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Single cell immune profiling of dengue virus patients reveals intact immune responses to Zika virus with enrichment of innate immune signatures
The genus Flavivirus contains many mosquito-borne human pathogens of global epidemiological importance such as dengue virus, West Nile virus, and Zika virus, which has recently emerged at epidemic levels. Infections with these viruses result in divergent clinical outcomes ranging from asymptomatic t...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082063/ https://www.ncbi.nlm.nih.gov/pubmed/32150565 http://dx.doi.org/10.1371/journal.pntd.0008112 |
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author | Zhao, Yujiao Amodio, Matthew Vander Wyk, Brent Gerritsen, Bram Kumar, Mahesh M. van Dijk, David Moon, Kevin Wang, Xiaomei Malawista, Anna Richards, Monique M. Cahill, Megan E. Desai, Anita Sivadasan, Jayasree Venkataswamy, Manjunatha M. Ravi, Vasanthapuram Fikrig, Erol Kumar, Priti Kleinstein, Steven H. Krishnaswamy, Smita Montgomery, Ruth R. |
author_facet | Zhao, Yujiao Amodio, Matthew Vander Wyk, Brent Gerritsen, Bram Kumar, Mahesh M. van Dijk, David Moon, Kevin Wang, Xiaomei Malawista, Anna Richards, Monique M. Cahill, Megan E. Desai, Anita Sivadasan, Jayasree Venkataswamy, Manjunatha M. Ravi, Vasanthapuram Fikrig, Erol Kumar, Priti Kleinstein, Steven H. Krishnaswamy, Smita Montgomery, Ruth R. |
author_sort | Zhao, Yujiao |
collection | PubMed |
description | The genus Flavivirus contains many mosquito-borne human pathogens of global epidemiological importance such as dengue virus, West Nile virus, and Zika virus, which has recently emerged at epidemic levels. Infections with these viruses result in divergent clinical outcomes ranging from asymptomatic to fatal. Myriad factors influence infection severity including exposure, immune status and pathogen/host genetics. Furthermore, pre-existing infection may skew immune pathways or divert immune resources. We profiled immune cells from dengue virus-infected individuals by multiparameter mass cytometry (CyTOF) to define functional status. Elevations in IFNβ were noted in acute patients across the majority of cell types and were statistically elevated in 31 of 36 cell subsets. We quantified response to in vitro (re)infection with dengue or Zika viruses and detected a striking pattern of upregulation of responses to Zika infection by innate cell types which was not noted in response to dengue virus. Significance was discovered by statistical analysis as well as a neural network-based clustering approach which identified unusual cell subsets overlooked by conventional manual gating. Of public health importance, patient cells showed significant enrichment of innate cell responses to Zika virus indicating an intact and robust anti-Zika response despite the concurrent dengue infection. |
format | Online Article Text |
id | pubmed-7082063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-70820632020-03-24 Single cell immune profiling of dengue virus patients reveals intact immune responses to Zika virus with enrichment of innate immune signatures Zhao, Yujiao Amodio, Matthew Vander Wyk, Brent Gerritsen, Bram Kumar, Mahesh M. van Dijk, David Moon, Kevin Wang, Xiaomei Malawista, Anna Richards, Monique M. Cahill, Megan E. Desai, Anita Sivadasan, Jayasree Venkataswamy, Manjunatha M. Ravi, Vasanthapuram Fikrig, Erol Kumar, Priti Kleinstein, Steven H. Krishnaswamy, Smita Montgomery, Ruth R. PLoS Negl Trop Dis Research Article The genus Flavivirus contains many mosquito-borne human pathogens of global epidemiological importance such as dengue virus, West Nile virus, and Zika virus, which has recently emerged at epidemic levels. Infections with these viruses result in divergent clinical outcomes ranging from asymptomatic to fatal. Myriad factors influence infection severity including exposure, immune status and pathogen/host genetics. Furthermore, pre-existing infection may skew immune pathways or divert immune resources. We profiled immune cells from dengue virus-infected individuals by multiparameter mass cytometry (CyTOF) to define functional status. Elevations in IFNβ were noted in acute patients across the majority of cell types and were statistically elevated in 31 of 36 cell subsets. We quantified response to in vitro (re)infection with dengue or Zika viruses and detected a striking pattern of upregulation of responses to Zika infection by innate cell types which was not noted in response to dengue virus. Significance was discovered by statistical analysis as well as a neural network-based clustering approach which identified unusual cell subsets overlooked by conventional manual gating. Of public health importance, patient cells showed significant enrichment of innate cell responses to Zika virus indicating an intact and robust anti-Zika response despite the concurrent dengue infection. Public Library of Science 2020-03-09 /pmc/articles/PMC7082063/ /pubmed/32150565 http://dx.doi.org/10.1371/journal.pntd.0008112 Text en © 2020 Zhao et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Zhao, Yujiao Amodio, Matthew Vander Wyk, Brent Gerritsen, Bram Kumar, Mahesh M. van Dijk, David Moon, Kevin Wang, Xiaomei Malawista, Anna Richards, Monique M. Cahill, Megan E. Desai, Anita Sivadasan, Jayasree Venkataswamy, Manjunatha M. Ravi, Vasanthapuram Fikrig, Erol Kumar, Priti Kleinstein, Steven H. Krishnaswamy, Smita Montgomery, Ruth R. Single cell immune profiling of dengue virus patients reveals intact immune responses to Zika virus with enrichment of innate immune signatures |
title | Single cell immune profiling of dengue virus patients reveals intact immune responses to Zika virus with enrichment of innate immune signatures |
title_full | Single cell immune profiling of dengue virus patients reveals intact immune responses to Zika virus with enrichment of innate immune signatures |
title_fullStr | Single cell immune profiling of dengue virus patients reveals intact immune responses to Zika virus with enrichment of innate immune signatures |
title_full_unstemmed | Single cell immune profiling of dengue virus patients reveals intact immune responses to Zika virus with enrichment of innate immune signatures |
title_short | Single cell immune profiling of dengue virus patients reveals intact immune responses to Zika virus with enrichment of innate immune signatures |
title_sort | single cell immune profiling of dengue virus patients reveals intact immune responses to zika virus with enrichment of innate immune signatures |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082063/ https://www.ncbi.nlm.nih.gov/pubmed/32150565 http://dx.doi.org/10.1371/journal.pntd.0008112 |
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