Correlation of the lung microbiota with metabolic profiles in bronchoalveolar lavage fluid in HIV infection
Background While 16S ribosomal RNA (rRNA) sequencing has been used to characterize the lung’s bacterial microbiota in human immunodeficiency virus (HIV)-infected individuals, taxonomic studies provide limited information on bacterial function and impact on the host. Metabolic profiles can provide fu...
Ausführliche Beschreibung
Autor*in: |
Cribbs, Sushma K. [verfasserIn] Uppal, Karan [verfasserIn] Li, Shuzhao [verfasserIn] Jones, Dean P. [verfasserIn] Huang, Laurence [verfasserIn] Tipton, Laura [verfasserIn] Fitch, Adam [verfasserIn] Greenblatt, Ruth M. [verfasserIn] Kingsley, Lawrence [verfasserIn] Guidot, David M. [verfasserIn] Ghedin, Elodie [verfasserIn] Morris, Alison [verfasserIn] |
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E-Artikel |
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Englisch |
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2016 |
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Übergeordnetes Werk: |
Enthalten in: Microbiome - London : Biomed Central, 2013, 4(2016), 1 vom: 20. Jan. |
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Übergeordnetes Werk: |
volume:4 ; year:2016 ; number:1 ; day:20 ; month:01 |
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DOI / URN: |
10.1186/s40168-016-0147-4 |
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Katalog-ID: |
SPR03322384X |
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245 | 1 | 0 | |a Correlation of the lung microbiota with metabolic profiles in bronchoalveolar lavage fluid in HIV infection |
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520 | |a Background While 16S ribosomal RNA (rRNA) sequencing has been used to characterize the lung’s bacterial microbiota in human immunodeficiency virus (HIV)-infected individuals, taxonomic studies provide limited information on bacterial function and impact on the host. Metabolic profiles can provide functional information on host-microbe interactions in the lungs. We investigated the relationship between the respiratory microbiota and metabolic profiles in the bronchoalveolar lavage fluid of HIV-infected and HIV-uninfected outpatients. Results Targeted sequencing of the 16S rRNA gene was used to analyze the bacterial community structure and liquid chromatography-high-resolution mass spectrometry was used to detect features in bronchoalveolar lavage fluid. Global integration of all metabolic features with microbial species was done using sparse partial least squares regression. Thirty-nine HIV-infected subjects and 20 HIV-uninfected controls without acute respiratory symptoms were enrolled. Twelve mass-to-charge ratio (m/z) features from C18 analysis were significantly different between HIV-infected individuals and controls (false discovery rate (FDR) = 0.2); another 79 features were identified by network analysis. Further metabolite analysis demonstrated that four features were significantly overrepresented in the bronchoalveolar lavage (BAL) fluid of HIV-infected individuals compared to HIV-uninfected, including cystine, two complex carbohydrates, and 3,5-dibromo-l-tyrosine. There were 231 m/z features significantly associated with peripheral blood CD4 cell counts identified using sparse partial least squares regression (sPLS) at a variable importance on projection (VIP) threshold of 2. Twenty-five percent of these 91 m/z features were associated with various microbial species. Bacteria from families Caulobacteraceae, Staphylococcaceae, Nocardioidaceae, and genus Streptococcus were associated with the greatest number of features. Glycerophospholipid and lineolate pathways correlated with these bacteria. Conclusions In bronchoalveolar lavage fluid, specific metabolic profiles correlated with bacterial organisms known to play a role in the pathogenesis of pneumonia in HIV-infected individuals. These findings suggest that microbial communities and their interactions with the host may have functional metabolic impact in the lung. | ||
650 | 4 | |a HIV |7 (dpeaa)DE-He213 | |
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650 | 4 | |a Metabolomics |7 (dpeaa)DE-He213 | |
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700 | 1 | |a Uppal, Karan |e verfasserin |4 aut | |
700 | 1 | |a Li, Shuzhao |e verfasserin |4 aut | |
700 | 1 | |a Jones, Dean P. |e verfasserin |4 aut | |
700 | 1 | |a Huang, Laurence |e verfasserin |4 aut | |
700 | 1 | |a Tipton, Laura |e verfasserin |4 aut | |
700 | 1 | |a Fitch, Adam |e verfasserin |4 aut | |
700 | 1 | |a Greenblatt, Ruth M. |e verfasserin |4 aut | |
700 | 1 | |a Kingsley, Lawrence |e verfasserin |4 aut | |
700 | 1 | |a Guidot, David M. |e verfasserin |4 aut | |
700 | 1 | |a Ghedin, Elodie |e verfasserin |4 aut | |
700 | 1 | |a Morris, Alison |e verfasserin |4 aut | |
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10.1186/s40168-016-0147-4 doi (DE-627)SPR03322384X (SPR)s40168-016-0147-4-e DE-627 ger DE-627 rakwb eng 570 ASE Cribbs, Sushma K. verfasserin aut Correlation of the lung microbiota with metabolic profiles in bronchoalveolar lavage fluid in HIV infection 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background While 16S ribosomal RNA (rRNA) sequencing has been used to characterize the lung’s bacterial microbiota in human immunodeficiency virus (HIV)-infected individuals, taxonomic studies provide limited information on bacterial function and impact on the host. Metabolic profiles can provide functional information on host-microbe interactions in the lungs. We investigated the relationship between the respiratory microbiota and metabolic profiles in the bronchoalveolar lavage fluid of HIV-infected and HIV-uninfected outpatients. Results Targeted sequencing of the 16S rRNA gene was used to analyze the bacterial community structure and liquid chromatography-high-resolution mass spectrometry was used to detect features in bronchoalveolar lavage fluid. Global integration of all metabolic features with microbial species was done using sparse partial least squares regression. Thirty-nine HIV-infected subjects and 20 HIV-uninfected controls without acute respiratory symptoms were enrolled. Twelve mass-to-charge ratio (m/z) features from C18 analysis were significantly different between HIV-infected individuals and controls (false discovery rate (FDR) = 0.2); another 79 features were identified by network analysis. Further metabolite analysis demonstrated that four features were significantly overrepresented in the bronchoalveolar lavage (BAL) fluid of HIV-infected individuals compared to HIV-uninfected, including cystine, two complex carbohydrates, and 3,5-dibromo-l-tyrosine. There were 231 m/z features significantly associated with peripheral blood CD4 cell counts identified using sparse partial least squares regression (sPLS) at a variable importance on projection (VIP) threshold of 2. Twenty-five percent of these 91 m/z features were associated with various microbial species. Bacteria from families Caulobacteraceae, Staphylococcaceae, Nocardioidaceae, and genus Streptococcus were associated with the greatest number of features. Glycerophospholipid and lineolate pathways correlated with these bacteria. Conclusions In bronchoalveolar lavage fluid, specific metabolic profiles correlated with bacterial organisms known to play a role in the pathogenesis of pneumonia in HIV-infected individuals. These findings suggest that microbial communities and their interactions with the host may have functional metabolic impact in the lung. HIV (dpeaa)DE-He213 Lung (dpeaa)DE-He213 Metabolomics (dpeaa)DE-He213 Microbiota (dpeaa)DE-He213 Bronchoalveolar lavage (dpeaa)DE-He213 Uppal, Karan verfasserin aut Li, Shuzhao verfasserin aut Jones, Dean P. verfasserin aut Huang, Laurence verfasserin aut Tipton, Laura verfasserin aut Fitch, Adam verfasserin aut Greenblatt, Ruth M. verfasserin aut Kingsley, Lawrence verfasserin aut Guidot, David M. verfasserin aut Ghedin, Elodie verfasserin aut Morris, Alison verfasserin aut Enthalten in Microbiome London : Biomed Central, 2013 4(2016), 1 vom: 20. Jan. (DE-627)734146140 (DE-600)2697425-3 2049-2618 nnns volume:4 year:2016 number:1 day:20 month:01 https://dx.doi.org/10.1186/s40168-016-0147-4 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2016 1 20 01 |
spelling |
10.1186/s40168-016-0147-4 doi (DE-627)SPR03322384X (SPR)s40168-016-0147-4-e DE-627 ger DE-627 rakwb eng 570 ASE Cribbs, Sushma K. verfasserin aut Correlation of the lung microbiota with metabolic profiles in bronchoalveolar lavage fluid in HIV infection 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background While 16S ribosomal RNA (rRNA) sequencing has been used to characterize the lung’s bacterial microbiota in human immunodeficiency virus (HIV)-infected individuals, taxonomic studies provide limited information on bacterial function and impact on the host. Metabolic profiles can provide functional information on host-microbe interactions in the lungs. We investigated the relationship between the respiratory microbiota and metabolic profiles in the bronchoalveolar lavage fluid of HIV-infected and HIV-uninfected outpatients. Results Targeted sequencing of the 16S rRNA gene was used to analyze the bacterial community structure and liquid chromatography-high-resolution mass spectrometry was used to detect features in bronchoalveolar lavage fluid. Global integration of all metabolic features with microbial species was done using sparse partial least squares regression. Thirty-nine HIV-infected subjects and 20 HIV-uninfected controls without acute respiratory symptoms were enrolled. Twelve mass-to-charge ratio (m/z) features from C18 analysis were significantly different between HIV-infected individuals and controls (false discovery rate (FDR) = 0.2); another 79 features were identified by network analysis. Further metabolite analysis demonstrated that four features were significantly overrepresented in the bronchoalveolar lavage (BAL) fluid of HIV-infected individuals compared to HIV-uninfected, including cystine, two complex carbohydrates, and 3,5-dibromo-l-tyrosine. There were 231 m/z features significantly associated with peripheral blood CD4 cell counts identified using sparse partial least squares regression (sPLS) at a variable importance on projection (VIP) threshold of 2. Twenty-five percent of these 91 m/z features were associated with various microbial species. Bacteria from families Caulobacteraceae, Staphylococcaceae, Nocardioidaceae, and genus Streptococcus were associated with the greatest number of features. Glycerophospholipid and lineolate pathways correlated with these bacteria. Conclusions In bronchoalveolar lavage fluid, specific metabolic profiles correlated with bacterial organisms known to play a role in the pathogenesis of pneumonia in HIV-infected individuals. These findings suggest that microbial communities and their interactions with the host may have functional metabolic impact in the lung. HIV (dpeaa)DE-He213 Lung (dpeaa)DE-He213 Metabolomics (dpeaa)DE-He213 Microbiota (dpeaa)DE-He213 Bronchoalveolar lavage (dpeaa)DE-He213 Uppal, Karan verfasserin aut Li, Shuzhao verfasserin aut Jones, Dean P. verfasserin aut Huang, Laurence verfasserin aut Tipton, Laura verfasserin aut Fitch, Adam verfasserin aut Greenblatt, Ruth M. verfasserin aut Kingsley, Lawrence verfasserin aut Guidot, David M. verfasserin aut Ghedin, Elodie verfasserin aut Morris, Alison verfasserin aut Enthalten in Microbiome London : Biomed Central, 2013 4(2016), 1 vom: 20. Jan. (DE-627)734146140 (DE-600)2697425-3 2049-2618 nnns volume:4 year:2016 number:1 day:20 month:01 https://dx.doi.org/10.1186/s40168-016-0147-4 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2016 1 20 01 |
allfields_unstemmed |
10.1186/s40168-016-0147-4 doi (DE-627)SPR03322384X (SPR)s40168-016-0147-4-e DE-627 ger DE-627 rakwb eng 570 ASE Cribbs, Sushma K. verfasserin aut Correlation of the lung microbiota with metabolic profiles in bronchoalveolar lavage fluid in HIV infection 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background While 16S ribosomal RNA (rRNA) sequencing has been used to characterize the lung’s bacterial microbiota in human immunodeficiency virus (HIV)-infected individuals, taxonomic studies provide limited information on bacterial function and impact on the host. Metabolic profiles can provide functional information on host-microbe interactions in the lungs. We investigated the relationship between the respiratory microbiota and metabolic profiles in the bronchoalveolar lavage fluid of HIV-infected and HIV-uninfected outpatients. Results Targeted sequencing of the 16S rRNA gene was used to analyze the bacterial community structure and liquid chromatography-high-resolution mass spectrometry was used to detect features in bronchoalveolar lavage fluid. Global integration of all metabolic features with microbial species was done using sparse partial least squares regression. Thirty-nine HIV-infected subjects and 20 HIV-uninfected controls without acute respiratory symptoms were enrolled. Twelve mass-to-charge ratio (m/z) features from C18 analysis were significantly different between HIV-infected individuals and controls (false discovery rate (FDR) = 0.2); another 79 features were identified by network analysis. Further metabolite analysis demonstrated that four features were significantly overrepresented in the bronchoalveolar lavage (BAL) fluid of HIV-infected individuals compared to HIV-uninfected, including cystine, two complex carbohydrates, and 3,5-dibromo-l-tyrosine. There were 231 m/z features significantly associated with peripheral blood CD4 cell counts identified using sparse partial least squares regression (sPLS) at a variable importance on projection (VIP) threshold of 2. Twenty-five percent of these 91 m/z features were associated with various microbial species. Bacteria from families Caulobacteraceae, Staphylococcaceae, Nocardioidaceae, and genus Streptococcus were associated with the greatest number of features. Glycerophospholipid and lineolate pathways correlated with these bacteria. Conclusions In bronchoalveolar lavage fluid, specific metabolic profiles correlated with bacterial organisms known to play a role in the pathogenesis of pneumonia in HIV-infected individuals. These findings suggest that microbial communities and their interactions with the host may have functional metabolic impact in the lung. HIV (dpeaa)DE-He213 Lung (dpeaa)DE-He213 Metabolomics (dpeaa)DE-He213 Microbiota (dpeaa)DE-He213 Bronchoalveolar lavage (dpeaa)DE-He213 Uppal, Karan verfasserin aut Li, Shuzhao verfasserin aut Jones, Dean P. verfasserin aut Huang, Laurence verfasserin aut Tipton, Laura verfasserin aut Fitch, Adam verfasserin aut Greenblatt, Ruth M. verfasserin aut Kingsley, Lawrence verfasserin aut Guidot, David M. verfasserin aut Ghedin, Elodie verfasserin aut Morris, Alison verfasserin aut Enthalten in Microbiome London : Biomed Central, 2013 4(2016), 1 vom: 20. Jan. (DE-627)734146140 (DE-600)2697425-3 2049-2618 nnns volume:4 year:2016 number:1 day:20 month:01 https://dx.doi.org/10.1186/s40168-016-0147-4 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2016 1 20 01 |
allfieldsGer |
10.1186/s40168-016-0147-4 doi (DE-627)SPR03322384X (SPR)s40168-016-0147-4-e DE-627 ger DE-627 rakwb eng 570 ASE Cribbs, Sushma K. verfasserin aut Correlation of the lung microbiota with metabolic profiles in bronchoalveolar lavage fluid in HIV infection 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background While 16S ribosomal RNA (rRNA) sequencing has been used to characterize the lung’s bacterial microbiota in human immunodeficiency virus (HIV)-infected individuals, taxonomic studies provide limited information on bacterial function and impact on the host. Metabolic profiles can provide functional information on host-microbe interactions in the lungs. We investigated the relationship between the respiratory microbiota and metabolic profiles in the bronchoalveolar lavage fluid of HIV-infected and HIV-uninfected outpatients. Results Targeted sequencing of the 16S rRNA gene was used to analyze the bacterial community structure and liquid chromatography-high-resolution mass spectrometry was used to detect features in bronchoalveolar lavage fluid. Global integration of all metabolic features with microbial species was done using sparse partial least squares regression. Thirty-nine HIV-infected subjects and 20 HIV-uninfected controls without acute respiratory symptoms were enrolled. Twelve mass-to-charge ratio (m/z) features from C18 analysis were significantly different between HIV-infected individuals and controls (false discovery rate (FDR) = 0.2); another 79 features were identified by network analysis. Further metabolite analysis demonstrated that four features were significantly overrepresented in the bronchoalveolar lavage (BAL) fluid of HIV-infected individuals compared to HIV-uninfected, including cystine, two complex carbohydrates, and 3,5-dibromo-l-tyrosine. There were 231 m/z features significantly associated with peripheral blood CD4 cell counts identified using sparse partial least squares regression (sPLS) at a variable importance on projection (VIP) threshold of 2. Twenty-five percent of these 91 m/z features were associated with various microbial species. Bacteria from families Caulobacteraceae, Staphylococcaceae, Nocardioidaceae, and genus Streptococcus were associated with the greatest number of features. Glycerophospholipid and lineolate pathways correlated with these bacteria. Conclusions In bronchoalveolar lavage fluid, specific metabolic profiles correlated with bacterial organisms known to play a role in the pathogenesis of pneumonia in HIV-infected individuals. These findings suggest that microbial communities and their interactions with the host may have functional metabolic impact in the lung. HIV (dpeaa)DE-He213 Lung (dpeaa)DE-He213 Metabolomics (dpeaa)DE-He213 Microbiota (dpeaa)DE-He213 Bronchoalveolar lavage (dpeaa)DE-He213 Uppal, Karan verfasserin aut Li, Shuzhao verfasserin aut Jones, Dean P. verfasserin aut Huang, Laurence verfasserin aut Tipton, Laura verfasserin aut Fitch, Adam verfasserin aut Greenblatt, Ruth M. verfasserin aut Kingsley, Lawrence verfasserin aut Guidot, David M. verfasserin aut Ghedin, Elodie verfasserin aut Morris, Alison verfasserin aut Enthalten in Microbiome London : Biomed Central, 2013 4(2016), 1 vom: 20. Jan. (DE-627)734146140 (DE-600)2697425-3 2049-2618 nnns volume:4 year:2016 number:1 day:20 month:01 https://dx.doi.org/10.1186/s40168-016-0147-4 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2016 1 20 01 |
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10.1186/s40168-016-0147-4 doi (DE-627)SPR03322384X (SPR)s40168-016-0147-4-e DE-627 ger DE-627 rakwb eng 570 ASE Cribbs, Sushma K. verfasserin aut Correlation of the lung microbiota with metabolic profiles in bronchoalveolar lavage fluid in HIV infection 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background While 16S ribosomal RNA (rRNA) sequencing has been used to characterize the lung’s bacterial microbiota in human immunodeficiency virus (HIV)-infected individuals, taxonomic studies provide limited information on bacterial function and impact on the host. Metabolic profiles can provide functional information on host-microbe interactions in the lungs. We investigated the relationship between the respiratory microbiota and metabolic profiles in the bronchoalveolar lavage fluid of HIV-infected and HIV-uninfected outpatients. Results Targeted sequencing of the 16S rRNA gene was used to analyze the bacterial community structure and liquid chromatography-high-resolution mass spectrometry was used to detect features in bronchoalveolar lavage fluid. Global integration of all metabolic features with microbial species was done using sparse partial least squares regression. Thirty-nine HIV-infected subjects and 20 HIV-uninfected controls without acute respiratory symptoms were enrolled. Twelve mass-to-charge ratio (m/z) features from C18 analysis were significantly different between HIV-infected individuals and controls (false discovery rate (FDR) = 0.2); another 79 features were identified by network analysis. Further metabolite analysis demonstrated that four features were significantly overrepresented in the bronchoalveolar lavage (BAL) fluid of HIV-infected individuals compared to HIV-uninfected, including cystine, two complex carbohydrates, and 3,5-dibromo-l-tyrosine. There were 231 m/z features significantly associated with peripheral blood CD4 cell counts identified using sparse partial least squares regression (sPLS) at a variable importance on projection (VIP) threshold of 2. Twenty-five percent of these 91 m/z features were associated with various microbial species. Bacteria from families Caulobacteraceae, Staphylococcaceae, Nocardioidaceae, and genus Streptococcus were associated with the greatest number of features. Glycerophospholipid and lineolate pathways correlated with these bacteria. Conclusions In bronchoalveolar lavage fluid, specific metabolic profiles correlated with bacterial organisms known to play a role in the pathogenesis of pneumonia in HIV-infected individuals. These findings suggest that microbial communities and their interactions with the host may have functional metabolic impact in the lung. HIV (dpeaa)DE-He213 Lung (dpeaa)DE-He213 Metabolomics (dpeaa)DE-He213 Microbiota (dpeaa)DE-He213 Bronchoalveolar lavage (dpeaa)DE-He213 Uppal, Karan verfasserin aut Li, Shuzhao verfasserin aut Jones, Dean P. verfasserin aut Huang, Laurence verfasserin aut Tipton, Laura verfasserin aut Fitch, Adam verfasserin aut Greenblatt, Ruth M. verfasserin aut Kingsley, Lawrence verfasserin aut Guidot, David M. verfasserin aut Ghedin, Elodie verfasserin aut Morris, Alison verfasserin aut Enthalten in Microbiome London : Biomed Central, 2013 4(2016), 1 vom: 20. Jan. (DE-627)734146140 (DE-600)2697425-3 2049-2618 nnns volume:4 year:2016 number:1 day:20 month:01 https://dx.doi.org/10.1186/s40168-016-0147-4 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2016 1 20 01 |
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Correlation of the lung microbiota with metabolic profiles in bronchoalveolar lavage fluid in HIV infection |
abstract |
Background While 16S ribosomal RNA (rRNA) sequencing has been used to characterize the lung’s bacterial microbiota in human immunodeficiency virus (HIV)-infected individuals, taxonomic studies provide limited information on bacterial function and impact on the host. Metabolic profiles can provide functional information on host-microbe interactions in the lungs. We investigated the relationship between the respiratory microbiota and metabolic profiles in the bronchoalveolar lavage fluid of HIV-infected and HIV-uninfected outpatients. Results Targeted sequencing of the 16S rRNA gene was used to analyze the bacterial community structure and liquid chromatography-high-resolution mass spectrometry was used to detect features in bronchoalveolar lavage fluid. Global integration of all metabolic features with microbial species was done using sparse partial least squares regression. Thirty-nine HIV-infected subjects and 20 HIV-uninfected controls without acute respiratory symptoms were enrolled. Twelve mass-to-charge ratio (m/z) features from C18 analysis were significantly different between HIV-infected individuals and controls (false discovery rate (FDR) = 0.2); another 79 features were identified by network analysis. Further metabolite analysis demonstrated that four features were significantly overrepresented in the bronchoalveolar lavage (BAL) fluid of HIV-infected individuals compared to HIV-uninfected, including cystine, two complex carbohydrates, and 3,5-dibromo-l-tyrosine. There were 231 m/z features significantly associated with peripheral blood CD4 cell counts identified using sparse partial least squares regression (sPLS) at a variable importance on projection (VIP) threshold of 2. Twenty-five percent of these 91 m/z features were associated with various microbial species. Bacteria from families Caulobacteraceae, Staphylococcaceae, Nocardioidaceae, and genus Streptococcus were associated with the greatest number of features. Glycerophospholipid and lineolate pathways correlated with these bacteria. Conclusions In bronchoalveolar lavage fluid, specific metabolic profiles correlated with bacterial organisms known to play a role in the pathogenesis of pneumonia in HIV-infected individuals. These findings suggest that microbial communities and their interactions with the host may have functional metabolic impact in the lung. |
abstractGer |
Background While 16S ribosomal RNA (rRNA) sequencing has been used to characterize the lung’s bacterial microbiota in human immunodeficiency virus (HIV)-infected individuals, taxonomic studies provide limited information on bacterial function and impact on the host. Metabolic profiles can provide functional information on host-microbe interactions in the lungs. We investigated the relationship between the respiratory microbiota and metabolic profiles in the bronchoalveolar lavage fluid of HIV-infected and HIV-uninfected outpatients. Results Targeted sequencing of the 16S rRNA gene was used to analyze the bacterial community structure and liquid chromatography-high-resolution mass spectrometry was used to detect features in bronchoalveolar lavage fluid. Global integration of all metabolic features with microbial species was done using sparse partial least squares regression. Thirty-nine HIV-infected subjects and 20 HIV-uninfected controls without acute respiratory symptoms were enrolled. Twelve mass-to-charge ratio (m/z) features from C18 analysis were significantly different between HIV-infected individuals and controls (false discovery rate (FDR) = 0.2); another 79 features were identified by network analysis. Further metabolite analysis demonstrated that four features were significantly overrepresented in the bronchoalveolar lavage (BAL) fluid of HIV-infected individuals compared to HIV-uninfected, including cystine, two complex carbohydrates, and 3,5-dibromo-l-tyrosine. There were 231 m/z features significantly associated with peripheral blood CD4 cell counts identified using sparse partial least squares regression (sPLS) at a variable importance on projection (VIP) threshold of 2. Twenty-five percent of these 91 m/z features were associated with various microbial species. Bacteria from families Caulobacteraceae, Staphylococcaceae, Nocardioidaceae, and genus Streptococcus were associated with the greatest number of features. Glycerophospholipid and lineolate pathways correlated with these bacteria. Conclusions In bronchoalveolar lavage fluid, specific metabolic profiles correlated with bacterial organisms known to play a role in the pathogenesis of pneumonia in HIV-infected individuals. These findings suggest that microbial communities and their interactions with the host may have functional metabolic impact in the lung. |
abstract_unstemmed |
Background While 16S ribosomal RNA (rRNA) sequencing has been used to characterize the lung’s bacterial microbiota in human immunodeficiency virus (HIV)-infected individuals, taxonomic studies provide limited information on bacterial function and impact on the host. Metabolic profiles can provide functional information on host-microbe interactions in the lungs. We investigated the relationship between the respiratory microbiota and metabolic profiles in the bronchoalveolar lavage fluid of HIV-infected and HIV-uninfected outpatients. Results Targeted sequencing of the 16S rRNA gene was used to analyze the bacterial community structure and liquid chromatography-high-resolution mass spectrometry was used to detect features in bronchoalveolar lavage fluid. Global integration of all metabolic features with microbial species was done using sparse partial least squares regression. Thirty-nine HIV-infected subjects and 20 HIV-uninfected controls without acute respiratory symptoms were enrolled. Twelve mass-to-charge ratio (m/z) features from C18 analysis were significantly different between HIV-infected individuals and controls (false discovery rate (FDR) = 0.2); another 79 features were identified by network analysis. Further metabolite analysis demonstrated that four features were significantly overrepresented in the bronchoalveolar lavage (BAL) fluid of HIV-infected individuals compared to HIV-uninfected, including cystine, two complex carbohydrates, and 3,5-dibromo-l-tyrosine. There were 231 m/z features significantly associated with peripheral blood CD4 cell counts identified using sparse partial least squares regression (sPLS) at a variable importance on projection (VIP) threshold of 2. Twenty-five percent of these 91 m/z features were associated with various microbial species. Bacteria from families Caulobacteraceae, Staphylococcaceae, Nocardioidaceae, and genus Streptococcus were associated with the greatest number of features. Glycerophospholipid and lineolate pathways correlated with these bacteria. Conclusions In bronchoalveolar lavage fluid, specific metabolic profiles correlated with bacterial organisms known to play a role in the pathogenesis of pneumonia in HIV-infected individuals. These findings suggest that microbial communities and their interactions with the host may have functional metabolic impact in the lung. |
collection_details |
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container_issue |
1 |
title_short |
Correlation of the lung microbiota with metabolic profiles in bronchoalveolar lavage fluid in HIV infection |
url |
https://dx.doi.org/10.1186/s40168-016-0147-4 |
remote_bool |
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author2 |
Uppal, Karan Li, Shuzhao Jones, Dean P. Huang, Laurence Tipton, Laura Fitch, Adam Greenblatt, Ruth M. Kingsley, Lawrence Guidot, David M. Ghedin, Elodie Morris, Alison |
author2Str |
Uppal, Karan Li, Shuzhao Jones, Dean P. Huang, Laurence Tipton, Laura Fitch, Adam Greenblatt, Ruth M. Kingsley, Lawrence Guidot, David M. Ghedin, Elodie Morris, Alison |
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doi_str |
10.1186/s40168-016-0147-4 |
up_date |
2024-07-03T17:24:11.607Z |
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