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The effects of cycled inhaled aztreonam on the cystic fibrosis (CF) lung microbiome.
Heirali, Alya A; Acosta, Nicole; Storey, Douglas G; Workentine, Matthew L; Somayaji, Ranjani; Laforest-Lapointe, Isabelle; Leung, Winnie; Quon, Bradley S; Berthiaume, Yves; Rabin, Harvey R; Waddell, Barbara J; Rossi, Laura; Surette, Michael G; Parkins, Michael D.
Afiliação
  • Heirali AA; Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, AB, Canada.
  • Acosta N; Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, AB, Canada.
  • Storey DG; Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, AB, Canada; Department of Biological Sciences, University of Calgary, Calgary, AB, Canada.
  • Workentine ML; Faculty of Veterinary Medicine, University of Calgary, Calgary, AB, Canada.
  • Somayaji R; Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, AB, Canada; Department of Medicine, University of Calgary, Calgary, AB, Canada.
  • Laforest-Lapointe I; Departments of Physiology & Pharmacology, University of Calgary, Calgary, AB, Canada; Department of Pediatrics, University of Calgary, Alberta, Canada.
  • Leung W; Department of Medicine, University of Alberta, Edmonton, AB, Canada.
  • Quon BS; Department of Medicine and Centre for Heart Lung Innovation, University of British Columbia, Vancouver, BC, Canada.
  • Berthiaume Y; Institut de recherches cliniques de Montreal and Department of Medicine, Universite de Montreal, QB, Canada.
  • Rabin HR; Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, AB, Canada; Department of Medicine, University of Calgary, Calgary, AB, Canada.
  • Waddell BJ; Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, AB, Canada.
  • Rossi L; Department of Medicine, McMaster University, Hamilton, ON, Canada.
  • Surette MG; Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, AB, Canada; Department of Medicine, McMaster University, Hamilton, ON, Canada.
  • Parkins MD; Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, AB, Canada; Department of Medicine, University of Calgary, Calgary, AB, Canada. Electronic address: mdparkin@ucalgary.ca.
J Cyst Fibros ; 18(6): 829-837, 2019 11.
Article em En | MEDLINE | ID: mdl-30857926
ABSTRACT

BACKGROUND:

To improve clinical outcomes, cystic fibrosis (CF) patients with chronic Pseudomonas aeruginosa infections are prescribed inhaled anti-pseudomonal antibiotics. Although, a diverse microbial community exists within CF airways, little is known about how the CF microbiota influences patient outcomes. We hypothesized that organisms within the CF microbiota are affected by inhaled-antibiotics and baseline microbiome may be used to predict therapeutic response.

METHODS:

Adults with chronic P. aeruginosa infection from four clinics were observed during a single 28-day on/off inhaled-aztreonam cycle. Patients performed serial sputum collection, CF-respiratory infection symptom scores (CRISS), and spirometry. Patients achieving a decrease of ≥2 CRISS by day 28 were categorized as subjective responders (SR). The airway microbiome was defined by Illumina MiSeq analysis of the 16S rRNA gene.

RESULTS:

Thirty-seven patients (median 37.4 years and FEV1 44% predicted) were enrolled. No significant cohort-wide changes in the microbiome were observed between on/off AZLI cycles in either alpha- or beta-diversity metrics. However, at an individual level shifts were apparent. Twenty-one patients (57%) were SR and fourteen patients did not subjectively respond. While alpha-diversity metrics did not associate with response, patients who did not subjectively respond had a higher abundance of Staphylococcus and Streptococcus, and lower abundance of Haemophilus.

CONCLUSIONS:

The CF microbiome is relatively resilient to AZLI perturbations. However, associated changes were observed at the individual patient level. The relative abundance of key "off-target" organisms associated with subjective improvements suggesting that the microbiome may be used as a tool to predict patient response - potentially improving outcomes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pseudomonas aeruginosa / Infecções por Pseudomonas / Aztreonam / Fibrose Cística / Autoavaliação Diagnóstica / Microbiota / Pulmão Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: J Cyst Fibros Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pseudomonas aeruginosa / Infecções por Pseudomonas / Aztreonam / Fibrose Cística / Autoavaliação Diagnóstica / Microbiota / Pulmão Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: J Cyst Fibros Ano de publicação: 2019 Tipo de documento: Article