Cargando…

Previous exposure to dengue virus is associated with increased Zika virus burden at the maternal-fetal interface in rhesus macaques

Concerns have arisen that pre-existing immunity to dengue virus (DENV) could enhance Zika virus (ZIKV) disease, due to the homology between ZIKV and DENV and the observation of antibody-dependent enhancement (ADE) among DENV serotypes. To date, no study has examined the impact of pre-existing DENV i...

Descripción completa

Detalles Bibliográficos
Autores principales: Crooks, Chelsea M., Weiler, Andrea M., Rybarczyk, Sierra L., Bliss, Mason I., Jaeger, Anna S., Murphy, Megan E., Simmons, Heather A., Mejia, Andres, Fritsch, Michael K., Hayes, Jennifer M., Eickhoff, Jens C., Mitzey, Ann M., Razo, Elaina, Braun, Katarina M., Brown, Elizabeth A., Yamamoto, Keisuke, Shepherd, Phoenix M., Possell, Amber, Weaver, Kara, Antony, Kathleen M., Morgan, Terry K., Newman, Christina M., Dudley, Dawn M., Schultz-Darken, Nancy, Peterson, Eric, Katzelnick, Leah C., Balmaseda, Angel, Harris, Eva, O’Connor, David H., Mohr, Emma L., Golos, Thaddeus G., Friedrich, Thomas C., Aliota, Matthew T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357128/
https://www.ncbi.nlm.nih.gov/pubmed/34329306
http://dx.doi.org/10.1371/journal.pntd.0009641
_version_ 1783737079147003904
author Crooks, Chelsea M.
Weiler, Andrea M.
Rybarczyk, Sierra L.
Bliss, Mason I.
Jaeger, Anna S.
Murphy, Megan E.
Simmons, Heather A.
Mejia, Andres
Fritsch, Michael K.
Hayes, Jennifer M.
Eickhoff, Jens C.
Mitzey, Ann M.
Razo, Elaina
Braun, Katarina M.
Brown, Elizabeth A.
Yamamoto, Keisuke
Shepherd, Phoenix M.
Possell, Amber
Weaver, Kara
Antony, Kathleen M.
Morgan, Terry K.
Newman, Christina M.
Dudley, Dawn M.
Schultz-Darken, Nancy
Peterson, Eric
Katzelnick, Leah C.
Balmaseda, Angel
Harris, Eva
O’Connor, David H.
Mohr, Emma L.
Golos, Thaddeus G.
Friedrich, Thomas C.
Aliota, Matthew T.
author_facet Crooks, Chelsea M.
Weiler, Andrea M.
Rybarczyk, Sierra L.
Bliss, Mason I.
Jaeger, Anna S.
Murphy, Megan E.
Simmons, Heather A.
Mejia, Andres
Fritsch, Michael K.
Hayes, Jennifer M.
Eickhoff, Jens C.
Mitzey, Ann M.
Razo, Elaina
Braun, Katarina M.
Brown, Elizabeth A.
Yamamoto, Keisuke
Shepherd, Phoenix M.
Possell, Amber
Weaver, Kara
Antony, Kathleen M.
Morgan, Terry K.
Newman, Christina M.
Dudley, Dawn M.
Schultz-Darken, Nancy
Peterson, Eric
Katzelnick, Leah C.
Balmaseda, Angel
Harris, Eva
O’Connor, David H.
Mohr, Emma L.
Golos, Thaddeus G.
Friedrich, Thomas C.
Aliota, Matthew T.
author_sort Crooks, Chelsea M.
collection PubMed
description Concerns have arisen that pre-existing immunity to dengue virus (DENV) could enhance Zika virus (ZIKV) disease, due to the homology between ZIKV and DENV and the observation of antibody-dependent enhancement (ADE) among DENV serotypes. To date, no study has examined the impact of pre-existing DENV immunity on ZIKV pathogenesis during pregnancy in a translational non-human primate model. Here we show that macaques with a prior DENV-2 exposure had a higher burden of ZIKV vRNA in maternal-fetal interface tissues as compared to DENV-naive macaques. However, pre-existing DENV immunity had no detectable impact on ZIKV replication kinetics in maternal plasma, and all pregnancies progressed to term without adverse outcomes or gross fetal abnormalities detectable at delivery. Understanding the risks of ADE to pregnant women worldwide is critical as vaccines against DENV and ZIKV are developed and licensed and as DENV and ZIKV continue to circulate.
format Online
Article
Text
id pubmed-8357128
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-83571282021-08-12 Previous exposure to dengue virus is associated with increased Zika virus burden at the maternal-fetal interface in rhesus macaques Crooks, Chelsea M. Weiler, Andrea M. Rybarczyk, Sierra L. Bliss, Mason I. Jaeger, Anna S. Murphy, Megan E. Simmons, Heather A. Mejia, Andres Fritsch, Michael K. Hayes, Jennifer M. Eickhoff, Jens C. Mitzey, Ann M. Razo, Elaina Braun, Katarina M. Brown, Elizabeth A. Yamamoto, Keisuke Shepherd, Phoenix M. Possell, Amber Weaver, Kara Antony, Kathleen M. Morgan, Terry K. Newman, Christina M. Dudley, Dawn M. Schultz-Darken, Nancy Peterson, Eric Katzelnick, Leah C. Balmaseda, Angel Harris, Eva O’Connor, David H. Mohr, Emma L. Golos, Thaddeus G. Friedrich, Thomas C. Aliota, Matthew T. PLoS Negl Trop Dis Research Article Concerns have arisen that pre-existing immunity to dengue virus (DENV) could enhance Zika virus (ZIKV) disease, due to the homology between ZIKV and DENV and the observation of antibody-dependent enhancement (ADE) among DENV serotypes. To date, no study has examined the impact of pre-existing DENV immunity on ZIKV pathogenesis during pregnancy in a translational non-human primate model. Here we show that macaques with a prior DENV-2 exposure had a higher burden of ZIKV vRNA in maternal-fetal interface tissues as compared to DENV-naive macaques. However, pre-existing DENV immunity had no detectable impact on ZIKV replication kinetics in maternal plasma, and all pregnancies progressed to term without adverse outcomes or gross fetal abnormalities detectable at delivery. Understanding the risks of ADE to pregnant women worldwide is critical as vaccines against DENV and ZIKV are developed and licensed and as DENV and ZIKV continue to circulate. Public Library of Science 2021-07-30 /pmc/articles/PMC8357128/ /pubmed/34329306 http://dx.doi.org/10.1371/journal.pntd.0009641 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Crooks, Chelsea M.
Weiler, Andrea M.
Rybarczyk, Sierra L.
Bliss, Mason I.
Jaeger, Anna S.
Murphy, Megan E.
Simmons, Heather A.
Mejia, Andres
Fritsch, Michael K.
Hayes, Jennifer M.
Eickhoff, Jens C.
Mitzey, Ann M.
Razo, Elaina
Braun, Katarina M.
Brown, Elizabeth A.
Yamamoto, Keisuke
Shepherd, Phoenix M.
Possell, Amber
Weaver, Kara
Antony, Kathleen M.
Morgan, Terry K.
Newman, Christina M.
Dudley, Dawn M.
Schultz-Darken, Nancy
Peterson, Eric
Katzelnick, Leah C.
Balmaseda, Angel
Harris, Eva
O’Connor, David H.
Mohr, Emma L.
Golos, Thaddeus G.
Friedrich, Thomas C.
Aliota, Matthew T.
Previous exposure to dengue virus is associated with increased Zika virus burden at the maternal-fetal interface in rhesus macaques
title Previous exposure to dengue virus is associated with increased Zika virus burden at the maternal-fetal interface in rhesus macaques
title_full Previous exposure to dengue virus is associated with increased Zika virus burden at the maternal-fetal interface in rhesus macaques
title_fullStr Previous exposure to dengue virus is associated with increased Zika virus burden at the maternal-fetal interface in rhesus macaques
title_full_unstemmed Previous exposure to dengue virus is associated with increased Zika virus burden at the maternal-fetal interface in rhesus macaques
title_short Previous exposure to dengue virus is associated with increased Zika virus burden at the maternal-fetal interface in rhesus macaques
title_sort previous exposure to dengue virus is associated with increased zika virus burden at the maternal-fetal interface in rhesus macaques
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357128/
https://www.ncbi.nlm.nih.gov/pubmed/34329306
http://dx.doi.org/10.1371/journal.pntd.0009641
work_keys_str_mv AT crookschelseam previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT weilerandream previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT rybarczyksierral previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT blissmasoni previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT jaegerannas previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT murphymegane previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT simmonsheathera previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT mejiaandres previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT fritschmichaelk previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT hayesjenniferm previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT eickhoffjensc previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT mitzeyannm previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT razoelaina previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT braunkatarinam previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT brownelizabetha previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT yamamotokeisuke previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT shepherdphoenixm previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT possellamber previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT weaverkara previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT antonykathleenm previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT morganterryk previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT newmanchristinam previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT dudleydawnm previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT schultzdarkennancy previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT petersoneric previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT katzelnickleahc previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT balmasedaangel previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT harriseva previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT oconnordavidh previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT mohremmal previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT golosthaddeusg previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT friedrichthomasc previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques
AT aliotamatthewt previousexposuretodenguevirusisassociatedwithincreasedzikavirusburdenatthematernalfetalinterfaceinrhesusmacaques