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Susceptibility of Xenopus Laevis Tadpoles to Infection by the Ranavirus Frog-Virus 3 Correlates with a Reduced and Delayed Innate Immune Response in Comparison with Adult Frogs

Overview
Journal Virology
Specialty Microbiology
Date 2012 Jul 24
PMID 22819836
Citations 46
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Abstract

Xenopus laevis adults mount effective immune responses to ranavirus Frog Virus 3 (FV3) infections and clear the pathogen within 2-3 weeks. In contrast, most tadpoles cannot clear FV3 and succumb to infections within a month. While larval susceptibility has been attributed to ineffective adaptive immunity, the contribution of innate immune components has not been addressed. Accordingly, we performed a comprehensive gene expression analysis on FV3-infected tadpoles and adults. In comparison to adults, leukocytes and tissues of infected tadpoles exhibited modest (10-100 time lower than adult) and delayed (3 day later than adult) increase in expression of inflammation-associated (TNF-α, IL-1β and IFN-γ) and antiviral (Mx1) genes. In contrast, these genes were readily and robustly upregulated in tadpoles upon bacterial stimulation. Furthermore, greater proportions of larval than adult PLs were infected by FV3. Our study suggests that tadpole susceptibility to FV3 infection is partially due to poor virus-elicited innate immune responses.

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References
1.
Jorgensen J, Johansen A, Hegseth M, Zou J, Robertsen B, Collet B . A recombinant CHSE-214 cell line expressing an Mx1 promoter-reporter system responds to both interferon type I and type II from salmonids and represents a versatile tool to study the IFN-system in teleost fish. Fish Shellfish Immunol. 2007; 23(6):1294-303. DOI: 10.1016/j.fsi.2007.07.008. View

2.
Campbell S, McBeath A, Secombes C, Snow M, Collet B . Interferon response following infection with genetically similar isolates of viral haemorrhagic septicaemia virus (VHSV) exhibiting contrasting virulence in rainbow trout. Fish Shellfish Immunol. 2010; 30(1):287-94. DOI: 10.1016/j.fsi.2010.10.021. View

3.
Morales H, Robert J . Characterization of primary and memory CD8 T-cell responses against ranavirus (FV3) in Xenopus laevis. J Virol. 2006; 81(5):2240-8. PMC: 1865961. DOI: 10.1128/JVI.01104-06. View

4.
Cilloniz C, Pantin-Jackwood M, Ni C, Carter V, Korth M, Swayne D . Molecular signatures associated with Mx1-mediated resistance to highly pathogenic influenza virus infection: mechanisms of survival. J Virol. 2011; 86(5):2437-46. PMC: 3302269. DOI: 10.1128/JVI.06156-11. View

5.
Robertsen B . The interferon system of teleost fish. Fish Shellfish Immunol. 2005; 20(2):172-91. DOI: 10.1016/j.fsi.2005.01.010. View