Culture enriched molecular profiling of the cystic fibrosis airway microbiome
The microbiome of the respiratory tract, including the nasopharyngeal and oropharyngeal microbiota, is a dynamic community of microorganisms that is highly diverse. The cystic fibrosis (CF) airway microbiome refers to the polymicrobial communities present in the lower airways of CF patients. It is c...
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description | The microbiome of the respiratory tract, including the nasopharyngeal and oropharyngeal microbiota, is a dynamic community of microorganisms that is highly diverse. The cystic fibrosis (CF) airway microbiome refers to the polymicrobial communities present in the lower airways of CF patients. It is comprised of chronic opportunistic pathogens (such as Pseudomonas aeruginosa) and a variety of organisms derived mostly from the normal microbiota of the upper respiratory tract. The complexity of these communities has been inferred primarily from culture independent molecular profiling. As with most microbial communities it is generally assumed that most of the organisms present are not readily cultured. Our culture collection generated using more extensive cultivation approaches, reveals a more complex microbial community than that obtained by conventional CF culture methods. To directly evaluate the cultivability of the airway microbiome, we examined six samples in depth using culture-enriched molecular profiling which combines culture-based methods with the molecular profiling methods of terminal restriction fragment length polymorphisms and 16S rRNA gene sequencing. We demonstrate that combining culture-dependent and culture-independent approaches enhances the sensitivity of either approach alone. Our techniques were able to cultivate 43 of the 48 families detected by deep sequencing; the five families recovered solely by culture-independent approaches were all present at very low abundance ( |
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The cystic fibrosis (CF) airway microbiome refers to the polymicrobial communities present in the lower airways of CF patients. It is comprised of chronic opportunistic pathogens (such as Pseudomonas aeruginosa) and a variety of organisms derived mostly from the normal microbiota of the upper respiratory tract. The complexity of these communities has been inferred primarily from culture independent molecular profiling. As with most microbial communities it is generally assumed that most of the organisms present are not readily cultured. Our culture collection generated using more extensive cultivation approaches, reveals a more complex microbial community than that obtained by conventional CF culture methods. To directly evaluate the cultivability of the airway microbiome, we examined six samples in depth using culture-enriched molecular profiling which combines culture-based methods with the molecular profiling methods of terminal restriction fragment length polymorphisms and 16S rRNA gene sequencing. We demonstrate that combining culture-dependent and culture-independent approaches enhances the sensitivity of either approach alone. Our techniques were able to cultivate 43 of the 48 families detected by deep sequencing; the five families recovered solely by culture-independent approaches were all present at very low abundance (<0.002% total reads). 46% of the molecular signatures detected by culture from the six patients were only identified in an anaerobic environment, suggesting that a large proportion of the cultured airway community is composed of obligate anaerobes. Most significantly, using 20 growth conditions per specimen, half of which included anaerobic cultivation and extended incubation times we demonstrate that the majority of bacteria present can be cultured.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0022702</identifier><identifier>PMID: 21829484</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acids ; Anaerobes ; Anaerobic conditions ; Antibiotics ; Bacteria ; Bacteria - classification ; Bacteria - genetics ; Bacteria - growth & development ; Biofilms ; Biology ; Communities ; Complexity ; Cultivation ; Culture ; Cystic fibrosis ; Cystic Fibrosis - genetics ; Cystic Fibrosis - microbiology ; Diabetes ; DNA Barcoding, Taxonomic ; Foot diseases ; Gene sequencing ; Genetic polymorphisms ; Growth conditions ; Humans ; Infections ; Infectious diseases ; Leg ulcers ; Medicine ; Metagenome - genetics ; Microbial activity ; Microbiota (Symbiotic organisms) ; Microorganisms ; Opportunist infection ; Patients ; Polymorphism, Restriction Fragment Length ; Proteobacteria ; Pseudomonas aeruginosa ; Respiratory System - microbiology ; Respiratory tract ; RNA ; RNA, Ribosomal, 16S - genetics ; rRNA 16S ; Salmonella ; Sensitivity enhancement ; Sputum - microbiology ; Testing laboratories ; Wound healing</subject><ispartof>PloS one, 2011-07, Vol.6 (7), p.e22702-e22702</ispartof><rights>COPYRIGHT 2011 Public Library of Science</rights><rights>2011 Sibley et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://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>Sibley et al. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c757t-6b371c6133ad0d710a1b5ccfa479389c1049ce7f6ea85e2b953811d0e1e64df63</citedby><cites>FETCH-LOGICAL-c757t-6b371c6133ad0d710a1b5ccfa479389c1049ce7f6ea85e2b953811d0e1e64df63</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/PMC3145661/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3145661/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,2103,2929,23871,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21829484$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Planet, Paul J.</contributor><creatorcontrib>Sibley, Christopher D</creatorcontrib><creatorcontrib>Grinwis, Margot E</creatorcontrib><creatorcontrib>Field, Tyler R</creatorcontrib><creatorcontrib>Eshaghurshan, Christina S</creatorcontrib><creatorcontrib>Faria, Monica M</creatorcontrib><creatorcontrib>Dowd, Scot E</creatorcontrib><creatorcontrib>Parkins, Michael D</creatorcontrib><creatorcontrib>Rabin, Harvey R</creatorcontrib><creatorcontrib>Surette, Michael G</creatorcontrib><title>Culture enriched molecular profiling of the cystic fibrosis airway microbiome</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The microbiome of the respiratory tract, including the nasopharyngeal and oropharyngeal microbiota, is a dynamic community of microorganisms that is highly diverse. 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The cystic fibrosis (CF) airway microbiome refers to the polymicrobial communities present in the lower airways of CF patients. It is comprised of chronic opportunistic pathogens (such as Pseudomonas aeruginosa) and a variety of organisms derived mostly from the normal microbiota of the upper respiratory tract. The complexity of these communities has been inferred primarily from culture independent molecular profiling. As with most microbial communities it is generally assumed that most of the organisms present are not readily cultured. Our culture collection generated using more extensive cultivation approaches, reveals a more complex microbial community than that obtained by conventional CF culture methods. To directly evaluate the cultivability of the airway microbiome, we examined six samples in depth using culture-enriched molecular profiling which combines culture-based methods with the molecular profiling methods of terminal restriction fragment length polymorphisms and 16S rRNA gene sequencing. We demonstrate that combining culture-dependent and culture-independent approaches enhances the sensitivity of either approach alone. Our techniques were able to cultivate 43 of the 48 families detected by deep sequencing; the five families recovered solely by culture-independent approaches were all present at very low abundance (<0.002% total reads). 46% of the molecular signatures detected by culture from the six patients were only identified in an anaerobic environment, suggesting that a large proportion of the cultured airway community is composed of obligate anaerobes. Most significantly, using 20 growth conditions per specimen, half of which included anaerobic cultivation and extended incubation times we demonstrate that the majority of bacteria present can be cultured.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>21829484</pmid><doi>10.1371/journal.pone.0022702</doi><tpages>e22702</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acids Anaerobes Anaerobic conditions Antibiotics Bacteria Bacteria - classification Bacteria - genetics Bacteria - growth & development Biofilms Biology Communities Complexity Cultivation Culture Cystic fibrosis Cystic Fibrosis - genetics Cystic Fibrosis - microbiology Diabetes DNA Barcoding, Taxonomic Foot diseases Gene sequencing Genetic polymorphisms Growth conditions Humans Infections Infectious diseases Leg ulcers Medicine Metagenome - genetics Microbial activity Microbiota (Symbiotic organisms) Microorganisms Opportunist infection Patients Polymorphism, Restriction Fragment Length Proteobacteria Pseudomonas aeruginosa Respiratory System - microbiology Respiratory tract RNA RNA, Ribosomal, 16S - genetics rRNA 16S Salmonella Sensitivity enhancement Sputum - microbiology Testing laboratories Wound healing |
title | Culture enriched molecular profiling of the cystic fibrosis airway microbiome |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-13T04%3A58%3A00IST&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=Culture%20enriched%20molecular%20profiling%20of%20the%20cystic%20fibrosis%20airway%20microbiome&rft.jtitle=PloS%20one&rft.au=Sibley,%20Christopher%20D&rft.date=2011-07-28&rft.volume=6&rft.issue=7&rft.spage=e22702&rft.epage=e22702&rft.pages=e22702-e22702&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0022702&rft_dat=%3Cgale_plos_%3EA476883752%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=1306219131&rft_id=info:pmid/21829484&rft_galeid=A476883752&rft_doaj_id=oai_doaj_org_article_8f2d2091e9e84cb585bdff9906031cc8&rfr_iscdi=true |