Kinetics of baculovirus replication and release using real-time quantitative polymerase chain reaction


Autoria(s): Rosinski, Matthew; Reid, Steven; Nielsen, Lars Keld
Data(s)

01/01/2002

Resumo

The study of viral-based processes is hampered by (a) their complex, transient nature, (b) the instability of products, and (c) the lack of accurate diagnostic assays. Here, we describe the use of real-time quantitative polymerase chain reaction to characterize baculoviral infection. Baculovirus DNA content doubles every 1.7 h from 6 h post-infection until replication is halted at the onset of budding. No dynamic equilibrium exists between replication and release, and the kinetics are independent of the cell density at the time of infection. No more than 16% of the intracellular virus copies bud from the cell. (C) 2002 John Wiley & Sons, Inc. Biotechnol Bioeng 77: 476-480, 2002; DOI 10.1002/bit.10126.

Identificador

http://espace.library.uq.edu.au/view/UQ:62592

Idioma(s)

eng

Publicador

John Wiley & Sons Inc

Palavras-Chave #Biotechnology & Applied Microbiology #Real-time Quantitative Pcr #Baculovirus #Replication Kinetics #Insect Cell #Dna Polymerase #Viral Dynamics #Nuclear Polyhedrosis-virus #Viral-dna Synthesis #Spodoptera-frugiperda #Insect Cells #Infection #Assay #Pcr #C1 #270805 Genetic Engineering and Enzyme Technology #670403 Treatments (e.g. chemicals, antibiotics)
Tipo

Journal Article