Skip to main content
Top
Published in: BMC Pulmonary Medicine 1/2017

Open Access 01-12-2017 | Research article

Antibiotic perturbation of mixed-strain Pseudomonas aeruginosa infection in patients with cystic fibrosis

Authors: Anna S. Tai, Laura J. Sherrard, Timothy J. Kidd, Kay A. Ramsay, Cameron Buckley, Melanie Syrmis, Keith Grimwood, Scott C. Bell, David M. Whiley

Published in: BMC Pulmonary Medicine | Issue 1/2017

Login to get access

Abstract

Background

Pulmonary exacerbations in cystic fibrosis (CF) remain poorly understood and treatment is usually targeted at Pseudomonas aeruginosa. Within Australia a predominant shared P. aeruginosa strain (AUST-02) is associated with greater treatment needs. This single centre study assessed temporal shared strain population dynamics during and after antibiotic treatment of exacerbations.

Methods

Sputum was collected from 12 adult patients with a history of chronic AUST-02 infection at four time-points during and after treatment of an exacerbation. Forty-eight P. aeruginosa isolates within each sample underwent AUST-02 allele-specific PCR and SNP-based strain genotyping.

Results

Various commonly shared Australian strains (AUST-01, 0.1%; AUST-02, 54.3%; AUST-06, 36.6%; AUST-07, 4.6%; AUST-11, 4.3%) and two unique strains (0.1%) were identified from 45 sputum samples (2160 isolates). Based on within-patient relative abundance of strains, a “single-strain infection” (n = 7) or “mixed-strain infection” (n = 5) was assigned to each patient. A significant temporal variation in the P. aeruginosa population composition was found for those with mixed-strain infection (P < 0.001). Patients with mixed-strain infections had more long-term treatment requirements than those with single-strain infection. Moreover, despite both groups having similar lung function at study entry, patients with single-strain infection had greater improvement in FEV1% predicted following their exacerbation treatment (P = 0.02).

Conclusion

Pulmonary exacerbations may reveal multiple, unrelated P. aeruginosa strains whose relative abundance with one another may change rapidly, in a sustained and unpredictable manner.
Appendix
Available only for authorised users
Literature
1.
go back to reference Foundation CF. Cystic Fibrosis foundation patient registry 2012 annual data report. Bethesda: Cystic Fibrosis Foundation; 2013. Foundation CF. Cystic Fibrosis foundation patient registry 2012 annual data report. Bethesda: Cystic Fibrosis Foundation; 2013.
2.
go back to reference Sanders DB, Bittner RC, Rosenfeld M, Redding GJ, Goss CH. Pulmonary exacerbations are associated with subsequent FEV1 decline in both adults and children with cystic fibrosis. Pediatr Pulmonol. 2011;46(4):393–400.CrossRefPubMed Sanders DB, Bittner RC, Rosenfeld M, Redding GJ, Goss CH. Pulmonary exacerbations are associated with subsequent FEV1 decline in both adults and children with cystic fibrosis. Pediatr Pulmonol. 2011;46(4):393–400.CrossRefPubMed
3.
go back to reference Amadori A, Antonelli A, Balteri I, Schreiber A, Bugiani M, et al. Recurrent exacerbations affect FEV(1) decline in adult patients with cystic fibrosis. Respir Med. 2009;103(3):407–13.CrossRefPubMed Amadori A, Antonelli A, Balteri I, Schreiber A, Bugiani M, et al. Recurrent exacerbations affect FEV(1) decline in adult patients with cystic fibrosis. Respir Med. 2009;103(3):407–13.CrossRefPubMed
4.
go back to reference Cogen J, Emerson J, Sanders DB, Ren C, Schechter MS, et al. Risk factors for lung function decline in a large cohort of young cystic fibrosis patients. Pediatr Pulmonol. 2015;50(8):763–70. Cogen J, Emerson J, Sanders DB, Ren C, Schechter MS, et al. Risk factors for lung function decline in a large cohort of young cystic fibrosis patients. Pediatr Pulmonol. 2015;50(8):763–70.
5.
go back to reference Solem CT, Vera-Llonch M, Liu S, Botteman M, Castiglione B. Impact of pulmonary exacerbations and lung function on generic health-related quality of life in patients with cystic fibrosis. Health Qual Life Outcomes. 2016;14:63.CrossRefPubMedPubMedCentral Solem CT, Vera-Llonch M, Liu S, Botteman M, Castiglione B. Impact of pulmonary exacerbations and lung function on generic health-related quality of life in patients with cystic fibrosis. Health Qual Life Outcomes. 2016;14:63.CrossRefPubMedPubMedCentral
6.
go back to reference de Boer K, Vandemheen KL, Tullis E, Doucette S, Fergusson D, et al. Exacerbation frequency and clinical outcomes in adult patients with cystic fibrosis. Thorax. 2011;66(8):680–5.CrossRefPubMed de Boer K, Vandemheen KL, Tullis E, Doucette S, Fergusson D, et al. Exacerbation frequency and clinical outcomes in adult patients with cystic fibrosis. Thorax. 2011;66(8):680–5.CrossRefPubMed
8.
go back to reference Ramsey BW, Pepe MS, Quan JM, Otto KL, Montgomery AB, et al. Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. Cystic fibrosis inhaled Tobramycin study group. N Engl J Med. 1999;340(1):23–30.CrossRefPubMed Ramsey BW, Pepe MS, Quan JM, Otto KL, Montgomery AB, et al. Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. Cystic fibrosis inhaled Tobramycin study group. N Engl J Med. 1999;340(1):23–30.CrossRefPubMed
9.
go back to reference Fuchs HJ, Borowitz DS, Christiansen DH, Morris EM, Nash ML, et al. Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme study group. N Engl J Med. 1994;331(10):637–42.CrossRefPubMed Fuchs HJ, Borowitz DS, Christiansen DH, Morris EM, Nash ML, et al. Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme study group. N Engl J Med. 1994;331(10):637–42.CrossRefPubMed
10.
go back to reference Doring G, Flume P, Heijerman H, Elborn JS, Consensus Study G. Treatment of lung infection in patients with cystic fibrosis: current and future strategies. J Cyst Fibros. 2012;11(6):461–79.CrossRefPubMed Doring G, Flume P, Heijerman H, Elborn JS, Consensus Study G. Treatment of lung infection in patients with cystic fibrosis: current and future strategies. J Cyst Fibros. 2012;11(6):461–79.CrossRefPubMed
11.
go back to reference Mowat E, Paterson S, Fothergill JL, Wright EA, Ledson MJ, et al. Pseudomonas aeruginosa population diversity and turnover in cystic fibrosis chronic infections. Am J Respir Crit Care Med. 2011;183(12):1674–9.CrossRefPubMed Mowat E, Paterson S, Fothergill JL, Wright EA, Ledson MJ, et al. Pseudomonas aeruginosa population diversity and turnover in cystic fibrosis chronic infections. Am J Respir Crit Care Med. 2011;183(12):1674–9.CrossRefPubMed
13.
go back to reference Kidd TJ, Ramsay KA, Hu H, Marks GB, Wainwright CE, et al. Shared Pseudomonas aeruginosa genotypes are common in Australian cystic fibrosis centres. Eur Respir J Physiology. 2013;41(5):1091–100.CrossRef Kidd TJ, Ramsay KA, Hu H, Marks GB, Wainwright CE, et al. Shared Pseudomonas aeruginosa genotypes are common in Australian cystic fibrosis centres. Eur Respir J Physiology. 2013;41(5):1091–100.CrossRef
14.
go back to reference Aaron SD, Vandemheen KL, Ramotar K, Giesbrecht-Lewis T, Tullis E, et al. Infection with transmissible strains of Pseudomonas aeruginosa and clinical outcomes in adults with cystic fibrosis. JAMA. 2010;304(19):2145–53.CrossRefPubMed Aaron SD, Vandemheen KL, Ramotar K, Giesbrecht-Lewis T, Tullis E, et al. Infection with transmissible strains of Pseudomonas aeruginosa and clinical outcomes in adults with cystic fibrosis. JAMA. 2010;304(19):2145–53.CrossRefPubMed
15.
go back to reference Aaron SD, Ramotar K, Ferris W, Vandemheen K, Saginur R, et al. Adult cystic fibrosis exacerbations and new strains of Pseudomonas aeruginosa. Am J Respir Crit Care Med. 2004;169(7):811–5.CrossRefPubMed Aaron SD, Ramotar K, Ferris W, Vandemheen K, Saginur R, et al. Adult cystic fibrosis exacerbations and new strains of Pseudomonas aeruginosa. Am J Respir Crit Care Med. 2004;169(7):811–5.CrossRefPubMed
16.
go back to reference Lee TW, Brownlee KG, Conway SP, Denton M, Littlewood JM. Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients. J Cyst Fibros. 2003;2(1):29–34.CrossRefPubMed Lee TW, Brownlee KG, Conway SP, Denton M, Littlewood JM. Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients. J Cyst Fibros. 2003;2(1):29–34.CrossRefPubMed
17.
go back to reference Ramsay KA, Sandhu H, Geake JB, Ballard E, O'Rourke P, et al. The changing prevalence of pulmonary infection in adults with cystic fibrosis: a longitudinal analysis. J Cyst Fibros. 2017;16(1):70–7.CrossRefPubMed Ramsay KA, Sandhu H, Geake JB, Ballard E, O'Rourke P, et al. The changing prevalence of pulmonary infection in adults with cystic fibrosis: a longitudinal analysis. J Cyst Fibros. 2017;16(1):70–7.CrossRefPubMed
18.
go back to reference Kidd TJ, Magalhaes RJ, Paynter S, Bell SC, Group ACI. The social network of cystic fibrosis centre care and shared Pseudomonas aeruginosa strain infection: a cross-sectional analysis. Lancet Respir Med. 2015;3(8):640–50.CrossRefPubMed Kidd TJ, Magalhaes RJ, Paynter S, Bell SC, Group ACI. The social network of cystic fibrosis centre care and shared Pseudomonas aeruginosa strain infection: a cross-sectional analysis. Lancet Respir Med. 2015;3(8):640–50.CrossRefPubMed
19.
go back to reference Hankinson JL, Odencrantz JR, Fedan KB. Spirometric reference values from a sample of the general U.S. population. Am J Respir Crit Care Med. 1999;159(1):179–87.CrossRefPubMed Hankinson JL, Odencrantz JR, Fedan KB. Spirometric reference values from a sample of the general U.S. population. Am J Respir Crit Care Med. 1999;159(1):179–87.CrossRefPubMed
20.
go back to reference Kidd TJ, Ramsay KA, Hu H, Bye PT, Elkins MR, et al. Low rates of Pseudomonas aeruginosa misidentification in isolates from cystic fibrosis patients. J Clin Microbiol. 2009;47(5):1503–9.CrossRefPubMedPubMedCentral Kidd TJ, Ramsay KA, Hu H, Bye PT, Elkins MR, et al. Low rates of Pseudomonas aeruginosa misidentification in isolates from cystic fibrosis patients. J Clin Microbiol. 2009;47(5):1503–9.CrossRefPubMedPubMedCentral
21.
go back to reference Anuj SN, Whiley DM, Kidd TJ, Ramsay KA, Bell SC, et al. Rapid single-nucleotide polymorphism-based identification of clonal Pseudomonas aeruginosa isolates from patients with cystic fibrosis by the use of real-time PCR and high-resolution melting curve analysis. Clin Microbiol Infect. 2011;17(9):1403–8.CrossRefPubMed Anuj SN, Whiley DM, Kidd TJ, Ramsay KA, Bell SC, et al. Rapid single-nucleotide polymorphism-based identification of clonal Pseudomonas aeruginosa isolates from patients with cystic fibrosis by the use of real-time PCR and high-resolution melting curve analysis. Clin Microbiol Infect. 2011;17(9):1403–8.CrossRefPubMed
22.
go back to reference Syrmis MW, Kidd TJ, Moser RJ, Ramsay KA, Gibson KM, et al. A comparison of two informative SNP-based strategies for typing Pseudomonas aeruginosa isolates from patients with cystic fibrosis. BMC Infect Dis. 2014;14(1):307.CrossRefPubMedPubMedCentral Syrmis MW, Kidd TJ, Moser RJ, Ramsay KA, Gibson KM, et al. A comparison of two informative SNP-based strategies for typing Pseudomonas aeruginosa isolates from patients with cystic fibrosis. BMC Infect Dis. 2014;14(1):307.CrossRefPubMedPubMedCentral
23.
go back to reference CLSI. Clinical and laboratory standards institute. Performance standards for antimicrobial susceptibility testing; twenty-third informational supplement. CLSI document M100-S23. Wayne: Clinical and Laboratory Standards Institute; 2013. p. 2013. CLSI. Clinical and laboratory standards institute. Performance standards for antimicrobial susceptibility testing; twenty-third informational supplement. CLSI document M100-S23. Wayne: Clinical and Laboratory Standards Institute; 2013. p. 2013.
24.
go back to reference Fyfe JA, Govan JR. Alginate synthesis in mucoid Pseudomonas aeruginosa: a chromosomal locus involved in control. J Gen Microbiol. 1980;119(2):443–50.PubMed Fyfe JA, Govan JR. Alginate synthesis in mucoid Pseudomonas aeruginosa: a chromosomal locus involved in control. J Gen Microbiol. 1980;119(2):443–50.PubMed
25.
go back to reference D'Argenio DA, Wu M, Hoffman LR, Kulasekara HD, Deziel E, et al. Growth phenotypes of Pseudomonas aeruginosa lasR mutants adapted to the airways of cystic fibrosis patients. Mol Microbiol. 2007;64(2):512–33.CrossRefPubMedPubMedCentral D'Argenio DA, Wu M, Hoffman LR, Kulasekara HD, Deziel E, et al. Growth phenotypes of Pseudomonas aeruginosa lasR mutants adapted to the airways of cystic fibrosis patients. Mol Microbiol. 2007;64(2):512–33.CrossRefPubMedPubMedCentral
26.
go back to reference Williams D, Evans B, Haldenby S, Walshaw MJ, Brockhurst MA, et al. Divergent, coexisting Pseudomonas aeruginosa lineages in chronic cystic fibrosis lung infections. Am J Respir Crit Care Med. 2015;191(7):775–85.CrossRefPubMedPubMedCentral Williams D, Evans B, Haldenby S, Walshaw MJ, Brockhurst MA, et al. Divergent, coexisting Pseudomonas aeruginosa lineages in chronic cystic fibrosis lung infections. Am J Respir Crit Care Med. 2015;191(7):775–85.CrossRefPubMedPubMedCentral
27.
go back to reference Jones AM, Dodd ME, Doherty CJ, Govan JR, Webb AK. Increased treatment requirements of patients with cystic fibrosis who harbour a highly transmissible strain of Pseudomonas aeruginosa. Thorax. 2002;57(11):924–5.CrossRefPubMedPubMedCentral Jones AM, Dodd ME, Doherty CJ, Govan JR, Webb AK. Increased treatment requirements of patients with cystic fibrosis who harbour a highly transmissible strain of Pseudomonas aeruginosa. Thorax. 2002;57(11):924–5.CrossRefPubMedPubMedCentral
28.
go back to reference Duong J, Booth SC, McCartney NK, Rabin HR, Parkins MD, et al. Phenotypic and genotypic comparison of epidemic and non-epidemic strains of Pseudomonas aeruginosa from individuals with cystic fibrosis. PLoS One. 2015;10(11):e0143466.CrossRefPubMedPubMedCentral Duong J, Booth SC, McCartney NK, Rabin HR, Parkins MD, et al. Phenotypic and genotypic comparison of epidemic and non-epidemic strains of Pseudomonas aeruginosa from individuals with cystic fibrosis. PLoS One. 2015;10(11):e0143466.CrossRefPubMedPubMedCentral
29.
go back to reference Griffiths AL, Jamsen K, Carlin JB, Grimwood K, Carzino R, et al. Effects of segregation on an epidemic Pseudomonas aeruginosa strain in a cystic fibrosis clinic. Am J Respir Crit Care Med. 2005;171(9):1020–5.CrossRefPubMed Griffiths AL, Jamsen K, Carlin JB, Grimwood K, Carzino R, et al. Effects of segregation on an epidemic Pseudomonas aeruginosa strain in a cystic fibrosis clinic. Am J Respir Crit Care Med. 2005;171(9):1020–5.CrossRefPubMed
30.
go back to reference George PM, Banya W, Pareek N, Bilton D, Cullinan P, et al. Improved survival at low lung function in cystic fibrosis: cohort study from 1990 to 2007. BMJ. 2011;342:d1008.CrossRefPubMedPubMedCentral George PM, Banya W, Pareek N, Bilton D, Cullinan P, et al. Improved survival at low lung function in cystic fibrosis: cohort study from 1990 to 2007. BMJ. 2011;342:d1008.CrossRefPubMedPubMedCentral
31.
go back to reference Smith DJ, Badrick AC, Zakrzewski M, Krause L, Bell SC, et al. Pyrosequencing reveals transient cystic fibrosis lung microbiome changes with intravenous antibiotics. Eur Respir J. 2014;44(4):922–30.CrossRefPubMed Smith DJ, Badrick AC, Zakrzewski M, Krause L, Bell SC, et al. Pyrosequencing reveals transient cystic fibrosis lung microbiome changes with intravenous antibiotics. Eur Respir J. 2014;44(4):922–30.CrossRefPubMed
32.
go back to reference Price KE, Hampton TH, Gifford AH, Dolben EL, Hogan DA, et al. Unique microbial communities persist in individual cystic fibrosis patients throughout a clinical exacerbation. Microbiome. 2013;1(1):27.CrossRefPubMedPubMedCentral Price KE, Hampton TH, Gifford AH, Dolben EL, Hogan DA, et al. Unique microbial communities persist in individual cystic fibrosis patients throughout a clinical exacerbation. Microbiome. 2013;1(1):27.CrossRefPubMedPubMedCentral
33.
go back to reference Diaz Caballero J, Clark ST, Coburn B, Zhang Y, Wang PW, et al. Selective sweeps and parallel Pathoadaptation drive Pseudomonas aeruginosa evolution in the cystic fibrosis lung. MBio. 2015;6(5) Diaz Caballero J, Clark ST, Coburn B, Zhang Y, Wang PW, et al. Selective sweeps and parallel Pathoadaptation drive Pseudomonas aeruginosa evolution in the cystic fibrosis lung. MBio. 2015;6(5)
34.
go back to reference Workentine ML, Sibley CD, Glezerson B, Purighalla S, Norgaard-Gron JC, et al. Phenotypic heterogeneity of Pseudomonas aeruginosa populations in a cystic fibrosis patient. PLoS One. 2013;8(4):e60225.CrossRefPubMedPubMedCentral Workentine ML, Sibley CD, Glezerson B, Purighalla S, Norgaard-Gron JC, et al. Phenotypic heterogeneity of Pseudomonas aeruginosa populations in a cystic fibrosis patient. PLoS One. 2013;8(4):e60225.CrossRefPubMedPubMedCentral
35.
go back to reference Cramer N, Klockgether J, Wrasman K, Schmidt M, Davenport CF, et al. Microevolution of the major common Pseudomonas aeruginosa clones C and PA14 in cystic fibrosis lungs. Environ Microbiol. 2011;13(7):1690–704.CrossRefPubMed Cramer N, Klockgether J, Wrasman K, Schmidt M, Davenport CF, et al. Microevolution of the major common Pseudomonas aeruginosa clones C and PA14 in cystic fibrosis lungs. Environ Microbiol. 2011;13(7):1690–704.CrossRefPubMed
36.
go back to reference Marvig RL, Sommer LM, Molin S, Johansen HK. Convergent evolution and adaptation of Pseudomonas aeruginosa within patients with cystic fibrosis. Nat Genet. 2015;47(1):57–64.CrossRefPubMed Marvig RL, Sommer LM, Molin S, Johansen HK. Convergent evolution and adaptation of Pseudomonas aeruginosa within patients with cystic fibrosis. Nat Genet. 2015;47(1):57–64.CrossRefPubMed
37.
go back to reference Jorth P, Staudinger BJ, Wu X, Hisert KB, Hayden H, et al. Regional isolation drives bacterial diversification within cystic fibrosis lungs. Cell Host Microbe. 2015;18(3):307–19.CrossRefPubMedPubMedCentral Jorth P, Staudinger BJ, Wu X, Hisert KB, Hayden H, et al. Regional isolation drives bacterial diversification within cystic fibrosis lungs. Cell Host Microbe. 2015;18(3):307–19.CrossRefPubMedPubMedCentral
38.
go back to reference Smith AL, Fiel SB, Mayer-Hamblett N, Ramsey B, Burns JL. Susceptibility testing of Pseudomonas aeruginosa isolates and clinical response to parenteral antibiotic administration: lack of association in cystic fibrosis. Chest. 2003;123(5):1495–502.CrossRefPubMed Smith AL, Fiel SB, Mayer-Hamblett N, Ramsey B, Burns JL. Susceptibility testing of Pseudomonas aeruginosa isolates and clinical response to parenteral antibiotic administration: lack of association in cystic fibrosis. Chest. 2003;123(5):1495–502.CrossRefPubMed
39.
go back to reference Hurley MN, Ariff AH, Bertenshaw C, Bhatt J, Smyth AR. Results of antibiotic susceptibility testing do not influence clinical outcome in children with cystic fibrosis. J Cyst Fibro. 2012;11(4):288–92.CrossRef Hurley MN, Ariff AH, Bertenshaw C, Bhatt J, Smyth AR. Results of antibiotic susceptibility testing do not influence clinical outcome in children with cystic fibrosis. J Cyst Fibro. 2012;11(4):288–92.CrossRef
40.
go back to reference Parkins MD, Rendall JC, Elborn JS. Incidence and risk factors for pulmonary exacerbation treatment failures in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa. Chest. 2012;141(2):485–93.CrossRefPubMed Parkins MD, Rendall JC, Elborn JS. Incidence and risk factors for pulmonary exacerbation treatment failures in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa. Chest. 2012;141(2):485–93.CrossRefPubMed
41.
go back to reference Fothergill JL, Mowat E, Ledson MJ, Walshaw MJ, Winstanley C. Fluctuations in phenotypes and genotypes within populations of Pseudomonas aeruginosa in the cystic fibrosis lung during pulmonary exacerbations. J Med Microbiol. 2010;59(Pt 4):472–81.CrossRefPubMed Fothergill JL, Mowat E, Ledson MJ, Walshaw MJ, Winstanley C. Fluctuations in phenotypes and genotypes within populations of Pseudomonas aeruginosa in the cystic fibrosis lung during pulmonary exacerbations. J Med Microbiol. 2010;59(Pt 4):472–81.CrossRefPubMed
42.
go back to reference Hatch RA, Schiller NL. Alginate lyase promotes diffusion of aminoglycosides through the extracellular polysaccharide of mucoid Pseudomonas aeruginosa. Antimicrob Agents Chemother. 1998;42(4):974–7.PubMedPubMedCentral Hatch RA, Schiller NL. Alginate lyase promotes diffusion of aminoglycosides through the extracellular polysaccharide of mucoid Pseudomonas aeruginosa. Antimicrob Agents Chemother. 1998;42(4):974–7.PubMedPubMedCentral
43.
go back to reference Parad RB, Gerard CJ, Zurakowski D, Nichols DP, Pier GB. Pulmonary outcome in cystic fibrosis is influenced primarily by mucoid Pseudomonas aeruginosa infection and immune status and only modestly by genotype. Infect Immun. 1999;67(9):4744–50.PubMedPubMedCentral Parad RB, Gerard CJ, Zurakowski D, Nichols DP, Pier GB. Pulmonary outcome in cystic fibrosis is influenced primarily by mucoid Pseudomonas aeruginosa infection and immune status and only modestly by genotype. Infect Immun. 1999;67(9):4744–50.PubMedPubMedCentral
44.
go back to reference Barclay ML, Begg EJ, Chambers ST, Thornley PE, Pattemore PK, et al. Adaptive resistance to tobramycin in Pseudomonas aeruginosa lung infection in cystic fibrosis. J Antimicrob Chemother. 1996;37(6):1155–64.CrossRefPubMed Barclay ML, Begg EJ, Chambers ST, Thornley PE, Pattemore PK, et al. Adaptive resistance to tobramycin in Pseudomonas aeruginosa lung infection in cystic fibrosis. J Antimicrob Chemother. 1996;37(6):1155–64.CrossRefPubMed
45.
go back to reference Boucher JC, Yu H, Mudd MH, Deretic V. Mucoid Pseudomonas aeruginosa in cystic fibrosis: characterization of muc mutations in clinical isolates and analysis of clearance in a mouse model of respiratory infection. Infect Immun. 1997;65(9):3838–46.PubMedPubMedCentral Boucher JC, Yu H, Mudd MH, Deretic V. Mucoid Pseudomonas aeruginosa in cystic fibrosis: characterization of muc mutations in clinical isolates and analysis of clearance in a mouse model of respiratory infection. Infect Immun. 1997;65(9):3838–46.PubMedPubMedCentral
46.
go back to reference Goolaerts A, Lafargue M, Song Y, Miyazawa B, Arjomandi M, et al. PAI-1 is an essential component of the pulmonary host response during Pseudomonas aeruginosa pneumonia in mice. Thorax. 2011;66(9):788–96.CrossRefPubMedPubMedCentral Goolaerts A, Lafargue M, Song Y, Miyazawa B, Arjomandi M, et al. PAI-1 is an essential component of the pulmonary host response during Pseudomonas aeruginosa pneumonia in mice. Thorax. 2011;66(9):788–96.CrossRefPubMedPubMedCentral
47.
go back to reference de Lima CD, Calegari-Silva TC, Pereira RM, Santos SA, Lopes UG, et al. ExoU activates NF-kappaB and increases IL-8/KC secretion during Pseudomonas aeruginosa infection. PLoS One. 2012;7(7):e41772.CrossRefPubMedPubMedCentral de Lima CD, Calegari-Silva TC, Pereira RM, Santos SA, Lopes UG, et al. ExoU activates NF-kappaB and increases IL-8/KC secretion during Pseudomonas aeruginosa infection. PLoS One. 2012;7(7):e41772.CrossRefPubMedPubMedCentral
48.
go back to reference Baldan R, Cigana C, Testa F, Bianconi I, De Simone M, et al. Adaptation of Pseudomonas aeruginosa in cystic fibrosis airways influences virulence of Staphylococcus aureus in vitro and murine models of co-infection. PLoS One. 2014;9(3):e89614.CrossRefPubMedPubMedCentral Baldan R, Cigana C, Testa F, Bianconi I, De Simone M, et al. Adaptation of Pseudomonas aeruginosa in cystic fibrosis airways influences virulence of Staphylococcus aureus in vitro and murine models of co-infection. PLoS One. 2014;9(3):e89614.CrossRefPubMedPubMedCentral
49.
go back to reference Nixon GM, Armstrong DS, Carzino R, Carlin JB, Olinsky A, et al. Clinical outcome after early Pseudomonas aeruginosa infection in cystic fibrosis. J Pediatr. 2001;138(5):699–704.CrossRefPubMed Nixon GM, Armstrong DS, Carzino R, Carlin JB, Olinsky A, et al. Clinical outcome after early Pseudomonas aeruginosa infection in cystic fibrosis. J Pediatr. 2001;138(5):699–704.CrossRefPubMed
50.
go back to reference Aaron SD, Kottachchi D, Ferris WJ, Vandemheen KL, St Denis ML, et al. Sputum versus bronchoscopy for diagnosis of Pseudomonas aeruginosa biofilms in cystic fibrosis. Eur Respir J Physiology. 2004;24(4):631–7.CrossRef Aaron SD, Kottachchi D, Ferris WJ, Vandemheen KL, St Denis ML, et al. Sputum versus bronchoscopy for diagnosis of Pseudomonas aeruginosa biofilms in cystic fibrosis. Eur Respir J Physiology. 2004;24(4):631–7.CrossRef
51.
go back to reference Tai AS, Bell SC, Kidd TJ, Trembizki E, Buckley C, et al. Genotypic diversity within a single Pseudomonas aeruginosa strain commonly shared by Australian patients with cystic fibrosis. PLoS One. 2015;10(12):e0144022.CrossRefPubMedPubMedCentral Tai AS, Bell SC, Kidd TJ, Trembizki E, Buckley C, et al. Genotypic diversity within a single Pseudomonas aeruginosa strain commonly shared by Australian patients with cystic fibrosis. PLoS One. 2015;10(12):e0144022.CrossRefPubMedPubMedCentral
Metadata
Title
Antibiotic perturbation of mixed-strain Pseudomonas aeruginosa infection in patients with cystic fibrosis
Authors
Anna S. Tai
Laura J. Sherrard
Timothy J. Kidd
Kay A. Ramsay
Cameron Buckley
Melanie Syrmis
Keith Grimwood
Scott C. Bell
David M. Whiley
Publication date
01-12-2017
Publisher
BioMed Central
Published in
BMC Pulmonary Medicine / Issue 1/2017
Electronic ISSN: 1471-2466
DOI
https://doi.org/10.1186/s12890-017-0482-7

Other articles of this Issue 1/2017

BMC Pulmonary Medicine 1/2017 Go to the issue