Dear Amanda,
nice to hear from you. You are still very active with ranaviruses. I will start next year with some surveils (Ranavirus, mycobacteria) in Germany,
Austria and France for that.
Unfortunately I do not have grants for this nice meeting in Australia. Secondly at this period I will be in China, work there in a lab (projects).
Sven
Dr. Dr. habil. Sven M. Bergmann,
diplomate
ECAAH
OIE Reference Laboratory for KHVD
NRL für die KHV-I
NRL für Muschelkrankheiten
Dr. med. vet. Dr. habil. agri. sci. – Fischereiwissenschaften
Fachtierarzt für Fische
Certified Veterinary Specialist for Aquaculture and for Fisheries Science
Institut für Infektionsmedizin
Institute of Infectology
___________________________________________
Friedrich-Loeffler-Institut
Bundesforschungsinstitut für Tiergesundheit
Federal Research Institute for Animal Health
Südufer 10 | 17493 Greifswald - Insel Riems
Tel: +49 38351 7 1103 Labor und 71150 Büro | Fax: +49 38351 7 1226
http://www.fli.de/
Von: Global Ranavirus Consortium <[log in to unmask]>
Im Auftrag von Duffus, Amanda
Gesendet: Mittwoch, 6. Februar 2019 19:25
An: [log in to unmask]
Betreff: Call for Abstracts - 5th International Symposium on Ranaviruses
WEBSITE COMING SOON!
CALL FOR ABSTRACTS
5th INTERNATIONAL SYMPOSIUM ON RANAVIRUSES
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Location: James Cook University, Townsville, Australia
Dates: June 4th to 6th, 2019
Abstracts on all topics relating to ranaviruses are being solicited for the 5th ISR.
Abstract Submission Date: Friday March 1, 2019
Abstracts should be formatted in accordance with the example below. Presenter’s name should be underlined and text must be a maximum of 250 words (excluding title, authors and affiliations)
and in MS Word format.
Submissions should be sent to
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PLEASE INDICATE if you prefer to give an oral presentation or a poster in your email with your submission.
Inquiries about abstract submission should be made to Dr. Duffus and Dr. Forzan, Co-Chairs of the Scientific Committee at
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Inquiries about the symposium should be made to Dr. Ellen Ariel ([log in to unmask]).
IMPORTANT VISA NOTICE: All visitors require a visa to enter Australia. Visa type depends on your country of citizenship, processing times range from
24 hours to 30 days. Visit the Australian Government Dept. of Home Affairs website (link: https://immi.homeaffairs.gov.au/visas/getting-a-visa/visa-finder)
and choose either "holiday" or "attend an event", then enter your country of citizenship, and you will be directed to the type of visa you should apply for.
SAMPLE ABSTRACT
The three dimensional structure and morphogenesis of Singapore grouper iridovirus
B. Tran1, D-H. Chen2, Y. Liu1,
J. Wu3, C. Wah2, and C. Hew1, 3
1Mechanobiology Institute Singapore, National University of Singapore,
Singapore. 2Baylor College of Medicine, Houston, TX, USA. 3Department of Biological Sciences, National University of Singapore, Singapore.
Singapore grouper iridovirus (SGIV), a major pathogen in grouper aquaculture, was first isolated in 1998 from brown-spotted grouper. In the past decade, we carried
out the viral genomic, transcriptomic, proteomic and lipidomic studies, dissected its molecular compositions and revealed its gene expression profiles. Our results show that the complex virion contains a dsDNA genome of 140,131 bp, at least 44 structural proteins
and 220 lipid species. How these molecules are assembled to form a viral particle is unknown. Recent advances in cryoEM/ET technology and computational power have made it possible to examine the structure and morphogenesis of large complex viruses in three
dimensions. We took more than 1000 frames with an FEI Titan Krios microscope and selected about 6000 particles for 3D reconstruction. A subnano resolution map was obtained, which reveals: 1) hexamers and pentamers distributed on a T = 247 icosahedral lattice;
2) an irregular lipid bilayer between the capsid shell and viral core; 3) anchor proteins located between the capsid shell and the inner lipid bilayer.
High-pressure freezing and freeze substitution were used to prepare SGIV-infected cells for electron microscopy. The viral capsid precursors first appear as closed membrane structures, then develop into headphone shape structures and capsid shells. We
identified viral intermediates showing that the viral DNA is packaged into viral capsid during capsid formation.
Knockdown of MCP disrupts the viral morphogenesis and diminishes the production of viral particles, while
knockdown of viral DNA core protein leads to reduction of viral titer and deformities in viral particles.