A Global Comparison of Bactericera cockerelli (Hemiptera: Triozidae) Microbial Communities
The potato psyllid (Bactericera cockerelli Sulc) is an economically important insect pest of solanaceous crops such as potato, tomato, pepper, and tobacco. Historically, the potato psyllid's range included central United States, Mexico, and California; more recently, populations of this insect...
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description | The potato psyllid (Bactericera cockerelli Sulc) is an economically important insect pest of solanaceous crops such as potato, tomato, pepper, and tobacco. Historically, the potato psyllid's range included central United States, Mexico, and California; more recently, populations of this insect have been reported in Central America, the Pacific Northwest, and New Zealand. Like most phytophagous insects, potato psyllids require symbiotic bacteria to compensate for nutritional deficiencies in their diet. Potato psyllids harbor the primary symbiont, Candidatus Carsonella ruddii, and may also harbor many secondary symbionts such as Wolbachia sp., Sodalis sp., Pseudomonas sp., and others. These secondary symbionts can have an effect on reproduction, nutrition, immune response, and resistances to heat or pesticides. To identify regional differences in potato psyllid bacterial symbionts, 454 pyrosequencing was performed using generic 16S rRNA gene primers. Analysis was performed using the Qiime 1.6.0 software suite, ARB Silva, and R. Operational taxonomic units were then grouped at 97% identity. Representative sequences were classified to genus using the ARB SILVA database. Potato psyllids collected in California contained a less diverse microbial community than those collected in the central United States and Central America. The crop variety, collection year, and haplotype did not seem to affect the microbial community in potato psyllids. The primary difference between psyllids in different regions was the presence and overall bacterial community composition of Candidatus Carsonella ruddii and Wolbachia. |
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Historically, the potato psyllid's range included central United States, Mexico, and California; more recently, populations of this insect have been reported in Central America, the Pacific Northwest, and New Zealand. Like most phytophagous insects, potato psyllids require symbiotic bacteria to compensate for nutritional deficiencies in their diet. Potato psyllids harbor the primary symbiont, Candidatus Carsonella ruddii, and may also harbor many secondary symbionts such as Wolbachia sp., Sodalis sp., Pseudomonas sp., and others. These secondary symbionts can have an effect on reproduction, nutrition, immune response, and resistances to heat or pesticides. To identify regional differences in potato psyllid bacterial symbionts, 454 pyrosequencing was performed using generic 16S rRNA gene primers. Analysis was performed using the Qiime 1.6.0 software suite, ARB Silva, and R. Operational taxonomic units were then grouped at 97% identity. Representative sequences were classified to genus using the ARB SILVA database. Potato psyllids collected in California contained a less diverse microbial community than those collected in the central United States and Central America. The crop variety, collection year, and haplotype did not seem to affect the microbial community in potato psyllids. The primary difference between psyllids in different regions was the presence and overall bacterial community composition of Candidatus Carsonella ruddii and Wolbachia.</description><identifier>ISSN: 0046-225X</identifier><identifier>EISSN: 1938-2936</identifier><identifier>DOI: 10.1603/EN13256</identifier><identifier>PMID: 24517908</identifier><language>eng</language><publisher>England: Entomological Society of America</publisher><subject>Animal Distribution - physiology ; Animals ; bacterial communities ; Bactericera cockerelli ; Base Sequence ; Biota ; California ; Candidatus Carsonella ruddii ; Central America ; community structure ; computer software ; crops ; cultivars ; diet ; genes ; Haplotypes ; heat tolerance ; Hemiptera ; Hemiptera - genetics ; Hemiptera - microbiology ; immune response ; insect pests ; INSECT–SYMBIONT INTERACTIONS ; Mexico ; microbiome ; microsymbionts ; Molecular Sequence Data ; New Zealand ; Nicaragua ; nutrient deficiencies ; pepper ; pesticides ; phytophagous insects ; population ; potato psyllid ; potatoes ; Pseudomonas ; reproduction ; ribosomal RNA ; sequence analysis ; Sequence Analysis, DNA ; Sodalis ; Species Specificity ; Symbiosis ; tobacco ; tomatoes ; Triozidae ; United States ; Wolbachia</subject><ispartof>Environmental entomology, 2014-04, Vol.43 (2), p.344-352</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b368t-44856a2bda0517cee005fef57da696b89bc86f3340225c71b35e98cafdfb29763</citedby><cites>FETCH-LOGICAL-b368t-44856a2bda0517cee005fef57da696b89bc86f3340225c71b35e98cafdfb29763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24517908$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arp, Alex</creatorcontrib><creatorcontrib>Munyaneza, Joseph E</creatorcontrib><creatorcontrib>Crosslin, James M</creatorcontrib><creatorcontrib>Trumble, John</creatorcontrib><creatorcontrib>Bextine, Blake</creatorcontrib><title>A Global Comparison of Bactericera cockerelli (Hemiptera: Triozidae) Microbial Communities</title><title>Environmental entomology</title><addtitle>Environ Entomol</addtitle><description>The potato psyllid (Bactericera cockerelli Sulc) is an economically important insect pest of solanaceous crops such as potato, tomato, pepper, and tobacco. Historically, the potato psyllid's range included central United States, Mexico, and California; more recently, populations of this insect have been reported in Central America, the Pacific Northwest, and New Zealand. Like most phytophagous insects, potato psyllids require symbiotic bacteria to compensate for nutritional deficiencies in their diet. Potato psyllids harbor the primary symbiont, Candidatus Carsonella ruddii, and may also harbor many secondary symbionts such as Wolbachia sp., Sodalis sp., Pseudomonas sp., and others. These secondary symbionts can have an effect on reproduction, nutrition, immune response, and resistances to heat or pesticides. To identify regional differences in potato psyllid bacterial symbionts, 454 pyrosequencing was performed using generic 16S rRNA gene primers. Analysis was performed using the Qiime 1.6.0 software suite, ARB Silva, and R. Operational taxonomic units were then grouped at 97% identity. Representative sequences were classified to genus using the ARB SILVA database. Potato psyllids collected in California contained a less diverse microbial community than those collected in the central United States and Central America. The crop variety, collection year, and haplotype did not seem to affect the microbial community in potato psyllids. The primary difference between psyllids in different regions was the presence and overall bacterial community composition of Candidatus Carsonella ruddii and Wolbachia.</description><subject>Animal Distribution - physiology</subject><subject>Animals</subject><subject>bacterial communities</subject><subject>Bactericera cockerelli</subject><subject>Base Sequence</subject><subject>Biota</subject><subject>California</subject><subject>Candidatus Carsonella ruddii</subject><subject>Central America</subject><subject>community structure</subject><subject>computer software</subject><subject>crops</subject><subject>cultivars</subject><subject>diet</subject><subject>genes</subject><subject>Haplotypes</subject><subject>heat tolerance</subject><subject>Hemiptera</subject><subject>Hemiptera - genetics</subject><subject>Hemiptera - microbiology</subject><subject>immune response</subject><subject>insect pests</subject><subject>INSECT–SYMBIONT INTERACTIONS</subject><subject>Mexico</subject><subject>microbiome</subject><subject>microsymbionts</subject><subject>Molecular Sequence Data</subject><subject>New Zealand</subject><subject>Nicaragua</subject><subject>nutrient deficiencies</subject><subject>pepper</subject><subject>pesticides</subject><subject>phytophagous insects</subject><subject>population</subject><subject>potato psyllid</subject><subject>potatoes</subject><subject>Pseudomonas</subject><subject>reproduction</subject><subject>ribosomal RNA</subject><subject>sequence analysis</subject><subject>Sequence Analysis, DNA</subject><subject>Sodalis</subject><subject>Species Specificity</subject><subject>Symbiosis</subject><subject>tobacco</subject><subject>tomatoes</subject><subject>Triozidae</subject><subject>United States</subject><subject>Wolbachia</subject><issn>0046-225X</issn><issn>1938-2936</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE9PGzEQxa0K1ASo-AawFwQctvWftdfuLUSBVErpoUGqelnZ3nFl2I1TOzmUT4-jDb0h5jKH-enNew-hU4I_E4HZl9k9YZSLD2hMFJMlVUwcoDHGlSgp5b9G6CilR5xH0vojGtGKk1phOUa_J8VdF4zuimno1zr6FFZFcMWNthuI3kLUhQ32CSJ0nS-u5tD7db7or8Uy-vDsWw3XxXdvYzB-UOm3K7_xkE7QodNdgk_7fYwebmfL6bxc_Lj7Np0sSsOE3JRVJbnQ1LQaZ1MWAGPuwPG61UIJI5WxUjjGKpyT2JoYxkFJq13rDFW1YMfoatBdx_B3C2nT9D7ZbFevIGxTQ3e5aypr_i5KOFFUYFLVGb0c0JwspQiuWUff6_ivIbjZdd7sO8_k2V50a3po_3OvJWfgfACcDo3-kztuHn5SnEUwZkpSlomLgTA-hBW8-eoFslSPcQ</recordid><startdate>20140401</startdate><enddate>20140401</enddate><creator>Arp, Alex</creator><creator>Munyaneza, Joseph E</creator><creator>Crosslin, James M</creator><creator>Trumble, John</creator><creator>Bextine, Blake</creator><general>Entomological Society of America</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20140401</creationdate><title>A Global Comparison of Bactericera cockerelli (Hemiptera: Triozidae) Microbial Communities</title><author>Arp, Alex ; Munyaneza, Joseph E ; Crosslin, James M ; Trumble, John ; Bextine, Blake</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b368t-44856a2bda0517cee005fef57da696b89bc86f3340225c71b35e98cafdfb29763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animal Distribution - physiology</topic><topic>Animals</topic><topic>bacterial communities</topic><topic>Bactericera cockerelli</topic><topic>Base Sequence</topic><topic>Biota</topic><topic>California</topic><topic>Candidatus Carsonella ruddii</topic><topic>Central America</topic><topic>community structure</topic><topic>computer software</topic><topic>crops</topic><topic>cultivars</topic><topic>diet</topic><topic>genes</topic><topic>Haplotypes</topic><topic>heat tolerance</topic><topic>Hemiptera</topic><topic>Hemiptera - genetics</topic><topic>Hemiptera - microbiology</topic><topic>immune response</topic><topic>insect pests</topic><topic>INSECT–SYMBIONT INTERACTIONS</topic><topic>Mexico</topic><topic>microbiome</topic><topic>microsymbionts</topic><topic>Molecular Sequence Data</topic><topic>New Zealand</topic><topic>Nicaragua</topic><topic>nutrient deficiencies</topic><topic>pepper</topic><topic>pesticides</topic><topic>phytophagous insects</topic><topic>population</topic><topic>potato psyllid</topic><topic>potatoes</topic><topic>Pseudomonas</topic><topic>reproduction</topic><topic>ribosomal RNA</topic><topic>sequence analysis</topic><topic>Sequence Analysis, DNA</topic><topic>Sodalis</topic><topic>Species Specificity</topic><topic>Symbiosis</topic><topic>tobacco</topic><topic>tomatoes</topic><topic>Triozidae</topic><topic>United States</topic><topic>Wolbachia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arp, Alex</creatorcontrib><creatorcontrib>Munyaneza, Joseph E</creatorcontrib><creatorcontrib>Crosslin, James M</creatorcontrib><creatorcontrib>Trumble, John</creatorcontrib><creatorcontrib>Bextine, Blake</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Environmental entomology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arp, Alex</au><au>Munyaneza, Joseph E</au><au>Crosslin, James M</au><au>Trumble, John</au><au>Bextine, Blake</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Global Comparison of Bactericera cockerelli (Hemiptera: Triozidae) Microbial Communities</atitle><jtitle>Environmental entomology</jtitle><addtitle>Environ Entomol</addtitle><date>2014-04-01</date><risdate>2014</risdate><volume>43</volume><issue>2</issue><spage>344</spage><epage>352</epage><pages>344-352</pages><issn>0046-225X</issn><eissn>1938-2936</eissn><abstract>The potato psyllid (Bactericera cockerelli Sulc) is an economically important insect pest of solanaceous crops such as potato, tomato, pepper, and tobacco. Historically, the potato psyllid's range included central United States, Mexico, and California; more recently, populations of this insect have been reported in Central America, the Pacific Northwest, and New Zealand. Like most phytophagous insects, potato psyllids require symbiotic bacteria to compensate for nutritional deficiencies in their diet. Potato psyllids harbor the primary symbiont, Candidatus Carsonella ruddii, and may also harbor many secondary symbionts such as Wolbachia sp., Sodalis sp., Pseudomonas sp., and others. These secondary symbionts can have an effect on reproduction, nutrition, immune response, and resistances to heat or pesticides. To identify regional differences in potato psyllid bacterial symbionts, 454 pyrosequencing was performed using generic 16S rRNA gene primers. Analysis was performed using the Qiime 1.6.0 software suite, ARB Silva, and R. Operational taxonomic units were then grouped at 97% identity. Representative sequences were classified to genus using the ARB SILVA database. Potato psyllids collected in California contained a less diverse microbial community than those collected in the central United States and Central America. The crop variety, collection year, and haplotype did not seem to affect the microbial community in potato psyllids. The primary difference between psyllids in different regions was the presence and overall bacterial community composition of Candidatus Carsonella ruddii and Wolbachia.</abstract><cop>England</cop><pub>Entomological Society of America</pub><pmid>24517908</pmid><doi>10.1603/EN13256</doi><tpages>9</tpages></addata></record> |
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source | MEDLINE; Oxford University Press Journals All Titles (1996-Current) |
subjects | Animal Distribution - physiology Animals bacterial communities Bactericera cockerelli Base Sequence Biota California Candidatus Carsonella ruddii Central America community structure computer software crops cultivars diet genes Haplotypes heat tolerance Hemiptera Hemiptera - genetics Hemiptera - microbiology immune response insect pests INSECT–SYMBIONT INTERACTIONS Mexico microbiome microsymbionts Molecular Sequence Data New Zealand Nicaragua nutrient deficiencies pepper pesticides phytophagous insects population potato psyllid potatoes Pseudomonas reproduction ribosomal RNA sequence analysis Sequence Analysis, DNA Sodalis Species Specificity Symbiosis tobacco tomatoes Triozidae United States Wolbachia |
title | A Global Comparison of Bactericera cockerelli (Hemiptera: Triozidae) Microbial Communities |
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