Lung-enriched Organisms and Aberrant Bacterial and Fungal Respiratory Microbiota after Lung Transplant

Long-term survival after lung transplantation is limited by infectious complications and by bronchiolitis obliterans syndrome (BOS), a form of chronic rejection linked in part to microbial triggers. To define microbial populations in the respiratory tract of transplant patients comprehensively using...

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Published inAmerican journal of respiratory and critical care medicine Vol. 186; no. 6; pp. 536 - 545
Main Authors Charlson, Emily S., Diamond, Joshua M., Bittinger, Kyle, Fitzgerald, Ayannah S., Yadav, Anjana, Haas, Andrew R., Bushman, Frederic D., Collman, Ronald G.
Format Journal Article
LanguageEnglish
Published New York, NY American Thoracic Society 15.09.2012
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Abstract Long-term survival after lung transplantation is limited by infectious complications and by bronchiolitis obliterans syndrome (BOS), a form of chronic rejection linked in part to microbial triggers. To define microbial populations in the respiratory tract of transplant patients comprehensively using unbiased high-density sequencing. Lung was sampled by bronchoalveolar lavage (BAL) and upper respiratory tract by oropharyngeal wash (OW). Bacterial 16S rDNA and fungal internal transcribed spacer sequencing was used to profile organisms present. Outlier analysis plots defining taxa enriched in lung relative to OW were used to identify bacteria enriched in lung against a background of oropharyngeal carryover. Lung transplant recipients had higher bacterial burden in BAL than control subjects, frequent appearance of dominant organisms, greater distance between communities in BAL and OW indicating more distinct populations, and decreased respiratory tract microbial richness and diversity. Fungal populations were typically dominated by Candida in both sites or by Aspergillus in BAL but not OW. 16S outlier analysis identified lung-enriched taxa indicating bacteria replicating in the lower respiratory tract. In some cases this confirmed respiratory cultures but in others revealed enrichment by anaerobic organisms or mixed outgrowth of upper respiratory flora and provided quantitative data on relative abundances of bacteria found by culture. Respiratory tract microbial communities in lung transplant recipients differ in structure and composition from healthy subjects. Outlier analysis can identify specific bacteria replicating in lung. These findings provide novel approaches to address the relationship between microbial communities and transplant outcome and aid in assessing lung infections.
AbstractList Long-term survival after lung transplantation is limited by infectious complications and by bronchiolitis obliterans syndrome (BOS), a form of chronic rejection linked in part to microbial triggers.RATIONALELong-term survival after lung transplantation is limited by infectious complications and by bronchiolitis obliterans syndrome (BOS), a form of chronic rejection linked in part to microbial triggers.To define microbial populations in the respiratory tract of transplant patients comprehensively using unbiased high-density sequencing.OBJECTIVESTo define microbial populations in the respiratory tract of transplant patients comprehensively using unbiased high-density sequencing.Lung was sampled by bronchoalveolar lavage (BAL) and upper respiratory tract by oropharyngeal wash (OW). Bacterial 16S rDNA and fungal internal transcribed spacer sequencing was used to profile organisms present. Outlier analysis plots defining taxa enriched in lung relative to OW were used to identify bacteria enriched in lung against a background of oropharyngeal carryover.METHODSLung was sampled by bronchoalveolar lavage (BAL) and upper respiratory tract by oropharyngeal wash (OW). Bacterial 16S rDNA and fungal internal transcribed spacer sequencing was used to profile organisms present. Outlier analysis plots defining taxa enriched in lung relative to OW were used to identify bacteria enriched in lung against a background of oropharyngeal carryover.Lung transplant recipients had higher bacterial burden in BAL than control subjects, frequent appearance of dominant organisms, greater distance between communities in BAL and OW indicating more distinct populations, and decreased respiratory tract microbial richness and diversity. Fungal populations were typically dominated by Candida in both sites or by Aspergillus in BAL but not OW. 16S outlier analysis identified lung-enriched taxa indicating bacteria replicating in the lower respiratory tract. In some cases this confirmed respiratory cultures but in others revealed enrichment by anaerobic organisms or mixed outgrowth of upper respiratory flora and provided quantitative data on relative abundances of bacteria found by culture.MEASUREMENTS AND MAIN RESULTSLung transplant recipients had higher bacterial burden in BAL than control subjects, frequent appearance of dominant organisms, greater distance between communities in BAL and OW indicating more distinct populations, and decreased respiratory tract microbial richness and diversity. Fungal populations were typically dominated by Candida in both sites or by Aspergillus in BAL but not OW. 16S outlier analysis identified lung-enriched taxa indicating bacteria replicating in the lower respiratory tract. In some cases this confirmed respiratory cultures but in others revealed enrichment by anaerobic organisms or mixed outgrowth of upper respiratory flora and provided quantitative data on relative abundances of bacteria found by culture.Respiratory tract microbial communities in lung transplant recipients differ in structure and composition from healthy subjects. Outlier analysis can identify specific bacteria replicating in lung. These findings provide novel approaches to address the relationship between microbial communities and transplant outcome and aid in assessing lung infections.CONCLUSIONSRespiratory tract microbial communities in lung transplant recipients differ in structure and composition from healthy subjects. Outlier analysis can identify specific bacteria replicating in lung. These findings provide novel approaches to address the relationship between microbial communities and transplant outcome and aid in assessing lung infections.
Long-term survival after lung transplantation is limited by infectious complications and by bronchiolitis obliterans syndrome (BOS), a form of chronic rejection linked in part to microbial triggers. To define microbial populations in the respiratory tract of transplant patients comprehensively using unbiased high-density sequencing. Lung was sampled by bronchoalveolar lavage (BAL) and upper respiratory tract by oropharyngeal wash (OW). Bacterial 16S rDNA and fungal internal transcribed spacer sequencing was used to profile organisms present. Outlier analysis plots defining taxa enriched in lung relative to OW were used to identify bacteria enriched in lung against a background of oropharyngeal carryover. Lung transplant recipients had higher bacterial burden in BAL than control subjects, frequent appearance of dominant organisms, greater distance between communities in BAL and OW indicating more distinct populations, and decreased respiratory tract microbial richness and diversity. Fungal populations were typically dominated by Candida in both sites or by Aspergillus in BAL but not OW. 16S outlier analysis identified lung-enriched taxa indicating bacteria replicating in the lower respiratory tract. In some cases this confirmed respiratory cultures but in others revealed enrichment by anaerobic organisms or mixed outgrowth of upper respiratory flora and provided quantitative data on relative abundances of bacteria found by culture. Respiratory tract microbial communities in lung transplant recipients differ in structure and composition from healthy subjects. Outlier analysis can identify specific bacteria replicating in lung. These findings provide novel approaches to address the relationship between microbial communities and transplant outcome and aid in assessing lung infections.
Long-term survival after lung transplantation is limited by infectious complications and by bronchiolitis obliterans syndrome (BOS), a form of chronic rejection linked in part to microbial triggers. To define microbial populations in the respiratory tract of transplant patients comprehensively using unbiased high-density sequencing. Lung was sampled by bronchoalveolar lavage (BAL) and upper respiratory tract by oropharyngeal wash (OW). Bacterial 16S rDNA and fungal internal transcribed spacer sequencing was used to profile organisms present. Outlier analysis plots defining taxa enriched in lung relative to OW were used to identify bacteria enriched in lung against a background of oropharyngeal carryover. Lung transplant recipients had higher bacterial burden in BAL than control subjects, frequent appearance of dominant organisms, greater distance between communities in BAL and OW indicating more distinct populations, and decreased respiratory tract microbial richness and diversity. Fungal populations were typically dominated by Candida in both sites or by Aspergillus in BAL but not OW. 16S outlier analysis identified lung-enriched taxa indicating bacteria replicating in the lower respiratory tract. In some cases this confirmed respiratory cultures but in others revealed enrichment by anaerobic organisms or mixed outgrowth of upper respiratory flora and provided quantitative data on relative abundances of bacteria found by culture. Respiratory tract microbial communities in lung transplant recipients differ in structure and composition from healthy subjects. Outlier analysis can identify specific bacteria replicating in lung. These findings provide novel approaches to address the relationship between microbial communities and transplant outcome and aid in assessing lung infections.
Rationale : Long-term survival after lung transplantation is limited by infectious complications and by bronchiolitis obliterans syndrome (BOS), a form of chronic rejection linked in part to microbial triggers. Objectives : To define microbial populations in the respiratory tract of transplant patients comprehensively using unbiased high-density sequencing. Methods : Lung was sampled by bronchoalveolar lavage (BAL) and upper respiratory tract by oropharyngeal wash (OW). Bacterial 16S rDNA and fungal internal transcribed spacer sequencing was used to profile organisms present. Outlier analysis plots defining taxa enriched in lung relative to OW were used to identify bacteria enriched in lung against a background of oropharyngeal carryover. Measurements and Main Results : Lung transplant recipients had higher bacterial burden in BAL than control subjects, frequent appearance of dominant organisms, greater distance between communities in BAL and OW indicating more distinct populations, and decreased respiratory tract microbial richness and diversity. Fungal populations were typically dominated by Candida in both sites or by Aspergillus in BAL but not OW. 16S outlier analysis identified lung-enriched taxa indicating bacteria replicating in the lower respiratory tract. In some cases this confirmed respiratory cultures but in others revealed enrichment by anaerobic organisms or mixed outgrowth of upper respiratory flora and provided quantitative data on relative abundances of bacteria found by culture. Conclusions : Respiratory tract microbial communities in lung transplant recipients differ in structure and composition from healthy subjects. Outlier analysis can identify specific bacteria replicating in lung. These findings provide novel approaches to address the relationship between microbial communities and transplant outcome and aid in assessing lung infections.
Author Diamond, Joshua M.
Charlson, Emily S.
Fitzgerald, Ayannah S.
Bittinger, Kyle
Collman, Ronald G.
Yadav, Anjana
Haas, Andrew R.
Bushman, Frederic D.
Author_xml – sequence: 1
  givenname: Emily S.
  surname: Charlson
  fullname: Charlson, Emily S.
  organization: Pulmonary, Allergy and Critical Care Division, Department of Medicine, and, Department of Microbiology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania
– sequence: 2
  givenname: Joshua M.
  surname: Diamond
  fullname: Diamond, Joshua M.
  organization: Pulmonary, Allergy and Critical Care Division, Department of Medicine, and
– sequence: 3
  givenname: Kyle
  surname: Bittinger
  fullname: Bittinger, Kyle
  organization: Department of Microbiology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania
– sequence: 4
  givenname: Ayannah S.
  surname: Fitzgerald
  fullname: Fitzgerald, Ayannah S.
  organization: Pulmonary, Allergy and Critical Care Division, Department of Medicine, and
– sequence: 5
  givenname: Anjana
  surname: Yadav
  fullname: Yadav, Anjana
  organization: Pulmonary, Allergy and Critical Care Division, Department of Medicine, and
– sequence: 6
  givenname: Andrew R.
  surname: Haas
  fullname: Haas, Andrew R.
  organization: Pulmonary, Allergy and Critical Care Division, Department of Medicine, and
– sequence: 7
  givenname: Frederic D.
  surname: Bushman
  fullname: Bushman, Frederic D.
  organization: Department of Microbiology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania
– sequence: 8
  givenname: Ronald G.
  surname: Collman
  fullname: Collman, Ronald G.
  organization: Pulmonary, Allergy and Critical Care Division, Department of Medicine, and, Department of Microbiology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26399394$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/22798321$$D View this record in MEDLINE/PubMed
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Issue 6
Keywords Infection
Intensive care
bronchiolitis obliterans syndrome
Respiratory disease
Bacteriosis
Bronchus disease
ITS
Bronchiolitis obliterans
microbiome
Resuscitation
16S
Language English
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Snippet Long-term survival after lung transplantation is limited by infectious complications and by bronchiolitis obliterans syndrome (BOS), a form of chronic...
Rationale : Long-term survival after lung transplantation is limited by infectious complications and by bronchiolitis obliterans syndrome (BOS), a form of...
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StartPage 536
SubjectTerms Adult
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Bacteria
Biological and medical sciences
Bronchiolitis Obliterans - microbiology
Bronchiolitis Obliterans - physiopathology
Bronchoalveolar Lavage Fluid - microbiology
Bronchoscopy
Bronchoscopy - methods
Candidiasis, Invasive - epidemiology
Candidiasis, Invasive - physiopathology
Case-Control Studies
DNA, Bacterial - analysis
DNA, Bacterial - genetics
DNA, Fungal - analysis
DNA, Fungal - genetics
Emergency and intensive respiratory care
Female
Follow-Up Studies
Gene amplification
Graft Rejection - epidemiology
Graft Rejection - microbiology
Gram-Negative Bacterial Infections - microbiology
Gram-Negative Bacterial Infections - physiopathology
Gram-Positive Bacterial Infections - microbiology
Gram-Positive Bacterial Infections - physiopathology
Humans
Incidence
Infections
Intensive care medicine
Invasive Pulmonary Aspergillosis - epidemiology
Invasive Pulmonary Aspergillosis - physiopathology
Lavage
Likelihood Functions
Lung Transplantation - adverse effects
Lung Transplantation - methods
Lung transplants
Male
Medical sciences
Metagenome
Microbiota
Middle Aged
Monte Carlo Method
Postoperative Complications - microbiology
Postoperative Complications - physiopathology
Respiratory Tract Infections - microbiology
Respiratory Tract Infections - physiopathology
Risk Assessment
Sampling Studies
Statistics, Nonparametric
Taxonomy
Title Lung-enriched Organisms and Aberrant Bacterial and Fungal Respiratory Microbiota after Lung Transplant
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Volume 186
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