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The effects of inhaled aztreonam on the cystic fibrosis lung microbiome
被引:45
|作者:
Heirali, Alya A.
[1
]
Workentine, Matthew L.
[2
]
Acosta, Nicole
[1
]
Poonja, Ali
[1
]
Storey, Douglas G.
[1
,3
]
Somayaji, Ranjani
[1
,4
]
Rabin, Harvey R.
[1
,4
]
Whelan, Fiona J.
[5
]
Surette, Michael G.
[1
,5
]
Parkins, Michael D.
[1
,4
]
机构:
[1] Univ Calgary, Dept Microbiol Immunol & Infect Dis, Calgary, AB, Canada
[2] Univ Calgary, Fac Vet Med, Calgary, AB, Canada
[3] Univ Calgary, Dept Biol Sci, Calgary, AB, Canada
[4] Univ Calgary, Dept Med, 3330 Hosp Dr NW, Calgary, AB, Canada
[5] McMaster Univ, Dept Biochem & Biomed Sci, Hamilton, ON, Canada
来源:
基金:
加拿大健康研究院;
关键词:
Microbiota;
AZLI;
Inhaled antibiotics;
Pseudomonas aeruginosa;
Prevotella;
Fusobacterium;
PSEUDOMONAS-AERUGINOSA;
PULMONARY EXACERBATION;
AIRWAY PSEUDOMONAS;
GENDER-DIFFERENCES;
RESPIRATORY-TRACT;
DISEASE;
SAFETY;
LYSINE;
COMMUNITIES;
TOBRAMYCIN;
D O I:
10.1186/s40168-017-0265-7
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Background: Aztreonam lysine for inhalation (AZLI) is an inhaled antibiotic used to treat chronic Pseudomonas aeruginosa infection in CF. AZLI improves lung function and quality of life, and reduces exacerbations-improvements attributed to its antipseudomonal activity. Given the extremely high aztreonam concentrations achieved in the lower airways by nebulization, we speculate this may extend its spectrum of activity to other organisms. As such, we sought to determine if AZLI affects the CF lung microbiome and whether community constituents can be used to predict treatment responsiveness. Methods: Patients were included if they had chronic P. aeruginosa infection and repeated sputum samples collected before and after AZLI. Sputum DNA was extracted, and the V3-hypervariable region of the 16S ribosomal RNA (rRNA) gene amplified and sequenced. Results: Twenty-four patients naive to AZLI contributed 162 samples. The cohort had a median age of 37. 1 years, and a median FEV1 of 44% predicted. Fourteen patients were a priori defined as responders for achieving >= 3% FEV1 improvement following initiation. No significant changes in alpha diversity were noted following AZLI. Furthermore, beta diversity demonstrated clustering with respect to patients, but had no association with AZLI use. However, we did observe a decline in the relative abundance of several individual operational taxonomic units (OTUs) following AZLI initiation suggesting that specific sub-populations of organisms may be impacted. Patients with higher abundance of Staphylococcus and anaerobic organisms including Prevotella and Fusobacterium were less likely to respond to therapy. Conclusions: Results from our study suggest potential alternate/additional mechanisms by which AZLI functions. Moreover, our study suggests that the CF microbiota may be used as a biomarker to predict patient responsiveness to therapy suggesting the microbiome may be harnessed for the personalization of therapies.
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