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Host preferences inhibit transmission from potential superspreader host species

Host species that are particularly abundant, infectious and/or infected tend to contribute disproportionately to symbiont (parasite or mutualist) maintenance in multi-host systems. Therefore, in a facultative multi-host system where two host species had high densities, high symbiont infestation inte...

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Autores principales: Hopkins, Skylar R., McGregor, Cari M., Belden, Lisa K., Wojdak, Jeremy M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8965418/
https://www.ncbi.nlm.nih.gov/pubmed/35350859
http://dx.doi.org/10.1098/rspb.2022.0084
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author Hopkins, Skylar R.
McGregor, Cari M.
Belden, Lisa K.
Wojdak, Jeremy M.
author_facet Hopkins, Skylar R.
McGregor, Cari M.
Belden, Lisa K.
Wojdak, Jeremy M.
author_sort Hopkins, Skylar R.
collection PubMed
description Host species that are particularly abundant, infectious and/or infected tend to contribute disproportionately to symbiont (parasite or mutualist) maintenance in multi-host systems. Therefore, in a facultative multi-host system where two host species had high densities, high symbiont infestation intensities and high infestation prevalence, we expected interspecific transmission rates to be high. Instead, we found that interspecific symbiont transmission rates to caged sentinel hosts were an order of magnitude lower than intraspecific transmission rates in the wild. Using laboratory experiments to decompose transmission rates, we found that opportunities for interspecific transmission were frequent, where interspecific and intraspecific contact rate functions were statistically indistinguishable. However, most interspecific contacts did not lead to transmission events owing to a previously unrecognized transmission barrier: strong host preferences. During laboratory choice experiments, the symbiont preferred staying on or dispersing to its current host species, even though the oligochaete symbiont is a globally distributed host generalist that can survive and reproduce on many snail host species. These surprising results suggest that when managing symbiont transmission, identifying key host species is still important, but it may be equally important to identify and manage transmission barriers that keep potential superspreader host species in check.
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spelling pubmed-89654182022-04-10 Host preferences inhibit transmission from potential superspreader host species Hopkins, Skylar R. McGregor, Cari M. Belden, Lisa K. Wojdak, Jeremy M. Proc Biol Sci Ecology Host species that are particularly abundant, infectious and/or infected tend to contribute disproportionately to symbiont (parasite or mutualist) maintenance in multi-host systems. Therefore, in a facultative multi-host system where two host species had high densities, high symbiont infestation intensities and high infestation prevalence, we expected interspecific transmission rates to be high. Instead, we found that interspecific symbiont transmission rates to caged sentinel hosts were an order of magnitude lower than intraspecific transmission rates in the wild. Using laboratory experiments to decompose transmission rates, we found that opportunities for interspecific transmission were frequent, where interspecific and intraspecific contact rate functions were statistically indistinguishable. However, most interspecific contacts did not lead to transmission events owing to a previously unrecognized transmission barrier: strong host preferences. During laboratory choice experiments, the symbiont preferred staying on or dispersing to its current host species, even though the oligochaete symbiont is a globally distributed host generalist that can survive and reproduce on many snail host species. These surprising results suggest that when managing symbiont transmission, identifying key host species is still important, but it may be equally important to identify and manage transmission barriers that keep potential superspreader host species in check. The Royal Society 2022-03-30 2022-03-30 /pmc/articles/PMC8965418/ /pubmed/35350859 http://dx.doi.org/10.1098/rspb.2022.0084 Text en © 2022 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
Hopkins, Skylar R.
McGregor, Cari M.
Belden, Lisa K.
Wojdak, Jeremy M.
Host preferences inhibit transmission from potential superspreader host species
title Host preferences inhibit transmission from potential superspreader host species
title_full Host preferences inhibit transmission from potential superspreader host species
title_fullStr Host preferences inhibit transmission from potential superspreader host species
title_full_unstemmed Host preferences inhibit transmission from potential superspreader host species
title_short Host preferences inhibit transmission from potential superspreader host species
title_sort host preferences inhibit transmission from potential superspreader host species
topic Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8965418/
https://www.ncbi.nlm.nih.gov/pubmed/35350859
http://dx.doi.org/10.1098/rspb.2022.0084
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