The Microbiome of Ehrlichia-Infected and Uninfected Lone Star Ticks (Amblyomma americanum)
The Lone Star tick, Amblyomma americanum, transmits several bacterial pathogens including species of Anaplasma and Ehrlichia. Amblyomma americanum also hosts a number of non-pathogenic bacterial endosymbionts. Recent studies of other arthropod and insect vectors have documented that commensal microf...
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description | The Lone Star tick, Amblyomma americanum, transmits several bacterial pathogens including species of Anaplasma and Ehrlichia. Amblyomma americanum also hosts a number of non-pathogenic bacterial endosymbionts. Recent studies of other arthropod and insect vectors have documented that commensal microflora can influence transmission of vector-borne pathogens; however, little is known about tick microbiomes and their possible influence on tick-borne diseases. Our objective was to compare bacterial communities associated with A. americanum, comparing Anaplasma/Ehrlichia -infected and uninfected ticks. Field-collected questing specimens (n = 50) were used in the analyses, of which 17 were identified as Anaplasma/Ehrlichia infected based on PCR amplification and sequencing of groEL genes. Bacterial communities from each specimen were characterized using Illumina sequencing of 16S rRNA gene amplicon libraries. There was a broad range in diversity between samples, with inverse Simpson's Diversity indices ranging from 1.28-89.5. There were no statistical differences in the overall microbial community structure between PCR diagnosed Anaplasma/Ehrlichia-positive and negative ticks, but there were differences based on collection method (P < 0.05), collection site (P < 0.05), and sex (P < 0.1) suggesting that environmental factors may structure A. americanum microbiomes. Interestingly, there was not always agreement between Illumina sequencing and PCR diagnostics: Ehrlichia was identified in 16S rRNA gene libraries from three PCR-negative specimens; conversely, Ehrlichia was not found in libraries of six PCR-positive ticks. Illumina sequencing also helped identify co-infections, for example, one specimen had both Ehrlichia and Anaplasma. Other taxa of interest in these specimens included Coxiella, Borrelia, and Rickettsia. Identification of bacterial community differences between specimens of a single tick species from a single geographical site indicates that intra-species differences in microbiomes were not due solely to pathogen presence/absence, but may be also driven by vector life history factors, including environment, life stage, population structure, and host choice. |
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Amblyomma americanum also hosts a number of non-pathogenic bacterial endosymbionts. Recent studies of other arthropod and insect vectors have documented that commensal microflora can influence transmission of vector-borne pathogens; however, little is known about tick microbiomes and their possible influence on tick-borne diseases. Our objective was to compare bacterial communities associated with A. americanum, comparing Anaplasma/Ehrlichia -infected and uninfected ticks. Field-collected questing specimens (n = 50) were used in the analyses, of which 17 were identified as Anaplasma/Ehrlichia infected based on PCR amplification and sequencing of groEL genes. Bacterial communities from each specimen were characterized using Illumina sequencing of 16S rRNA gene amplicon libraries. There was a broad range in diversity between samples, with inverse Simpson's Diversity indices ranging from 1.28-89.5. There were no statistical differences in the overall microbial community structure between PCR diagnosed Anaplasma/Ehrlichia-positive and negative ticks, but there were differences based on collection method (P < 0.05), collection site (P < 0.05), and sex (P < 0.1) suggesting that environmental factors may structure A. americanum microbiomes. Interestingly, there was not always agreement between Illumina sequencing and PCR diagnostics: Ehrlichia was identified in 16S rRNA gene libraries from three PCR-negative specimens; conversely, Ehrlichia was not found in libraries of six PCR-positive ticks. Illumina sequencing also helped identify co-infections, for example, one specimen had both Ehrlichia and Anaplasma. Other taxa of interest in these specimens included Coxiella, Borrelia, and Rickettsia. Identification of bacterial community differences between specimens of a single tick species from a single geographical site indicates that intra-species differences in microbiomes were not due solely to pathogen presence/absence, but may be also driven by vector life history factors, including environment, life stage, population structure, and host choice.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0146651</identifier><identifier>PMID: 26751816</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Amblyomma americanum ; Analysis ; Anaplasma ; Animals ; Arachnids ; Bacteria ; Collection ; Communities ; Community structure ; Deoxyribonucleic acid ; Dermacentor variabilis ; Developmental stages ; Disease transmission ; Diseases and pests ; Diversity indices ; DNA ; DNA, Bacterial - analysis ; Ecosystem ; Ehrlichia ; Endosymbionts ; Environmental factors ; Ethanol ; Female ; Gene libraries ; Gene sequencing ; Genetic aspects ; Health aspects ; Infections ; Insects ; Ixodes scapularis ; Life history ; Male ; Microbiomes ; Microbiota ; Microbiota (Symbiotic organisms) ; Microflora ; Microorganisms ; Parasitic diseases ; Pathogens ; Physiological aspects ; Plasmodium ; Polymerase Chain Reaction ; Population (statistical) ; Population structure ; Proteins ; Rickettsia ; Risk factors ; RNA, Ribosomal, 16S - genetics ; rRNA 16S ; Soil sciences ; Species ; Species Specificity ; Statistical analysis ; Statistical methods ; Studies ; Tick-borne diseases ; Tick-Borne Diseases - microbiology ; Ticks ; Ticks - microbiology ; Vector-borne diseases ; Vectors ; Viral infections</subject><ispartof>PloS one, 2016-01, Vol.11 (1), p.e0146651-e0146651</ispartof><rights>COPYRIGHT 2016 Public Library of Science</rights><rights>2016 Trout Fryxell, DeBruyn. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2016 Trout Fryxell, DeBruyn 2016 Trout Fryxell, DeBruyn</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-ec05b9879ac3c38eea7ac3a011c5d6857a43c2424ac46a8f4d840a878243b1bf3</citedby><cites>FETCH-LOGICAL-c692t-ec05b9879ac3c38eea7ac3a011c5d6857a43c2424ac46a8f4d840a878243b1bf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709196/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709196/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26751816$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Stevenson, Brian</contributor><creatorcontrib>Trout Fryxell, R T</creatorcontrib><creatorcontrib>DeBruyn, J M</creatorcontrib><title>The Microbiome of Ehrlichia-Infected and Uninfected Lone Star Ticks (Amblyomma americanum)</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The Lone Star tick, Amblyomma americanum, transmits several bacterial pathogens including species of Anaplasma and Ehrlichia. Amblyomma americanum also hosts a number of non-pathogenic bacterial endosymbionts. Recent studies of other arthropod and insect vectors have documented that commensal microflora can influence transmission of vector-borne pathogens; however, little is known about tick microbiomes and their possible influence on tick-borne diseases. Our objective was to compare bacterial communities associated with A. americanum, comparing Anaplasma/Ehrlichia -infected and uninfected ticks. Field-collected questing specimens (n = 50) were used in the analyses, of which 17 were identified as Anaplasma/Ehrlichia infected based on PCR amplification and sequencing of groEL genes. Bacterial communities from each specimen were characterized using Illumina sequencing of 16S rRNA gene amplicon libraries. There was a broad range in diversity between samples, with inverse Simpson's Diversity indices ranging from 1.28-89.5. There were no statistical differences in the overall microbial community structure between PCR diagnosed Anaplasma/Ehrlichia-positive and negative ticks, but there were differences based on collection method (P < 0.05), collection site (P < 0.05), and sex (P < 0.1) suggesting that environmental factors may structure A. americanum microbiomes. Interestingly, there was not always agreement between Illumina sequencing and PCR diagnostics: Ehrlichia was identified in 16S rRNA gene libraries from three PCR-negative specimens; conversely, Ehrlichia was not found in libraries of six PCR-positive ticks. Illumina sequencing also helped identify co-infections, for example, one specimen had both Ehrlichia and Anaplasma. Other taxa of interest in these specimens included Coxiella, Borrelia, and Rickettsia. Identification of bacterial community differences between specimens of a single tick species from a single geographical site indicates that intra-species differences in microbiomes were not due solely to pathogen presence/absence, but may be also driven by vector life history factors, including environment, life stage, population structure, and host choice.</description><subject>Amblyomma americanum</subject><subject>Analysis</subject><subject>Anaplasma</subject><subject>Animals</subject><subject>Arachnids</subject><subject>Bacteria</subject><subject>Collection</subject><subject>Communities</subject><subject>Community structure</subject><subject>Deoxyribonucleic acid</subject><subject>Dermacentor variabilis</subject><subject>Developmental stages</subject><subject>Disease transmission</subject><subject>Diseases and pests</subject><subject>Diversity indices</subject><subject>DNA</subject><subject>DNA, Bacterial - analysis</subject><subject>Ecosystem</subject><subject>Ehrlichia</subject><subject>Endosymbionts</subject><subject>Environmental factors</subject><subject>Ethanol</subject><subject>Female</subject><subject>Gene libraries</subject><subject>Gene sequencing</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Infections</subject><subject>Insects</subject><subject>Ixodes scapularis</subject><subject>Life history</subject><subject>Male</subject><subject>Microbiomes</subject><subject>Microbiota</subject><subject>Microbiota (Symbiotic organisms)</subject><subject>Microflora</subject><subject>Microorganisms</subject><subject>Parasitic diseases</subject><subject>Pathogens</subject><subject>Physiological aspects</subject><subject>Plasmodium</subject><subject>Polymerase Chain Reaction</subject><subject>Population (statistical)</subject><subject>Population structure</subject><subject>Proteins</subject><subject>Rickettsia</subject><subject>Risk factors</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>rRNA 16S</subject><subject>Soil sciences</subject><subject>Species</subject><subject>Species Specificity</subject><subject>Statistical analysis</subject><subject>Statistical methods</subject><subject>Studies</subject><subject>Tick-borne diseases</subject><subject>Tick-Borne Diseases - microbiology</subject><subject>Ticks</subject><subject>Ticks - microbiology</subject><subject>Vector-borne diseases</subject><subject>Vectors</subject><subject>Viral infections</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNk11v0zAUhiMEYqPwDxBEQkLbRYsdO_64QaqmAZWKJrGOC26sE8dpPJK42Ali_x53TacW7QL5wo79vO-Jz_FJktcYzTDh-MOtG3wHzWzjOjNDmDKW4yfJKZYkm7IMkacH65PkRQi3COVEMPY8OckYz7HA7DT5sapN-tVq7wrrWpO6Kr2sfWN1bWG66Cqje1Om0JXpTWf3n8sYMr3uwacrq3-G9GzeFs2da1tIoTXeauiG9vxl8qyCJphX4zxJbj5dri6-TJdXnxcX8-VUM5n1U6NRXkjBJWiiiTAGeFwBwljnJRM5B0p0RjMKmjIQFS0FRSC4yCgpcFGRSfJ257tpXFBjWoLCPM-5pDTHkVjsiNLBrdp424K_Uw6sut9wfq3A91Y3Jqq40MTQUpqSZphKUZhCc54BlvdHk-TjGG0oWlNq0_UemiPT45PO1mrtfivKkcSSRYOz0cC7X4MJvWpt0KZpoDNu2P43QyKXWUYi-u4f9PHbjdQa4gVikVyMq7emak6JZAhRJiI1e4SKozSt1bGglY37R4LzI0FkevOnX8MQglpcf_t_9ur7Mfv-gK0NNH0dXDP01nXhGKQ7MD7OELypHpKMkdq2wD4batsCamyBKHtzWKAH0f7Nk78Ov_-i</recordid><startdate>20160111</startdate><enddate>20160111</enddate><creator>Trout Fryxell, R T</creator><creator>DeBruyn, J M</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20160111</creationdate><title>The Microbiome of Ehrlichia-Infected and Uninfected Lone Star Ticks (Amblyomma americanum)</title><author>Trout Fryxell, R T ; DeBruyn, J M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-ec05b9879ac3c38eea7ac3a011c5d6857a43c2424ac46a8f4d840a878243b1bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Amblyomma americanum</topic><topic>Analysis</topic><topic>Anaplasma</topic><topic>Animals</topic><topic>Arachnids</topic><topic>Bacteria</topic><topic>Collection</topic><topic>Communities</topic><topic>Community structure</topic><topic>Deoxyribonucleic acid</topic><topic>Dermacentor variabilis</topic><topic>Developmental stages</topic><topic>Disease transmission</topic><topic>Diseases and pests</topic><topic>Diversity indices</topic><topic>DNA</topic><topic>DNA, Bacterial - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Trout Fryxell, R T</au><au>DeBruyn, J M</au><au>Stevenson, Brian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Microbiome of Ehrlichia-Infected and Uninfected Lone Star Ticks (Amblyomma americanum)</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2016-01-11</date><risdate>2016</risdate><volume>11</volume><issue>1</issue><spage>e0146651</spage><epage>e0146651</epage><pages>e0146651-e0146651</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The Lone Star tick, Amblyomma americanum, transmits several bacterial pathogens including species of Anaplasma and Ehrlichia. Amblyomma americanum also hosts a number of non-pathogenic bacterial endosymbionts. Recent studies of other arthropod and insect vectors have documented that commensal microflora can influence transmission of vector-borne pathogens; however, little is known about tick microbiomes and their possible influence on tick-borne diseases. Our objective was to compare bacterial communities associated with A. americanum, comparing Anaplasma/Ehrlichia -infected and uninfected ticks. Field-collected questing specimens (n = 50) were used in the analyses, of which 17 were identified as Anaplasma/Ehrlichia infected based on PCR amplification and sequencing of groEL genes. Bacterial communities from each specimen were characterized using Illumina sequencing of 16S rRNA gene amplicon libraries. There was a broad range in diversity between samples, with inverse Simpson's Diversity indices ranging from 1.28-89.5. There were no statistical differences in the overall microbial community structure between PCR diagnosed Anaplasma/Ehrlichia-positive and negative ticks, but there were differences based on collection method (P < 0.05), collection site (P < 0.05), and sex (P < 0.1) suggesting that environmental factors may structure A. americanum microbiomes. Interestingly, there was not always agreement between Illumina sequencing and PCR diagnostics: Ehrlichia was identified in 16S rRNA gene libraries from three PCR-negative specimens; conversely, Ehrlichia was not found in libraries of six PCR-positive ticks. Illumina sequencing also helped identify co-infections, for example, one specimen had both Ehrlichia and Anaplasma. Other taxa of interest in these specimens included Coxiella, Borrelia, and Rickettsia. Identification of bacterial community differences between specimens of a single tick species from a single geographical site indicates that intra-species differences in microbiomes were not due solely to pathogen presence/absence, but may be also driven by vector life history factors, including environment, life stage, population structure, and host choice.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26751816</pmid><doi>10.1371/journal.pone.0146651</doi><oa>free_for_read</oa></addata></record> |
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subjects | Amblyomma americanum Analysis Anaplasma Animals Arachnids Bacteria Collection Communities Community structure Deoxyribonucleic acid Dermacentor variabilis Developmental stages Disease transmission Diseases and pests Diversity indices DNA DNA, Bacterial - analysis Ecosystem Ehrlichia Endosymbionts Environmental factors Ethanol Female Gene libraries Gene sequencing Genetic aspects Health aspects Infections Insects Ixodes scapularis Life history Male Microbiomes Microbiota Microbiota (Symbiotic organisms) Microflora Microorganisms Parasitic diseases Pathogens Physiological aspects Plasmodium Polymerase Chain Reaction Population (statistical) Population structure Proteins Rickettsia Risk factors RNA, Ribosomal, 16S - genetics rRNA 16S Soil sciences Species Species Specificity Statistical analysis Statistical methods Studies Tick-borne diseases Tick-Borne Diseases - microbiology Ticks Ticks - microbiology Vector-borne diseases Vectors Viral infections |
title | The Microbiome of Ehrlichia-Infected and Uninfected Lone Star Ticks (Amblyomma americanum) |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T22%3A41%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Microbiome%20of%20Ehrlichia-Infected%20and%20Uninfected%20Lone%20Star%20Ticks%20(Amblyomma%20americanum)&rft.jtitle=PloS%20one&rft.au=Trout%20Fryxell,%20R%20T&rft.date=2016-01-11&rft.volume=11&rft.issue=1&rft.spage=e0146651&rft.epage=e0146651&rft.pages=e0146651-e0146651&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0146651&rft_dat=%3Cgale_plos_%3EA439600468%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1755794451&rft_id=info:pmid/26751816&rft_galeid=A439600468&rft_doaj_id=oai_doaj_org_article_1778c3e4d9ed421498bebc772a19778c&rfr_iscdi=true |