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Journal of Clinical Microbiology, March 2006, p. 833-836, Vol. 44, No. 3
0095-1137/06/$08.00+0     doi:10.1128/JCM.44.3.833-836.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Chronic Colonization with Pandoraea apista in Cystic Fibrosis Patients Determined by Repetitive-Element-Sequence PCR

R. M. Atkinson,1,{dagger} J. J. LiPuma,2 D. B. Rosenbluth,3 and W. M. Dunne Jr.1*

Departments of Pathology and Immunology,1 Internal Medicine, Washington University School of Medicine, St. Louis, Missouri,3 Department of Pediatrics, University of Michigan School of Medicine, Ann Arbor, Michigan2

Received 26 October 2005/ Returned for modification 16 December 2005/ Accepted 5 January 2006

Pandoraea apista is recovered with increasing frequency from the lungs of patients with cystic fibrosis (CF) and may represent an emerging pathogen (I. M. Jorgensen et al., Pediatr. Pulmonol. 36:439-446, 2003). We identified two CF patients from our hospital whose sputum specimens were culture positive for P. apista over the course of several years. Repetitive-element-sequence PCR was employed to determine whether sequential isolates that were recovered from these patients represented a single clone and whether each patient had been chronically colonized with the same strain. Banding patterns generated with ERIC primers, REP primers, and BOX primers showed that individual patient isolates had a high degree of similarity (>97%) and were considered identical. However, only the banding patterns from the ERIC primers and BOX primers were able to show that the strains from patients I and II were unique (similarity indices of 79.8% and 70.0%, respectively). We concluded that all strains of P. apista from patient I were identical, as were all strains from patient II, establishing chronic colonization. Only two of the three methods employed indicate that the strains from the two patients are distinct. This implied that the organism was not transferred from one patient to the other, suggesting that the choice of methodology could generate misleading results when examining person-to-person transmission regarding this organism.


* Corresponding author. Mailing address: Washington University School of Medicine, Department of Pathology and Immunology, Division of Laboratory Medicine, Campus Box 8118, 660 S. Euclid Ave., St. Louis, MO 63110. Phone: (314) 362-2998. Fax: (314) 362-1462. E-mail: dunne{at}pathbox.wustl.edu.

{dagger} Present address: Division of Infectious Diseases, Wadsworth Center, New York State Department of Health, Albany, NY 12201.


Journal of Clinical Microbiology, March 2006, p. 833-836, Vol. 44, No. 3
0095-1137/06/$08.00+0     doi:10.1128/JCM.44.3.833-836.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.




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