Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1999-1-25
pubmed:abstractText
The aim of this study was to compare conventional enterovirus isolation with rapid detection of enteroviral RNA by a reverse transcription-nested polymerase chain reaction (RT-nPCR) method amplifying the 5' nontranslated region of the enteroviral genome in specimens from patients with aseptic meningitis. Reference enterovirus strains and clinical enterovirus isolates were analyzed to evaluate assay sensitivity and specificity. All known enteroviral serotypes tested, but one (echovirus type 22), were detected by RT-nPCR. A series of unrelated viral isolates as well as CSF samples from patients with meningitis/encephalitis or neurological syndromes unrelated to enterovirus infection were included as controls. A total of 47 specimens (31 CSF, 12 rectal swabs, 4 throat swabs) from 30 patients with aseptic meningitis were available for the study. Of the 31 CSF samples tested from 30 patients, 17 from 17 patients (54.8%) were positive by RT-nPCR, while only 10 from 10 patients (32.2%) were positive by culture. Thus, RT-nPCR allowed diagnosis of enterovirus meningitis in 7 additional patients compared to cell culture. The cytopathic effect was observed 5-15 days after inoculation of CSF specimens onto cell cultures, while direct detection of viral RNA in CSF samples by RT-nPCR permitted diagnosis of enteroviral meningitis within 1-2 days. On the whole, viral isolation was positive in 12/47 (25.5%) specimens, whereas viral RNA was detected by RT-nPCR in 11 additional samples (23/47, 48.9%). Specimens of the control group were consistently negative by both viral isolation and RT-nPCR. Restriction endonuclease analysis of PCR products (RFLP) was applied to differentiate poliovirus (PV) from non-polio enteroviruses (NPEV). All enterovirus strains detected in clinical samples (n = 23) were identified as NPEV by RFLP. Clinical isolates were typed by neutralization as echovirus type 30 (n = 6), while 6 were not typed. In conclusion, detection of enteroviral RNA in CSF by RT-nPCR allows: i) rapid diagnosis of enteroviral meningitis; ii) increased sensitivity with respect to virus isolation; iii) differentiation between PV and NPEV infections of the central nervous system.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1121-7138
pubmed:author
pubmed:issnType
Print
pubmed:volume
21
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
343-51
pubmed:dateRevised
2011-2-25
pubmed:meshHeading
pubmed-meshheading:9812315-Adolescent, pubmed-meshheading:9812315-Adult, pubmed-meshheading:9812315-Animals, pubmed-meshheading:9812315-Cercopithecus aethiops, pubmed-meshheading:9812315-Child, pubmed-meshheading:9812315-Child, Preschool, pubmed-meshheading:9812315-Disease Outbreaks, pubmed-meshheading:9812315-Electrophoresis, Polyacrylamide Gel, pubmed-meshheading:9812315-Enterovirus, pubmed-meshheading:9812315-Enterovirus B, Human, pubmed-meshheading:9812315-Enterovirus Infections, pubmed-meshheading:9812315-Female, pubmed-meshheading:9812315-Humans, pubmed-meshheading:9812315-Infant, pubmed-meshheading:9812315-Male, pubmed-meshheading:9812315-Meningitis, Aseptic, pubmed-meshheading:9812315-Middle Aged, pubmed-meshheading:9812315-Neutralization Tests, pubmed-meshheading:9812315-Poliovirus, pubmed-meshheading:9812315-Polymorphism, Restriction Fragment Length, pubmed-meshheading:9812315-RNA, Viral, pubmed-meshheading:9812315-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:9812315-Vero Cells
pubmed:year
1998
pubmed:articleTitle
Rapid detection of enteroviral RNA in cerebrospinal fluid (CSF) from patients with aseptic meningitis by reverse transcription-nested polymerase chain reaction.
pubmed:affiliation
Servizio di Virologia, IRCCS Policlinico San Matteo, Pavia, Italy.
pubmed:publicationType
Journal Article, Comparative Study