Phylogeography of Diaphorina citri (Hemiptera: Liviidae) and its primary endosymbiont, ‘Candidatus Carsonella ruddii’: an evolutionary approach to host–endosymbiont interaction

BACKGROUND In insects, little is known about the co‐evolution between their primary endosymbionts and hosts at the intraspecific level. This study examined co‐diversification between the notorious agricultural pest Diaphorina citri and its primary endosymbionts (P‐endosymbiont), ‘Candidatus Carsonel...

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Veröffentlicht in:Pest management science 2018-09, Vol.74 (9), p.2185-2194
Hauptverfasser: Wang, Yanjing, Lu, Jinming, Beattie, George AC, Islam, Mohammad R, Om, Namgay, Dao, Hang T, Van Nguyen, Liem, Zaka, Syed M, Guo, Jun, Tian, Mingyi, Deng, Xiaoling, Tan, Shunyun, Holford, Paul, He, Yurong, Cen, Yijing
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container_end_page 2194
container_issue 9
container_start_page 2185
container_title Pest management science
container_volume 74
creator Wang, Yanjing
Lu, Jinming
Beattie, George AC
Islam, Mohammad R
Om, Namgay
Dao, Hang T
Van Nguyen, Liem
Zaka, Syed M
Guo, Jun
Tian, Mingyi
Deng, Xiaoling
Tan, Shunyun
Holford, Paul
He, Yurong
Cen, Yijing
description BACKGROUND In insects, little is known about the co‐evolution between their primary endosymbionts and hosts at the intraspecific level. This study examined co‐diversification between the notorious agricultural pest Diaphorina citri and its primary endosymbionts (P‐endosymbiont), ‘Candidatus Carsonella ruddii’ at the population level. RESULTS Maximum likelihood, haplotype network, principal components and Bayesian clustering identified three lineages for D. citri and its P‐endosymbiont: a Western clade containing individuals from Pakistan, Bhutan (Phuentsholing), Vietnam (Son La), USA, Myanmar and China (Ruili, Yunnan); a Central clade, with accessions originating from Southwest China, Bhutan (Tsirang) and Bangladesh; and an Eastern clade containing individuals from Southeast Asia, and East and South China. A more diverse genetic structure was apparent in the host mitochondrial DNA than their P‐endosymbionts; however, the two sets of data were strongly congruent. CONCLUSION This study provides evidence for the co‐diversification of D. citri and its P‐endosymbiont during the migration from South Asia to East and Southeast Asia. We also suggest that the P‐endosymbiont may facilitate investigations into the genealogy and migration history of the host. The biogeography of D. citri and its P‐endosymbiont indicated that D. citri colonized and underwent a secondary dispersal from South Asia to East and Southeast Asia. © 2018 Society of Chemical Industry This study provides evidence for the co‐diversification of Diaphorina citri and its P‐endosymbiont during the invasion process from South Asia to East and Southeast Asia.
doi_str_mv 10.1002/ps.4917
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This study examined co‐diversification between the notorious agricultural pest Diaphorina citri and its primary endosymbionts (P‐endosymbiont), ‘Candidatus Carsonella ruddii’ at the population level. RESULTS Maximum likelihood, haplotype network, principal components and Bayesian clustering identified three lineages for D. citri and its P‐endosymbiont: a Western clade containing individuals from Pakistan, Bhutan (Phuentsholing), Vietnam (Son La), USA, Myanmar and China (Ruili, Yunnan); a Central clade, with accessions originating from Southwest China, Bhutan (Tsirang) and Bangladesh; and an Eastern clade containing individuals from Southeast Asia, and East and South China. A more diverse genetic structure was apparent in the host mitochondrial DNA than their P‐endosymbionts; however, the two sets of data were strongly congruent. CONCLUSION This study provides evidence for the co‐diversification of D. citri and its P‐endosymbiont during the migration from South Asia to East and Southeast Asia. We also suggest that the P‐endosymbiont may facilitate investigations into the genealogy and migration history of the host. The biogeography of D. citri and its P‐endosymbiont indicated that D. citri colonized and underwent a secondary dispersal from South Asia to East and Southeast Asia. © 2018 Society of Chemical Industry This study provides evidence for the co‐diversification of Diaphorina citri and its P‐endosymbiont during the invasion process from South Asia to East and Southeast Asia.</description><identifier>ISSN: 1526-498X</identifier><identifier>EISSN: 1526-4998</identifier><identifier>DOI: 10.1002/ps.4917</identifier><identifier>PMID: 29575777</identifier><language>eng</language><publisher>Chichester, UK: John Wiley &amp; Sons, Ltd</publisher><subject>Bayesian analysis ; Biogeography ; Candidatus Carsonella ruddii ; Clustering ; co‐divergence ; co‐phylogeny ; Deoxyribonucleic acid ; Diaphorina citri ; Dispersal ; DNA ; Endosymbionts ; Genealogy ; Genetic diversity ; Genetic structure ; Insects ; Migration ; Mitochondrial DNA ; Organic chemistry</subject><ispartof>Pest management science, 2018-09, Vol.74 (9), p.2185-2194</ispartof><rights>2018 Society of Chemical Industry</rights><rights>2018 Society of Chemical Industry.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3457-f412cd5e6d443ff37af959e0bb2af7815da4104952205c67cc3d3a0dbaf2ae5e3</citedby><cites>FETCH-LOGICAL-c3457-f412cd5e6d443ff37af959e0bb2af7815da4104952205c67cc3d3a0dbaf2ae5e3</cites><orcidid>0000-0003-2931-0910</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fps.4917$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fps.4917$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29575777$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Yanjing</creatorcontrib><creatorcontrib>Lu, Jinming</creatorcontrib><creatorcontrib>Beattie, George AC</creatorcontrib><creatorcontrib>Islam, Mohammad R</creatorcontrib><creatorcontrib>Om, Namgay</creatorcontrib><creatorcontrib>Dao, Hang T</creatorcontrib><creatorcontrib>Van Nguyen, Liem</creatorcontrib><creatorcontrib>Zaka, Syed M</creatorcontrib><creatorcontrib>Guo, Jun</creatorcontrib><creatorcontrib>Tian, Mingyi</creatorcontrib><creatorcontrib>Deng, Xiaoling</creatorcontrib><creatorcontrib>Tan, Shunyun</creatorcontrib><creatorcontrib>Holford, Paul</creatorcontrib><creatorcontrib>He, Yurong</creatorcontrib><creatorcontrib>Cen, Yijing</creatorcontrib><title>Phylogeography of Diaphorina citri (Hemiptera: Liviidae) and its primary endosymbiont, ‘Candidatus Carsonella ruddii’: an evolutionary approach to host–endosymbiont interaction</title><title>Pest management science</title><addtitle>Pest Manag Sci</addtitle><description>BACKGROUND In insects, little is known about the co‐evolution between their primary endosymbionts and hosts at the intraspecific level. This study examined co‐diversification between the notorious agricultural pest Diaphorina citri and its primary endosymbionts (P‐endosymbiont), ‘Candidatus Carsonella ruddii’ at the population level. RESULTS Maximum likelihood, haplotype network, principal components and Bayesian clustering identified three lineages for D. citri and its P‐endosymbiont: a Western clade containing individuals from Pakistan, Bhutan (Phuentsholing), Vietnam (Son La), USA, Myanmar and China (Ruili, Yunnan); a Central clade, with accessions originating from Southwest China, Bhutan (Tsirang) and Bangladesh; and an Eastern clade containing individuals from Southeast Asia, and East and South China. A more diverse genetic structure was apparent in the host mitochondrial DNA than their P‐endosymbionts; however, the two sets of data were strongly congruent. 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This study examined co‐diversification between the notorious agricultural pest Diaphorina citri and its primary endosymbionts (P‐endosymbiont), ‘Candidatus Carsonella ruddii’ at the population level. RESULTS Maximum likelihood, haplotype network, principal components and Bayesian clustering identified three lineages for D. citri and its P‐endosymbiont: a Western clade containing individuals from Pakistan, Bhutan (Phuentsholing), Vietnam (Son La), USA, Myanmar and China (Ruili, Yunnan); a Central clade, with accessions originating from Southwest China, Bhutan (Tsirang) and Bangladesh; and an Eastern clade containing individuals from Southeast Asia, and East and South China. A more diverse genetic structure was apparent in the host mitochondrial DNA than their P‐endosymbionts; however, the two sets of data were strongly congruent. CONCLUSION This study provides evidence for the co‐diversification of D. citri and its P‐endosymbiont during the migration from South Asia to East and Southeast Asia. We also suggest that the P‐endosymbiont may facilitate investigations into the genealogy and migration history of the host. The biogeography of D. citri and its P‐endosymbiont indicated that D. citri colonized and underwent a secondary dispersal from South Asia to East and Southeast Asia. © 2018 Society of Chemical Industry This study provides evidence for the co‐diversification of Diaphorina citri and its P‐endosymbiont during the invasion process from South Asia to East and Southeast Asia.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>29575777</pmid><doi>10.1002/ps.4917</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-2931-0910</orcidid></addata></record>
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subjects Bayesian analysis
Biogeography
Candidatus Carsonella ruddii
Clustering
co‐divergence
co‐phylogeny
Deoxyribonucleic acid
Diaphorina citri
Dispersal
DNA
Endosymbionts
Genealogy
Genetic diversity
Genetic structure
Insects
Migration
Mitochondrial DNA
Organic chemistry
title Phylogeography of Diaphorina citri (Hemiptera: Liviidae) and its primary endosymbiont, ‘Candidatus Carsonella ruddii’: an evolutionary approach to host–endosymbiont interaction
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