Literature DB >> 1317878

Propagation of adenovirus types 40 and 41 in the PLC/PRF/5 primary liver carcinoma cell line.

W O Grabow1, D L Puttergill, A Bosch.   

Abstract

The sensitivity of cell cultures to adenovirus types 40 and 41 (Ad40/41) was compared by means of cell culture infectious dose (ID50) assays using monolayer cultures in microtitre plates. The PLC/PRF/5 cell line derived from a primary human hepatocellular carcinoma was 100 times more sensitive to a laboratory strain of Ad41, and 10 times more sensitive to a laboratory strain of Ad40 and two Ad41 stool isolates, than Graham 293 and Chang conjunctival cells commonly used for the propagation of these viruses. In microtitre plate titration assays PLC/PRF/5 cells retained an optimal condition for longer and displayed cytopathogenic effects earlier and more clearly than the other cell lines. In contrast to previously used cells, PLC/PRF/5 cells also proved successful for the quantitation of Ad41, but not Ad40, by conventional plaque assays. The reason for the exceptional susceptibility of PLC/PRF/5 cells has not been elucidated, but the findings open attractive new doors for research on Ad40/41.

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Year:  1992        PMID: 1317878     DOI: 10.1016/0166-0934(92)90047-h

Source DB:  PubMed          Journal:  J Virol Methods        ISSN: 0166-0934            Impact factor:   2.014


  15 in total

1.  Effect of host cells on low- and medium-pressure UV inactivation of adenoviruses.

Authors:  Huiling Guo; Xiaona Chu; Jiangyong Hu
Journal:  Appl Environ Microbiol       Date:  2010-09-17       Impact factor: 4.792

2.  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

3.  Application of PCR-based methods to assess the infectivity of enteric viruses in environmental samples.

Authors:  Roberto A Rodríguez; Ian L Pepper; Charles P Gerba
Journal:  Appl Environ Microbiol       Date:  2008-11-14       Impact factor: 4.792

4.  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

5.  Comparative Assessment of BGM and PLC/PRF/5 Cell Lines for Enteric Virus Detection in Biosolids.

Authors:  Sherif Abd-Elmaksoud; Nohelia Castro-Del Campo; Charles P Gerba; Ian L Pepper; Kelly R Bright
Journal:  Food Environ Virol       Date:  2019-01-23       Impact factor: 2.778

6.  The impact of combined sewage overflows on the viral contamination of receiving waters.

Authors:  Roberto A Rodríguez; Patricia M Gundy; Geeta K Rijal; Charles P Gerba
Journal:  Food Environ Virol       Date:  2012-01-14       Impact factor: 2.778

7.  Molecular epidemiology of group A rotaviruses in water sources and selected raw vegetables in southern Africa.

Authors:  W B van Zyl; N A Page; W O K Grabow; A D Steele; M B Taylor
Journal:  Appl Environ Microbiol       Date:  2006-07       Impact factor: 4.792

8.  Subgroup F adenovirus growth in foetal intestinal organ cultures.

Authors:  C T Tiemessen; M Ujfalusi; A H Kidd
Journal:  Arch Virol       Date:  1993       Impact factor: 2.574

9.  A rapid Q-PCR titration protocol for adenovirus and helper-dependent adenovirus vectors that produces biologically relevant results.

Authors:  Sean D Gallaher; Arnold J Berk
Journal:  J Virol Methods       Date:  2013-04-26       Impact factor: 2.014

10.  Chlorine inactivation of adenovirus type 40 and feline calicivirus.

Authors:  Jeanette A Thurston-Enriquez; Charles N Haas; Joseph Jacangelo; Charles P Gerba
Journal:  Appl Environ Microbiol       Date:  2003-07       Impact factor: 4.792

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