Cargando…
Experimental assessment of cross-species transmission in a natural multihost–multivector–multipathogen community
Vector-borne pathogens, many of which cause major suffering worldwide, often circulate in diverse wildlife communities comprising multiple reservoir host and/or vector species. However, the complexities of these systems make it challenging to determine the contributions these different species make...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10646469/ https://www.ncbi.nlm.nih.gov/pubmed/37964529 http://dx.doi.org/10.1098/rspb.2023.1900 |
_version_ | 1785147449392758784 |
---|---|
author | Fenton, Andy Withenshaw, Susan M. Devevey, Godefroy Morris, Alexandra Erazo, Diana Pedersen, Amy B. |
author_facet | Fenton, Andy Withenshaw, Susan M. Devevey, Godefroy Morris, Alexandra Erazo, Diana Pedersen, Amy B. |
author_sort | Fenton, Andy |
collection | PubMed |
description | Vector-borne pathogens, many of which cause major suffering worldwide, often circulate in diverse wildlife communities comprising multiple reservoir host and/or vector species. However, the complexities of these systems make it challenging to determine the contributions these different species make to transmission. We experimentally manipulated transmission within a natural multihost–multipathogen–multivector system, by blocking flea-borne pathogen transmission from either of two co-occurring host species (bank voles and wood mice). Through genetic analysis of the resulting infections in the hosts and vectors, we show that both host species likely act together to maintain the overall flea community, but cross-species pathogen transmission is relatively rare—most pathogens were predominantly found in only one host species, and there were few cases where targeted treatment affected pathogens in the other host species. However, we do provide experimental evidence of some reservoir–spillover dynamics whereby reductions of some infections in one host species are achieved by blocking transmission from the other host species. Overall, despite the apparent complexity of such systems, we show there can be ‘covert simplicity’, whereby pathogen transmission is primarily dominated by single host species, potentially facilitating the targeting of key hosts for control, even in diverse ecological communities. |
format | Online Article Text |
id | pubmed-10646469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-106464692023-11-15 Experimental assessment of cross-species transmission in a natural multihost–multivector–multipathogen community Fenton, Andy Withenshaw, Susan M. Devevey, Godefroy Morris, Alexandra Erazo, Diana Pedersen, Amy B. Proc Biol Sci Ecology Vector-borne pathogens, many of which cause major suffering worldwide, often circulate in diverse wildlife communities comprising multiple reservoir host and/or vector species. However, the complexities of these systems make it challenging to determine the contributions these different species make to transmission. We experimentally manipulated transmission within a natural multihost–multipathogen–multivector system, by blocking flea-borne pathogen transmission from either of two co-occurring host species (bank voles and wood mice). Through genetic analysis of the resulting infections in the hosts and vectors, we show that both host species likely act together to maintain the overall flea community, but cross-species pathogen transmission is relatively rare—most pathogens were predominantly found in only one host species, and there were few cases where targeted treatment affected pathogens in the other host species. However, we do provide experimental evidence of some reservoir–spillover dynamics whereby reductions of some infections in one host species are achieved by blocking transmission from the other host species. Overall, despite the apparent complexity of such systems, we show there can be ‘covert simplicity’, whereby pathogen transmission is primarily dominated by single host species, potentially facilitating the targeting of key hosts for control, even in diverse ecological communities. The Royal Society 2023-11-15 /pmc/articles/PMC10646469/ /pubmed/37964529 http://dx.doi.org/10.1098/rspb.2023.1900 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Ecology Fenton, Andy Withenshaw, Susan M. Devevey, Godefroy Morris, Alexandra Erazo, Diana Pedersen, Amy B. Experimental assessment of cross-species transmission in a natural multihost–multivector–multipathogen community |
title | Experimental assessment of cross-species transmission in a natural multihost–multivector–multipathogen community |
title_full | Experimental assessment of cross-species transmission in a natural multihost–multivector–multipathogen community |
title_fullStr | Experimental assessment of cross-species transmission in a natural multihost–multivector–multipathogen community |
title_full_unstemmed | Experimental assessment of cross-species transmission in a natural multihost–multivector–multipathogen community |
title_short | Experimental assessment of cross-species transmission in a natural multihost–multivector–multipathogen community |
title_sort | experimental assessment of cross-species transmission in a natural multihost–multivector–multipathogen community |
topic | Ecology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10646469/ https://www.ncbi.nlm.nih.gov/pubmed/37964529 http://dx.doi.org/10.1098/rspb.2023.1900 |
work_keys_str_mv | AT fentonandy experimentalassessmentofcrossspeciestransmissioninanaturalmultihostmultivectormultipathogencommunity AT withenshawsusanm experimentalassessmentofcrossspeciestransmissioninanaturalmultihostmultivectormultipathogencommunity AT deveveygodefroy experimentalassessmentofcrossspeciestransmissioninanaturalmultihostmultivectormultipathogencommunity AT morrisalexandra experimentalassessmentofcrossspeciestransmissioninanaturalmultihostmultivectormultipathogencommunity AT erazodiana experimentalassessmentofcrossspeciestransmissioninanaturalmultihostmultivectormultipathogencommunity AT pedersenamyb experimentalassessmentofcrossspeciestransmissioninanaturalmultihostmultivectormultipathogencommunity |