Viral vectors
Viral vectors are tools commonly used by molecular biologists to deliver genetic material into cells. This process can be performed inside a living organism (in vivo) or in cell culture (in vitro). Viruses have evolved specialized molecular mechanisms to efficiently transport their genomes inside the cells they infect. Delivery of genes by a virus is termed transduction and the infected cells are described as transduced.
Types of viral vectors[edit | edit source]
There are several types of viral vectors that can be used for gene delivery. These include retroviral vectors, lentiviral vectors, adenoviral vectors, adeno-associated viral vectors, and herpes simplex viral vectors.
Retroviral vectors[edit | edit source]
retroviral vectors are derived from retroviruses. They have the ability to integrate their genetic material into the genome of the host cell, which allows for long-term expression of the transgene.
Lentiviral vectors[edit | edit source]
Lentiviral vectors are a type of retrovirus that can infect both dividing and non-dividing cells. This makes them useful for gene delivery to tissues with slow cell turnover, such as the brain.
Adenoviral vectors[edit | edit source]
Adenoviral vectors are derived from adenoviruses. They do not integrate their genetic material into the host genome and are therefore used for short-term expression of the transgene.
Adeno-associated viral vectors[edit | edit source]
Adeno-associated viral vectors are derived from the adeno-associated virus. They can infect both dividing and non-dividing cells and can result in long-term expression of the transgene.
Herpes simplex viral vectors[edit | edit source]
Herpes simplex viral vectors are derived from the herpes simplex virus. They have a large capacity for foreign genetic material but can be cytotoxic.
Applications[edit | edit source]
Viral vectors have many applications in biotechnology, including gene therapy, vaccine development, and basic biological research.
Safety and ethical considerations[edit | edit source]
The use of viral vectors for gene delivery raises several safety and ethical considerations, including the potential for immunogenicity, oncogenesis, and off-target effects.
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Contributors: Prab R. Tumpati, MD