Literature DB >> 7852976

Use of the colonic carcinoma cell line CaCo-2 for in vivo amplification and detection of enteric viruses.

R M Pintó1, J M Diez, A Bosch.   

Abstract

The use of the continuous cell line CaCo-2 as an in vivo amplification system for the detection of fastidious human enteric viruses is reported. CaCo-2 cells showed an increased sensitivity to laboratory strains of group A rotavirus 3, reovirus 3, astrovirus 1, poliovirus 1, coxsackievirus A 24, enterovirus 70, and adenovirus 5, 40 and 41, when compared to a routine host cell line for each virus. Nucleic acids from wild-type infectious rotavirus, astrovirus, and adenovirus 40 in stool samples of patients with acute gastroenteritis could be amplified after infection of CaCo-2 cells with trypsin-pre-treated virus inocula. Virus diagnosis was carried out subsequently by dot-blot hybridisation with specific cDNA probes. An amplification factor between 10 and 1,000x was obtained by infection of CaCo-2 cells, thus enabling specific detection of low numbers of a wide range of enteric viruses, and the differentiation between infectious and noninfectious particles.

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Year:  1994        PMID: 7852976     DOI: 10.1002/jmv.1890440317

Source DB:  PubMed          Journal:  J Med Virol        ISSN: 0146-6615            Impact factor:   2.327


  32 in total

1.  C-terminal nsP1a protein of human astrovirus colocalizes with the endoplasmic reticulum and viral RNA.

Authors:  Susana Guix; Santiago Caballero; Albert Bosch; Rosa M Pintó
Journal:  J Virol       Date:  2004-12       Impact factor: 5.103

2.  Removal of astrovirus from water and sewage treatment plants, evaluated by a competitive reverse transcription-PCR.

Authors:  Waled Morsy El-Senousy; Susana Guix; Islem Abid; Rosa M Pintó; Albert Bosch
Journal:  Appl Environ Microbiol       Date:  2006-11-03       Impact factor: 4.792

3.  Detection of infectious astroviruses in water.

Authors:  R M Pinto; F X Abad; R Gajardo; A Bosch
Journal:  Appl Environ Microbiol       Date:  1996-05       Impact factor: 4.792

4.  Comparison of BGM and PLC/PRC/5 cell lines for total culturable viral assay of treated sewage.

Authors:  Roberto A Rodríguez; Patricia M Gundy; Charles P Gerba
Journal:  Appl Environ Microbiol       Date:  2008-03-07       Impact factor: 4.792

5.  Flow cytometry detection of infectious rotaviruses in environmental and clinical samples.

Authors:  F X Abad; R M Pintó; A Bosch
Journal:  Appl Environ Microbiol       Date:  1998-07       Impact factor: 4.792

6.  Astrovirus survival in drinking water.

Authors:  F X Abad; R M Pintó; C Villena; R Gajardo; A Bosch
Journal:  Appl Environ Microbiol       Date:  1997-08       Impact factor: 4.792

7.  Rapid diagnosis of enterovirus infection by a new one-step reverse transcription-PCR assay.

Authors:  H H Kessler; B Santner; H Rabenau; A Berger; A Vince; C Lewinski; B Weber; K Pierer; D Stuenzner; E Marth; H W Doerr
Journal:  J Clin Microbiol       Date:  1997-04       Impact factor: 5.948

8.  Evaluation of Natural Compounds of Plant Origin for Inactivation of Enteric Viruses.

Authors:  G Sánchez; R Aznar
Journal:  Food Environ Virol       Date:  2015-01-31       Impact factor: 2.778

9.  An assay combining cell culture with reverse transcriptase PCR to detect and determine the infectivity of waterborne Cryptosporidium parvum.

Authors:  P A Rochelle; D M Ferguson; T J Handojo; R De Leon; M H Stewart; R L Wolfe
Journal:  Appl Environ Microbiol       Date:  1997-05       Impact factor: 4.792

10.  Capsid region involved in hepatitis A virus binding to glycophorin A of the erythrocyte membrane.

Authors:  Glòria Sánchez; Lluís Aragonès; M Isabel Costafreda; Enric Ribes; Albert Bosch; Rosa M Pintó
Journal:  J Virol       Date:  2004-09       Impact factor: 5.103

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