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On-Demand Patient-Specific Phenotype-to-Genotype Ebola Virus Characterization.
Beitzel, Brett F; Radoshitzky, Sheli R; Di Paola, Nicholas; Brannan, Jennifer M; Kimmel, David; Caviness, Katie; Soloveva, Veronica; Yu, Shuiqing; Postnikova, Elena N; Finch, Courtney L; Liu, Hu; Prugar, Laura; Bakken, Russell; Dye, John M; Kugelman, Jeffrey R; Cunningham, James M; Sanchez-Lockhart, Mariano; Kuhn, Jens H; Palacios, Gustavo.
Afiliación
  • Beitzel BF; United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD 21702, USA.
  • Radoshitzky SR; United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD 21702, USA.
  • Di Paola N; The Geneva Foundation, Tacoma, WA 98402, USA.
  • Brannan JM; United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD 21702, USA.
  • Kimmel D; United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD 21702, USA.
  • Caviness K; United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD 21702, USA.
  • Soloveva V; United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD 21702, USA.
  • Yu S; United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD 21702, USA.
  • Postnikova EN; Integrated Research Facility at Fort Detrick (IRF-Frederick), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Fort Detrick, Frederick, MD 21702, USA.
  • Finch CL; Integrated Research Facility at Fort Detrick (IRF-Frederick), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Fort Detrick, Frederick, MD 21702, USA.
  • Liu H; Integrated Research Facility at Fort Detrick (IRF-Frederick), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Fort Detrick, Frederick, MD 21702, USA.
  • Prugar L; Department of Medicine, Brigham and Women's Hospital and Department of Microbiology, Harvard Medical School, Boston, MA 02115, USA.
  • Bakken R; United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD 21702, USA.
  • Dye JM; United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD 21702, USA.
  • Kugelman JR; United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD 21702, USA.
  • Cunningham JM; United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD 21702, USA.
  • Sanchez-Lockhart M; Department of Medicine, Brigham and Women's Hospital and Department of Microbiology, Harvard Medical School, Boston, MA 02115, USA.
  • Kuhn JH; United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD 21702, USA.
  • Palacios G; Integrated Research Facility at Fort Detrick (IRF-Frederick), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Fort Detrick, Frederick, MD 21702, USA.
Viruses ; 13(10)2021 10 06.
Article en En | MEDLINE | ID: mdl-34696439
ABSTRACT
Biosafety, biosecurity, logistical, political, and technical considerations can delay or prevent the wide dissemination of source material containing viable virus from the geographic origin of an outbreak to laboratories involved in developing medical countermeasures (MCMs). However, once virus genome sequence information is available from clinical samples, reverse-genetics systems can be used to generate virus stocks de novo to initiate MCM development. In this study, we developed a reverse-genetics system for natural isolates of Ebola virus (EBOV) variants Makona, Tumba, and Ituri, which have been challenging to obtain. These systems were generated starting solely with in silico genome sequence information and have been used successfully to produce recombinant stocks of each of the viruses for use in MCM testing. The antiviral activity of MCMs targeting viral entry varied depending on the recombinant virus isolate used. Collectively, selecting and synthetically engineering emerging EBOV variants and demonstrating their efficacy against available MCMs will be crucial for answering pressing public health and biosecurity concerns during Ebola disease (EBOD) outbreaks.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fiebre Hemorrágica Ebola / Ebolavirus / Genética Inversa Límite: Humans Idioma: En Revista: Viruses Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fiebre Hemorrágica Ebola / Ebolavirus / Genética Inversa Límite: Humans Idioma: En Revista: Viruses Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos