{"id":{"repo_id":"mo-state","oai_identifier":"oai:bearworks.missouristate.edu:theses-1069"},"canonical_url":"https://search.dev.ndltd.org/etd/mo-state/oai:bearworks.missouristate.edu:theses-1069","repository":{"repo_id":"mo-state","name":"Missouri State University","base_url":"https://bearworks.missouristate.edu/do/oai/"},"display":{"title":"Characterization of Attachment and Receptor Isolation of Infectious Pancreatic Necrosis Virus to Chse-214 Cells","abstract":"Infectious Pancreatic Necrosis Virus (IPNV) is a bisegmented, double stranded RNA virus with a protein capsid and no envelope and is classified in the group, Birnaviridae. Although much is known about viral genes and proteins, the initial stages of attachment to susceptible cells are not known and are the focus of this research. The attachment of ³⁵S methionine labelled viruses to Chinook Salmon Embryo cells (CHSE-214) was assayed after treatment of the monolayer with various proteolytic enzymes, reducing agents and specific blocking agents. IPNV attached optimally at a pH of 7.2-7.4 within 10 to 15 seconds at 23°c. Treatment of the monolayer with chyrotrypsin and neuraminidase decreased viral attachment at all concentrations tested. Protease at 8U/mL increased viral attachment, but higher concentrations reduced attachment. Fewer viruses absorbed to Concanavalin A, lentil or fetuin treated cells, indicating the cellular receptor sites may contain a structural sialo-glycoprotein similar to glycophorin A. The IPNV receptor is suggested to reside in a coated pit covered by a masking protein, which is removed by low concentrations of protease. Preliminary research suggests the receptor protein is solubilized by mild detergent treatment and will react with labelled viruses in vitro.","abstract_html":"Infectious Pancreatic Necrosis Virus (IPNV) is a bisegmented, double stranded RNA virus with a protein capsid and no envelope and is classified in the group, Birnaviridae. Although much is known about viral genes and proteins, the initial stages of attachment to susceptible cells are not known and are the focus of this research. The attachment of ³⁵S methionine labelled viruses to Chinook Salmon Embryo cells (CHSE-214) was assayed after treatment of the monolayer with various proteolytic enzymes, reducing agents and specific blocking agents. IPNV attached optimally at a pH of 7.2-7.4 within 10 to 15 seconds at 23°c. Treatment of the monolayer with chyrotrypsin and neuraminidase decreased viral attachment at all concentrations tested. Protease at 8U/mL increased viral attachment, but higher concentrations reduced attachment. Fewer viruses absorbed to Concanavalin A, lentil or fetuin treated cells, indicating the cellular receptor sites may contain a structural sialo-glycoprotein similar to glycophorin A. The IPNV receptor is suggested to reside in a coated pit covered by a masking protein, which is removed by low concentrations of protease. Preliminary research suggests the receptor protein is solubilized by mild detergent treatment and will react with labelled viruses in vitro.","abstract_has_math":false,"creators":["Jones, Nora Sherry"],"institution":null,"degree_name":"Master of Science in Biology","degree_level":"Masters","degree_discipline":"Biology","degree_department":null,"school":null,"contributors":["Christopher Field"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1990,"date_issued":"1990-05-01T07:00:00Z","date_published":"1990-05-01T07:00:00Z","updated_at":"2026-07-24T03:14:59Z","subjects":["Biology"],"languages":[],"rights":["© Nora Sherry Jones"],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://bearworks.missouristate.edu/theses/68","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Christopher Field"]},{"key":"dc:creator","label":"Author","values":["Jones, Nora Sherry"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"thesis:degree_discipline","label":"Discipline","values":["Biology"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Masters"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science in Biology"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Biology"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:rights","label":"Dc Rights","values":["© Nora Sherry Jones"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://bearworks.missouristate.edu/theses/68"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Infectious Pancreatic Necrosis Virus (IPNV) is a bisegmented, double stranded RNA virus with a protein capsid and no envelope and is classified in the group, Birnaviridae. Although much is known about viral genes and proteins, the initial stages of attachment to susceptible cells are not known and are the focus of this research. The attachment of ³⁵S methionine labelled viruses to Chinook Salmon Embryo cells (CHSE-214) was assayed after treatment of the monolayer with various proteolytic enzymes, reducing agents and specific blocking agents. IPNV attached optimally at a pH of 7.2-7.4 within 10 to 15 seconds at 23°c. Treatment of the monolayer with chyrotrypsin and neuraminidase decreased viral attachment at all concentrations tested. Protease at 8U/mL increased viral attachment, but higher concentrations reduced attachment. Fewer viruses absorbed to Concanavalin A, lentil or fetuin treated cells, indicating the cellular receptor sites may contain a structural sialo-glycoprotein similar to glycophorin A. The IPNV receptor is suggested to reside in a coated pit covered by a masking protein, which is removed by low concentrations of protease. Preliminary research suggests the receptor protein is solubilized by mild detergent treatment and will react with labelled viruses in vitro."]},{"key":"dc:title","label":"Title","values":["Characterization of Attachment and Receptor Isolation of Infectious Pancreatic Necrosis Virus to Chse-214 Cells"]}]}],"canonical_facts":{"dc:contributor":["Christopher Field"],"dc:creator":["Jones, Nora Sherry"],"dc:description.abstract":["Infectious Pancreatic Necrosis Virus (IPNV) is a bisegmented, double stranded RNA virus with a protein capsid and no envelope and is classified in the group, Birnaviridae. Although much is known about viral genes and proteins, the initial stages of attachment to susceptible cells are not known and are the focus of this research. The attachment of ³⁵S methionine labelled viruses to Chinook Salmon Embryo cells (CHSE-214) was assayed after treatment of the monolayer with various proteolytic enzymes, reducing agents and specific blocking agents. IPNV attached optimally at a pH of 7.2-7.4 within 10 to 15 seconds at 23°c. Treatment of the monolayer with chyrotrypsin and neuraminidase decreased viral attachment at all concentrations tested. Protease at 8U/mL increased viral attachment, but higher concentrations reduced attachment. Fewer viruses absorbed to Concanavalin A, lentil or fetuin treated cells, indicating the cellular receptor sites may contain a structural sialo-glycoprotein similar to glycophorin A. The IPNV receptor is suggested to reside in a coated pit covered by a masking protein, which is removed by low concentrations of protease. Preliminary research suggests the receptor protein is solubilized by mild detergent treatment and will react with labelled viruses in vitro."],"dc:identifier":["https://bearworks.missouristate.edu/theses/68"],"dc:rights":["© Nora Sherry Jones"],"dc:subject":["Biology"],"dc:title":["Characterization of Attachment and Receptor Isolation of Infectious Pancreatic Necrosis Virus to Chse-214 Cells"],"thesis:degree_discipline":["Biology"],"thesis:degree_level":["Masters"],"thesis:degree_name":["Master of Science in Biology"]},"updated_at":"2026-07-24T03:14:59Z"}