Diversification by host switching and dispersal shaped the diversity and distribution of avian malaria parasites in Amazonia
Understanding how pathogens and parasites diversify through time and space is fundamental to predicting emerging infectious diseases. Here, we use biogeographic, coevolutionary and phylogenetic analyses to describe the origin, diversity, and distribution of avian malaria parasites in the most divers...
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Veröffentlicht in: | Oikos 2018-09, Vol.127 (9), p.1233-1242 |
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creator | Fecchio, Alan Bell, Jeffrey Andrew Collins, Michael David Farias, Izeni Pires Trisos, Christopher Harry Tobias, Joseph Andrew Tkach, Vasyl Volodymyr Weckstein, Jason David Ricklefs, Robert Eric Batalha‐Filho, Henrique |
description | Understanding how pathogens and parasites diversify through time and space is fundamental to predicting emerging infectious diseases. Here, we use biogeographic, coevolutionary and phylogenetic analyses to describe the origin, diversity, and distribution of avian malaria parasites in the most diverse avifauna on Earth. We first performed phylogenetic analyses using the mitochondrial cytochrome b (cyt b) gene to determine relationships among parasite lineages. Then, we estimated divergence times and reconstructed ancestral areas to uncover how landscape evolution has shaped the diversification of Parahaemoproteus and Plasmodium in Amazonia. Finally, we assessed the coevolutionary patterns of diversification in this host–parasite system to determine how coevolution may have influenced the contemporary diversity of avian malaria parasites and their distribution among Amazonian birds.
Biogeographic analysis of 324 haemosporidian parasite lineages recovered from 4178 individual birds provided strong evidence that these parasites readily disperse across major Amazonian rivers and this has occurred with increasing frequency over the last five million years. We also recovered many duplication events within areas of endemism in Amazonia. Cophylogenetic analyses of these blood parasites and their avian hosts support a diversification history dominated by host switching. The ability of avian malaria parasites to disperse geographically and shift among avian hosts has played a major role in their radiation and has shaped the current distribution and diversity of these parasites across Amazonia. |
doi_str_mv | 10.1111/oik.05115 |
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Biogeographic analysis of 324 haemosporidian parasite lineages recovered from 4178 individual birds provided strong evidence that these parasites readily disperse across major Amazonian rivers and this has occurred with increasing frequency over the last five million years. We also recovered many duplication events within areas of endemism in Amazonia. Cophylogenetic analyses of these blood parasites and their avian hosts support a diversification history dominated by host switching. The ability of avian malaria parasites to disperse geographically and shift among avian hosts has played a major role in their radiation and has shaped the current distribution and diversity of these parasites across Amazonia.</description><identifier>ISSN: 0030-1299</identifier><identifier>EISSN: 1600-0706</identifier><identifier>DOI: 10.1111/oik.05115</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Avifauna ; Biogeography ; Birds ; Blood parasites ; Coevolution ; Current distribution ; Cytochrome ; Cytochrome b ; Cytochromes ; Dispersal ; Dispersion ; Distribution ; Divergence ; Diversification ; Earth ; Endemism ; Host alternation ; Hosts ; Human diseases ; Infectious diseases ; Landscape ; macroevolution ; Malaria ; Mitochondria ; parasite dispersal ; parasite diversity ; Parasites ; Pathogens ; Phylogenetics ; Phylogeny ; Radiation ; Rivers ; Switching ; Vector-borne diseases</subject><ispartof>Oikos, 2018-09, Vol.127 (9), p.1233-1242</ispartof><rights>2018 The Authors</rights><rights>Oikos © 2018 Nordic Society Oikos</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3975-7b7e793b67ab80bb049fce415ca3eb9ccbd78d9f8fe846080f83d432941e87263</citedby><cites>FETCH-LOGICAL-c3975-7b7e793b67ab80bb049fce415ca3eb9ccbd78d9f8fe846080f83d432941e87263</cites><orcidid>0000-0002-7319-0234</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1411,27901,27902</link.rule.ids></links><search><creatorcontrib>Fecchio, Alan</creatorcontrib><creatorcontrib>Bell, Jeffrey Andrew</creatorcontrib><creatorcontrib>Collins, Michael David</creatorcontrib><creatorcontrib>Farias, Izeni Pires</creatorcontrib><creatorcontrib>Trisos, Christopher Harry</creatorcontrib><creatorcontrib>Tobias, Joseph Andrew</creatorcontrib><creatorcontrib>Tkach, Vasyl Volodymyr</creatorcontrib><creatorcontrib>Weckstein, Jason David</creatorcontrib><creatorcontrib>Ricklefs, Robert Eric</creatorcontrib><creatorcontrib>Batalha‐Filho, Henrique</creatorcontrib><title>Diversification by host switching and dispersal shaped the diversity and distribution of avian malaria parasites in Amazonia</title><title>Oikos</title><description>Understanding how pathogens and parasites diversify through time and space is fundamental to predicting emerging infectious diseases. Here, we use biogeographic, coevolutionary and phylogenetic analyses to describe the origin, diversity, and distribution of avian malaria parasites in the most diverse avifauna on Earth. We first performed phylogenetic analyses using the mitochondrial cytochrome b (cyt b) gene to determine relationships among parasite lineages. Then, we estimated divergence times and reconstructed ancestral areas to uncover how landscape evolution has shaped the diversification of Parahaemoproteus and Plasmodium in Amazonia. Finally, we assessed the coevolutionary patterns of diversification in this host–parasite system to determine how coevolution may have influenced the contemporary diversity of avian malaria parasites and their distribution among Amazonian birds.
Biogeographic analysis of 324 haemosporidian parasite lineages recovered from 4178 individual birds provided strong evidence that these parasites readily disperse across major Amazonian rivers and this has occurred with increasing frequency over the last five million years. We also recovered many duplication events within areas of endemism in Amazonia. Cophylogenetic analyses of these blood parasites and their avian hosts support a diversification history dominated by host switching. The ability of avian malaria parasites to disperse geographically and shift among avian hosts has played a major role in their radiation and has shaped the current distribution and diversity of these parasites across Amazonia.</description><subject>Avifauna</subject><subject>Biogeography</subject><subject>Birds</subject><subject>Blood parasites</subject><subject>Coevolution</subject><subject>Current distribution</subject><subject>Cytochrome</subject><subject>Cytochrome b</subject><subject>Cytochromes</subject><subject>Dispersal</subject><subject>Dispersion</subject><subject>Distribution</subject><subject>Divergence</subject><subject>Diversification</subject><subject>Earth</subject><subject>Endemism</subject><subject>Host alternation</subject><subject>Hosts</subject><subject>Human diseases</subject><subject>Infectious diseases</subject><subject>Landscape</subject><subject>macroevolution</subject><subject>Malaria</subject><subject>Mitochondria</subject><subject>parasite dispersal</subject><subject>parasite diversity</subject><subject>Parasites</subject><subject>Pathogens</subject><subject>Phylogenetics</subject><subject>Phylogeny</subject><subject>Radiation</subject><subject>Rivers</subject><subject>Switching</subject><subject>Vector-borne diseases</subject><issn>0030-1299</issn><issn>1600-0706</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp10E1PwzAMBuAIgcQYHPgHkThx6HDatGmO0_iaQNoFzpHTpjSja0vSbSrix1M6OOKLJeuxLb2EXDKYsaFuGvs-g5ix-IhMWAIQgIDkmEwAIghYKOUpOfN-DQBCCD4hX7d2Z5y3hc2ws01NdU_LxnfU722XlbZ-o1jnNLe-HRhW1JfYmpx2pRmG42rX_5HOWb0drzQFxZ3Fmm6wQmeRtuhwoMZTW9P5Bj-b2uI5OSmw8ubit0_J6_3dy-IxeF49LBfz5yCLpIgDoYURMtKJQJ2C1sBlkRnO4gwjo2WW6VykuSzSwqQ8gRSKNMp5FErOTCrCJJqSq8Pd1jUfW-M7tW62rh5eqhCkEBI444O6PqjMNd47U6jW2Q26XjFQP-GqIVw1hjvY2cHubWX6_6FaLZ_GhW-QAH2P</recordid><startdate>201809</startdate><enddate>201809</enddate><creator>Fecchio, Alan</creator><creator>Bell, Jeffrey Andrew</creator><creator>Collins, Michael David</creator><creator>Farias, Izeni Pires</creator><creator>Trisos, Christopher Harry</creator><creator>Tobias, Joseph Andrew</creator><creator>Tkach, Vasyl Volodymyr</creator><creator>Weckstein, Jason David</creator><creator>Ricklefs, Robert Eric</creator><creator>Batalha‐Filho, Henrique</creator><general>Blackwell Publishing Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><orcidid>https://orcid.org/0000-0002-7319-0234</orcidid></search><sort><creationdate>201809</creationdate><title>Diversification by host switching and dispersal shaped the diversity and distribution of avian malaria parasites in Amazonia</title><author>Fecchio, Alan ; Bell, Jeffrey Andrew ; Collins, Michael David ; Farias, Izeni Pires ; Trisos, Christopher Harry ; Tobias, Joseph Andrew ; Tkach, Vasyl Volodymyr ; Weckstein, Jason David ; Ricklefs, Robert Eric ; Batalha‐Filho, Henrique</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3975-7b7e793b67ab80bb049fce415ca3eb9ccbd78d9f8fe846080f83d432941e87263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Avifauna</topic><topic>Biogeography</topic><topic>Birds</topic><topic>Blood parasites</topic><topic>Coevolution</topic><topic>Current distribution</topic><topic>Cytochrome</topic><topic>Cytochrome b</topic><topic>Cytochromes</topic><topic>Dispersal</topic><topic>Dispersion</topic><topic>Distribution</topic><topic>Divergence</topic><topic>Diversification</topic><topic>Earth</topic><topic>Endemism</topic><topic>Host alternation</topic><topic>Hosts</topic><topic>Human diseases</topic><topic>Infectious diseases</topic><topic>Landscape</topic><topic>macroevolution</topic><topic>Malaria</topic><topic>Mitochondria</topic><topic>parasite dispersal</topic><topic>parasite diversity</topic><topic>Parasites</topic><topic>Pathogens</topic><topic>Phylogenetics</topic><topic>Phylogeny</topic><topic>Radiation</topic><topic>Rivers</topic><topic>Switching</topic><topic>Vector-borne diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fecchio, Alan</creatorcontrib><creatorcontrib>Bell, Jeffrey Andrew</creatorcontrib><creatorcontrib>Collins, Michael David</creatorcontrib><creatorcontrib>Farias, Izeni Pires</creatorcontrib><creatorcontrib>Trisos, Christopher Harry</creatorcontrib><creatorcontrib>Tobias, Joseph Andrew</creatorcontrib><creatorcontrib>Tkach, Vasyl Volodymyr</creatorcontrib><creatorcontrib>Weckstein, Jason David</creatorcontrib><creatorcontrib>Ricklefs, Robert Eric</creatorcontrib><creatorcontrib>Batalha‐Filho, Henrique</creatorcontrib><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Oikos</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fecchio, Alan</au><au>Bell, Jeffrey Andrew</au><au>Collins, Michael David</au><au>Farias, Izeni Pires</au><au>Trisos, Christopher Harry</au><au>Tobias, Joseph Andrew</au><au>Tkach, Vasyl Volodymyr</au><au>Weckstein, Jason David</au><au>Ricklefs, Robert Eric</au><au>Batalha‐Filho, Henrique</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diversification by host switching and dispersal shaped the diversity and distribution of avian malaria parasites in Amazonia</atitle><jtitle>Oikos</jtitle><date>2018-09</date><risdate>2018</risdate><volume>127</volume><issue>9</issue><spage>1233</spage><epage>1242</epage><pages>1233-1242</pages><issn>0030-1299</issn><eissn>1600-0706</eissn><abstract>Understanding how pathogens and parasites diversify through time and space is fundamental to predicting emerging infectious diseases. Here, we use biogeographic, coevolutionary and phylogenetic analyses to describe the origin, diversity, and distribution of avian malaria parasites in the most diverse avifauna on Earth. We first performed phylogenetic analyses using the mitochondrial cytochrome b (cyt b) gene to determine relationships among parasite lineages. Then, we estimated divergence times and reconstructed ancestral areas to uncover how landscape evolution has shaped the diversification of Parahaemoproteus and Plasmodium in Amazonia. Finally, we assessed the coevolutionary patterns of diversification in this host–parasite system to determine how coevolution may have influenced the contemporary diversity of avian malaria parasites and their distribution among Amazonian birds.
Biogeographic analysis of 324 haemosporidian parasite lineages recovered from 4178 individual birds provided strong evidence that these parasites readily disperse across major Amazonian rivers and this has occurred with increasing frequency over the last five million years. We also recovered many duplication events within areas of endemism in Amazonia. Cophylogenetic analyses of these blood parasites and their avian hosts support a diversification history dominated by host switching. The ability of avian malaria parasites to disperse geographically and shift among avian hosts has played a major role in their radiation and has shaped the current distribution and diversity of these parasites across Amazonia.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1111/oik.05115</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-7319-0234</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Avifauna Biogeography Birds Blood parasites Coevolution Current distribution Cytochrome Cytochrome b Cytochromes Dispersal Dispersion Distribution Divergence Diversification Earth Endemism Host alternation Hosts Human diseases Infectious diseases Landscape macroevolution Malaria Mitochondria parasite dispersal parasite diversity Parasites Pathogens Phylogenetics Phylogeny Radiation Rivers Switching Vector-borne diseases |
title | Diversification by host switching and dispersal shaped the diversity and distribution of avian malaria parasites in Amazonia |
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