The impact of host genetic background in the Pseudomonas aeruginosa respiratory infections

被引:3
作者
Lore, Nicola Ivan [1 ,2 ]
Cigana, Cristina [1 ]
Sipione, Barbara [1 ,2 ]
Bragonzi, Alessandra [1 ]
机构
[1] IRCCS San Raffaele Sci Inst, Div Immunol Transplantat & Infect Dis, Infect & Cyst Fibrosis Unit, Milan, Italy
[2] Univ Vita Salute San Raffaele, Milan, Italy
关键词
INBRED MOUSE STRAINS; CYSTIC-FIBROSIS; COLLABORATIVE CROSS; LUNG INFECTION; IN-VITRO; MICE; RESISTANT; SUSCEPTIBILITY; SEVERITY; MODIFIER;
D O I
10.1007/s00335-018-9753-8
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
Understanding the significance of human genetic diversity in modulating host susceptibility to opportunistic infections is an emerging challenge in the field of respiratory illnesses. While it is recognized that diverse bacterial strains account for differential disease manifestations, emerging data indicate that host genetic diversity is an important determinant factor that influences the severity of opportunistic infections. With particular regard to respiratory illnesses mediated by the gram-negative bacterium Pseudomonas aeruginosa, diverse genetic background is also emerging as a key contributor. Human-genome-wide association studies are a common approach for determining the inter-individual genetic variation associated with variability of the pulmonary infections. Historically, diverse murine inbred mouse strains and ex-vivo cellular models were considered complementary to human studies for establishing the contribution of genetic background to P. aeruginosa respiratory infections. More recently, the development of a new mouse model of infection, mirroring human airway diseases, combined with innovative murine resource populations, modelling human genetic variation, provides additional insights into the mechanisms of genetic susceptibility. In this review, we cover the recent state of the art of human and animal studies and we discuss future potential challenges in the field of P. aeruginosa respiratory infections.
引用
收藏
页码:550 / 557
页数:8
相关论文
共 43 条
[11]   Modulatory Effect of the SLC9A3 Gene on Susceptibility to Infections and Pulmonary Function in Children With Cystic Fibrosis [J].
Dorfman, Ruslan ;
Taylor, Chelsea ;
Lin, Fan ;
Sun, Lei ;
Sandford, Andrew ;
Pare, Peter ;
Berthiaume, Yves ;
Corey, Mary ;
Durie, Peter ;
Zielenski, Julian .
PEDIATRIC PULMONOLOGY, 2011, 46 (04) :385-392
[12]   Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis [J].
Emond, Mary J. ;
Louie, Tin ;
Emerson, Julia ;
Chong, Jessica X. ;
Mathias, Rasika A. ;
Knowles, Michael R. ;
Rieder, Mark J. ;
Tabor, Holly K. ;
Nickerson, Debbie A. ;
Barnes, Kathleen C. ;
Go, Lung ;
Gibson, Ronald L. ;
Bamshad, Michael J. .
PLOS GENETICS, 2015, 11 (06)
[13]   Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis [J].
Emond, Mary J. ;
Louie, Tin ;
Emerson, Julia ;
Zhao, Wei ;
Mathias, Rasika A. ;
Knowles, Michael R. ;
Wright, Fred A. ;
Rieder, Mark J. ;
Tabor, Holly K. ;
Nickerson, Deborah A. ;
Barnes, Kathleen C. ;
Go, Lung ;
Gibson, Ronald L. ;
Bamshad, Michael J. .
NATURE GENETICS, 2012, 44 (08) :886-+
[14]   Modeling Host Genetic Regulation of Influenza Pathogenesis in the Collaborative Cross [J].
Ferris, Martin T. ;
Aylor, David L. ;
Bottomly, Daniel ;
Whitmore, Alan C. ;
Aicher, Lauri D. ;
Bell, Timothy A. ;
Bradel-Tretheway, Birgit ;
Bryan, Janine T. ;
Buus, Ryan J. ;
Gralinski, Lisa E. ;
Haagmans, Bart L. ;
McMillan, Leonard ;
Miller, Darla R. ;
Rosenzweig, Elizabeth ;
Valdar, William ;
Wang, Jeremy ;
Churchill, Gary A. ;
Threadgill, David W. ;
McWeeney, Shannon K. ;
Katze, Michael G. ;
de Villena, Fernando Pardo-Manuel ;
Baric, Ralph S. ;
Heise, Mark T. .
PLOS PATHOGENS, 2013, 9 (02)
[15]   IL8 gene as modifier of cystic fibrosis: unraveling the factors which influence clinical variability [J].
Furlan, Larissa Lazzarini ;
Lima Marson, Fernando Augusto ;
Ribeiro, Jose Dirceu ;
Bertuzzo, Carmen Silvia ;
Salomao Junior, Joao Batista ;
Silva Souza, Doroteia Rossi .
HUMAN GENETICS, 2016, 135 (08) :881-894
[16]   Pseudomonas aeruginosa: new insights into pathogenesis and host defenses [J].
Gellatly, Shaan L. ;
Hancock, Robert E. W. .
PATHOGENS AND DISEASE, 2013, 67 (03) :159-173
[17]   Genetic Diversity in the Collaborative Cross Model Recapitulates Human West Nile Virus Disease Outcomes [J].
Graham, Jessica B. ;
Thomas, Sunil ;
Swarts, Jessica ;
McMillan, Aimee A. ;
Ferris, Martin T. ;
Suthar, Mehul S. ;
Treuting, Piper M. ;
Ireton, Renee ;
Gale, Michael, Jr. ;
Lund, Jennifer M. .
MBIO, 2015, 6 (03) :1-11
[18]   Genome Wide Identification of SARS-CoV Susceptibility Loci Using the Collaborative Cross [J].
Gralinski, Lisa E. ;
Ferris, Martin T. ;
Aylor, David L. ;
Whitmore, Alan C. ;
Green, Richard ;
Frieman, Matthew B. ;
Deming, Damon ;
Menachery, Vineet D. ;
Miller, Darla R. ;
Buus, Ryan J. ;
Bell, Timothy A. ;
Churchill, Gary A. ;
Threadgill, David W. ;
Katze, Michael G. ;
McMillan, Leonard ;
Valdar, William ;
Heise, Mark T. ;
de Villena, Fernando Pardo-Manuel ;
Baric, Ralph S. .
PLOS GENETICS, 2015, 11 (10)
[19]   Forward genetic dissection of innate response to infection in inbred mouse strains: selected success stories [J].
Gruenheid, S. ;
Gros, P. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2010, 162 (03) :393-401
[20]   Polymorphisms in the lectin pathway genes as a possible cause of early chronic Pseudomonas aeruginosa colonization in cystic fibrosis patients [J].
Haerynck, F. ;
Van Steen, K. ;
Cattaert, T. ;
Loeys, B. ;
Van Daele, S. ;
Schelstraete, P. ;
Claes, K. ;
Van Thielen, M. ;
De Canck, I. ;
John, J. M. Mahachie ;
De Baets, F. .
HUMAN IMMUNOLOGY, 2012, 73 (11) :1175-1183