Literature DB >> 2671012

Routine viral culture for pediatric respiratory specimens submitted for direct immunofluorescence testing.

J G Blanding1, M G Hoshiko, H R Stutman.   

Abstract

From 1986 to 1987, 69 (25%) of 274 specimens from children with lower respiratory tract syndromes were positive for respiratory syncytial virus antigen by direct immunofluorescence assay (DFA). Comprehensive viral culture was performed on all 205 DFA-negative specimens, and 72 specimens yielded viruses; 5 specimens yielded multiple agents. Thus, 52% of specimens yielded a specific virus, supporting the routine use of viral culture. Isolates from the DFA-negative specimens included respiratory syncytial virus (n = 7), rhinovirus (n = 34), hemadsorbing viruses (n = 13), cytomegalovirus (n = 11), adenovirus (n = 8), enteroviruses (n = 3), and herpes simplex virus (n = 2). Although serologic confirmation is needed, cytomegalovirus may be an underappreciated cause of acute lower respiratory tract infection in normal children. Further studies must be conducted to document this possibility.

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Year:  1989        PMID: 2671012      PMCID: PMC267588          DOI: 10.1128/jcm.27.7.1438-1440.1989

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  11 in total

1.  Clinically useful method for the isolation of respiratory syncytial virus.

Authors:  C B Hall; R G Douglas
Journal:  J Infect Dis       Date:  1975-01       Impact factor: 5.226

2.  Epidemiology of cytomegaloviral infection in a heterogeneous population of pregnant women.

Authors:  S H Chandler; E R Alexander; K K Holmes
Journal:  J Infect Dis       Date:  1985-08       Impact factor: 5.226

3.  Enhanced isolation of respiratory syncytial virus in cell culture.

Authors:  M Q Arens; E M Swierkosz; R R Schmidt; T Armstrong; K A Rivetna
Journal:  J Clin Microbiol       Date:  1986-04       Impact factor: 5.948

Review 4.  Detection, pathogenesis, and therapy of respiratory syncytial virus infections.

Authors:  R C Welliver
Journal:  Clin Microbiol Rev       Date:  1988-01       Impact factor: 26.132

5.  Effect of incubation temperature on isolation of cytomegalovirus from fresh clinical specimens.

Authors:  W W Gregory; M A Menegus
Journal:  J Clin Microbiol       Date:  1983-10       Impact factor: 5.948

6.  Comparison of nasopharyngeal washings and swab specimens for diagnosis of respiratory syncytial virus by EIA, FAT, and cell culture.

Authors:  H B Masters; K O Weber; J R Groothuis; C G Wren; B A Lauer
Journal:  Diagn Microbiol Infect Dis       Date:  1987-10       Impact factor: 2.803

7.  Strategy for efficient detection of respiratory viruses in pediatric clinical specimens.

Authors:  M Q Arens; E M Swierkosz; R R Schmidt; T Armstrong; K A Rivetna
Journal:  Diagn Microbiol Infect Dis       Date:  1986-11       Impact factor: 2.803

8.  Comparison of nasopharyngeal aspirate and nasopharyngeal swab specimens for respiratory syncytial virus diagnosis by cell culture, indirect immunofluorescence assay, and enzyme-linked immunosorbent assay.

Authors:  G Ahluwalia; J Embree; P McNicol; B Law; G W Hammond
Journal:  J Clin Microbiol       Date:  1987-05       Impact factor: 5.948

9.  Adenovirus infections in young children.

Authors:  K M Edwards; J Thompson; J Paolini; P F Wright
Journal:  Pediatrics       Date:  1985-09       Impact factor: 7.124

10.  Comparison of direct immunofluorescent staining of clinical specimens for respiratory virus antigens with conventional isolation techniques.

Authors:  L Minnich; C G Ray
Journal:  J Clin Microbiol       Date:  1980-09       Impact factor: 5.948

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  13 in total

1.  Evaluation of R-Mix FreshCells in shell vials for detection of respiratory viruses.

Authors:  C K Fong; M K Lee; B P Griffith
Journal:  J Clin Microbiol       Date:  2000-12       Impact factor: 5.948

2.  Detection of respiratory syncytial virus in nasopharyngeal secretions by shell vial technique.

Authors:  M C Smith; C Creutz; Y T Huang
Journal:  J Clin Microbiol       Date:  1991-03       Impact factor: 5.948

3.  Comparison of enzyme-linked immunosorbent assay, indirect immunofluorescence assay, and virus isolation for detection of respiratory viruses in nasopharyngeal secretions.

Authors:  S Takimoto; M Grandien; M A Ishida; M S Pereira; T M Paiva; T Ishimaru; E M Makita; C H Martinez
Journal:  J Clin Microbiol       Date:  1991-03       Impact factor: 5.948

4.  Use of fluorescent-antibody staining of cytocentrifuge-prepared smears in combination with cell culture for direct detection of respiratory viruses.

Authors:  K M Doing; M A Jerkofsky; E G Dow; J A Jellison
Journal:  J Clin Microbiol       Date:  1998-07       Impact factor: 5.948

5.  Evaluation of direct immunofluorescence, dot-blot enzyme immunoassay, and shell-vial culture for detection of respiratory syncytial virus in patients with bronchiolitis.

Authors:  J Reina; M J Ros; J M Del Valle; I Blanco; M Munar
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1995-11       Impact factor: 3.267

6.  Evaluation of five methods for respiratory syncytial virus detection.

Authors:  D C Halstead; S Todd; G Fritch
Journal:  J Clin Microbiol       Date:  1990-05       Impact factor: 5.948

Review 7.  Mixed viral infections: detection and management.

Authors:  J L Waner
Journal:  Clin Microbiol Rev       Date:  1994-04       Impact factor: 26.132

8.  Rapid diagnosis of human parainfluenza virus type 1 infection by quantitative reverse transcription-PCR-enzyme hybridization assay.

Authors:  J Fan; K J Henrickson
Journal:  J Clin Microbiol       Date:  1996-08       Impact factor: 5.948

9.  Rapid detection of respiratory viruses by shell vial culture and direct staining by using pooled and individual monoclonal antibodies.

Authors:  S Matthey; D Nicholson; S Ruhs; B Alden; M Knock; K Schultz; A Schmuecker
Journal:  J Clin Microbiol       Date:  1992-03       Impact factor: 5.948

10.  Utility of a respiratory virus panel containing a monoclonal antibody pool for screening of respiratory specimens in nonpeak respiratory syncytial virus season.

Authors:  J C McDonald; P Quennec
Journal:  J Clin Microbiol       Date:  1993-10       Impact factor: 5.948

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