scholarly journals Single-Virus Tracking: From Imaging Methodologies to Virological Applications

2020 ◽  
Vol 120 (3) ◽  
pp. 1936-1979 ◽  
Author(s):  
Shu-Lin Liu ◽  
Zhi-Gang Wang ◽  
Hai-Yan Xie ◽  
An-An Liu ◽  
Don C. Lamb ◽  
...  
Molecules ◽  
2019 ◽  
Vol 24 (3) ◽  
pp. 481 ◽  
Author(s):  
Thorsten Müller ◽  
Volkan Sakin ◽  
Barbara Müller

The replication of a virus within its host cell involves numerous interactions between viral and cellular factors, which have to be tightly controlled in space and time. The intricate interplay between viral exploitation of cellular pathways and the intrinsic host defense mechanisms is difficult to unravel by traditional bulk approaches. In recent years, novel fluorescence microscopy techniques and single virus tracking have transformed the investigation of dynamic virus-host interactions. A prerequisite for the application of these imaging-based methods is the attachment of a fluorescent label to the structure of interest. However, their small size, limited coding capacity and multifunctional proteins render viruses particularly challenging targets for fluorescent labeling approaches. Click chemistry in conjunction with genetic code expansion provides virologists with a novel toolbox for site-specific, minimally invasive labeling of virion components, whose potential has just recently begun to be exploited. Here, we summarize recent achievements, current developments and future challenges for the labeling of viral nucleic acids, proteins, glycoproteins or lipids using click chemistry in order to study dynamic processes in virus-cell interactions.


ACS Nano ◽  
2017 ◽  
Vol 11 (5) ◽  
pp. 4395-4406 ◽  
Author(s):  
En-Ze Sun ◽  
An-An Liu ◽  
Zhi-Ling Zhang ◽  
Shu-Lin Liu ◽  
Zhi-Quan Tian ◽  
...  

Biomaterials ◽  
2014 ◽  
Vol 35 (7) ◽  
pp. 2295-2301 ◽  
Author(s):  
Li Wen ◽  
Yi Lin ◽  
Zhen-Hua Zheng ◽  
Zhi-Ling Zhang ◽  
Li-Juan Zhang ◽  
...  

mBio ◽  
2020 ◽  
Vol 11 (3) ◽  
Author(s):  
Li-Juan Zhang ◽  
Shaobo Wang ◽  
Li Xia ◽  
Cheng Lv ◽  
Hong-Wu Tang ◽  
...  

ABSTRACT Quantum dots (QDs) possess optical properties of superbright fluorescence, excellent photostability, narrow emission spectra, and optional colors. Labeled with QDs, single molecules/viruses can be rapidly and continuously imaged for a long time, providing more detailed information than when labeled with other fluorophores. While they are widely used to label proteins in single-molecule-tracking studies, QDs have rarely been used to study virus infection, mainly due to a lack of accepted labeling strategies. Here, we report a general method to mildly and readily label enveloped viruses with QDs. Lipid-biotin conjugates were used to recognize and mark viral lipid membranes, and streptavidin-QD conjugates were used to light them up. Such a method allowed enveloped viruses to be labeled in 2 h with specificity and efficiency up to 99% and 98%, respectively. The intact morphology and the native infectivity of viruses were preserved. With the aid of this QD labeling method, we lit wild-type and mutant Japanese encephalitis viruses up, tracked their infection in living Vero cells, and found that H144A and Q258A substitutions in the envelope protein did not affect the virus intracellular trafficking. The lipid-specific QD labeling method described in this study provides a handy and practical tool to readily “see” the viruses and follow their infection, facilitating the widespread use of single-virus tracking and the uncovering of complex infection mechanisms. IMPORTANCE Virus infection in host cells is a complex process comprising a large number of dynamic molecular events. Single-virus tracking is a versatile technique to study these events. To perform this technique, viruses must be fluorescently labeled to be visible to fluorescence microscopes. The quantum dot is a kind of fluorescent tag that has many unique optical properties. It has been widely used to label proteins in single-molecule-tracking studies but rarely used to study virus infection, mainly due to the lack of an accepted labeling method. In this study, we developed a lipid-specific method to readily, mildly, specifically, and efficiently label enveloped viruses with quantum dots by recognizing viral envelope lipids with lipid-biotin conjugates and recognizing these lipid-biotin conjugates with streptavidin-quantum dot conjugates. It is not only applicable to normal viruses, but also competent to label the key protein-mutated viruses and the inactivated highly virulent viruses, providing a powerful tool for single-virus tracking.


Viruses ◽  
2018 ◽  
Vol 10 (11) ◽  
pp. 632 ◽  
Author(s):  
Fujun Qin ◽  
Congrui Xu ◽  
Chengfeng Lei ◽  
Jia Hu ◽  
Xiulian Sun

The cell entry mechanism of Autographa californica multiple nucleopolyhedrovirus (AcMNPV) is not fully understood. Previous studies showed that AcMNPV entered host cells primarily through clathrin-mediated endocytosis, and could efficiently infect cells via fusion with the plasma membrane after a low-pH trigger. However, whether AcMNPV enters cells via these two pathways simultaneously, and the exact manner in which AcMNPV particles are internalized into cells remains unclear. In this study, using single-virus tracking, we observed that AcMNPV particles were first captured by pre-existing clathrin-coated pits (CCP), and were then delivered to early endosomes. Population-based analysis of single-virus tracking and quantitative electron microscopy demonstrated that the majority of particles were captured by CCPs and internalized via invagination. In contrast, a minority of virus particles were not delivered to CCPs, and were internalized through direct fusion with the plasma membrane without invagination. Quantitative electron microscopy also showed that, while inhibition of CCP assembly significantly impaired viral internalization, inhibition of endosomal acidification blocked virus particles out of vesicles. Collectively, these findings demonstrated that approximately 90% of AcMNPV particles entered cells through clathrin-mediated endocytosis and 10% entered via direct fusion with the plasma membrane. This study will lead toward a better understanding of AcMNPV infection.


Nano Today ◽  
2021 ◽  
Vol 40 ◽  
pp. 101271
Author(s):  
Hao-Yang Liu ◽  
Zhi-Gang Wang ◽  
Yusi Hu ◽  
Xue-Hui Shi ◽  
Hua-Jie Chen ◽  
...  

2019 ◽  
Vol 35 (4) ◽  
pp. 407-416
Author(s):  
Zhenpu Liang ◽  
Pengjuan Li ◽  
Caiping Wang ◽  
Deepali Singh ◽  
Xiaoxia Zhang

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