Author: Uhlenhaut, Christine; Cohen, Jeffrey I; Fedorko, Daniel; Nanda, Santosh; Krause, Philip R
                    Title: Use of a universal virus detection assay to identify human metapneumovirus in a hematopoietic stem cell transplant recipient with pneumonia of unknown origin.  Cord-id: z5s7pmf7  Document date: 2009_1_1
                    ID: z5s7pmf7
                    
                    Snippet: BACKGROUND Development of uncommon viral infections in immunocompromised transplant recipients can pose major diagnostic challenges. We present a case report of an immunocompromised patient suffering from pneumonia, for which the causative agent was not identified by routine methods. OBJECTIVES To identify the potential cause of the pneumonia using a degenerate oligonucleotide primer (DOP)-PCR assay that is designed to detect all viruses. STUDY DESIGN DOP-PCR was applied to bronchoalveolar lavag
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: BACKGROUND Development of uncommon viral infections in immunocompromised transplant recipients can pose major diagnostic challenges. We present a case report of an immunocompromised patient suffering from pneumonia, for which the causative agent was not identified by routine methods. OBJECTIVES To identify the potential cause of the pneumonia using a degenerate oligonucleotide primer (DOP)-PCR assay that is designed to detect all viruses. STUDY DESIGN DOP-PCR was applied to bronchoalveolar lavage fluid from this patient. Generic PCR products were cloned and sequenced. RESULTS The novel universal virus assay detected human metapneumovirus in the clinical sample. The finding was confirmed by two independent metapneumovirus specific PCRs targeting different regions of the viral genome. CONCLUSIONS The DOP-PCR was used to detect and identify the sequence of an unidentified virus. This study provides proof of concept for the use of clinically relevant specimens in this unbiased universal assay, which requires no previous viral sequence information.
 
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