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Title: Deletion of CD2-like gene from the genome of African swine fever virus strain Georgia does not attenuate virulence in swine

Journal Article · · Scientific Reports
 [1];  [2];  [2];  [3];  [3];  [4];  [5];  [6];  [6];  [7];  [7]; ORCiD logo [2]
  1. US Dept. of Homeland Security (DHS), Greenport, NY (United States). Plum Island Animal Disease Center. Agricultural Research Service (ARS); DOE/OSTI
  2. US Dept. of Homeland Security (DHS), Greenport, NY (United States). Plum Island Animal Disease Center. Agricultural Research Service (ARS)
  3. US Dept. of Homeland Security (DHS), Greenport, NY (United States). Plum Island Animal Disease Center. Agricultural Research Service (ARS); Univ. of Connecticut, Storrs, CT (United States). Dept. of Pathobiology and Veterinary Science
  4. Mississippi State Univ., Mississippi State, MS (United States). Dept. of Pathology and Population Medicine
  5. Kansas State Univ., Manhattan, KS (United States). Dept. of Anatomy and Physiology
  6. US Dept. of Homeland Security (DHS), Greenport, NY (United States). Plum Island Animal Disease Center. Agricultural Research Service (ARS); Oak Ridge Inst. for Science and Education (ORISE), Oak Ridge, TN (United States)
  7. US Dept. of Homeland Security (DHS), Greenport, NY (United States). Plum Island Animal Disease Center. Agricultural Research Service (ARS); Kansas State Univ., Manhattan, KS (United States). Dept. of Anatomy and Physiology

The CD2-like African swine fever virus (ASFV) gene 8DR, (also known as EP402R) encodes for a structural transmembrane glycoprotein that has been shown to mediate hemadsorption and be involved in host immunomodulation as well as the induction of protective immune response. In addition, several natural ASFV isolates showing decreased virulence in swine has been shown to be non-hemadsorbing suggesting an association between altered or deleted forms of 8DR and virus attenuation. Here we demonstrate that deletion of 8DR gene from the genome of ASFV Georgia2010 isolate (ASFV-G-Δ8DR) does not significantly alter the virulence of the virus. ASFV-G-Δ8DR inoculated intramuscularly or intranasally (in a range of 102 to 104TCID50) produced a clinical disease in domestic pigs indistinguishable from that induced by the same doses of the virulent parental ASFV Georgia2010 isolate. In addition, viremia values in ASFV-G-Δ8DR do not differ from those detected in animals infected with parental virus. Therefore, deletion of 8DR gene is not associated with a noticeable decrease in virulence of the ASFV Georgia isolate.

Research Organization:
Oak Ridge Inst. for Science and Education (ORISE), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Biological and Environmental Research (BER). Biological Systems Science Division
Grant/Contract Number:
SC0014664
OSTI ID:
1629662
Journal Information:
Scientific Reports, Journal Name: Scientific Reports Journal Issue: 1 Vol. 10; ISSN 2045-2322
Publisher:
Nature Publishing GroupCopyright Statement
Country of Publication:
United States
Language:
English

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African swine fever: how can global spread be prevented?
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journal September 2009
African swine fever virus NL gene is not required for virus virulence. journal October 1998
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An African Swine Fever Virus ERV1-ALRHomologue, 9GL, Affects Virion Maturation and Viral Growth in Macrophages and Viral Virulence in Swine journal February 2000
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