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Feng Yang

Researcher at State Oceanic Administration

Publications -  22
Citations -  734

Feng Yang is an academic researcher from State Oceanic Administration. The author has contributed to research in topics: White spot syndrome & Gene. The author has an hindex of 12, co-authored 18 publications receiving 592 citations.

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A simple and efficient method for purification of intact white spot syndrome virus (WSSV) viral particles.

TL;DR: A new simple and efficient method for isolation of intact WSSV viral particles from infected crayfish tissues with high yield was developed and it was found that purified viral particles were coated with integral envelope.
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Proteomic Analysis of the Major Envelope and Nucleocapsid Proteins of White Spot Syndrome Virus

TL;DR: The analysis of posttranslational modifications revealed that none of the WSSV structural proteins was glycosylated and that VP28 and VP19 were threonine phosphorylated, which should provide an important reference for future molecular studies of WSSVs morphogenesis.
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Isolation and preliminary characterization of a new pathogenic iridovirus from redclaw crayfish Cherax quadricarinatus.

TL;DR: Based on virion morphology, protein composition, DNA genome length, and MCP sequence relatedness, the virus identified has tentatively been named Cherax quadricarinatus iridovirus (CQIV), suggesting that CQIV poses a potential threat to cultured and wild crayfish and shrimp.
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White spot syndrome virus enters crayfish hematopoietic tissue cells via clathrin-mediated endocytosis

TL;DR: Analysis of the internalization of white spot syndrome virus using crayfish hematopoietic tissue (HPT) cells showed that WSSV virions were engulfed by cell membrane invaginations sharing the features of clathrin-coated pits and then internalized into coated cytoplasmic vesicles, indicating membrane cholesterol as well as dynamin is critical for efficient viral entry.
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VP24 Is a Chitin-Binding Protein Involved in White Spot Syndrome Virus Infection

TL;DR: It is demonstrated that WSSV virions can bind to chitin through one of the major envelope proteins (VP24) through the envelope protein VP24, indicating that binding of W SSV to ch itin through the viral envelope proteinVP24 is essential for WSSVs per os infection.