Population dynamics and transcriptomic responses of Pseudomonas aeruginosa in a complex laboratory microbial community
Pseudomonas aeruginosa tends to be among the dominant species in multi-species bacterial consortia in diverse environments. To understand P. aeruginosa’s physiology and interactions with co-existing bacterial species in different conditions, we established physiologically reproducible 18 species com...
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creator | Cheng, Yingying Yam, Joey Kuok Hoong Cai, Zhao Ding, Yichen Zhang, Lian-Hui Deng, Yinyue Yang, Liang |
description | Pseudomonas aeruginosa
tends to be among the dominant species in multi-species bacterial consortia in diverse environments. To understand
P. aeruginosa’s
physiology and interactions with co-existing bacterial species in different conditions, we established physiologically reproducible 18 species communities, and found that
P. aeruginosa
dominated in mixed-species biofilm communities but not in planktonic communities.
P. aeruginosa’s
H1 type VI secretion system was highly induced in mixed-species biofilm consortia, compared with its monospecies biofilm, which was further demonstrated to play a key role in
P. aeruginosa
's enhanced fitness over other bacterial species. In addition, the type IV pili and Psl exopolysaccharide were required for
P. aeruginosa
to compete with other bacterial species in the biofilm community. Our study showed that the physiology of
P. aeruginosa
is strongly affected by interspecies interactions, and both biofilm determinants and type VI secretion system contribute to higher
P. aeruginosa
's fitness over other species in complex biofilm communities.
Microbial ecology: transcriptome determinants for biofilm dominance
Pseudomonas aeruginosa
bacteria are highly adaptable and dominate different environments—notably biofilms—yet the biological and ecological factors that support this dominance are still poorly understood. Here, Yingying Cheng and Liang Yang at the Nanyang Technological University, Singapore, used multiplexed gene expression analysis of mixed-species microbial communities to monitor transcriptional changes in
P. aeruginosa
, and reveal the upregulation of the H1 type VI secretion system and the expression of the type IV pili and Psl exopolysaccharide as central events in establishing the dominance of
P. aeruginosa
over other bacterial species growing in biofilms. This work provides new insights into the factors that enhance the fitness of
P. aeruginosa
in multi-species communities, and exemplifies how transcriptome analyses can uncover the physiological properties that enable
P. aeruginosa
to overcome other microbial species and thrive in complex biofilms. |
doi_str_mv | 10.1038/s41522-018-0076-z |
format | Article |
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tends to be among the dominant species in multi-species bacterial consortia in diverse environments. To understand
P. aeruginosa’s
physiology and interactions with co-existing bacterial species in different conditions, we established physiologically reproducible 18 species communities, and found that
P. aeruginosa
dominated in mixed-species biofilm communities but not in planktonic communities.
P. aeruginosa’s
H1 type VI secretion system was highly induced in mixed-species biofilm consortia, compared with its monospecies biofilm, which was further demonstrated to play a key role in
P. aeruginosa
's enhanced fitness over other bacterial species. In addition, the type IV pili and Psl exopolysaccharide were required for
P. aeruginosa
to compete with other bacterial species in the biofilm community. Our study showed that the physiology of
P. aeruginosa
is strongly affected by interspecies interactions, and both biofilm determinants and type VI secretion system contribute to higher
P. aeruginosa
's fitness over other species in complex biofilm communities.
Microbial ecology: transcriptome determinants for biofilm dominance
Pseudomonas aeruginosa
bacteria are highly adaptable and dominate different environments—notably biofilms—yet the biological and ecological factors that support this dominance are still poorly understood. Here, Yingying Cheng and Liang Yang at the Nanyang Technological University, Singapore, used multiplexed gene expression analysis of mixed-species microbial communities to monitor transcriptional changes in
P. aeruginosa
, and reveal the upregulation of the H1 type VI secretion system and the expression of the type IV pili and Psl exopolysaccharide as central events in establishing the dominance of
P. aeruginosa
over other bacterial species growing in biofilms. This work provides new insights into the factors that enhance the fitness of
P. aeruginosa
in multi-species communities, and exemplifies how transcriptome analyses can uncover the physiological properties that enable
P. aeruginosa
to overcome other microbial species and thrive in complex biofilms.</description><identifier>ISSN: 2055-5008</identifier><identifier>EISSN: 2055-5008</identifier><identifier>DOI: 10.1038/s41522-018-0076-z</identifier><identifier>PMID: 30675369</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/1647/514/2254 ; 631/326/2565/2134 ; 631/326/46 ; Bacteria ; Biofilms ; Biomedical and Life Sciences ; Consortia ; Dominant species ; Exopolysaccharides ; Fitness ; Life Sciences ; Medical Microbiology ; Microbial Ecology ; Microbial Genetics and Genomics ; Microbiology ; Microbiomes ; Pathogens ; Physiology ; Pili ; Pseudomonas aeruginosa ; Secretion</subject><ispartof>NPJ biofilms and microbiomes, 2019-01, Vol.5 (1), p.1-1, Article 1</ispartof><rights>The Author(s) 2019</rights><rights>This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-14ae862ad9e21d82d1a0b0b3bc8cecf95838ee4529023647994e52c64f8b25e23</citedby><cites>FETCH-LOGICAL-c470t-14ae862ad9e21d82d1a0b0b3bc8cecf95838ee4529023647994e52c64f8b25e23</cites><orcidid>0000-0002-7698-8233 ; 0000-0002-2362-0128 ; 0000-0003-1511-0870</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334633/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334633/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27922,27923,41118,42187,51574,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30675369$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cheng, Yingying</creatorcontrib><creatorcontrib>Yam, Joey Kuok Hoong</creatorcontrib><creatorcontrib>Cai, Zhao</creatorcontrib><creatorcontrib>Ding, Yichen</creatorcontrib><creatorcontrib>Zhang, Lian-Hui</creatorcontrib><creatorcontrib>Deng, Yinyue</creatorcontrib><creatorcontrib>Yang, Liang</creatorcontrib><title>Population dynamics and transcriptomic responses of Pseudomonas aeruginosa in a complex laboratory microbial community</title><title>NPJ biofilms and microbiomes</title><addtitle>npj Biofilms Microbiomes</addtitle><addtitle>NPJ Biofilms Microbiomes</addtitle><description>Pseudomonas aeruginosa
tends to be among the dominant species in multi-species bacterial consortia in diverse environments. To understand
P. aeruginosa’s
physiology and interactions with co-existing bacterial species in different conditions, we established physiologically reproducible 18 species communities, and found that
P. aeruginosa
dominated in mixed-species biofilm communities but not in planktonic communities.
P. aeruginosa’s
H1 type VI secretion system was highly induced in mixed-species biofilm consortia, compared with its monospecies biofilm, which was further demonstrated to play a key role in
P. aeruginosa
's enhanced fitness over other bacterial species. In addition, the type IV pili and Psl exopolysaccharide were required for
P. aeruginosa
to compete with other bacterial species in the biofilm community. Our study showed that the physiology of
P. aeruginosa
is strongly affected by interspecies interactions, and both biofilm determinants and type VI secretion system contribute to higher
P. aeruginosa
's fitness over other species in complex biofilm communities.
Microbial ecology: transcriptome determinants for biofilm dominance
Pseudomonas aeruginosa
bacteria are highly adaptable and dominate different environments—notably biofilms—yet the biological and ecological factors that support this dominance are still poorly understood. Here, Yingying Cheng and Liang Yang at the Nanyang Technological University, Singapore, used multiplexed gene expression analysis of mixed-species microbial communities to monitor transcriptional changes in
P. aeruginosa
, and reveal the upregulation of the H1 type VI secretion system and the expression of the type IV pili and Psl exopolysaccharide as central events in establishing the dominance of
P. aeruginosa
over other bacterial species growing in biofilms. This work provides new insights into the factors that enhance the fitness of
P. aeruginosa
in multi-species communities, and exemplifies how transcriptome analyses can uncover the physiological properties that enable
P. aeruginosa
to overcome other microbial species and thrive in complex biofilms.</description><subject>631/1647/514/2254</subject><subject>631/326/2565/2134</subject><subject>631/326/46</subject><subject>Bacteria</subject><subject>Biofilms</subject><subject>Biomedical and Life Sciences</subject><subject>Consortia</subject><subject>Dominant species</subject><subject>Exopolysaccharides</subject><subject>Fitness</subject><subject>Life Sciences</subject><subject>Medical Microbiology</subject><subject>Microbial Ecology</subject><subject>Microbial Genetics and Genomics</subject><subject>Microbiology</subject><subject>Microbiomes</subject><subject>Pathogens</subject><subject>Physiology</subject><subject>Pili</subject><subject>Pseudomonas aeruginosa</subject><subject>Secretion</subject><issn>2055-5008</issn><issn>2055-5008</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kUtr3TAQhUVpaEKSH5BNEHTTjZvRy5Y3hRL6gkCzaNdClsc3CrbkSnboza-vLjevFroQEppvjnTmEHLG4D0DoS-yZIrzCpiuAJq6un9FjjgoVSkA_frF-ZCc5nwLAEzJRmj1hhwKqBsl6vaI3F3HeR3t4mOg_TbYybtMbejpkmzILvl5ieWOJsxzDBkzjQO9zrj2cYrBFhbTuvEhZkt9oJa6OM0j_qaj7WKyS0xbWvpT7Lwdd8VpDX7ZnpCDwY4ZTx_2Y_Lz86cfl1-rq-9fvl1-vKqcbGCpmLSoa277FjnrNe-ZhQ460Tnt0A2t0kIjSsVb4KKWTdtKVNzVctAdV8jFMfmw153XbsLeYSi-RjMnP9m0NdF683cl-BuziXemFkKWVQTePQik-GvFvJjJZ4fjaAPGNRvOmlYyUaZb0Lf_oLdxTaHYK1TdAGec7yi2p8pMck44PH2GgdkFa_bBmhKs2QVr7kvP-UsXTx2PMRaA74FcSmGD6fnp_6v-AZkisfE</recordid><startdate>20190114</startdate><enddate>20190114</enddate><creator>Cheng, Yingying</creator><creator>Yam, Joey Kuok Hoong</creator><creator>Cai, Zhao</creator><creator>Ding, Yichen</creator><creator>Zhang, Lian-Hui</creator><creator>Deng, Yinyue</creator><creator>Yang, Liang</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7698-8233</orcidid><orcidid>https://orcid.org/0000-0002-2362-0128</orcidid><orcidid>https://orcid.org/0000-0003-1511-0870</orcidid></search><sort><creationdate>20190114</creationdate><title>Population dynamics and transcriptomic responses of Pseudomonas aeruginosa in a complex laboratory microbial community</title><author>Cheng, Yingying ; 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tends to be among the dominant species in multi-species bacterial consortia in diverse environments. To understand
P. aeruginosa’s
physiology and interactions with co-existing bacterial species in different conditions, we established physiologically reproducible 18 species communities, and found that
P. aeruginosa
dominated in mixed-species biofilm communities but not in planktonic communities.
P. aeruginosa’s
H1 type VI secretion system was highly induced in mixed-species biofilm consortia, compared with its monospecies biofilm, which was further demonstrated to play a key role in
P. aeruginosa
's enhanced fitness over other bacterial species. In addition, the type IV pili and Psl exopolysaccharide were required for
P. aeruginosa
to compete with other bacterial species in the biofilm community. Our study showed that the physiology of
P. aeruginosa
is strongly affected by interspecies interactions, and both biofilm determinants and type VI secretion system contribute to higher
P. aeruginosa
's fitness over other species in complex biofilm communities.
Microbial ecology: transcriptome determinants for biofilm dominance
Pseudomonas aeruginosa
bacteria are highly adaptable and dominate different environments—notably biofilms—yet the biological and ecological factors that support this dominance are still poorly understood. Here, Yingying Cheng and Liang Yang at the Nanyang Technological University, Singapore, used multiplexed gene expression analysis of mixed-species microbial communities to monitor transcriptional changes in
P. aeruginosa
, and reveal the upregulation of the H1 type VI secretion system and the expression of the type IV pili and Psl exopolysaccharide as central events in establishing the dominance of
P. aeruginosa
over other bacterial species growing in biofilms. This work provides new insights into the factors that enhance the fitness of
P. aeruginosa
in multi-species communities, and exemplifies how transcriptome analyses can uncover the physiological properties that enable
P. aeruginosa
to overcome other microbial species and thrive in complex biofilms.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>30675369</pmid><doi>10.1038/s41522-018-0076-z</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-7698-8233</orcidid><orcidid>https://orcid.org/0000-0002-2362-0128</orcidid><orcidid>https://orcid.org/0000-0003-1511-0870</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/1647/514/2254 631/326/2565/2134 631/326/46 Bacteria Biofilms Biomedical and Life Sciences Consortia Dominant species Exopolysaccharides Fitness Life Sciences Medical Microbiology Microbial Ecology Microbial Genetics and Genomics Microbiology Microbiomes Pathogens Physiology Pili Pseudomonas aeruginosa Secretion |
title | Population dynamics and transcriptomic responses of Pseudomonas aeruginosa in a complex laboratory microbial community |
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