Detection of severe human metapneumovirus infection by real-time polymerase chain reaction and histopathological assessment

Kaharu C. Sumino, Eugene Agapov, Richard A. Pierce, Elbert P. Trulock, John D. Pfeifer, Jon H. Ritter, Monique Gaudreault-Keener, Gregory A. Storch, Michael J. Holtzman

Research output: Contribution to journalArticlepeer-review

76 Scopus citations

Abstract

Background. Infections with common respiratory tract viruses can cause high mortality, especially in immunocompromised hosts, but the impact of human metapneumovirus (hMPV) in this setting was previously unknown. Methods. We evaluated consecutive bronchoalveolar lavage and bronchial wash fluid samples from 688 patients-72% were immunocompromised and were predominantly lung transplant recipients-for hMPV by use of quantitative real-time polymerase chain reaction (PCR), and positive results were correlated with clinical outcome and results of viral cultures, in situ hybridization, and lung histopathological assessment. Results. Six cases of hMPV infection were identified, and they had a similar frequency and occurred in a similar age range as other paramyxoviral infections. Four of 6 infections occurred in immunocompromised patients. Infection was confirmed by in situ hybridization for the viral nucleocapsid gene. Histopathological assessment of lung tissue samples showed acute and organizing injury, and smudge cell formation was distinct from findings in infections with other paramyxoviruses. Each patient with high titers of hMPV exhibited a complicated clinical course requiring prolonged hospitalization. Conclusions. Our results provide in situ evidence of hMPV infection in humans and suggest that hMPV is a cause of clinically severe lower respiratory tract infection that can be detected during bronchoscopy by use of real-time PCR and routine histopathological assessment.

Original languageEnglish
Pages (from-to)1052-1060
Number of pages9
JournalJournal of Infectious Diseases
Volume192
Issue number6
DOIs
StatePublished - Sep 15 2005

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