Impact of Anaerobic Antibacterial Spectrum on Cystic Fibrosis Airway Microbiome Diversity and Pulmonary Function

被引:4
作者
Bozzella, Michael J. [1 ]
Chaney, Hollis [2 ,3 ]
Sami, Iman [2 ,3 ]
Koumbourlis, Anastassios [2 ,3 ]
Bost, James E. [3 ,4 ]
Zemanick, Edith T. [5 ]
Freishtat, Robert J. [3 ,6 ]
Crandall, Keith A. [7 ,8 ]
Hahn, Andrea [1 ,3 ]
机构
[1] Natl Childrens Hosp, Div Infect Dis, Washington, DC USA
[2] Natl Childrens Hosp, Div Pulm & Sleep Med, Washington, DC USA
[3] George Washington Univ, Sch Med & Hlth Sci, Washington, DC 20052 USA
[4] Natl Childrens Hosp, Div Biostat & Study Methodol, Washington, DC USA
[5] Univ Colorado Anschutz Med Campus, Dept Pediat, Aurora, CO USA
[6] Natl Childrens Hosp, Div Emergency Med, Washington, DC USA
[7] George Washington Univ, Milken Inst Sch Publ Hlth, Computat Biol Inst, Washington, DC USA
[8] George Washington Univ, Milken Inst Sch Publ Hlth, Dept Biostat & Bioinformat, Washington, DC USA
关键词
anaerobes; cystic fibrosis; antibiotic spectrum; microbiome; pulmonary function; CHAIN FATTY-ACIDS; BACTERIA; CHILDREN; EXACERBATIONS; INFLAMMATION; ANTIBIOTICS; PSEUDOMONAS; SPUTUM;
D O I
10.1097/INF.0000000000003211
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: The role of anaerobic organisms in the cystic fibrosis (CF) lung microbiome is unclear. Our objectives were to investigate the effect of broad (BS) versus narrow (NS) spectrum antianaerobic antibiotic activity on lung microbiome diversity and pulmonary function, hypothesizing that BS antibiotics would cause greater change in microbiome diversity without a significant improvement in lung function. Methods: Pulmonary function tests and respiratory samples were collected prospectively in persons with CF before and after treatment for pulmonary exacerbations. Treatment antibiotics were classified as BS or NS. Gene sequencing data from 16S rRNA were used for diversity analysis and bacterial genera classification. We compared the effects of BS versus NS on diversity indices, lung function and anaerobic/aerobic ratios. Statistical significance was determined by multilevel mixed-effects generalized linear models and mixed-effects regression models. Results: Twenty patients, 6-20 years of age, experienced 30 exacerbations. BS therapy had a greater effect on beta diversity than NS therapy when comparing time points before antibiotics to after and at recovery. After antibiotics, the NS therapy group had a greater return toward baseline forced expiratory volume at 1 second and forced expiratory flow 25%-75% values than the BS group. The ratio of anaerobic/aerobic organisms showed a predominance of anaerobes in the NS group with aerobes dominating in the BS group. Conclusions: BS antianaerobic therapy had a greater and possibly longer lasting effect on the lung microbiome of persons with CF, without achieving the recovery of pulmonary function seen with the NS therapy. Specific antibiotic therapies may affect disease progression by changing the airway microbiome.
引用
收藏
页码:962 / 968
页数:7
相关论文
共 40 条
  • [1] Fluctuations in airway bacterial communities associated with clinical states and disease stages in cystic fibrosis
    Carmody, Lisa A.
    Caverly, Lindsay J.
    Foster, Bridget K.
    Rogers, Mary A. M.
    Kalikin, Linda M.
    Simon, Richard H.
    VanDevanter, Donald R.
    LiPuma, John J.
    [J]. PLOS ONE, 2018, 13 (03):
  • [2] Carmody Lisa A, 2013, Ann Am Thorac Soc, V10, P179, DOI 10.1513/AnnalsATS.201211-107OC
  • [3] Chmiel James F, 2014, Ann Am Thorac Soc, V11, P1120, DOI 10.1513/AnnalsATS.201402-050AS
  • [4] Lung microbiota across age and disease stage in cystic fibrosis
    Coburn, Bryan
    Wang, Pauline W.
    Caballero, Julio Diaz
    Clark, Shawn T.
    Brahma, Vijaya
    Donaldson, Sylva
    Zhang, Yu
    Surendra, Anu
    Gong, Yunchen
    Tullis, D. Elizabeth
    Yau, Yvonne C. W.
    Waters, Valerie J.
    Hwang, David M.
    Guttman, David S.
    [J]. SCIENTIFIC REPORTS, 2015, 5
  • [5] Cox MJ, 2010, PLOS ONE, V5, DOI [10.1371/journal.pone.0011044, 10.1371/journal.pone.0012132]
  • [6] Dose optimisation of antibiotics in children: application of pharmacokinetics/pharmacodynamics in paediatrics
    Downes, Kevin J.
    Hahn, Andrea
    Wiles, Jason
    Courter, Joshua D.
    Vinks, Alexander A.
    [J]. INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2014, 43 (03) : 223 - 230
  • [7] abc Sputum DNA sequencing in cystic fibrosis: non-invasive access to the lung microbiome and to pathogen details
    Feigelman, Rounak
    Kahlert, Christian R.
    Baty, Florent
    Rassouli, Frank
    Kleiner, Rebekka L.
    Kohler, Philipp
    Brutsche, Martin H.
    von Mering, Christian
    [J]. MICROBIOME, 2017, 5
  • [8] Rapid Detection of Emerging Pathogens and Loss of Microbial Diversity Associated with Severe Lung Disease in Cystic Fibrosis
    Flight, William G.
    Smith, Ann
    Paisey, Christopher
    Marchesi, Julian R.
    Bull, Matthew J.
    Norville, Phillip J.
    Mutton, Ken J.
    Webb, A. Kevin
    Bright-Thomas, Rowland J.
    Jones, Andrew M.
    Mahenthiralingam, Eshwar
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2015, 53 (07) : 2022 - 2029
  • [9] EFFECT OF AEROSOLIZED RECOMBINANT HUMAN DNASE ON EXACERBATIONS OF RESPIRATORY SYMPTOMS AND ON PULMONARY-FUNCTION IN PATIENTS WITH CYSTIC-FIBROSIS
    FUCHS, HJ
    BOROWITZ, DS
    CHRISTIANSEN, DH
    MORRIS, EM
    NASH, ML
    RAMSEY, BW
    ROSENSTEIN, BJ
    SMITH, AL
    WOHL, ME
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (10) : 637 - 642
  • [10] Short-chain fatty acids affect cystic fibrosis airway inflammation and bacterial growth
    Ghorbani, Peyman
    Santhakumar, Prisila
    Hu, Qingda
    Djiadeu, Pascal
    Wolever, Thomas M. S.
    Palaniyar, Nades
    Grasemann, Hartmut
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2015, 46 (04) : 1033 - 1045