Journal
FUTURE MICROBIOLOGY
Volume 11, Issue 5, Pages 631-641Publisher
FUTURE MEDICINE LTD
DOI: 10.2217/fmb.16.11
Keywords
Acinetobacter baumannii; antibody; bacteriophage; cyclophosphamide; mouse model; pneumonia
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Funding
- Particular Clinical Applied Research of the Capital of China [Z121107001012127]
- China Mega-Project on Infectious Disease Prevention [2013ZX10004-605, 2013ZX10004-607, 2013ZX10004-217, 2011ZX10004-001]
- National Hi-Tech Research and Development (863) Program of China [2014AA021402, 2012AA022-003]
- National Natural Science Foundation of China [81572045]
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Aim: With the emergence of drug-resistant bacteria, finding alternative agents to treat antibiotic-resistant bacterial infections is imperative. Materials & methods: A mouse pneumonia model was developed by combining cyclophosphamide pretreatment and Acinetobacter baumannii challenge, and a lytic bacteriophage was evaluated for its therapeutic efficacy in this model by examining the survival rate, bacterial load in the lung and lung pathology. Results: Intranasal instillation with bacteriophage rescued 100% of mice following lethal challenge with A. baumannii. Phage treatment reduced bacterial load in the lung. Microcomputed tomography indicated a reduction in lung inflammation in mice given phage. Conclusion: This research demonstrates that intranasal application of bacteriophage is viable, and could provide complete protection from pneumonia caused by A. baumannii.
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