Cargando…

Tissue tropism and transmission ecology predict virulence of human RNA viruses

Novel infectious diseases continue to emerge within human populations. Predictive studies have begun to identify pathogen traits associated with emergence. However, emerging pathogens vary widely in virulence, a key determinant of their ultimate risk to public health. Here, we use structured literat...

Descripción completa

Detalles Bibliográficos
Autores principales: Brierley, Liam, Pedersen, Amy B., Woolhouse, Mark E. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879112/
https://www.ncbi.nlm.nih.gov/pubmed/31770368
http://dx.doi.org/10.1371/journal.pbio.3000206
_version_ 1783473556151074816
author Brierley, Liam
Pedersen, Amy B.
Woolhouse, Mark E. J.
author_facet Brierley, Liam
Pedersen, Amy B.
Woolhouse, Mark E. J.
author_sort Brierley, Liam
collection PubMed
description Novel infectious diseases continue to emerge within human populations. Predictive studies have begun to identify pathogen traits associated with emergence. However, emerging pathogens vary widely in virulence, a key determinant of their ultimate risk to public health. Here, we use structured literature searches to review the virulence of each of the 214 known human-infective RNA virus species. We then use a machine learning framework to determine whether viral virulence can be predicted by ecological traits, including human-to-human transmissibility, transmission routes, tissue tropisms, and host range. Using severity of clinical disease as a measurement of virulence, we identified potential risk factors using predictive classification tree and random forest ensemble models. The random forest approach predicted literature-assigned disease severity of test data with mean accuracy of 89.4% compared to a null accuracy of 74.2%. In addition to viral taxonomy, the ability to cause systemic infection was the strongest predictor of severe disease. Further notable predictors of severe disease included having neural and/or renal tropism, direct contact or respiratory transmission, and limited (0 < R(0) ≤ 1) human-to-human transmissibility. We present a novel, to our knowledge, comparative perspective on the virulence of all currently known human RNA virus species. The risk factors identified may provide novel perspectives in understanding the evolution of virulence and elucidating molecular virulence mechanisms. These risk factors could also improve planning and preparedness in public health strategies as part of a predictive framework for novel human infections.
format Online
Article
Text
id pubmed-6879112
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-68791122019-12-08 Tissue tropism and transmission ecology predict virulence of human RNA viruses Brierley, Liam Pedersen, Amy B. Woolhouse, Mark E. J. PLoS Biol Research Article Novel infectious diseases continue to emerge within human populations. Predictive studies have begun to identify pathogen traits associated with emergence. However, emerging pathogens vary widely in virulence, a key determinant of their ultimate risk to public health. Here, we use structured literature searches to review the virulence of each of the 214 known human-infective RNA virus species. We then use a machine learning framework to determine whether viral virulence can be predicted by ecological traits, including human-to-human transmissibility, transmission routes, tissue tropisms, and host range. Using severity of clinical disease as a measurement of virulence, we identified potential risk factors using predictive classification tree and random forest ensemble models. The random forest approach predicted literature-assigned disease severity of test data with mean accuracy of 89.4% compared to a null accuracy of 74.2%. In addition to viral taxonomy, the ability to cause systemic infection was the strongest predictor of severe disease. Further notable predictors of severe disease included having neural and/or renal tropism, direct contact or respiratory transmission, and limited (0 < R(0) ≤ 1) human-to-human transmissibility. We present a novel, to our knowledge, comparative perspective on the virulence of all currently known human RNA virus species. The risk factors identified may provide novel perspectives in understanding the evolution of virulence and elucidating molecular virulence mechanisms. These risk factors could also improve planning and preparedness in public health strategies as part of a predictive framework for novel human infections. Public Library of Science 2019-11-26 /pmc/articles/PMC6879112/ /pubmed/31770368 http://dx.doi.org/10.1371/journal.pbio.3000206 Text en © 2019 Brierley 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
Brierley, Liam
Pedersen, Amy B.
Woolhouse, Mark E. J.
Tissue tropism and transmission ecology predict virulence of human RNA viruses
title Tissue tropism and transmission ecology predict virulence of human RNA viruses
title_full Tissue tropism and transmission ecology predict virulence of human RNA viruses
title_fullStr Tissue tropism and transmission ecology predict virulence of human RNA viruses
title_full_unstemmed Tissue tropism and transmission ecology predict virulence of human RNA viruses
title_short Tissue tropism and transmission ecology predict virulence of human RNA viruses
title_sort tissue tropism and transmission ecology predict virulence of human rna viruses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879112/
https://www.ncbi.nlm.nih.gov/pubmed/31770368
http://dx.doi.org/10.1371/journal.pbio.3000206
work_keys_str_mv AT brierleyliam tissuetropismandtransmissionecologypredictvirulenceofhumanrnaviruses
AT pedersenamyb tissuetropismandtransmissionecologypredictvirulenceofhumanrnaviruses
AT woolhousemarkej tissuetropismandtransmissionecologypredictvirulenceofhumanrnaviruses