Insights into host-pathogen interactions from state-of-the-art animal models of respiratory Pseudomonas aeruginosa infections

被引:21
作者
Lorenz, Anne [1 ]
Pawar, Vinay [2 ,3 ,4 ]
Haeussler, Susanne [1 ,2 ]
Weiss, Siegfried [3 ,4 ]
机构
[1] TWINCORE GmbH, Ctr Clin & Expt Infect Res, Inst Mol Bacteriol, Hannover, Germany
[2] Helmholtz Ctr Infect Res, Dept Mol Bacteriol, Inhoffenstr 7, D-38124 Braunschweig, Germany
[3] Helmholtz Ctr Infect Res, Dept Mol Immunol, Braunschweig, Germany
[4] Hannover Med Sch, Inst Immunol, Hannover, Germany
关键词
animal models; biofilm; host-pathogen interaction; in vivo infections; P; aeruginosa; INHALED NITRIC-OXIDE; FIBROSIS LUNG INFECTION; CYSTIC-FIBROSIS; CAENORHABDITIS-ELEGANS; GENETIC ADAPTATION; ENHANCED EFFICACY; BIOFILM FORMATION; INNATE IMMUNITY; RAT MODEL; VIRULENCE;
D O I
10.1002/1873-3468.12454
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pseudomonas aeruginosa is an important opportunistic pathogen that can cause acute respiratory infections in immunocompetent patients or chronic infections in immunocompromised individuals and in patients with cystic fibrosis. When acquiring the chronic infection state, bacteria are encapsulated within biofilm structures enabling them to withstand diverse environmental assaults, including immune reactions and antimicrobial therapy. Understanding the molecular interactions within the bacteria, as well as with the host or other bacteria, is essential for developing innovative treatment strategies. Such knowledge might be accumulated in vitro. However, it is ultimately necessary to confirm these findings in vivo. In the present Review, we describe state-of-the-art in vivo models that allow studying P. aeruginosa infections in molecular detail. The portrayed mammalian models exclusively focus on respiratory infections. The data obtained by alternative animal models which lack lung tissue, often provide molecular insights that are easily transferable to mammals. Importantly, these surrogate in vivo systems reveal complex molecular interactions of P. aeruginosa with the host. Herein, we also provide a critical assessment of the advantages and disadvantages of such models.
引用
收藏
页码:3941 / 3959
页数:19
相关论文
共 129 条
  • [1] Caenorhabditis elegans as a host for the study of host-pathogen interactions
    Aballay, A
    Ausubel, FM
    [J]. CURRENT OPINION IN MICROBIOLOGY, 2002, 5 (01) : 97 - 101
  • [2] Enhanced efficacy of putative efflux pump inhibitor/antibiotic combination treatments versus MDR strains of Pseudomonas aeruginosa in a Galleria mellonella in vivo infection model
    Adamson, Dougal H.
    Krikstopaityte, Vasare
    Coote, Peter J.
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2015, 70 (08) : 2271 - 2278
  • [3] Inhaled nitric oxide increases endothelial permeability in Pseudomonas aeruginosa pneumonia
    Ader, Florence
    Le Berre, Rozenn
    Lancel, Steve
    Faure, Karine
    Viget, Nathalie B.
    Nowak, Emmanuel
    Neviere, Remi
    Guery, Benoit P.
    [J]. INTENSIVE CARE MEDICINE, 2007, 33 (03) : 503 - 510
  • [4] Alasil S. M., 2015, INT J BACTERIOL, V2015
  • [5] Efficacy of Liposomal Bismuth-Ethanedithiol-Loaded Tobramycin after Intratracheal Administration in Rats with Pulmonary Pseudomonas aeruginosa Infection
    Alhariri, Moayad
    Omri, Abdelwahab
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2013, 57 (01) : 569 - 578
  • [6] The natural history of Caenorhabditis elegans research
    Ankeny, RA
    [J]. NATURE REVIEWS GENETICS, 2001, 2 (06) : 474 - 479
  • [7] [Anonymous], 2012, G3 BETHESDA
  • [8] Adaptation of Pseudomonas aeruginosa in Cystic Fibrosis Airways Influences Virulence of Staphylococcus aureus In Vitro and Murine Models of Co-Infection
    Baldan, Rossella
    Cigana, Cristina
    Testa, Francesca
    Bianconi, Irene
    De Simone, Maura
    Pellin, Danilo
    Di Serio, Clelia
    Bragonzi, Alessandra
    Cirillo, Daniela M.
    [J]. PLOS ONE, 2014, 9 (03):
  • [9] Norovirus Triggered Microbiota-driven Mucosal Inflammation in Interleukin 10-deficient Mice
    Basic, Marijana
    Keubler, Lydia M.
    Buettner, Manuela
    Achard, Marcel
    Breves, Gerhard
    Schroeder, Bernd
    Smoczek, Anna
    Joerns, Anne
    Wedekind, Dirk
    Zschemisch, Nils H.
    Guenther, Claudia
    Neumann, Detlef
    Lienenklaus, Stefan
    Weiss, Siegfried
    Hornef, Mathias W.
    Maehler, Michael
    Bleich, Andre
    [J]. INFLAMMATORY BOWEL DISEASES, 2014, 20 (03) : 431 - 443
  • [10] IL-22 exacerbates weight loss in a murine model of chronic pulmonary Pseudomonas aeruginosa infection
    Bayes, Hannah K.
    Ritchie, Neil D.
    Ward, Christopher
    Corris, Paul A.
    Brodlie, Malcolm
    Evans, Thomas J.
    [J]. JOURNAL OF CYSTIC FIBROSIS, 2016, 15 (06) : 759 - 768