A170: Achromobacter xyloxocidans
a new emerging microorganism in cystic fibrosis.
C.R. Hansen, T. Pressler, C. Koch, H.K. Johansen, N. Hoiby
Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
Aspergillus fumigatus and other Fungal infections
A217: Aspergillus fumigatus
an airway pathogen in CF – not only ABPA
K.G. Brownlee , M. Denton , S. Conway
Regional Paediatric Cystic Fibrosis Centre, St. James’s University Hospital, Leeds, United Kingdom, Department of Microbiology, Leeds Teaching Hospitals, Leeds, United KingdomA236: Report of a case of Paecilomyces lilacinus (P. lilacinus) infection in a CF patient.
G.A. Loeuille , F. Delepoulle , I. Joly-Durand , V. Montagne
Cystic fibrosis center, Dunkerque, France, Laboratory of parasitology and mycology, Lille, FranceA216: Frequency of sensitization to Aspergillus fumigatus and its influence to the patients with cystic fibrosis (CF)
I. Loukou, V. Talanti, M. Liatsis, M. Kanariou, S. Doudounakis
CF Centre, Aghia Sophia Children’s Hospital, Athens, GreeceA177: SAP virulence gene expression of C. albicans sputum isolates from CF patients.
F.-M. Muller , S. Salvenmoser , R. Hess , M. Wiebel , C. Gil-Lamaignere
Pad. Pneumolgie, Mukoviszidose u. Infektiologie, Heidelberg, Germany, CF- Ambulanz, Thoraxklinik, Heidelberg, GermanyA171: Risk factors for allergic bronchopulmonary aspergillosis and sensitisation to Aspergillus fumigatus in patients with cystic fibrosis.
N. Ritz, R.A. Ammann, C. Casaulta, F. Schoni-Affolter, M.H. Schoni
Department of Paediatrics, Universitiy of Berne, Berne, SwitzerlandA169: Scedosporium apiospermum sputum isolation in cystic fibrosis.
M. Wickremasinghe, K. Gyi, A. Hall, M. Hodson
Royal Brompton Hospital, London, United Kingdom
Burkholderia Cepacia and other Burkholderia species
A162: Investigation of the interaction of
B. cepacia complex with lung epithelial cells in vitro.
CE Duff , T Mullen , PG Murphy , M Callaghan , S McClean
Institute of Technology, Tallaght, Dubline, Ireland Adelaide, Meath and Incorporating National Children’s Hospital, Tallaght, Dublin, IrelandA128: Burkholderia cepacia-an infrequent cause of a sepsis in a non-CF patient
A. Holcikova , P. Drevinek , D. Burgetova
Pediatric Infectious Clinic, Masaryk University, Brno, Czech Republic, Pediatric Clinic, Charles University, Prague, Czech Republic, Microbiology Department, University Hospital, Brno, Czech RepublicA6: The role of insertion sequences in the genomic plasticity of the Burkholderia cepacia complex
D.T. Kenna , H. Yesilkaya , K.J. Forbes , V.A. Barcus , J.R.W. Govan
University of Edinburgh, Edinburgh, United Kingdom, University of Aberdeen, Aberdeen, United KingdomA132: Burkholderia cepacia
infection and clinical course in cystic fibrosis patients.
L. Pereira, S. Correia, C. Nascimento, T. Bandeira, C. Barreto.
Santa Maria Hospital, Lisbon, Portugal, Instituto Superior Tecnico, Lisbon, PortugalA126: Clinical follow-up of 122 Italian cystic fibrosis patients with B. cepacia complex infection
G. Taccetti , M. Ambroni , B. Assael , A. Cosimi , D. Costantini , M.L. Furnari , R. Gagliardini , G.L. Grzinchich , A. Manca , A. Negri , G. Pizzamiglio , F. Poli , V. Raia , G. Tuccio , P. Vandamme
Italian Cystic Fibrosis Study Group, Palermo, Italy, Laboratorium voor Microbiologie, Universiteit Gent, Gent, BelgiumA127: Novel strategy for the isolation of
Burkholderia cepacia complex from the environment
E. Vanlaere, T. Coenye, E. Samyn, J. Govan, F. De Baets, K. De Boeck, C. Knoop, P. Vandamme
University of Ghent, Ghent, BelgiumA131: Factors affecting the survival rate in
Burkholderia cenocepacia infected Czech CF patients.
D. Zemkova , P. Drevınek , J. Bartosova , L. Fila , V. Vavrova
Clinic of Pulmonology, Prague, Czech RepublicA183:CmaxSS-MIC ratio, as a predictor of CF patients infected with
Burkholderia cenocepacia.
D. Zemkova , P. Drevinek , J. Bartosova , L. Fila , V. Vavrova
Paediatric Dept, 2nd Medical School, Prague, Czech Republic, Adult Pulmonology Dept, University Hospital Motol, Prague, Czech Republic
A154: In children with cystic fibrosis can bacteria isolated from spirometry filters guide clinical management? J.L. Hartley , J.H.M. Rees , M.C.J. Rudolf
Royal Shrewsbury Hospital, Shrewsbury, United Kingdom, Birmingham Children’s Hospital, Birmingham, United Kingdom, Leeds General Infirmary, Leeds, United KingdomA116: Chronological timing of respiratory pathogen acquisition in infants with CF in Northern Ireland.
C.A. Kavanagh, A.J.M. Reid
Royal Belfast Hospital For Sick Children, Belfast, United KingdomA184: The analysis of the isolated microorganisms from the respiratory tract of CF children treated in Children’s Memorial Health Institute 1999–2003.
K.S. Semczuk, H.D. Dmenska, D.D. Dzierzanowska, P.G. Gutkowski, M.M.Modrzewska, E.G. Gabinska, H.Z. Zareba
Warsaw, Poland
Infection, Incidence and Diagnosis
A235: Unusual respiratory bacterial pathogens in a cystic fibrosis adult patients unit.
E. Inglezos, P. Boura, M. Kanellopoulou, M. Skarmoutsou, E. Papafrangas, F.Apostolopoulou.
Sismanoglio General Hospital, Maroussi-Athens, GreeceA139: Fingerprinting of cystic fibrosis sputum metagenome reveals unique amplicon length heterogeneity (ALH) profiles for each patient.
S. Miller , D. Mills , T. Pressler , C. Koch , K. Mathee
Florida International university, Department of Biological Sciences, Miami, United States, The National University Hospital (Rigshospitalet), Department of Pediatrics, Copenhagen, DenmarkA164: Identification of interacting groups of bacterial species colonising the CF lung, through statistical analysis of T-RFLP profiles.
G.B. Rogers , M.P. Carroll , P.M. Hockey , K.D. Bruce
Southampton General Hospital, Southampton, United Kingdom, King’s College London, London, United Kingdom
A168: Inquilinus limosus
: an unusual bacterium recovered in two French patients sputum with cystic fibrosis.
R. Chiron , F. Counil , F. Bremont , C. Segonds , E. Jumas-Bilak , H. Jean-Pierre , H. Marchandin
CHU Arnaud de Villeneuve, Montpellier, France, CHU Rangueil, Toulouse, France, Faculte de Pharmacie, Montpellier, France
A151: Pseudomonas aeruginosa
in water of public outdoor and indoor swimming pools and bathroom water taps of patients with cystic fibrosis during the hot summer 2003.
J. Barben , G. Hafen , J. Schmid
Paediatric Pulmonology, Children’s Hospital, St. Gallen, Switzerland, Official Food Control Laboratory, St. Gallen, SwitzerlandA175: Detection of volatile compounds released by Pseudomonas aeruginosa in vitro by selected ion flow tube mass spectrometry (SIFT-MS).
W.D. Carroll , D. Smith , T.S. Wang , P. Spanel , P.A. Alcock , W. Lenney
Academic Department of Paediatrics, University Hospital of North Staffordshire, Stoke-on-Trent, United Kingdom, Centre for Science & Technology in Medicine, Keele University, Keele, United Kingdom, J. Heyrovsky Institute of Physcial Chemistry, Academy of Sciences, Prague, Czech Republic, Department of Medical
Microbiology, University Hospital of North Staffordshire, Stoke-on-Trent, United KingdomA186: Real-time PCR detects non cultivable Pseudomonas aeruginosa in the early phase of CF lung colonisation.
G. Couetdic, F. El’Garch, J. Schneider, C. Millardet, M.L. Dalphin, J.C. Dalphin, P. Plesiat
Hopital Jean Minjoz, Besancon, FranceA185: The Liverpool epidemic strain of Pseudomonas aeruginosa; 8 years after initial identification.
E.A. Gaillard , H.L. Wallace , L.J. Heaf , S. Panagea , P. Shears , E.F. Burrows , P. Garnett , J.J. Cottrell , M.J. Walshaw , M.J. Ledson , J.M. Couriel , R.L. Smyth , C.A. Hart , K.W. Southern , D.P. Heaf
Royal Liverpool Children’s Hospital, Liverpool, United Kingdom, Institute of Child Health, University of Liverpool, Liverpool, United Kingdom, Medical Microbiology, University of Liverpool, Liverpool, United Kingdom, Cardiothoracic Centre Adult CF Unit, Liverpool, United KingdomA134: Longitudinal surveillance for Pseudomonas aeruginosa cross-infection at an adult cystic fibrosis centre.
A.M. Jones , C.M. Smith , M.E. Dodd , C.J. Doherty , J.R.W. Govan , A.K. Webb
Manchester Adult Cystic Fibrosis Centre, Manchester, United Kingdom, Medical Microbiology, Edinburgh, United KingdomA439: Genotyping Pseudomonas aeruginosa isolates by pulsed field gel electrophoresis (PFGE) and randomly amplified polymorphic DNA (RAPD) techniques
D. Jyothish , M. Desai , N. West , P. Weller , J. Clarke , M. Mehmi , C. Powell , K. Hinton , A. Hilton , P. Lambert
Birmingham Children’s Hospital NHS Trust, Birmingham, United Kingdom, Aston University, Birmingham, United KingdomA155: Characterization of poxB, a chromosomal-encoded Pseudomonas aeruginosa oxacillinase.
K.F. Kong , S. Jayawardena , A. del Puerto , L. Wiehlmann , U. Laabs , B. Tuemmler , K. Mathee
Florida International University, Miami, United States, Klinische Forschergruppe, Medizinische Hochschule Hannover, Hannover, GermanyA167: Maintenance of high adherence capacity of Pseudomonas aeruginosa cystic fibrosis isolates during chronic infection is associated with more severe lung disease.
U. Laabs , P. Gudowius , L. Wiehlmann , A.S. Limpert , A. Filloux , Tummler , S. de Bentzmann
CNRS IBSM UPR9027, Marseille, France, Medizinische Hochschule Hannover, Hannover, Germany, Universitats kinderklinik, Dusseldorf, GermanyA136: Identification and prevalence of DNA markers specific to a multiresistant and transmissible clone of Pseudomonas aeruginosa
D.A. Miller , A.M. Jones , A.K. Webb , J.R.W. Govan , D.P. Speert , C. Smith E. Mahenthiralingam
Cardiff School of Biosciences, Cardiff University, Cardiff, United Kingdom, Bradbury CF Unit, Wythenshawe Hospital, Manchester, United Kingdom, Medical Microbiology, University of Edinburgh, Edinburgh, United Kingdom, Dept. of Paediatrics, University of British Columbia, Vancouver, CanadaA156: Effect of pH on inorganic polyphosphate accumulation in Pseudomonas aeruginosa and Burkholderia cepacia isolates from patients with cystic fibrosis.
T.F. Moriarty , C. Laverty , A. Mullan , J. McGrath , J.S. Elborn , M.M. Tunney
School of Biology and Biochemistry, Queen’s University, Belfast, United Kingdom, Respiratory Medicine Research Group, Queen’s University, Belfast, United Kingdom, Belfast City Hospital, Belfast, United KingdomA153: Domestic washing machines: a reservoir for Pseudomonas aeruginosa?
T.L. Pitt, H. Englender, H.M. Aucken.
Laboratory of HealthCare Associated Infection, SRMD,HPA Colindale, London,United KingdomA133: Use of multilocus restriction typing method to detect hypertransmissible P. aeruginosa strains from patients attending Cardiff CF clinics.
H.C. Ryley , J.L. Weeks , D.J. Shale , I.J.M. Doull
Dept of Medical Microbiology, UWCM, Cardif, United Kingdom, Section of Respiratory Disease, UWCM, Penarth, United Kingdom, Dept of Child Health, Cardiff, United KingdomA135: Characterisation of a diagnostic probe for the
Pseudomonas aeruginosa Liverpool CF epidemic strain. C.H. Smart, C.A. Hart, C. Winstanley
University of Liverpool, Liverpool, United KingdomA137: Clinical consequences of transmissible Pseudomonas aeruginosa infection in patients with cystic fibrosis—a 4 year prospective study
C.M. Smith, M.E. Dodd, A.K. Webb, A.M. Jones
Wythenshawe Hospital, Manchester, United KingdomA161: Effect of growth under anaerobic conditions on the antimicrobial susceptibility of
Pseudomonas aeruginosa isolates from cystic fibrosis patients.
M.M. Tunney , A. White , J.S. Elborn
Respiratory Medicine Research Group, Queen’s University, Belfast, United Kingdom, Belfast City Hospital, Belfast, United KingdomA440: Newly acquired Pseudomonas aeruginosa (P.a.) in Belgian CF patients:does the patients’ P.a. genotype correlate with environmental genotypes?
S. Van daele , F. De Baets , P. Schelstraete , L. Van Simaey , G. Claeys , M. Vaneechoutte
Pediatric Pulmonology,University Hospital, Gent, Belgium, Microbiology,University Hospital, Gent, BelgiumA443:
Pseudomonas aeruginosa DNA-fingerprinting register in Belgian CF patients: a one year survey
S. Van daele , M. Vaneechoutte , G. Claeys , P. Schelstraete , F. Haerynck , F. De Baets
Pedaitric Pulmonology,University Hospital, Gent, Belgium, Microbiology,University Hospital, Gent, BelgiumA174: Comparative proteomic analysis of planktonic and biofilm
Pseudomonas aeruginosa cells: identification of differentially expressed proteins.
S. Vilain, P. Cosette, D. Seyer, G.A. Junter, T. Jouenne.
UMR 6522 CNRS, IFRMP 23, Mont-Saint-Aignan, FranceA176: DNA chip for geno- and pathotyping of
Pseudomonas aeruginosa
L. Wiehlmann , G. Morales , B. Siebert , G. Wagner , P. Slickers , B. Tummler
Klinische Forschergruppe, OE 6710, Medizinische Hochschule Hannover, Hannover, Germany, Centro Nacional de Biotecnologia, Madrid, Spain, Clondiag Chip Technologies, Jena, GermanyA46: Pseudomonas aeruginosa adherence to murine nasal epithelium
T. Wodehouse , R. Farley , B. Wainwright , D.M. Geddes , J.C. Davies , E.W.F.W. Alton
Department of Gene Therapy at Imperial College London, UK CFGT Consortium, London, United Kingdom, Institute for Molecular Bioscience, University of Queensland, Brisbane, AustraliaA50: Binding of Pseudomonas aeruginosa to cystic fibrosis human nasal
epithelium
T. Wodehouse, L.A. Collins, D.M. Geddes, J.C. Davies, E.W.F.W. Alton
Department of Gene Therapy, Imperial College; UK CFGT Consortium, London,United Kingdom
A163: Fas-induced apoptosis of Staphylococcus aureus-infected airway epithelial cells
M.C.A. Da Silva , M.C. De Assis , J.-M. Zahm , E. Puchelle , M.C. Plotkowski
Institut of Microbiology, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil, Department of Microbiology and Immunology, State University of Rio de Janeiro, Rio de Janeiro, Brazil, INSERM U314, Reims, France.A165: Staphylococcus aureus
and airway epithelial cell interaction.
D. Gras , M. Da Silva , M. Milliot , J.M. Zahm , O. Bajolet , M.C. Plotkowski , E. Puchelle INSERM UMRS 514, Reims, France, Laboratoire de Bacteriologie-Virologie-Hygiene, CHU, Reims, France, Department of Microbiology, University of Rio Janeiro, Rio Janeiro, BrazilA148: Risk factors for MRSA colonization in patients with cystic fibrosis.
K. Nadesalingam , S.P. Conway , M. Denton
Department of Microbiology, Leeds Teaching Hospitals, Leeds, United Kingdom, Regional Cystic Fibrosis Unit, Leeds Teaching Hospitals, Leeds, United KingdomA149: Methicillin-resistant
Staphylococcus aureus (MRSA) in French CF patients : an epidemiologic approach.
C. Segonds , P. Clavel-Batut , K. Eydieux-Laporte , I. Le Thomas-Bories , E. Bingen , P. Mariani , N. Brahimi , S. Ravilly , G. Chabanon
Hopital Rangueil, Toulouse, France, Hopital Robert-Debre, Paris, France, Vaincre la Mucoviscidose, Paris, France
A172: Increasing prevalence of
Stenotrophomonas maltophilia in patients with cystic fibrosis.
J. Larsson Friden, M. Gilljam, B. Jonsson
Sahlgrenska University Hospital, Goteborg, Sweden ¨
A118: Does respiratory viral infections influence lung function and bacterial colonisation in children with CF?
H.V. Olesen , L.P. Nielsen , P.O. Schiotz
CF-centre West, Aarhus University Hospital, Skejby Sygehus, Aarhus, Denmark, Department of Clinical Microbiology, Odense University Hospital, Odense, DenmarkA247: Respiratory viruses in cystic fibrosis
D.S. Wat , C.M. Gelder , S. Hibbitts , I. Bowler , R. Evans , M. Pierrepoint , I.J. Doull
University of Wales College of Medicine, Cardiff, United Kingdom, Llandough Hospital, Penarth, United Kingdom, Royal Gwent Hospital, Newport, United Kingdom, Singleton Hospital, Swansea, United Kingdom, University Hospital ofWales, Cardiff, United Kingdom