Literature DB >> 16349700

Virustat, a device for continuous production of viruses.

H Jacobson1, L S Jacobson.   

Abstract

Methods for continuous production of viruses, and operation of the virustat, an apparatus in which such production was accomplished, were studied. Continuous production requires a separate continuous host growth chamber, such as the chemostat, and a multiunit virus growth chamber into which the virus-inoculated host cells are led. Successful continuous output of MS-2 and varphiX174 viruses, the latter in lysates, over periods of several days and at titers approximating those of batch lysates, was observed. Design problems include chamber sizes and flow rates, growth of resistant mutants within both virus and host growth chambers, clogging by lysis debris, and the phenomenon of self-inoculation. The latter represents virus growth in the first section of the chamber in excess of the washout rate, leading to lack of need for virus inoculation after an initial period. Use of the virustat for production and research purposes will require some attention to the formation of resistant bacterial colonies at pockets and surface sites of limited washout. With the virustat as a continuous virus production device, continuous purification methods are desirable. Research use of the virustat in continuous mutagenic population studies would require suppression of self-inoculation by use of many sections in the chamber, and improved servo control of host populations at low concentrations.

Entities:  

Year:  1966        PMID: 16349700      PMCID: PMC1058447          DOI: 10.1128/am.14.6.940-952.1966

Source DB:  PubMed          Journal:  Appl Microbiol        ISSN: 0003-6919


  6 in total

1.  MUTATION IN CONTINUOUS CULTURES. I. DEPENDENCE OF MUTATIONAL RESPONSE UPON GROWTH-LIMITING FACTORS.

Authors:  H E KUBITSCHEK; H E BENDIGKEIT
Journal:  Mutat Res       Date:  1964-07       Impact factor: 2.433

2.  The replication of bacteriophage MS2. 1. Transfer of parental nucleic acid to progeny phage.

Authors:  J E DAVIS; R L SINSHEIMER
Journal:  J Mol Biol       Date:  1963-03       Impact factor: 5.469

3.  Submerged culture of mammalian cells: the five liter fermentor.

Authors:  W F McLIMANS; F E GIARDINELLO; E V DAVIS; C J KUCERA; G W RAKE
Journal:  J Bacteriol       Date:  1957-12       Impact factor: 3.490

4.  Description of the chemostat.

Authors:  A NOVICK; L SZILARD
Journal:  Science       Date:  1950-12-15       Impact factor: 47.728

5.  Semi-conservative replication of DNA in a higher plant cell.

Authors:  P Filner
Journal:  Exp Cell Res       Date:  1965-08       Impact factor: 3.905

6.  A device for growing bacterial populations under steady state conditions.

Authors:  M S FOX; L SZILARD
Journal:  J Gen Physiol       Date:  1955-11-20       Impact factor: 4.086

  6 in total
  2 in total

Review 1.  Continuous cultivation of microorganisms. A review.

Authors:  I Málek; J Ricica
Journal:  Folia Microbiol (Praha)       Date:  1968       Impact factor: 2.099

Review 2.  Bioreactors for high cell density and continuous multi-stage cultivations: options for process intensification in cell culture-based viral vaccine production.

Authors:  Felipe Tapia; Daniel Vázquez-Ramírez; Yvonne Genzel; Udo Reichl
Journal:  Appl Microbiol Biotechnol       Date:  2016-01-13       Impact factor: 4.813

  2 in total

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