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Journal of Clinical Microbiology, February 2007, p. 324-328, Vol. 45, No. 2
0095-1137/07/$08.00+0     doi:10.1128/JCM.01173-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Relationship between Cytomegalovirus DNA Load in Epithelial Lining Fluid and Plasma of Lung Transplant Recipients and Analysis of Coinfection with Epstein-Barr Virus and Human Herpesvirus 6 in the Lung Compartment{triangledown}

Claudia C. Bauer,1* Peter Jaksch,2 Stephan W. Aberle,1 Heinrich Haber,3 Gyoergy Lang,2 Walter Klepetko,2 Hanns Hofmann,1 and Elisabeth Puchhammer-Stöckl1

Institute of Virology, Medical University of Vienna, Vienna, Austria,1 Department of Cardiothoracic Surgery, Medical University of Vienna, Vienna, Austria,2 Otto Wagner Hospital, Vienna, Austria3

Received 7 June 2006/ Returned for modification 8 August 2006/ Accepted 27 November 2006

Cytomegalovirus (CMV) is a significant cause of morbidity and mortality in lung transplant recipients (LTRs). The aim of the present study was to elucidate the relationship between the CMV DNA load in the lung compartment and that in plasma. For CMV load determination, the level of CMV DNA in plasma and bronchoalveolar lavage (BAL) samples was measured in a total of 97 paired BAL and plasma samples obtained from 25 LTRs. The original virus concentration in the epithelial lining fluid (ELF) was calculated from the BAL samples by correcting for dilution using the urea dilution method. In addition, the load of Epstein-Barr virus (EBV) and that of human herpesvirus 6 (HHV-6) DNA also were determined in BAL samples, recalculated for their concentrations in the ELF, and compared with the CMV DNA load. CMV DNA was found more frequently and at significantly higher levels in the lung compartment than in plasma (P < 0.001, Wilcoxon test), and the CMV load in the ELF was associated with symptomatic CMV disease. EBV and HHV-6 were detected in 43.6% and 21.7% of the ELF samples, respectively. A statistically significant association was found between the CMV and EBV DNA loads in the ELF (P < 0.001; Spearman's rho = 0.651). Thus, in LTRs, determination of the CMV DNA load in the lung compartment may be advantageous compared to monitoring only viremia. The significant relationship between EBV and CMV DNA loads in the ELF of LTRs and its clinical impact require further investigation.


* Corresponding author. Mailing address: Division of Clinical Virology, Institute of Virology, Medical University of Vienna, Allgemeines Krankenhaus 4P, Währinger Gürtel 18-20, A-1090 Vienna, Austria. Phone: 43-1-40400-5138. Fax: 43-1-40400-5135. E-mail: claudia.bauer{at}meduniwien.ac.at.

{triangledown} Published ahead of print on 6 December 2006.


Journal of Clinical Microbiology, February 2007, p. 324-328, Vol. 45, No. 2
0095-1137/07/$08.00+0     doi:10.1128/JCM.01173-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.







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