Abstract
The opportunistic pathogen Pseudomonas aeruginosa is a frequent colonizer of the airways of patients suffering from cystic fibrosis (CF). Depending on early treatment regimens, the colonization will, with high probability, develop into chronic infections sooner or later, and it is important to establish under which conditions the switch to chronic infection takes place. In association with a recently established sinus surgery treatment program for CF patients at the Copenhagen CF Center, colonization of the paranasal sinuses with P. aeruginosa has been investigated, paralleled by sampling of sputum from the same patients. On the basis of genotyping and phenotypic characterization including transcription profiling, the diversity of the P. aeruginosa populations in the sinuses and the lower airways was investigated and compared. The observations made from several children show that the paranasal sinuses constitute an important niche for the colonizing bacteria in many patients. The paranasal sinuses often harbor distinct bacterial subpopulations, and in the early colonization phases there seems to be a migration from the sinuses to the lower airways, suggesting that independent adaptation and evolution take place in the sinuses. Importantly, before the onset of chronic lung infection, lineages with mutations conferring a large fitness benefit in CF airways such as mucA and lasR as well as small colony variants and antibiotic-resistant clones are part of the sinus populations. Thus, the paranasal sinuses potentially constitute a protected niche of adapted clones of P. aeruginosa, which can intermittently seed the lungs and pave the way for subsequent chronic lung infections.
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References
Aanaes K, Rickelt LF, Johansen HK, von Buchwald C, Pressler T, Høiby N et al. (2011). Decreased mucosal oxygen tension in the maxillary sinuses in patients with cystic fibrosis. J Cyst Fibr 10: 114–120.
Andersen JB, Heydorn A, Hentzer M, Eberl L, Geisenberger O, Christensen BB et al. (2001). gfp-based N-acyl homoserine-lactone sensor systems for detection of bacterial communication. Appl Environ Microbiol 67: 575–585.
Boles BR, Thoendel M, Singh PK . (2005). Genetic variation in biofilms and the insurance effects of diversity. Microbiology 151: 2816–2818.
Brown MR, Foster JH . (1970). A simple diagnostic milk medium for Pseudomonas aeruginosa. J Clin Pathol 23: 172–177.
Burns JL, Gibson RL, McNamara S, Yim D, Emerson J, Rosenfeld M et al. (2001). Longitudinal assessment of Pseudomonas aeruginosa in young children with cystic fibrosis. J Infect Dis 183: 444–452.
Cabral DA, Loh BA, Speert DP . (1987). Mucoid Pseudomonas aeruginosa resists nonopsonic phagocytosis by human neutrophils and macrophages. Pediatr Res 22: 429–431.
Carenfelt C, Lundberg C . (1977). Purulent and non-purulent maxillary sinus secretions with respect to pO2, pCO2 and pH. Acta Otolaryngol 84: 138–144.
Coste A, Gilain L, Roger G, Sebbagh G, Lenoir G, Manach Y et al. (1995). Endoscopic and CT-scan evaluation of rhinosinusitis in cystic fibrosis. Rhinology 33: 152–156.
D'Argenio DA, Wu M, Hoffman LR, Kulasekara HD, Deziel E, Smith EE et al. (2007). Growth phenotypes of Pseudomonas aeruginosa lasR mutants adapted to the airways of cystic fibrosis patients. Mol Microbiol 64: 512–533.
Dacheux D, Attree I, Toussaint B . (2001). Expression of ExsA in trans confers type III secretion system-dependent cytotoxicity on noncytotoxic Pseudomonas aeruginosa cystic fibrosis isolates. Infect Immun 69: 538–542.
Demko CA, Byard PJ, Davis PB . (1995). Gender differences in cystic fibrosis: Pseudomonas aeruginosa infection. J Clin Epidemiol 48: 1041–1049.
Deretic V, Schurr MJ, Yu H . (1995). Pseudomonas aeruginosa, mucoidy and the chronic infection phenotype in cystic fibrosis. Trends Microbiol 3: 351–356.
DeVries CA, Ohman DE . (1994). Mucoid-to-nonmucoid conversion in alginate-producing Pseudomonas aeruginosa often results from spontaneous mutations in algT, encoding a putative alternate sigma factor, and shows evidence for autoregulation. J Bacteriol 176: 6677–6687.
Doring G, Taccetti G, Campana S, Festini F, Mascherini M . (2006). Eradication of Pseudomonas aeruginosa in cystic fibrosis patients. Eur Respir J 27: 653.
Dosanjh A, Lakhani S, Elashoff D, Chin C, Hsu V, Hilman B . (2000). A comparison of microbiologic flora of the sinuses and airway among cystic fibrosis patients with maxillary antrostomies. Pediatr Transplant 4: 182–185.
Gibson RL, Emerson J, McNamara S, Burns JL, Rosenfeld M, Yunker A et al. (2003). Significant microbiological effect of inhaled tobramycin in young children with cystic fibrosis. Am J Respir Crit Care Med 167: 841–849.
Gysin C, Alothman GA, Papsin BC . (2000). Sinonasal disease in cystic fibrosis: clinical characteristics, diagnosis, and management. Pediatr Pulmonol 30: 481–489.
Hancock RE, Mutharia LM, Chan L, Darveau RP, Speert DP, Pier GB . (1983). Pseudomonas aeruginosa isolates from patients with cystic fibrosis: a class of serum-sensitive, nontypable strains deficient in lipopolysaccharide O side chains. Infect Immun 42: 170–177.
Hansen SK, Rainey PB, Haagensen JA, Molin S . (2007). Evolution of species interactions in a biofilm community. Nature 445: 533–536.
Haussler S . (2004). Biofilm formation by the small colony variant phenotype of Pseudomonas aeruginosa. Environ Microbiol 6: 546–551.
Haussler S, Tummler B, Weissbrodt H, Rohde M, Steinmetz I . (1999). Small-colony variants of Pseudomonas aeruginosa in cystic fibrosis. Clin Infect Dis 29: 621–625.
Hentzer M, Riedel K, Rasmussen TB, Heydorn A, Andersen JB, Parsek MR et al. (2002). Inhibition of quorum sensing in Pseudomonas aeruginosa biofilm bacteria by a halogenated furanone compound. Microbiology 148: 87–102.
Hoffman LR, Kulasekara HD, Emerson J, Houston LS, Burns JL, Ramsey BW et al. (2009). Pseudomonas aeruginosa lasR mutants are associated with cystic fibrosis lung disease progression. J Cyst Fibros 8: 66–70.
Hoffman LR, Richardson AR, Houston LS, Kulasekara HD, Martens-Habbena W, Klausen M et al. (2010). Nutrient availability as a mechanism for selection of antibiotic tolerant Pseudomonas aeruginosa within the CF airway. PLoS Pathogen 6: e1000712.
Høiby N . (1974). Epidemiological investigations of the respiratory tract bacteriology in patients with cystic fibrosis. Acta Pathol Microbiol Scand B 82: 541–550.
Høiby N . (1977). Pseudomonas aeruginosa infection in cystic fibrosis. Diagnostic and prognostic significance of pseudomonas aeruginosa precipitins determined by means of crossed immunoelectrophoresis. A survey. Scand J Respir Dis 58: 65–79.
Høiby N, Frederiksen B . (2000). Microbiology of cystic fibrosis. In: Hodson ME, Geddes DM (eds). Cystic Fibrosis, 2nd edn. Arnold: London, United Kingdom, pp 83–107.
Høiby N, Frederiksen B, Pressler T . (2005). Eradication of early Pseudomonas aeruginosa infection. J Cyst Fibros 4(Suppl 2): 49–54.
Høiby N, Pedersen SS . (1989). Estimated risk of cross-infection with Pseudomonas aeruginosa in Danish cystic fibrosis patients. Acta Paediatr Scand 78: 395–404.
Holloway BW, Morgan AF . (1986). Genome organization in Pseudomonas. Annu Rev Microbiol 40: 79–105.
Huxley EJ, Viroslav J, Gray WR, Pierce AK . (1978). Pharyngeal aspiration in normal adults and patients with depressed consciousness. Am J Med 64: 564–568.
Jelsbak L, Johansen HK, Frost AL, Thogersen R, Thomsen LE, Ciofu O et al. (2007). Molecular epidemiology and dynamics of Pseudomonas aeruginosa populations in lungs of cystic fibrosis patients. Infect Immun 75: 2214–2224.
Jones JW, Parsons DS, Cuyler JP . (1993). The results of functional endoscopic sinus (FES) surgery on the symptoms of patients with cystic fibrosis. Int J Pediatr Otorhinolaryngol 28: 25–32.
Koch C . (2002). Early infection and progression of cystic fibrosis lung disease. Pediatr Pulmonol 34: 232–236.
Lam J, Chan R, Lam K, Costerton JW . (1980). Production of mucoid microcolonies by Pseudomonas aeruginosa within infected lungs in cystic fibrosis. Infect Immun 28: 546–556.
Low AS, MacKenzie FM, Gould IM, Booth IR . (2001). Protected environments allow parallel evolution of a bacterial pathogen in a patient subjected to long-term antibiotic therapy. Mol Microbiol 42: 619–630.
Mahenthiralingam E, Campbell ME, Speert DP . (1994). Nonmotility and phagocytic resistance of Pseudomonas aeruginosa isolates from chronically colonized patients with cystic fibrosis. Infect Immun 62: 596–605.
Mainz JG, Naehrlich L, Schien M, Kading M, Schiller I, Mayr S et al. (2009). Concordant genotype of upper and lower airways P aeruginosa and S. aureus isolates in cystic fibrosis. Thorax 64: 535–540.
Muhlebach MS, Miller MB, Moore C, Wedd JP, Drake AF, Leigh MW . (2006). Are lower airway or throat cultures predictive of sinus bacteriology in cystic fibrosis? Pediatr Pulmonol 41: 445–451.
Munck A, Bonacorsi S, Mariani-Kurkdjian P, Lebourgeois M, Gerardin M, Brahimi N et al. (2001). Genotypic characterization of Pseudomonas aeruginosa strains recovered from patients with cystic fibrosis after initial and subsequent colonization. Pediatr Pulmonol 32: 288–292.
Nguyen D, Singh PK . (2006). Evolving stealth: genetic adaptation of Pseudomonas aeruginosa during cystic fibrosis infections. Proc Natl Acad Sci USA 103: 8305–8306.
Nishioka GJ, Barbero GJ, Konig P, Parsons DS, Cook PR, Davis WE . (1995). Symptom outcome after functional endoscopic sinus surgery in patients with cystic fibrosis: a prospective study. Otolaryngol Head Neck Surg 113: 440–445.
Parad RB, Gerard CJ, Zurakowski D, Nichols DP, Pier GB . (1999). Pulmonary outcome in cystic fibrosis is influenced primarily by mucoid Pseudomonas aeruginosa infection and immune status and only modestly by genotype. Infect Immun 67: 4744–4750.
Poole K . (2004). Efflux-mediated multiresistance in Gram-negative bacteria. Clin Microbiol Infect 10: 12–26.
Pratt LA, Kolter R . (1998). Genetic analysis of Escherichia coli biofilm formation: roles of flagella, motility, chemotaxis and type I pili. Mol Microbiol 30: 285–293.
Rainey PB, Travisano M . (1998). Adaptive radiation in a heterogeneous environment. Nature 394: 69–72.
Rau MH, Hansen SK, Johansen HK, Thomsen LE, Workman CT, Nielsen KF et al. (2010). Early adaptive developments of Pseudomonas aeruginosa after the transition from life in the environment to persistent colonization in the airways of human cystic fibrosis hosts. Environ Microbiol 12: 1643–1658.
Robertson JM, Friedman EM, Rubin BK . (2008). Nasal and sinus disease in cystic fibrosis. Paediatr Respir Rev 9: 213–219.
Smith EE, Buckley DG, Wu Z, Saenphimmachak C, Hoffman LR, D'Argenio DA et al. (2006). Genetic adaptation by Pseudomonas aeruginosa to the airways of cystic fibrosis patients. Proc Natl Acad Sci USA 103: 8487–8492.
Starkey M, Hickman JH, Ma L, Zhang N, De Long S, Hinz A et al. (2009). Pseudomonas aeruginosa rugose small-colony variants have adaptations that likely promote persistence in the cystic fibrosis lung. J Bacteriol 191: 3492–3503.
Taccetti G, Campana S, Festini F, Mascherini M, Doring G . (2005). Early eradication therapy against Pseudomonas aeruginosa in cystic fibrosis patients. Eur Respir J 26: 458–461.
Taylor RF, Morgan DW, Nicholson PS, Mackay IS, Hodson ME, Pitt TL . (1992). Extrapulmonary sites of Pseudomonas aeruginosa in adults with cystic fibrosis. Thorax 47: 426–428.
Terry JM, Pina SE, Mattingly SJ . (1991). Environmental conditions which influence mucoid conversion Pseudomonas aeruginosa PAO1. Infect Immun 59: 471–477.
Terry JM, Pina SE, Mattingly SJ . (1992). Role of energy metabolism in conversion of nonmucoid Pseudomonas aeruginosa to the mucoid phenotype. Infect Immun 60: 1329–1335.
Thomassen MJ, Demko CA, Boxerbaum B, Stern RC, Kuchenbrod PJ . (1979). Multiple of isolates of Pseudomonas aeruginosa with differing antimicrobial susceptibility patterns from patients with cystic fibrosis. J Infect Dis 140: 873–880.
Wahba AH, Darrell JH . (1965). The identification of atypical strains of Pseudomonas aeruginosa. J Gen Microbiol 38: 329–342.
Wiehlmann L, Wagner G, Cramer N, Siebert B, Gudowius P, Morales G et al. (2007). Population structure of Pseudomonas aeruginosa. Proc Natl Acad Sci USA 104: 8101–8106.
Yang L, Haagensen JA, Jelsbak L, Johansen HK, Sternberg C, Høiby N et al. (2008). In situ growth rates and biofilm development of Pseudomonas aeruginosa populations in chronic lung infections. J Bacteriol 190: 2767–2776.
Yang L, Jelsbak L, Marvig RL, Damkiær S, Workman CT, Rau MH et al. (2011). Evolutionary dynamics of bacteria in a human host environment. Proc Natl Acad Sci USA 108: 7481–7466.
Yang L, Rybtke MT, Jakobsen TH, Hentzer M, Bjarnsholt T, Givskov M et al. (2009). Computer-aided identification of recognized drugs as Pseudomonas aeruginosa quorum-sensing inhibitors. Antimicrob Agents Chemother 53: 2432–2443.
Acknowledgements
We gratefully acknowledge Matthew Parsek and Liang Yang for experimental assistance and we also thank the nurses and doctors at the Copenhagen CF Center for their help in recruiting and preparing the patients for surgery. This work was supported by grants from the Danish Research Agency and the Lundbeck Foundation to SM.
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Hansen, S., Rau, M., Johansen, H. et al. Evolution and diversification of Pseudomonas aeruginosa in the paranasal sinuses of cystic fibrosis children have implications for chronic lung infection. ISME J 6, 31–45 (2012). https://doi.org/10.1038/ismej.2011.83
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DOI: https://doi.org/10.1038/ismej.2011.83
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