Study of camelpox virus pathogenesis in athymic nude mice.

Camelpox virus (CMLV) is the closest known orthopoxvirus genetically related to variola virus. So far, CMLV was restricted to camelids but, recently, three human cases of camelpox have been described in India, highlighting the need to pursue research on its pathogenesis, which has been hampered by t...

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Main Authors: Sophie Duraffour, Patrick Matthys, Joost J van den Oord, Tim De Schutter, Tania Mitera, Robert Snoeck, Graciela Andrei
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21738709/?tool=EBI
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author Sophie Duraffour
Patrick Matthys
Joost J van den Oord
Tim De Schutter
Tania Mitera
Robert Snoeck
Graciela Andrei
author_facet Sophie Duraffour
Patrick Matthys
Joost J van den Oord
Tim De Schutter
Tania Mitera
Robert Snoeck
Graciela Andrei
author_sort Sophie Duraffour
collection DOAJ
description Camelpox virus (CMLV) is the closest known orthopoxvirus genetically related to variola virus. So far, CMLV was restricted to camelids but, recently, three human cases of camelpox have been described in India, highlighting the need to pursue research on its pathogenesis, which has been hampered by the lack of small animal models. Here, we confirm that NMRI immunocompetent mice are resistant to intranasal (i.n.) CMLV infection. However, we demonstrate that CMLV induced a severe disease following i.n. challenge of athymic nude mice, which was accompanied with a failure in gaining weight, leading to euthanasia of the animals. On the other hand, intracutaneous (i.c.) infection resulted in disease development without impacting the body weight evolution. CMLV replication in tissues and body fluids was confirmed in the two models. We further analyzed innate immune and B cell responses induced in the spleen and draining lymph nodes after exposure to CMLV. In both models, strong increases in CD11b(+)F4/80(+) macrophages were seen in the spleen, while neutrophils, NK and B cell responses varied between the routes of infection. In the lymph nodes, the magnitude of CD11c(+)CD8α(+) lymphoid and CD11c(+)CD11b(+) myeloid dendritic cell responses increased in i.n. challenged animals. Analysis of cytokine profiles revealed significant increases of interleukin (IL)-6 and IL-18 in the sera of infected animals, while those of other cytokines were similar to uninfected controls. The efficacy of two antivirals (cidofovir or HPMPC, and its 2, 6-diaminopurine analog) was evaluated in both models. HPMPC was the most effective molecule affording 100% protection from morbidity. It appeared that both treatments did not affect immune cell responses or cytokine expression. In conclusion, we demonstrated that immunodeficient mice are permissive for CMLV propagation. These results provide a basis for studying the pathogenesis of CMLV, as well as for evaluating potential antiviral therapies in an immunodeficiency context.
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spelling doaj.art-76a1d5b7a49d4ac5aab40a344604e9ab2022-12-21T21:33:25ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0166e2156110.1371/journal.pone.0021561Study of camelpox virus pathogenesis in athymic nude mice.Sophie DuraffourPatrick MatthysJoost J van den OordTim De SchutterTania MiteraRobert SnoeckGraciela AndreiCamelpox virus (CMLV) is the closest known orthopoxvirus genetically related to variola virus. So far, CMLV was restricted to camelids but, recently, three human cases of camelpox have been described in India, highlighting the need to pursue research on its pathogenesis, which has been hampered by the lack of small animal models. Here, we confirm that NMRI immunocompetent mice are resistant to intranasal (i.n.) CMLV infection. However, we demonstrate that CMLV induced a severe disease following i.n. challenge of athymic nude mice, which was accompanied with a failure in gaining weight, leading to euthanasia of the animals. On the other hand, intracutaneous (i.c.) infection resulted in disease development without impacting the body weight evolution. CMLV replication in tissues and body fluids was confirmed in the two models. We further analyzed innate immune and B cell responses induced in the spleen and draining lymph nodes after exposure to CMLV. In both models, strong increases in CD11b(+)F4/80(+) macrophages were seen in the spleen, while neutrophils, NK and B cell responses varied between the routes of infection. In the lymph nodes, the magnitude of CD11c(+)CD8α(+) lymphoid and CD11c(+)CD11b(+) myeloid dendritic cell responses increased in i.n. challenged animals. Analysis of cytokine profiles revealed significant increases of interleukin (IL)-6 and IL-18 in the sera of infected animals, while those of other cytokines were similar to uninfected controls. The efficacy of two antivirals (cidofovir or HPMPC, and its 2, 6-diaminopurine analog) was evaluated in both models. HPMPC was the most effective molecule affording 100% protection from morbidity. It appeared that both treatments did not affect immune cell responses or cytokine expression. In conclusion, we demonstrated that immunodeficient mice are permissive for CMLV propagation. These results provide a basis for studying the pathogenesis of CMLV, as well as for evaluating potential antiviral therapies in an immunodeficiency context.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21738709/?tool=EBI
spellingShingle Sophie Duraffour
Patrick Matthys
Joost J van den Oord
Tim De Schutter
Tania Mitera
Robert Snoeck
Graciela Andrei
Study of camelpox virus pathogenesis in athymic nude mice.
PLoS ONE
title Study of camelpox virus pathogenesis in athymic nude mice.
title_full Study of camelpox virus pathogenesis in athymic nude mice.
title_fullStr Study of camelpox virus pathogenesis in athymic nude mice.
title_full_unstemmed Study of camelpox virus pathogenesis in athymic nude mice.
title_short Study of camelpox virus pathogenesis in athymic nude mice.
title_sort study of camelpox virus pathogenesis in athymic nude mice
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21738709/?tool=EBI
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