1980
DOI: 10.1136/jcp.33.5.484
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Detection of virus particles by electron microscopy with polyacrylamide hydrogel.

Abstract: SUMMARY The use of lyphogel to concentrate the number of virus particles in specimens for electron microscopic examination was studied in parallel with ultracentrifugation. One hundred faecal and urine samples were compared. Both methods had a similar sensitivity. Lyphogel was economical, simple, and rapid in use; in contrast to ultracentrifugation, it required relatively little material. The procedure could be done within a safety cabinet, and virus particles were morphologically undamaged by the process.

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Cited by 32 publications
(14 citation statements)
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“…The spectrum of clinical signs exhibited by patients with acute gastroenteritis included acute watery diarrhea, vomiting, abdominal cramps, and fever of various severity and in various combinations. All the specimens were investigated by EM [Whitby and Rodgers, 1980], latex agglutination for group A RV and AdV (Orion Diagnostica, Espoo, Finland), reverse transcription-polymerase chain reaction (RT-PCR) for NoV (Nanogen Advanced Diagnostics, Turin, Italy) [Ando et al, 1995;Vinjé and Koopmans, 1996;Yuen et al, 2001;Medici et al, 2005], and cell culture, before storage in balanced salt solution as 10% suspensions at À708C until use. Cytopathogenic agents were identified by EM, neutralization tests using Lim Benyesh-Melnick antisera pools [Melnick et al, 1973;Melnick and Wimberly, 1985] and/or polyacrylamide gel electrophoresis.…”
Section: Patients and Samplesmentioning
confidence: 99%
“…The spectrum of clinical signs exhibited by patients with acute gastroenteritis included acute watery diarrhea, vomiting, abdominal cramps, and fever of various severity and in various combinations. All the specimens were investigated by EM [Whitby and Rodgers, 1980], latex agglutination for group A RV and AdV (Orion Diagnostica, Espoo, Finland), reverse transcription-polymerase chain reaction (RT-PCR) for NoV (Nanogen Advanced Diagnostics, Turin, Italy) [Ando et al, 1995;Vinjé and Koopmans, 1996;Yuen et al, 2001;Medici et al, 2005], and cell culture, before storage in balanced salt solution as 10% suspensions at À708C until use. Cytopathogenic agents were identified by EM, neutralization tests using Lim Benyesh-Melnick antisera pools [Melnick et al, 1973;Melnick and Wimberly, 1985] and/or polyacrylamide gel electrophoresis.…”
Section: Patients and Samplesmentioning
confidence: 99%
“…Ten-percent stool suspensions in phosphate-buffered saline were submitted either to electron microscopy (EM) [Whitby and Rodgers, 1980] or conventional cell culture. Samples were stored at À208C until norovirus testing and/or further processing.…”
Section: Virological Investigationsmentioning
confidence: 99%
“…The sup ernatants were tested by commercia] Rotazyme EIA (Abbott L a b o r a t o r i e s ) ; in addition, formvar-carbon-coated 400 mesh grids for electron microsco~py were p r e p a r e d by the lyphogel m e t h o d (11) and examined for a m i n i m u m of 20 minutes in a Philips EM 300 ,electron microscope.…”
Section: Introductionmentioning
confidence: 99%