Virulent infection of outbred Hartley guinea pigs with recombinant Pichinde virus as a surrogate small animal model for human Lassa fever.


Journal

Virulence
ISSN: 2150-5608
Titre abrégé: Virulence
Pays: United States
ID NLM: 101531386

Informations de publication

Date de publication:
12 2020
Historique:
pubmed: 18 8 2020
medline: 20 7 2021
entrez: 18 8 2020
Statut: ppublish

Résumé

Arenaviruses, such as Lassa virus (LASV), can cause severe and fatal hemorrhagic fevers (e.g., Lassa fever, LF) in humans with no vaccines or therapeutics. Research on arenavirus-induced hemorrhagic fevers (AHFs) has been hampered by the highly virulent nature of these viral pathogens, which require high biocontainment laboratory, and the lack of an immune-competent small animal model that can recapitulate AHF disease and pathological features. Guinea pig infected with Pichinde virus (PICV), an arenavirus that does not cause disease in humans, has been established as a convenient surrogate animal model for AHFs as it can be handled in a conventional laboratory. The PICV strain P18, derived from sequential passaging of the virus 18 times in strain 13 inbred guinea pigs, causes severe febrile illness in guinea pigs that is reminiscent of lethal LF in humans. As inbred guinea pigs are not readily available and are difficult to maintain, outbred Hartley guinea pigs have been used but they show a high degree of disease heterogeneity upon virulent P18 PICV infection. Here, we describe an improved outbred guinea-pig infection model using recombinant rP18 PICV generated by reverse genetics technique followed by plaque purification, which consistently shows >90% mortality and virulent infection. Comprehensive virological, histopathological, and immunohistochemical analyses of the rP18-virus infected animals show similar features of human LASV infection. Our data demonstrate that this improved animal model can serve as a safe, affordable, and convenient surrogate small animal model for studying human LF pathogenesis and for evaluating efficacy of preventative or therapeutic approaches.

Identifiants

pubmed: 32799623
doi: 10.1080/21505594.2020.1809328
pmc: PMC7549944
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1131-1141

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI083409
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI093580
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI131586
Pays : United States
Organisme : NIAID NIH HHS
ID : U54 AI057157
Pays : United States

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Auteurs

Shuiyun Lan (S)

Department of Pathology and Laboratory Medicine, Emory University , Atlanta, GA, USA.

Wun-Ju Shieh (WJ)

Infectious Disease Pathology Branch, Centers for Disease Control and Prevention , Atlanta, GA, USA.

Qinfeng Huang (Q)

Department of Veterinary and Biomedical Sciences, College of Veterinary Medicine, University of Minnesota , St Paul, MN, USA.

Sherif R Zaki (SR)

Infectious Disease Pathology Branch, Centers for Disease Control and Prevention , Atlanta, GA, USA.

Yuying Liang (Y)

Department of Veterinary and Biomedical Sciences, College of Veterinary Medicine, University of Minnesota , St Paul, MN, USA.

Hinh Ly (H)

Department of Veterinary and Biomedical Sciences, College of Veterinary Medicine, University of Minnesota , St Paul, MN, USA.

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