Population structure and migration pattern of a conifer pathogen, Grosmannia clavigera, as influenced by its symbiont, the mountain pine beetle

We investigated the population structure of Grosmannia clavigera (Gc), a fungal symbiont of the mountain pine beetle (MPB) that plays a crucial role in the establishment and reproductive success of this pathogen. This insect–fungal complex has destroyed over 16 million ha of lodgepole pine forests i...

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Veröffentlicht in:Molecular ecology 2012-01, Vol.21 (1), p.71-86
Hauptverfasser: TSUI, CLEMENT K. M., ROE, AMANDA D., EL-KASSABY, YOUSRY A., RICE, ADRIANNE V., ALAMOUTI, SEPIDEH M., SPERLING, FELIX A. H., COOKE, JANICE E. K., BOHLMANN, JÖRG, HAMELIN, RICHARD C.
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container_issue 1
container_start_page 71
container_title Molecular ecology
container_volume 21
creator TSUI, CLEMENT K. M.
ROE, AMANDA D.
EL-KASSABY, YOUSRY A.
RICE, ADRIANNE V.
ALAMOUTI, SEPIDEH M.
SPERLING, FELIX A. H.
COOKE, JANICE E. K.
BOHLMANN, JÖRG
HAMELIN, RICHARD C.
description We investigated the population structure of Grosmannia clavigera (Gc), a fungal symbiont of the mountain pine beetle (MPB) that plays a crucial role in the establishment and reproductive success of this pathogen. This insect–fungal complex has destroyed over 16 million ha of lodgepole pine forests in Canada, the largest MPB epidemic in recorded history. During this current epidemic, MPB has expanded its range beyond historically recorded boundaries, both northward and eastward, and has now reached the jack pine of Alberta, potentially threatening the Canadian boreal forest. To better understand the dynamics between the beetle and its fungal symbiont, we sampled 19 populations in western North America and genotyped individuals from these populations with eight microsatellite markers. The fungus displayed high haplotype diversity, with over 250 unique haplotypes observed in 335 single spore isolates. Linkage equilibria in 13 of the 19 populations suggested that the fungus reproduces sexually. Bayesian clustering and distance analyses identified four genetic clusters that corresponded to four major geographical regions, which suggested that the epidemic arose from multiple geographical sources. A genetic cluster north of the Rocky Mountains, where the MPB has recently become established, experienced a population bottleneck, probably as a result of the recent range expansion. The two genetic clusters located north and west of the Rocky Mountains contained many fungal isolates admixed from all populations, possibly due to the massive movement of MPB during the epidemic. The general agreement in north–south differentiation of MPB and G. clavigera populations points to the fungal pathogen’s dependence on the movement of its insect vector. In addition, the patterns of diversity and the individual assignment tests of the fungal associate suggest that migration across the Rocky Mountains occurred via a northeastern corridor, in accordance with meteorological patterns and observation of MPB movement data. Our results highlight the potential of this pathogen for both expansion and sexual reproduction, and also identify some possible barriers to gene flow. Understanding the ecological and evolutionary dynamics of this fungus–beetle association is important for the modelling and prediction of MPB epidemics.
doi_str_mv 10.1111/j.1365-294X.2011.05366.x
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To better understand the dynamics between the beetle and its fungal symbiont, we sampled 19 populations in western North America and genotyped individuals from these populations with eight microsatellite markers. The fungus displayed high haplotype diversity, with over 250 unique haplotypes observed in 335 single spore isolates. Linkage equilibria in 13 of the 19 populations suggested that the fungus reproduces sexually. Bayesian clustering and distance analyses identified four genetic clusters that corresponded to four major geographical regions, which suggested that the epidemic arose from multiple geographical sources. A genetic cluster north of the Rocky Mountains, where the MPB has recently become established, experienced a population bottleneck, probably as a result of the recent range expansion. 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M.</au><au>ROE, AMANDA D.</au><au>EL-KASSABY, YOUSRY A.</au><au>RICE, ADRIANNE V.</au><au>ALAMOUTI, SEPIDEH M.</au><au>SPERLING, FELIX A. H.</au><au>COOKE, JANICE E. K.</au><au>BOHLMANN, JÖRG</au><au>HAMELIN, RICHARD C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Population structure and migration pattern of a conifer pathogen, Grosmannia clavigera, as influenced by its symbiont, the mountain pine beetle</atitle><jtitle>Molecular ecology</jtitle><addtitle>Mol Ecol</addtitle><date>2012-01</date><risdate>2012</risdate><volume>21</volume><issue>1</issue><spage>71</spage><epage>86</epage><pages>71-86</pages><issn>0962-1083</issn><eissn>1365-294X</eissn><abstract>We investigated the population structure of Grosmannia clavigera (Gc), a fungal symbiont of the mountain pine beetle (MPB) that plays a crucial role in the establishment and reproductive success of this pathogen. This insect–fungal complex has destroyed over 16 million ha of lodgepole pine forests in Canada, the largest MPB epidemic in recorded history. During this current epidemic, MPB has expanded its range beyond historically recorded boundaries, both northward and eastward, and has now reached the jack pine of Alberta, potentially threatening the Canadian boreal forest. To better understand the dynamics between the beetle and its fungal symbiont, we sampled 19 populations in western North America and genotyped individuals from these populations with eight microsatellite markers. The fungus displayed high haplotype diversity, with over 250 unique haplotypes observed in 335 single spore isolates. Linkage equilibria in 13 of the 19 populations suggested that the fungus reproduces sexually. Bayesian clustering and distance analyses identified four genetic clusters that corresponded to four major geographical regions, which suggested that the epidemic arose from multiple geographical sources. A genetic cluster north of the Rocky Mountains, where the MPB has recently become established, experienced a population bottleneck, probably as a result of the recent range expansion. The two genetic clusters located north and west of the Rocky Mountains contained many fungal isolates admixed from all populations, possibly due to the massive movement of MPB during the epidemic. The general agreement in north–south differentiation of MPB and G. clavigera populations points to the fungal pathogen’s dependence on the movement of its insect vector. In addition, the patterns of diversity and the individual assignment tests of the fungal associate suggest that migration across the Rocky Mountains occurred via a northeastern corridor, in accordance with meteorological patterns and observation of MPB movement data. Our results highlight the potential of this pathogen for both expansion and sexual reproduction, and also identify some possible barriers to gene flow. Understanding the ecological and evolutionary dynamics of this fungus–beetle association is important for the modelling and prediction of MPB epidemics.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22118059</pmid><doi>10.1111/j.1365-294X.2011.05366.x</doi><tpages>16</tpages></addata></record>
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subjects Alberta
Animal migration
Animals
approximate Bayesian computation
Bayesian analysis
Biological Evolution
Coleoptera - genetics
Coleoptera - pathogenicity
Computer Simulation
Coniferophyta - microbiology
demography
fungi
Haplotypes
insect dispersal
Insects
landscape
Linkage Disequilibrium
Microsatellite Repeats
migration
Ophiostomatales - genetics
Ophiostomatales - pathogenicity
Pathogens
Phylogeography
Pinus - metabolism
Pinus - microbiology
population genetics
Sequence Analysis, DNA
Symbiosis
Trees - microbiology
vector
title Population structure and migration pattern of a conifer pathogen, Grosmannia clavigera, as influenced by its symbiont, the mountain pine beetle
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