Enzyme-linked immunosorbent assay based on recombinant human group C rotavirus inner capsid protein (VP6) To detect human group C rotaviruses in fecal samples
Enzyme-linked immunosorbent assay based on recombinant human group C rotavirus inner capsid protein (VP6) To detect human group C rotaviruses in fecal samples
A recent study showed that 43% of a population in the United Kingdom were seropositive for group C rotavirus. The higher than expected incidence may be due to limited diagnosis of acute human group C rotavirus infections because no routine test is available. Human group C rotavirus infections are routinely diagnosed by electron microscopy (EM) and a negative group A rotavirus enzyme-linked immunosorbent assay (ELISA) result. An antigen-detection ELISA was developed with hyperimmune antibodies raised to human group C rotavirus recombinant VP6 (Bristol strain) expressed in insect cells. The assay was used to screen fecal samples to determine the prevalence of group C rotavirus infection. Samples positive by ELISA were confirmed by EM, polyacrylamide gel electrophoresis of double-stranded RNA, or detection of the VP6 gene by reverse transcription-PCR. Retrospective analysis indicated a 1 to 2% detection rate of positivity among samples from patients with acute diarrhea.
3178-3181
James, V.L.A.
7d989208-47a0-4f67-9b14-b67d74ca4bfe
Lambden, P.R.
e99ecc21-50d7-4a43-9e79-efba46592c77
Caul, E.O.
3ab60e6e-ca41-4196-a205-4c0075fd3767
Clarke, I.N.
ff6c9324-3547-4039-bb2c-10c0b3327a8b
November 1998
James, V.L.A.
7d989208-47a0-4f67-9b14-b67d74ca4bfe
Lambden, P.R.
e99ecc21-50d7-4a43-9e79-efba46592c77
Caul, E.O.
3ab60e6e-ca41-4196-a205-4c0075fd3767
Clarke, I.N.
ff6c9324-3547-4039-bb2c-10c0b3327a8b
James, V.L.A., Lambden, P.R., Caul, E.O. and Clarke, I.N.
(1998)
Enzyme-linked immunosorbent assay based on recombinant human group C rotavirus inner capsid protein (VP6) To detect human group C rotaviruses in fecal samples.
Journal of Clinical Microbiology, 36 (11), .
(PMID:9431910)
Abstract
A recent study showed that 43% of a population in the United Kingdom were seropositive for group C rotavirus. The higher than expected incidence may be due to limited diagnosis of acute human group C rotavirus infections because no routine test is available. Human group C rotavirus infections are routinely diagnosed by electron microscopy (EM) and a negative group A rotavirus enzyme-linked immunosorbent assay (ELISA) result. An antigen-detection ELISA was developed with hyperimmune antibodies raised to human group C rotavirus recombinant VP6 (Bristol strain) expressed in insect cells. The assay was used to screen fecal samples to determine the prevalence of group C rotavirus infection. Samples positive by ELISA were confirmed by EM, polyacrylamide gel electrophoresis of double-stranded RNA, or detection of the VP6 gene by reverse transcription-PCR. Retrospective analysis indicated a 1 to 2% detection rate of positivity among samples from patients with acute diarrhea.
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Published date: November 1998
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Local EPrints ID: 194257
URI: http://eprints.soton.ac.uk/id/eprint/194257
ISSN: 0095-1137
PURE UUID: daff28a5-75f0-4330-84eb-149c8c07fd3b
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Date deposited: 26 Jul 2011 12:23
Last modified: 23 Jul 2022 01:32
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Author:
V.L.A. James
Author:
P.R. Lambden
Author:
E.O. Caul
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