Abstract

Viral pathogens have adapted to the host organism to exploit the cellular machinery for virus replication and to modulate the host cells for efficient systemic dissemination and immune evasion. Much of our knowledge of the effects that virus infections have on cells originates from in vitro imaging studies using experimental culture systems consisting of cell lines and primary cells. Recently, intravital microscopy using multi-photon excitation of fluorophores has been applied to observe virus dissemination and pathogenesis in real-time under physiological conditions in living organisms. Critical steps during viral infection and pathogenesis could be studied by direct visualization of fluorescent virus particles, virus-infected cells, and the immune response to viral infection. In this review, I summarize the latest research on in vivo studies of viral infections using multi-photon intravital microscopy (MP-IVM). Initially, the underlying principle of multi-photon microscopy is introduced and experimental challenges during microsurgical animal preparation and fluorescent labeling strategies for intravital imaging are discussed. I will further highlight recent studies that combine MP-IVM with optogenetic tools and transcriptional analysis as a powerful approach to extend the significance of in vivo imaging studies of viral pathogens.

Highlights

  • Imaging studies under experimental in vitro conditions revealed exciting details of the replication cycle of many different viruses

  • Reporter viruses for cytoplasmic green fluorescent protein (GFP) expression have been used to study the dynamic behavior of retrovirus-infected cells in vivo, revealing important insights into the mechanism of how viruses establish infection, spread within target organs, and disseminate systemically in the host organism [30,31,62]

  • human immunodeficiency virus (HIV) have been analyzed in animal models using multi-photon intravital microscopy (MP-IVM) [123,144]

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Summary

Introduction

Imaging studies under experimental in vitro conditions revealed exciting details of the replication cycle of many different viruses. Live cell imaging using confocal laser-scanning or spinning-disk microscopy provided valuable dynamic information in three dimensions (3D) at the subcellular level of in vitro cultured cells [1,2]. Viruses such as the model virus simian virus-40 allowed researchers to unravel basic concepts in cell biology such as caveolar endocytosis, endosomal trafficking, and cellular transformation [3,4,5,6]. Bioluminescence imaging has been combined with micro-computed tomography to acquire

Multi-Photon Excitation Microscopy
Properties
Experimental
Challenges for Intravital Imaging
Animal Preparation for Short- and Long-Term Intravital Imaging
Labeling Strategies for Intravital Imaging
MP-IVM Studies of Virus Infection
HIV Nef Interferes with T Cell Diapedesis for Lymph Node Homing In Vivo
Combinations of MP-IVM
Optogenetic Manipulations of Protein Function and Cell Dynamics Using MP-IVM
Summary and Future Perspectives
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