Mapping genetic determinants of host susceptibility to Pseudomonas aeruginosa lung infection in mice

被引:12
作者
De Simone, Maura [1 ]
Spagnuolo, Lorenza [1 ]
Lore, Nicola Ivan [1 ]
Cigana, Cristina [1 ]
De Fino, Ida [1 ]
Broman, Karl W. [2 ]
Iraqi, Fuad A. [3 ]
Bragonzi, Alessandra [1 ]
机构
[1] IRCCS, San Raffaele Sci Inst, Infect & Cyst Fibrosis Unit, Milan, Italy
[2] Univ Wisconsin, Dept Biostat & Med Informat, Madison, WI USA
[3] Tel Aviv Univ, Sackler Fac Med, Dept Clin Microbiol & Immunol, IL-69978 Tel Aviv, Israel
关键词
P; aeruginosa; Pneumonia; Linkage analysis; Murine model; Host susceptibility; QTL mapping; Candidate genes; QUANTITATIVE TRAIT LOCI; GASTROINTESTINAL NEMATODE INFECTIONS; SUBSTANCE-P; CONTROLLING RESISTANCE; CANDIDATE GENES; MODIFIER GENES; DISEASE; PRIORITIZATION; DISSECTION; STRAINS;
D O I
10.1186/s12864-016-2676-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: P. aeruginosa is one of the top three causes of opportunistic human bacterial infections. The remarkable variability in the clinical outcomes of this infection is thought to be associated with genetic predisposition. However, the genes underlying host susceptibility to P. aeruginosa infection are still largely unknown. Results: As a step towards mapping these genes, we applied a genome wide linkage analysis approach to a mouse model. A large F2 intercross population, obtained by mating P. aeruginosa-resistant C3H/HeOuJ, and susceptible A/J mice, was used for quantitative trait locus (QTL) mapping. The F2 progenies were challenged with a P. aeruginosa clinical strain and monitored for the survival time up to 7 days post-infection, as a disease phenotype associated trait. Selected phenotypic extremes of the F2 distribution were genotyped with high-density single nucleotide polymorphic (SNP) markers, and subsequently QTL analysis was performed. A significant locus was mapped on chromosome 6 and was named P. aeruginosa infection resistance locus 1 (Pairl1). The most promising candidate genes, including Dok1, Tacr1, Cd207, Clec4f, Gp9, Gata2, Foxp1, are related to pathogen sensing, neutrophils and macrophages recruitment and inflammatory processes. Conclusions: We propose a set of genes involved in the pathogenesis of P. aeruginosa infection that may be explored to complement human studies.
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页数:8
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