1. Marked increase in incidence of Achromobacter xylosoxidans infections caused by sporadic acquisition from the environment 
Winnie Ridderberg, Karen E.M. Bendstrup, Hanne V. Olesen, Søren Jensen-Fangel, Niels Nørskov-Lauritsen 
Journal of Cystic Fibrosis 
Volume 10, Issue 6, Pages (December 2011)
DOI: /j.jcf
Copyright © 2011 European Cystic Fibrosis Society Terms and Conditions

2. Fig. 1
Pulsed field gel electrophoresis of SpeI digested genomic DNA from 15 isolates of A. xylosoxidans collected during 2009 from 15 CF patients. Five patients had been infected for more than six years (a–e), five patients had been infected for two to three years (f–j), and five patients experienced a first-time identification of A. xylosoxidans in 2009 (k–o). Four patients carry strains with identical macro restriction profiles (c–f). Lanes M: molecular marker.
Journal of Cystic Fibrosis  , DOI: ( /j.jcf )
Copyright © 2011 European Cystic Fibrosis Society Terms and Conditions

3. Fig. 2
Pulsed field gel electrophoresis of SpeI digested genomic DNA from twenty two isolates of A. xylosoxidans cultured from airway secretions from a CF patient between 2003 and Lanes 1–2: 2003, 3–6: 2005, 7–10: 2006, 11–14: 2007, 15–18: 2008, 19–22: Lanes M: molecular marker.
Journal of Cystic Fibrosis  , DOI: ( /j.jcf )
Copyright © 2011 European Cystic Fibrosis Society Terms and Conditions

4. Fig. 3
Pulsed field gel electrophoresis of SpeI digested genomic DNA from isolates of A. xylosoxidans. A. Isolates from a CF patient who underwent lung transplantation in B. Isolates from a CF patient who underwent lung transplantation in Lanes M: molecular marker.
Journal of Cystic Fibrosis  , DOI: ( /j.jcf )
Copyright © 2011 European Cystic Fibrosis Society Terms and Conditions