Key result
Near-infrared fluorophore-labeled adenovirus allowed real-time in vivo tracking in mice, showing virus entering the heart within 500 milliseconds and bulk distribution completing within 3 minutes.
Why the study?
Does near-infrared fluorophore labeling allow real-time in vivo tracking of systemic adenovirus infection in mice?
Does near-infrared fluorophore labeling allow real-time in vivo tracking of systemic adenovirus infection in mice?
Near-infrared fluorophore labeling enables real-time, in vivo tracking of the rapid initial distribution of systemically injected viruses in mice.
Answers are grounded in this paper and cite their sources.
Enables real-time viral tracking in mouse models; leaves open translation to human gene therapy or other vectors.
The distribution of viruses and gene therapy vectors is difficult to assess in a living organism. For instance, trafficking in murine models can usually only be assessed after sacrificing the animal for tissue sectioning or extraction. These assays are laborious requiring whole animal sectioning to ascertain tissue localization. They also obviate the ability to perform longitudinal or kinetic studies in one animal. To track viruses after systemic infection, we have labeled adenoviruses with a near-infrared (NIR) fluorophore and imaged these after intravenous injection in mice. Imaging was able to track and quantitate virus particles entering the jugular vein simultaneous with injection, appearing in the heart within 500 milliseconds, distributing in the bloodstream and throughout the animal within 7 seconds, and that the bulk of virus distribution was essentially complete within 3 minutes. These data provide the first in vivo real-time tracking of the rapid initial events of systemic virus infection.
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Hofherr et al. (2011) studied this question. IR800-labeled adenovirus vs. Free IR800 dye or unlabeled adenovirus was evaluated on Real-time biodistribution of virus particles. Near-infrared fluorophore-labeled adenovirus allowed real-time in vivo tracking in mice, showing virus entering the heart within 500 milliseconds and bulk distribution completing within 3 minutes.
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