Literature DB >> 26908211

Comparison of lentiviruses pseudotyped with S proteins from coronaviruses and cell tropisms of porcine coronaviruses.

Jingjing Wang1,2, Feng Deng1,2, Gang Ye1,2, Wanyu Dong1,2, Anjun Zheng1,2, Qigai He1,2,3, Guiqing Peng4,5,6.   

Abstract

The surface glycoproteins of coronaviruses play an important role in receptor binding and cell entry. Different coronaviruses interact with their specific receptors to enter host cells. Lentiviruses pseudotyped with their spike proteins (S) were compared to analyze the entry efficiency of various coronaviruses. Our results indicated that S proteins from different coronaviruses displayed varied abilities to mediate pseudotyped virus infection. Furthermore, the cell tropisms of porcine epidemic diarrhea virus (PEDV) and transmissible gastroenteritis virus (TGEV) have been characterized by live and pseudotyped viruses. Both live and pseudoviruses could infected Vero- CCL-81 (monkey kidney), Huh-7 (human liver), and PK-15 (pig kidney) cells efficiently. CCL94 (cat kidney) cells could be infected efficiently by TGEV but not PEDV. Overall, our study provides new insights into the mechanisms of viral entry and forms a basis for antiviral drug screening.

Entities:  

Keywords:  Coronavirus; cell entry; pseudotyped virus; receptor binding; spike proteins

Mesh:

Substances:

Year:  2016        PMID: 26908211      PMCID: PMC7090623          DOI: 10.1007/s12250-015-3690-4

Source DB:  PubMed          Journal:  Virol Sin        ISSN: 1995-820X            Impact factor:   4.327


  24 in total

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5.  Mutational analysis of aminopeptidase N, a receptor for several group 1 coronaviruses, identifies key determinants of viral host range.

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6.  The coronavirus spike protein is a class I virus fusion protein: structural and functional characterization of the fusion core complex.

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7.  Comparison of vesicular stomatitis virus pseudotyped with the S proteins from a porcine and a human coronavirus.

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Review 6.  Recent Developments in SARS-CoV-2 Neutralizing Antibody Detection Methods.

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7.  Peptide-Based Membrane Fusion Inhibitors Targeting HCoV-229E Spike Protein HR1 and HR2 Domains.

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8.  Evaluation of SARS-CoV-2 neutralizing antibodies using a CPE-based colorimetric live virus micro-neutralization assay in human serum samples.

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Review 9.  Deciphering the biology of porcine epidemic diarrhea virus in the era of reverse genetics.

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  9 in total

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