TY - JOUR
T1 - Facilitative priority effects drive parasite assembly under coinfection
AU - Halliday, Fletcher W.
AU - Penczykowski, Rachel M.
AU - Barrès, Benoit
AU - Eck, Jenalle L.
AU - Numminen, Elina
AU - Laine, Anna Liisa
N1 - Funding Information:
We thank P. Hyttinen, S. Neggazi, M. Kirjokangas and S. Sallinen for assistance with field and lab work. We thank J. Loehr and other staff at the Lammi Biological Station for facilitating the common garden experiment. We also thank the Nåtö Biological Station for housing in Åland. We thank K. Raveala, S. Parratt and A. Sims for additional assistance, including the processing of genetic samples. The Institute of Biotechnology and Institute for Molecular Medicine at the University of Helsinki are acknowledged for carrying out the DNA extractions and for genotyping samples, respectively. This work was supported by the University of Zürich and by grants from the Academy of Finland (no. 296686) to A.-L.L. and the European Research Council (Consolidator Grant RESISTANCE 724508) to A.-L.L.
Publisher Copyright:
© 2020, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2020/11/1
Y1 - 2020/11/1
N2 - Host individuals are often coinfected with diverse parasite assemblages, resulting in complex interactions among parasites within hosts. Within hosts, priority effects occur when the infection sequence alters the outcome of interactions among parasites. Yet, the role of host immunity in this process remains poorly understood. We hypothesized that the host response to the first infection could generate priority effects among parasites, altering the assembly of later-arriving strains during epidemics. We tested this by infecting sentinel host genotypes of Plantago lanceolata with strains of the fungal parasite Podosphaera plantaginis and measuring susceptibility to subsequent infection during experimental and natural epidemics. In these experiments, prior infection by one strain often increased susceptibility to other strains, and these facilitative priority effects altered the structure of parasite assemblages, but this effect depended on host genotype, host population and parasite genotype. Thus, host genotype, spatial structure and priority effects among strains all independently altered parasite assembly. Using a fine-scale survey and sampling of infections on wild hosts in several populations, we then identified a signal of facilitative priority effects, which altered parasite assembly during natural epidemics. Together, these results provide evidence that within-host priority effects of early-arriving strains can drive parasite assembly, with implications for how strain diversity is spatially and temporally distributed during epidemics.
AB - Host individuals are often coinfected with diverse parasite assemblages, resulting in complex interactions among parasites within hosts. Within hosts, priority effects occur when the infection sequence alters the outcome of interactions among parasites. Yet, the role of host immunity in this process remains poorly understood. We hypothesized that the host response to the first infection could generate priority effects among parasites, altering the assembly of later-arriving strains during epidemics. We tested this by infecting sentinel host genotypes of Plantago lanceolata with strains of the fungal parasite Podosphaera plantaginis and measuring susceptibility to subsequent infection during experimental and natural epidemics. In these experiments, prior infection by one strain often increased susceptibility to other strains, and these facilitative priority effects altered the structure of parasite assemblages, but this effect depended on host genotype, host population and parasite genotype. Thus, host genotype, spatial structure and priority effects among strains all independently altered parasite assembly. Using a fine-scale survey and sampling of infections on wild hosts in several populations, we then identified a signal of facilitative priority effects, which altered parasite assembly during natural epidemics. Together, these results provide evidence that within-host priority effects of early-arriving strains can drive parasite assembly, with implications for how strain diversity is spatially and temporally distributed during epidemics.
UR - http://www.scopus.com/inward/record.url?scp=85089966455&partnerID=8YFLogxK
U2 - 10.1038/s41559-020-01289-9
DO - 10.1038/s41559-020-01289-9
M3 - Article
C2 - 32868915
AN - SCOPUS:85089966455
SN - 2397-334X
VL - 4
SP - 1510
EP - 1521
JO - Nature Ecology and Evolution
JF - Nature Ecology and Evolution
IS - 11
ER -