. J Virol. 1997 Apr;71(4):3293-8. doi: 10.1128/JVI.71.4.3293-3298.1997. J Virol. 1997. PMID: 9060698 Free PMC article. - Development of a recombinant adenovirus vector production system free of replication-competent adenovirus by utilizing a packaging size limit of the viral genome.
Suzuki T, Sasaki T, Yano K, Sakurai F, Kawabata K, Kondoh M, Hayakawa T, Yagi K, Mizuguchi H. Suzuki T, et al. Virus Res. 2011 Jun;158(1-2):154-60. doi: 10.1016/j.virusres.2011.03.026. Epub 2011 Apr 4. Virus Res. 2011. PMID: 21470569 - Foreign gene expression by human adenovirus type 5-based vectors studied using firefly luciferase and bacterial beta-galactosidase genes as reporters.
Mittal SK, Bett AJ, Prevec L, Graham FL. Mittal SK, et al. Virology. 1995 Jun 20;210(1):226-30. doi: 10.1006/viro.1995.1337. Virology. 1995. PMID: 7793076 - Adenovirus vectors as potential vaccines against herpes simplex virus.
Johnson DC. Johnson DC. Rev Infect Dis. 1991 Nov-Dec;13 Suppl 11:S912-6. doi: 10.1093/clind/13.supplement_11.s912. Rev Infect Dis. 1991. PMID: 1664127 Review. - On the stability of sequences inserted into viral genomes.
Willemsen A, Zwart MP. Willemsen A, et al. Virus Evol. 2019 Nov 14;5(2):vez045. doi: 10.1093/ve/vez045. eCollection 2019 Jul. Virus Evol. 2019. PMID: 31741748 Free PMC article. Review.
Cited by
- Construction and Stability of All-in-One Adenovirus Vectors Simultaneously Expressing Four and Eight Multiplex Guide RNAs and Cas9 Nickase.
Nakahara T, Tabata H, Kato Y, Fuse R, Nakamura M, Yamaji M, Hattori N, Kiyono T, Saito I, Nakanishi T. Nakahara T, et al. Int J Mol Sci. 2024 Aug 12;25(16):8783. doi: 10.3390/ijms25168783. Int J Mol Sci. 2024. PMID: 39201470 Free PMC article. - One-Step Genetic Modification by Embryonic Doral Aorta Injection of Adenoviral CRISPR/Cas9 Vector in Chicken.
Qin C, Jiang S, Xu K, Zhu J, Wang L, Yang W, Xiao F, Yang K, Huang Q, Meng H. Qin C, et al. Int J Mol Sci. 2024 Aug 9;25(16):8692. doi: 10.3390/ijms25168692. Int J Mol Sci. 2024. PMID: 39201387 Free PMC article. - User-Friendly Replication-Competent MAdV-1 Vector System with a Cloning Capacity of 3.3 Kilobases.
Zhang Z, Guo X, Hou W, Zou X, Wang Y, Liu S, Lu Z. Zhang Z, et al. Viruses. 2024 May 11;16(5):761. doi: 10.3390/v16050761. Viruses. 2024. PMID: 38793642 Free PMC article. - Expanding the Scope of Adenoviral Vectors by Utilizing Novel Tools for Recombination and Vector Rescue.
Fischer J, Fedotova A, Bühler C, Darriba L, Schreiner S, Ruzsics Z. Fischer J, et al. Viruses. 2024 Apr 23;16(5):658. doi: 10.3390/v16050658. Viruses. 2024. PMID: 38793540 Free PMC article. - Expanding the adenovirus toolbox: reporter viruses for studying the dynamics of human adenovirus replication.
King CR, Dodge MJ, MacNeil KM, Tessier TM, Mymryk JS, Mehle A. King CR, et al. J Virol. 2024 May 14;98(5):e0020724. doi: 10.1128/jvi.00207-24. Epub 2024 Apr 19. J Virol. 2024. PMID: 38639487 Free PMC article.
References
- Adv Exp Med Biol. 1991;309B:61-6 - PubMed
- Rev Infect Dis. 1991 Nov-Dec;13 Suppl 11:S912-6 - PubMed
- Arch Virol. 1992;123(1-2):169-79 - PubMed
- Proc Natl Acad Sci U S A. 1992 Apr 1;89(7):2581-4 - PubMed
- Curr Top Microbiol Immunol. 1992;158:39-66 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources