» Articles » PMID: 23624118

A Rapid Q-PCR Titration Protocol for Adenovirus and Helper-dependent Adenovirus Vectors That Produces Biologically Relevant Results

Overview
Journal J Virol Methods
Specialty Microbiology
Date 2013 Apr 30
PMID 23624118
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Adenoviruses are employed in the study of cellular processes and as expression vectors used in gene therapy. The success and reproducibility of these studies is dependent in part on having accurate and meaningful titers of replication competent and helper-dependent adenovirus stocks, which is problematic due to the use of varied and divergent titration protocols. Physical titration methods, which quantify the total number of viral particles, are used by many, but are poor at estimating activity. Biological titration methods, such as plaque assays, are more biologically relevant, but are time consuming and not applicable to helper-dependent gene therapy vectors. To address this, a protocol was developed called "infectious genome titration" in which viral DNA is isolated from the nuclei of cells ~3 h post-infection, and then quantified by Q-PCR. This approach ensures that only biologically active virions are counted as part of the titer determination. This approach is rapid, robust, sensitive, reproducible, and applicable to all forms of adenovirus. Unlike other Q-PCR-based methods, titers determined by this protocol are well correlated with biological activity.

Citing Articles

Targeting host O-linked glycan biosynthesis affects Ebola virus replication efficiency and reveals differential GalNAc-T acceptor site preferences on the Ebola virus glycoprotein.

Bagdonaite I, Abdurahman S, Mirandola M, Pasqual D, Frank M, Narimatsu Y J Virol. 2024; 98(6):e0052424.

PMID: 38757972 PMC: 11237518. DOI: 10.1128/jvi.00524-24.


An optimized protocol for the generation and monitoring of conditional orthotopic lung cancer in the KP mouse model using an adeno-associated virus vector compatible with biosafety level 1.

Deng H, Ge H, Dubey C, Losmanova T, Medova M, Konstantinidou G Cancer Immunol Immunother. 2023; 72(12):4457-4470.

PMID: 37796299 PMC: 10700219. DOI: 10.1007/s00262-023-03542-z.


Rapid and stain-free quantification of viral plaque via lens-free holography and deep learning.

Liu T, Li Y, Koydemir H, Zhang Y, Yang E, Eryilmaz M Nat Biomed Eng. 2023; 7(8):1040-1052.

PMID: 37349390 PMC: 10427422. DOI: 10.1038/s41551-023-01057-7.


NEAT1-SOD2 Axis Confers Sorafenib and Lenvatinib Resistance by Activating AKT in Liver Cancer Cell Lines.

Tsuchiya H, Shinonaga R, Sakaguchi H, Kitagawa Y, Yoshida K Curr Issues Mol Biol. 2023; 45(2):1073-1085.

PMID: 36826016 PMC: 9955465. DOI: 10.3390/cimb45020071.


NEAT1 Confers Radioresistance to Hepatocellular Carcinoma Cells by Inducing PINK1/Parkin-Mediated Mitophagy.

Tsuchiya H, Shinonaga R, Sakaguchi H, Kitagawa Y, Yoshida K, Shiota G Int J Mol Sci. 2022; 23(22).

PMID: 36430876 PMC: 9692527. DOI: 10.3390/ijms232214397.


References
1.
Rots M, Curiel D, Gerritsen W, Haisma H . Targeted cancer gene therapy: the flexibility of adenoviral gene therapy vectors. J Control Release. 2003; 87(1-3):159-65. DOI: 10.1016/s0168-3659(02)00360-7. View

2.
Dorigo O, Gil J, Gallaher S, Tan B, Castro M, Lowenstein P . Development of a novel helper-dependent adenovirus-Epstein-Barr virus hybrid system for the stable transformation of mammalian cells. J Virol. 2004; 78(12):6556-66. PMC: 416543. DOI: 10.1128/JVI.78.12.6556-6566.2004. View

3.
Philipson L . Adenovirus assay by the fluorescent cell-counting procedure. Virology. 1961; 15:263-8. DOI: 10.1016/0042-6822(61)90357-9. View

4.
Harui A, Suzuki S, Kochanek S, Mitani K . Frequency and stability of chromosomal integration of adenovirus vectors. J Virol. 1999; 73(7):6141-6. PMC: 112682. DOI: 10.1128/JVI.73.7.6141-6146.1999. View

5.
Dai Y, Schwarz E, Gu D, Zhang W, Sarvetnick N, Verma I . Cellular and humoral immune responses to adenoviral vectors containing factor IX gene: tolerization of factor IX and vector antigens allows for long-term expression. Proc Natl Acad Sci U S A. 1995; 92(5):1401-5. PMC: 42527. DOI: 10.1073/pnas.92.5.1401. View