Bacteriophages Can Treat and Prevent Pseudomonas aeruginosa Lung Infections

被引:244
作者
Debarbieux, Laurent [1 ]
Leduc, Dominique [2 ]
Maura, Damien [1 ]
Morello, Eric [1 ]
Criscuolo, Alexis [1 ]
Grossi, Olivier [3 ]
Balloy, Viviane [2 ]
Touqui, Lhousseine [2 ]
机构
[1] Inst Pasteur, Dept Microbiol, Mol Biol Gene Extremophiles Unit, F-75724 Paris, France
[2] Inst Pasteur, Dept Infect & Epidemiol, Innate Host Def & Inflammat Unit, F-75724 Paris, France
[3] Ctr Hosp Univ Hotel Dieu, Serv Malad Infect & Trop, Nantes, France
关键词
PHAGE THERAPY; BIOFILMS; EFFICACY; SEPSIS; MICE;
D O I
10.1086/651135
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antibiotic-resistant bacteria threaten life worldwide. Although new antibiotics are scarce, the use of bacteriophages, viruses that infect bacteria, is rarely proposed as a means of offsetting this shortage. Doubt also remains widespread about the efficacy of phage therapy despite recent encouraging results. Using a bioluminescent Pseudomonas aeruginosa strain, we monitored and quantified the efficacy of a bacteriophage treatment in mice during acute lung infection. Bacteriophage treatment not only was effective in saving animals from lethal infection, but also was able to prevent lung infection when given 24 h before bacterial infection, thereby extending the potential use of bacteriophages as therapeutic agents to combat bacterial lung infection.
引用
收藏
页码:1096 / 1104
页数:9
相关论文
共 35 条
[1]   5500 Phages examined in the electron microscope [J].
Ackermann, H. -W. .
ARCHIVES OF VIROLOGY, 2007, 152 (02) :227-243
[2]  
Ackermann Hans-W., 2009, V501, P113, DOI 10.1007/978-1-60327-164-6_12
[3]   Stress molecules in sepsis and systemic inflammatory response syndrome [J].
Adib-Conquy, Minou ;
Cavaillon, Jean-Marc .
FEBS LETTERS, 2007, 581 (19) :3723-3733
[4]   Evidence for spread of a clonal strain of Pseudomonas aeruginosa among cystic fibrosis clinics [J].
Armstrong, D ;
Bell, S ;
Robinson, M ;
Bye, P ;
Rose, B ;
Harbour, C ;
Lee, C ;
Service, H ;
Nissen, M ;
Syrmis, M ;
Wainwright, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (05) :2266-2267
[5]   The role of flagellin versus motility in acute lung disease caused by Pseudomonas aeruginosa [J].
Balloy, Viviane ;
Verma, Amrisha ;
Kuravi, Sudha ;
Si-Tahar, Mustapha ;
Chignard, Michel ;
Ramphal, Reuben .
JOURNAL OF INFECTIOUS DISEASES, 2007, 196 (02) :289-296
[6]   Bacteriophage therapy and prophylaxis: Rediscovery and renewed assessment of potential [J].
Barrow, PA ;
Soothill, JS .
TRENDS IN MICROBIOLOGY, 1997, 5 (07) :268-271
[7]  
Boulanger Pascale, 2009, V502, P227, DOI 10.1007/978-1-60327-565-1_13
[8]   Phage therapy:: the Escherichia coli experience [J].
Brüssow, H .
MICROBIOLOGY-SGM, 2005, 151 :2133-2140
[9]   Quantitative Models of In Vitro Bacteriophage-Host Dynamics and Their Application to Phage Therapy [J].
Cairns, Benjamin J. ;
Timms, Andrew R. ;
Jansen, Vincent A. A. ;
Connerton, Ian F. ;
Payne, Robert J. H. .
PLOS PATHOGENS, 2009, 5 (01)
[10]   The future of bacteriophage biology [J].
Campbell, A .
NATURE REVIEWS GENETICS, 2003, 4 (06) :471-477