Cargando…

Evolution of resistance to single and combined floral phytochemicals by a bumble bee parasite

Repeated exposure to inhibitory compounds can drive the evolution of resistance, which weakens chemical defence against antagonists. Floral phytochemicals in nectar and pollen have antimicrobial properties that can ameliorate infection in pollinators, but evolved resistance among parasites could dim...

Descripción completa

Detalles Bibliográficos
Autores principales: Palmer‐Young, E. C., Sadd, B. M., Adler, L. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324628/
https://www.ncbi.nlm.nih.gov/pubmed/27783434
http://dx.doi.org/10.1111/jeb.13002
_version_ 1782510240741195776
author Palmer‐Young, E. C.
Sadd, B. M.
Adler, L. S.
author_facet Palmer‐Young, E. C.
Sadd, B. M.
Adler, L. S.
author_sort Palmer‐Young, E. C.
collection PubMed
description Repeated exposure to inhibitory compounds can drive the evolution of resistance, which weakens chemical defence against antagonists. Floral phytochemicals in nectar and pollen have antimicrobial properties that can ameliorate infection in pollinators, but evolved resistance among parasites could diminish the medicinal efficacy of phytochemicals. However, multicompound blends, which occur in nectar and pollen, present simultaneous chemical challenges that may slow resistance evolution. We assessed evolution of resistance by the common bumble bee gut parasite Crithidia bombi to two floral phytochemicals, singly and combined, over 6 weeks (~100 generations) of chronic exposure. Resistance of C. bombi increased under single and combined phytochemical exposure, without any associated costs of reduced growth under phytochemical‐free conditions. After 6 weeks’ exposure, phytochemical concentrations that initially inhibited growth by > 50%, and exceeded concentrations in floral nectar, had minimal effects on evolved parasite lines. Unexpectedly, the phytochemical combination did not impede resistance evolution compared to single compounds. These results demonstrate that repeated phytochemical exposure, which could occur in homogeneous floral landscapes or with therapeutic phytochemical treatment of managed hives, can cause rapid evolution of resistance in pollinator parasites. We discuss possible explanations for submaximal phytochemical resistance in natural populations. Evolved resistance could diminish the antiparasitic value of phytochemical ingestion, weakening an important natural defence against infection.
format Online
Article
Text
id pubmed-5324628
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-53246282017-03-08 Evolution of resistance to single and combined floral phytochemicals by a bumble bee parasite Palmer‐Young, E. C. Sadd, B. M. Adler, L. S. J Evol Biol Research Papers Repeated exposure to inhibitory compounds can drive the evolution of resistance, which weakens chemical defence against antagonists. Floral phytochemicals in nectar and pollen have antimicrobial properties that can ameliorate infection in pollinators, but evolved resistance among parasites could diminish the medicinal efficacy of phytochemicals. However, multicompound blends, which occur in nectar and pollen, present simultaneous chemical challenges that may slow resistance evolution. We assessed evolution of resistance by the common bumble bee gut parasite Crithidia bombi to two floral phytochemicals, singly and combined, over 6 weeks (~100 generations) of chronic exposure. Resistance of C. bombi increased under single and combined phytochemical exposure, without any associated costs of reduced growth under phytochemical‐free conditions. After 6 weeks’ exposure, phytochemical concentrations that initially inhibited growth by > 50%, and exceeded concentrations in floral nectar, had minimal effects on evolved parasite lines. Unexpectedly, the phytochemical combination did not impede resistance evolution compared to single compounds. These results demonstrate that repeated phytochemical exposure, which could occur in homogeneous floral landscapes or with therapeutic phytochemical treatment of managed hives, can cause rapid evolution of resistance in pollinator parasites. We discuss possible explanations for submaximal phytochemical resistance in natural populations. Evolved resistance could diminish the antiparasitic value of phytochemical ingestion, weakening an important natural defence against infection. John Wiley and Sons Inc. 2016-11-23 2017-02 /pmc/articles/PMC5324628/ /pubmed/27783434 http://dx.doi.org/10.1111/jeb.13002 Text en © 2016 The Authors. Journal of Evolutionary Biology Published by John Wiley & Sons ltd on behalf of European Society for Evolutionary Biology. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Palmer‐Young, E. C.
Sadd, B. M.
Adler, L. S.
Evolution of resistance to single and combined floral phytochemicals by a bumble bee parasite
title Evolution of resistance to single and combined floral phytochemicals by a bumble bee parasite
title_full Evolution of resistance to single and combined floral phytochemicals by a bumble bee parasite
title_fullStr Evolution of resistance to single and combined floral phytochemicals by a bumble bee parasite
title_full_unstemmed Evolution of resistance to single and combined floral phytochemicals by a bumble bee parasite
title_short Evolution of resistance to single and combined floral phytochemicals by a bumble bee parasite
title_sort evolution of resistance to single and combined floral phytochemicals by a bumble bee parasite
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324628/
https://www.ncbi.nlm.nih.gov/pubmed/27783434
http://dx.doi.org/10.1111/jeb.13002
work_keys_str_mv AT palmeryoungec evolutionofresistancetosingleandcombinedfloralphytochemicalsbyabumblebeeparasite
AT saddbm evolutionofresistancetosingleandcombinedfloralphytochemicalsbyabumblebeeparasite
AT adlerls evolutionofresistancetosingleandcombinedfloralphytochemicalsbyabumblebeeparasite