Abstract
A reverse transcriptase polymerase chain reaction (RT-PCR) was used to detect a human cytomegalovirus (HCMV) late mRNA in peripheral blood leukocytes (PBL) of 102 human immunodeficiency virus-infected individuals. The clinical value of this new technique for the diagnosis of acute HCMV disease was evaluated in comparison with viral culture and direct amplification of viral DNA (PCR). The sensitivity of the RT-PCR was slightly lower than that of the two other methods, but its specificity was 94%, compared to 55 and 32% for culture and PCR, respectively. Transcription of this late mRNA is linked to viral replication, and its detection in PBL confirms that these cells can support a complete viral cycle. The relationship between complete replicative cycles and HCMV disease makes RT-PCR a useful clinical tool.
MeSH Terms
AIDS-Related Opportunistic Infections/diagnosis,microbiology
Adult
Base Sequence
Cytomegalovirus/genetics,isolation & purification
Cytomegalovirus Infections/complications,diagnosis,microbiology
DNA, Viral/blood,genetics
Evaluation Studies as Topic
Female
Humans
Male
Molecular Sequence Data
Polymerase Chain Reaction/methods,statistics & numerical data
RNA, Messenger/blood
RNA, Viral/blood
Sensitivity and Specificity
Viremia/complications,diagnosis,microbiology
Virus Cultivation/statistics & numerical data
Chemicals
DNA, Viral
RNA, Messenger
RNA, Viral
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Gozlan J
Service de Bactériologie-Virologie, Hôpital Saint-Antoine, Paris, France.
Salord J M
Chouaïd C
Duvivier C
Picard O
Meyohas M C
Petit J C
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