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Decade-long bacterial community dynamics in cystic fibrosis airways
Open accessAbstract
The structure and dynamics of bacterial communities in the airways of persons with cystic fibrosis (CF) remain largely unknown. We characterized the bacterial communities in 126 sputum samples representing serial collections spanning 8-9 y from six age-matched male CF patients. Sputum DNA was analyzed by bar-coded pyrosequencing of the V3-V5 hypervariable region of the 16S rRNA gene, defining 662 operational taxonomic units (OTUs) from >633,000 sequences. Bacterial community diversity decreased significantly over time in patients with typically progressive lung disease but remained relatively stable in patients with a mild lung disease phenotype. Antibiotic use, rather than patient age or lung function, was the primary driver of decreasing diversity. Interpatient variability in community structure exceeded intrapatient variability in serial samples. Antibiotic treatment was associated with pronounced shifts in community structure, but communities showed both short- and long-term resilience after antibiotic perturbation. There was a positive correlation between OTU occurrence and relative abundance, with a small number of persistent OTUs accounting for the greatest abundance. Significant changes in community structure, diversity, or total bacterial density at the time of pulmonary exacerbation were not observed. Despite decreasing community diversity in patients with progressive disease, total bacterial density remained relatively stable over time. These findings show the critical relationship between airway bacterial community structure, disease stage, and clinical state at the time of sample collection. These features are the key parameters with which to assess the complex ecology of the CF airway.
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“With remarkable consistency, all studies report no increase in bacterial burden and no decrease in community diversity during exacerbations.”
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Schloss, P. D., Westcott, S. L., Ryabin, T., Hall, J. R., Hartmann, M., Hollister, E. B., Lesniewski, R. A., Oakley, B. B., Parks, D. H., Robinson, C. J., et al. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01541-09 · Cited by 19,549
Self-citationA new method for non-parametric multivariate analysis of variance
Anderson, M. J. (2001) · Austral Ecology · doi:10.1111/j.1442-9993.2001.01070.pp.x · Cited by 13,828
Nadkarni, M. A., Martin, F. E., Jacques, N. A., & Hunter, N. (2002) · Microbiology · doi:10.1099/00221287-148-1-257 · Cited by 1,931
Detection of Anaerobic Bacteria in High Numbers in Sputum from Patients with Cystic Fibrosis
Tunney, M. M., Field, T. R., Moriarty, T. F., Patrick, S., Doering, G., Muhlebach, M. S., Wolfgang, M. C., Boucher, R. C., Gilpin, D. F., McDowell, A., et al. (2008) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200708-1151oc · Cited by 466
Airway Microbiota and Pathogen Abundance in Age-Stratified Cystic Fibrosis Patients
Cox, M. J., Allgaier, M., Taylor, B., Baek, M. S., Huang, Y. J., Daly, R. A., Karaöz, U., Andersen, G. L., Brown, R., Fujimura, K. E., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011044 · Cited by 458
Harris, J. K., Groote, M. A. D., Sagel, S. D., Zemanick, E. T., Kapsner, R. K., Penvari, C., Kaess, H., Deterding, R. R., Accurso, F. J., & Pace, N. R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709804104 · Cited by 373
Rogers, G. B., Carroll, M. P., Serisier, D. J., Hockey, P., Jones, G., & Bruce, K. D. (2004) · Journal of Clinical Microbiology · doi:10.1128/jcm.42.11.5176-5183.2004 · Cited by 316
Sibley, C. D., Parkins, M. D., Rabin, H. R., Duan, K., Nørgaard, J. C., & Surette, M. G. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804326105 · Cited by 311
Partitioning core and satellite taxa from within cystic fibrosis lung bacterial communities
Gast, C., Walker, A. W., Stressmann, F. A., Rogers, G. B., Scott, P., Daniels, T. W. V., Carroll, M. P., Parkhill, J., & Bruce, K. D. (2010) · The ISME Journal · doi:10.1038/ismej.2010.175 · Cited by 265
Klepac‐Ceraj, V., Lemon, K. P., Martin, T. R., Allgaier, M., Kembel, S. W., Knapp, A. A., Lory, S., Brodie, E., Lynch, S. V., Bohannan, B. J. M., et al. (2010) · Environmental Microbiology · doi:10.1111/j.1462-2920.2010.02173.x · Cited by 219
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Self-citationO’Toole, G. A., Crabbé, A., Kümmerli, R., LiPuma, J. J., Bomberger, J. M., Davies, J. C., Limoli, D. H., Phelan, V. V., Bliska, J. B., DePas, W. H., et al. (2021) · mBio · doi:10.1128/mbio.01763-21 · Cited by 50
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Mall, M. A., Criner, G. J., Miravitlles, M., Rowe, S. M., Vogelmeier, C. F., Rowlands, D. J., Schoenberger, M., & Altman, P. (2022) · European Respiratory Journal · doi:10.1183/13993003.01307-2022 · Cited by 52
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Peleg, A. Y., Choo, J. M., Langan, K. M., Edgeworth, D. M., Keating, D., Wilson, J. W., Rogers, G. B., & Kotsimbos, T. C. (2017) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2017.08.002 · Cited by 53
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Barraza, J. P., & Whiteley, M. (2021) · mBio · doi:10.1128/mbio.00047-21 · Cited by 48
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Millares, L., Pérez‐Brocal, V., Ferrari, R. G., Gallego, M., Pomares, X., García-Núñez, M., Montón, C., Capilla, S., Monsó, E., & Moyá, A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144448 · Cited by 48
Zemanick, E. T., & Hoffman, L. R. (2016) · Pediatric Clinics of North America · doi:10.1016/j.pcl.2016.04.003 · Cited by 47
Perault, A. I., Chandler, C. E., Rasko, D. A., Ernst, R. K., Wolfgang, M. C., & Cotter, P. A. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.06.019 · Cited by 47
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Hwang, G. (2022) · Environmental Microbiology Reports · doi:10.1111/1758-2229.13053 · Cited by 47
Antibiotic resistance in chronic respiratory diseases: from susceptibility testing to the resistome
Pailhories, H., Herrmann, J., Velo‐Suárez, L., Lamoureux, C., Beauruelle, C., Burgel, P., & Héry-Arnaud, G. (2022) · European Respiratory Review · doi:10.1183/16000617.0259-2021 · Cited by 46
Pezzulo, A. A., Kelly, P. H., Nassar, B. S., Rutland, C. J., Gansemer, N. D., Dohrn, C. L., Costello, A. J., Stoltz, D. A., & Zabner, J. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.01752-13 · Cited by 47
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Acosta, N., Whelan, F., Somayaji, R., Poonja, A., Surette, M. G., Rabin, H. R., & Parkins, M. D. (2017) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201609-668oc · Cited by 46
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Saeed, A., Bosch, A., Bettiol, M., González, D. N., Erben, M. F., & Lamberti, Y. (2018) · Molecules · doi:10.3390/molecules23051158 · Cited by 46
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Cystic fibrosis respiratory microbiota: unraveling complexity to inform clinical practice
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The airway microbiota in early cystic fibrosis lung disease
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Scott, J. E., & O’Toole, G. A. (2019) · Journal of Bacteriology · doi:10.1128/jb.00115-19 · Cited by 44
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Jansen, G., Mahrt, N., Tüeffers, L., Barbosa, C., Harjes, M., Adolph, G., Friedrichs, A. K., Krenz-Weinreich, A., Rosenstiel, P. C., & Schulenburg, H. (2016) · Evolution Medicine and Public Health · doi:10.1093/emph/eow016 · Cited by 40
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Zhao, J., Cheng, W., He, X., & Liu, Y. (2018) · Microbial Pathogenesis · doi:10.1016/j.micpath.2018.09.010 · Cited by 39
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Stokell, J. R., Gharaibeh, R. Z., Hamp, T. J., Zapata, M. J., Fodor, A. A., & Steck, T. R. (2014) · Journal of Clinical Microbiology · doi:10.1128/jcm.02555-14 · Cited by 40
Acquisition and adaptation of the airway microbiota in the early life of cystic fibrosis patients
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Héry-Arnaud, G., Boutin, S., Cuthbertson, L., Elborn, J. S., & Tunney, M. M. (2018) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2018.11.003 · Cited by 37
Caverly, L. J., Carmody, L. A., Haig, S., Kotlarz, N., Kalikin, L. M., Raskin, L. M., & LiPuma, J. J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0153876 · Cited by 37
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Bacci, G., Paganin, P., Lopez, L., Vanni, C., Dalmastri, C., Cantale, C., Daddiego, L., Perrotta, G., Dolce, D., Morelli, P., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0156807 · Cited by 38
Lu, J., Carmody, L. A., Opron, K., Simon, R. H., Kalikin, L. M., Caverly, L. J., & LiPuma, J. J. (2020) · mSystems · doi:10.1128/msystems.00296-20 · Cited by 39
Self-citationLux, C. A., Mackenzie, B. W., Johnston, J. J., Zoing, M., Biswas, K., Taylor, M. W., & Douglas, R. G. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.595555 · Cited by 36
Stefanie Widder, A., Zhao, J., Carmody, L. A., Zhang, Q., Kalikin, L. M., Schloss, P. D., & LiPuma, J. J. (2021) · The ISME Journal · doi:10.1038/s41396-021-01129-z · Cited by 36
Self-citationOrmerod, K. L., George, N., Fraser, J. A., Wainwright, C. E., & Hugenholtz, P. (2015) · PeerJ · doi:10.7717/peerj.1223 · Cited by 36
Palmer, G. C., & Whiteley, M. (2015) · Microbiology Spectrum · doi:10.1128/microbiolspec.mbp-0003-2014 · Cited by 37
Clark, S. T., Guttman, D. S., & Hwang, D. M. (2018) · FEMS Microbiology Letters · doi:10.1093/femsle/fny026 · Cited by 36
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Dyamenahalli, K. U., Garg, G., Shupp, J. W., Kuprys, P. V., Choudhry, M. A., & Kovacs, E. J. (2019) · Journal of Burn Care & Research · doi:10.1093/jbcr/irz055 · Cited by 39
McDermott, A. J., Frank, C. R., Falkowski, N. R., McDonald, R. A., Young, V. B., & Huffnagle, G. B. (2014) · Gut Microbes · doi:10.4161/gmic.29964 · Cited by 36
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Sherrard, L. J., Schaible, B., Graham, K., McGrath, S., McIlreavey, L., Hatch, J., Wolfgang, M. C., Muhlebach, M. S., Gilpin, D. F., Schneiders, T., et al. (2014) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dku192 · Cited by 33
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Price, K. E., Naimie, A. A., Griffin, E. F., Bay, C., & O’Toole, G. A. (2015) · Journal of Bacteriology · doi:10.1128/jb.00705-15 · Cited by 32
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Hurley, M. N., Fogarty, A., McKeever, T. M., Goss, C. H., Rosenfeld, M., & Smyth, A. R. (2017) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201705-376oc · Cited by 31
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Pienkowska, K., Pust, M., Gessner, M., Gaedcke, S., Thavarasa, A., Rosenboom, I., Losada, P. M., Minso, R., Arnold, C., Hedtfeld, S., et al. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.03633-22 · Cited by 31
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Syed, S. A., Whelan, F., Waddell, B. J. M., Rabin, H. R., Parkins, M. D., & Surette, M. G. (2016) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201606-431oc · Cited by 31
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Schmidt, A., Belaaouaj, A., Bissinger, R., Koller, G., Malleret, L., D'Orazio, C., Facchinelli, M., Schulte-Hubbert, B., Molinaro, A., Holst, O., et al. (2014) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2014.03.004 · Cited by 30
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Vandeplassche, E., Sass, A. M., Ostyn, L., Burmølle, M., Kragh, K. N., Bjarnsholt, T., Coenye, T., & Crabbé, A. (2020) · Biofilm · doi:10.1016/j.bioflm.2020.100031 · Cited by 30
Duncan, R. P., Moustafa, D. A., Lewin, G. R., Diggle, F. L., Bomberger, J. M., Whiteley, M., & Goldberg, J. B. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2406234121 · Cited by 29
Selin, C., Stietz, M. S., Blanchard, J., Gehrke, S. S., Bernard, S., Hall, D. G., Brown, E. D., & Cardona, S. T. (2015) · PLoS ONE · doi:10.1371/journal.pone.0128587 · Cited by 29
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Alsayed, A. R., Abed, A. I., Khader, H. A., Al-Shdifat, L., Hasoun, L., Al‐Rshaidat, M. M. D., Alkhatib, M., & Zihlif, M. A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24044086 · Cited by 32
Ralstonia mannitolilytica in cystic fibrosis: A new predictor of worse outcomes
Coman, I., Bilodeau, L., Lavoie, A., Carricart, M., Tremblay, F., Zlosnik, J. E. A., & Berthiaume, Y. (2016) · Respiratory Medicine Case Reports · doi:10.1016/j.rmcr.2016.11.014 · Cited by 29
Microbial diversity within the airway microbiome in chronic pediatric lung diseases
Hahn, A., Warnken, S., Pérez‐Losada, M., Freishtat, R. J., & Crandall, K. A. (2017) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2017.12.006 · Cited by 33
Interaction betweenPseudomonas aeruginosaandAspergillus fumigatusin cystic fibrosis
Zhao, J., & Yu, W. (2018) · PeerJ · doi:10.7717/peerj.5931 · Cited by 30
Self-citationSputum microbiota in adults with CF associates with response to inhaled tobramycin
Heirali, A., Thornton, C. S., Acosta, N., Somayaji, R., Laforest‐Lapointe, I., Storey, D. G., Rabin, H. R., Waddell, B. J. M., Rossi, L., Arrieta, M., et al. (2020) · Thorax · doi:10.1136/thoraxjnl-2019-214191 · Cited by 29
Kramer, R., Sauer‐Heilborn, A., Welte, T., Jáuregui, R., Brettar, I., Guzmán, C. A., & Höfle, M. G. (2015) · PLoS ONE · doi:10.1371/journal.pone.0117436 · Cited by 29
Hahn, A., Whiteson, K., Davis, T. J., Phan, J. L., Sami, I. R., Koumbourlis, A. C., Freishtat, R. J., Crandall, K. A., & Bean, H. D. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00174 · Cited by 28
Potential Contributions of Anaerobes in Cystic Fibrosis Airways
Thornton, C. S., & Surette, M. G. (2020) · Journal of Clinical Microbiology · doi:10.1128/jcm.01813-19 · Cited by 29
Vandeplassche, E., Coenye, T., & Crabbé, A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0187540 · Cited by 27
The sputum microbiome associated with different sub-types of AECOPD in a Chinese cohort
Wang, J., Chai, J., Sun, L., Zhao, J., & Chang, C. H. (2020) · BMC Infectious Diseases · doi:10.1186/s12879-020-05313-y · Cited by 27
Self-citationBeck, J. M. (2014) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201306-188mg · Cited by 29
The microbiome of the upper airways: focus on chronic rhinosinusitis
Chalermwatanachai, T., Pereira, L. C. V., & Bachert, C. (2015) · World Allergy Organization Journal · doi:10.1186/s40413-014-0048-6 · Cited by 27
Data Mining of Lung Microbiota in Cystic Fibrosis Patients
Li, J., Hao, C., Ren, L., Xiao, Y. B., Wang, J., & Qin, X. (2016) · PLoS ONE · doi:10.1371/journal.pone.0164510 · Cited by 28
Self-citationThe effects of cycled inhaled aztreonam on the cystic fibrosis (CF) lung microbiome
Heirali, A., Acosta, N., Storey, D. G., Workentine, M. L., Somayaji, R., Laforest‐Lapointe, I., Leung, W. M., Quon, B. S., Berthiaume, Y., Rabin, H. R., et al. (2019) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2019.02.010 · Cited by 27
Longitudinal development of the airway microbiota in infants with cystic fibrosis
Ahmed, B., Cox, M. J., Cuthbertson, L., James, P. L., Cookson, W., Davies, J. C., Moffatt, M. F., & Bush, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-41597-0 · Cited by 27
Metadata
- Authors
- Zhao, J., Schloss, P. D., Kalikin, L. M., Carmody, L. A., Foster, B. K., Petrosino, J. F., Cavalcoli, J. D., VanDevanter, D. R., Murray, S., Li, J. Z., Young, V. B., & LiPuma, J. J.
- Affiliations
- University of Michigan (US)
- Microbiology and Immunology,
- Baylor College of Medicine (US)
- Case Western Reserve University (US)
- Biostatistics and
- Human Genetics, and
- ORCID
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2012-03-26
- Volume
- 109
- Issue
- 15
- Pages
- 5809-5814
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3326496
- OpenAlex
- W2094167812
- Cited by
- 599
- References
- 18
- Citations by year
- 2026: 12 · 2025: 18 · 2024: 32 · 2023: 31 · 2022: 37 · 2021: 41 · 2020: 57 · 2019: 57 · 2018: 40 · 2017: 39 · 2016: 50 · 2015: 61 · 2014: 63 · 2013: 43 · 2012: 18
- FWCI
- 47.73
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Deep Blue (University of Michigan) (submittedVersion)
- Funders
- National Institutes of Health (5rc1hl100809-02)
- National Heart, Lung, and Blood Institute (U01HL098961, RC1-HL100809, 1RC1HL100809-01)
- National Human Genome Research Institute (R01HG005975, R01HG004906)
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK034933, P30DK027651)
- National Center for Research Resources (UL1RR024986)
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Cystic Fibrosis Research Advances
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
- Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
- Keywords
- cystic fibrosis, sputum microbiome, bacterial diversity, antibiotic therapy, community resilience, pulmonary exacerbations, disease progression, 16S rRNA gene sequencing, interpatient variability
- MeSH terms
- Adolescent, Adult, Aging, Anti-Bacterial Agents, Bacteria, Cystic Fibrosis, Humans, Lung, Male, Respiratory Function Tests, Sputum, Disease Progression, Principal Component Analysis, Biodiversity, Metagenome, Young Adult, Bacterial Load
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