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Analysis of respiratory syncytial virus in clinical samples by reverse transcriptase-polymerase chain reaction restriction mapping

Valdivia, A ; Savón, C ; Chacón, D ; Sarmiento Pérez, L LU ; Morier, L ; Otero, A ; Soto, Y ; Oropesa, S and Goyenechea, A (1997) In Memorias do Instituto Oswaldo Cruz 92(3). p.93-389
Abstract

The aim of this study was to develop a polymerase chain reaction (PCR) for the detection of respiratory syncytial virus (RSV) genomes. The primers were designed from published sequences and selected from conserved regions of the genome encoding for the N protein of subgroups A and B of RSV. PCR was applied to 20 specimens from children admitted to the respiratory ward of "William Soler" Pediatric Hospital in Havana City with a clinical diagnosis of bronchiolitis. The PCR was compared with viral isolation and with an indirect immunofluorescence technique that employs monoclonal antibodies of subgroups A and B. Of 20 nasopharyngeal exudates, 10 were found positive by the three assayed methods. In only two cases, samples that yielded... (More)

The aim of this study was to develop a polymerase chain reaction (PCR) for the detection of respiratory syncytial virus (RSV) genomes. The primers were designed from published sequences and selected from conserved regions of the genome encoding for the N protein of subgroups A and B of RSV. PCR was applied to 20 specimens from children admitted to the respiratory ward of "William Soler" Pediatric Hospital in Havana City with a clinical diagnosis of bronchiolitis. The PCR was compared with viral isolation and with an indirect immunofluorescence technique that employs monoclonal antibodies of subgroups A and B. Of 20 nasopharyngeal exudates, 10 were found positive by the three assayed methods. In only two cases, samples that yielded positive RNA-PCR were found negative by indirect immunofluorescence and cell culture. Considering viral isolation as the "gold standard" technique, RNA-PCR had 100% sensitivity and 80% specificity. RNA-PCR is a specific and sensitive technique for the detection of the RSV genome. Technical advantages are discussed.

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author
; ; ; ; ; ; ; and
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Humans, Polymerase Chain Reaction, RNA-Directed DNA Polymerase, Respiratory Syncytial Virus Infections/diagnosis, Respiratory Syncytial Virus, Human/genetics, Restriction Mapping
in
Memorias do Instituto Oswaldo Cruz
volume
92
issue
3
pages
5 pages
publisher
Fundacao Oswaldo Cruz
external identifiers
  • scopus:0031129669
  • pmid:9332606
ISSN
0074-0276
DOI
10.1590/s0074-02761997000300015
language
English
LU publication?
no
id
76466786-6529-4631-995b-ff5ac2eeea19
date added to LUP
2019-07-08 15:50:37
date last changed
2024-01-01 15:49:55
@article{76466786-6529-4631-995b-ff5ac2eeea19,
  abstract     = {{<p>The aim of this study was to develop a polymerase chain reaction (PCR) for the detection of respiratory syncytial virus (RSV) genomes. The primers were designed from published sequences and selected from conserved regions of the genome encoding for the N protein of subgroups A and B of RSV. PCR was applied to 20 specimens from children admitted to the respiratory ward of "William Soler" Pediatric Hospital in Havana City with a clinical diagnosis of bronchiolitis. The PCR was compared with viral isolation and with an indirect immunofluorescence technique that employs monoclonal antibodies of subgroups A and B. Of 20 nasopharyngeal exudates, 10 were found positive by the three assayed methods. In only two cases, samples that yielded positive RNA-PCR were found negative by indirect immunofluorescence and cell culture. Considering viral isolation as the "gold standard" technique, RNA-PCR had 100% sensitivity and 80% specificity. RNA-PCR is a specific and sensitive technique for the detection of the RSV genome. Technical advantages are discussed.</p>}},
  author       = {{Valdivia, A and Savón, C and Chacón, D and Sarmiento Pérez, L and Morier, L and Otero, A and Soto, Y and Oropesa, S and Goyenechea, A}},
  issn         = {{0074-0276}},
  keywords     = {{Humans; Polymerase Chain Reaction; RNA-Directed DNA Polymerase; Respiratory Syncytial Virus Infections/diagnosis; Respiratory Syncytial Virus, Human/genetics; Restriction Mapping}},
  language     = {{eng}},
  month        = {{05}},
  number       = {{3}},
  pages        = {{93--389}},
  publisher    = {{Fundacao Oswaldo Cruz}},
  series       = {{Memorias do Instituto Oswaldo Cruz}},
  title        = {{Analysis of respiratory syncytial virus in clinical samples by reverse transcriptase-polymerase chain reaction restriction mapping}},
  url          = {{http://dx.doi.org/10.1590/s0074-02761997000300015}},
  doi          = {{10.1590/s0074-02761997000300015}},
  volume       = {{92}},
  year         = {{1997}},
}