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Spillover, hybridization, and persistence in schistosome transmission dynamics at the human–animal interface
Zoonotic spillover and hybridization of parasites are major emerging public and veterinary health concerns at the interface of infectious disease biology, evolution, and control. Schistosomiasis is a neglected tropical disease of global importance caused by parasites of the Schistosoma genus, and th...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8521685/ https://www.ncbi.nlm.nih.gov/pubmed/34615712 http://dx.doi.org/10.1073/pnas.2110711118 |
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author | Borlase, Anna Rudge, James W. Léger, Elsa Diouf, Nicolas D. Fall, Cheikh B. Diop, Samba D. Catalano, Stefano Sène, Mariama Webster, Joanne P. |
author_facet | Borlase, Anna Rudge, James W. Léger, Elsa Diouf, Nicolas D. Fall, Cheikh B. Diop, Samba D. Catalano, Stefano Sène, Mariama Webster, Joanne P. |
author_sort | Borlase, Anna |
collection | PubMed |
description | Zoonotic spillover and hybridization of parasites are major emerging public and veterinary health concerns at the interface of infectious disease biology, evolution, and control. Schistosomiasis is a neglected tropical disease of global importance caused by parasites of the Schistosoma genus, and the Schistosoma spp. system within Africa represents a key example of a system where spillover of animal parasites into human populations has enabled formation of hybrids. Combining model-based approaches and analyses of parasitological, molecular, and epidemiological data from northern Senegal, a region with a high prevalence of schistosome hybrids, we aimed to unravel the transmission dynamics of this complex multihost, multiparasite system. Using Bayesian methods and by estimating the basic reproduction number (R(0)), we evaluate the frequency of zoonotic spillover of Schistosoma bovis from livestock and the potential for onward transmission of hybrid S. bovis × S. haematobium offspring within human populations. We estimate R(0) of hybrid schistosomes to be greater than the critical threshold of one (1.76; 95% CI 1.59 to 1.99), demonstrating the potential for hybridization to facilitate spread and establishment of schistosomiasis beyond its original geographical boundaries. We estimate R(0) for S. bovis to be greater than one in cattle (1.43; 95% CI 1.24 to 1.85) but not in other ruminants, confirming cattle as the primary zoonotic reservoir. Through longitudinal simulations, we also show that where S. bovis and S. haematobium are coendemic (in livestock and humans respectively), the relative importance of zoonotic transmission is predicted to increase as the disease in humans nears elimination. |
format | Online Article Text |
id | pubmed-8521685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-85216852021-10-27 Spillover, hybridization, and persistence in schistosome transmission dynamics at the human–animal interface Borlase, Anna Rudge, James W. Léger, Elsa Diouf, Nicolas D. Fall, Cheikh B. Diop, Samba D. Catalano, Stefano Sène, Mariama Webster, Joanne P. Proc Natl Acad Sci U S A Biological Sciences Zoonotic spillover and hybridization of parasites are major emerging public and veterinary health concerns at the interface of infectious disease biology, evolution, and control. Schistosomiasis is a neglected tropical disease of global importance caused by parasites of the Schistosoma genus, and the Schistosoma spp. system within Africa represents a key example of a system where spillover of animal parasites into human populations has enabled formation of hybrids. Combining model-based approaches and analyses of parasitological, molecular, and epidemiological data from northern Senegal, a region with a high prevalence of schistosome hybrids, we aimed to unravel the transmission dynamics of this complex multihost, multiparasite system. Using Bayesian methods and by estimating the basic reproduction number (R(0)), we evaluate the frequency of zoonotic spillover of Schistosoma bovis from livestock and the potential for onward transmission of hybrid S. bovis × S. haematobium offspring within human populations. We estimate R(0) of hybrid schistosomes to be greater than the critical threshold of one (1.76; 95% CI 1.59 to 1.99), demonstrating the potential for hybridization to facilitate spread and establishment of schistosomiasis beyond its original geographical boundaries. We estimate R(0) for S. bovis to be greater than one in cattle (1.43; 95% CI 1.24 to 1.85) but not in other ruminants, confirming cattle as the primary zoonotic reservoir. Through longitudinal simulations, we also show that where S. bovis and S. haematobium are coendemic (in livestock and humans respectively), the relative importance of zoonotic transmission is predicted to increase as the disease in humans nears elimination. National Academy of Sciences 2021-10-12 2021-10-06 /pmc/articles/PMC8521685/ /pubmed/34615712 http://dx.doi.org/10.1073/pnas.2110711118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Biological Sciences Borlase, Anna Rudge, James W. Léger, Elsa Diouf, Nicolas D. Fall, Cheikh B. Diop, Samba D. Catalano, Stefano Sène, Mariama Webster, Joanne P. Spillover, hybridization, and persistence in schistosome transmission dynamics at the human–animal interface |
title | Spillover, hybridization, and persistence in schistosome transmission dynamics at the human–animal interface |
title_full | Spillover, hybridization, and persistence in schistosome transmission dynamics at the human–animal interface |
title_fullStr | Spillover, hybridization, and persistence in schistosome transmission dynamics at the human–animal interface |
title_full_unstemmed | Spillover, hybridization, and persistence in schistosome transmission dynamics at the human–animal interface |
title_short | Spillover, hybridization, and persistence in schistosome transmission dynamics at the human–animal interface |
title_sort | spillover, hybridization, and persistence in schistosome transmission dynamics at the human–animal interface |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8521685/ https://www.ncbi.nlm.nih.gov/pubmed/34615712 http://dx.doi.org/10.1073/pnas.2110711118 |
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