Literature DB >> 4967775

Nature of the carrier state of bacteriophage SP-10 in Bacillus subtilis.

M Kawakami, O E Landman.   

Abstract

Although the association of phage SP-10 with Bacillus subtilis W-23-S(r) persists in heat- and antiserum-resistant form through the spore stage, it is unstable in vegetative cells and frequently terminates in loss of the carried phage or in lysis. On low-tonicity media, the plating efficiency of carrier cells is low. However, high concentrations of succinate or sucrose or a slowed growth rate preserve viability: on 0.48 m succinate-agar, the viable count per optical density unit is the same as that of a noncarrier control culture. Carrier clones retain phage on 0.48 m succinate-agar. At higher succinate levels, many colonies emerge free of phage; at 1 m succinate, all are cured, probably because high succinate inhibits reinfection. Growth of carrier cells in liquid medium with antiphage serum results in rapid curing; events in such cultures with and without succinate were studied quantitatively by tracing the emergence of sensitive cells, the multiplication and induction of carrier cells, and the sensitivity of carrier cells to superinfection with virulent phage. During log phase, 40 to 70% of the carrier cells became sensitive to virulent phage, although the same cells were insensitive during lag and stationary phase. Apparently, fluctuations in repressor levels are responsible. Spontaneous induction of carrier cells followed a qualitatively similar pattern, perhaps in response to changes in level of the same repressor. Production of sensitive segregants by carrier followed a different course, presumably because the repressor does not affect segregation. Many sensitive cells were found two to three divisions after inoculation in antiserum medium. This suggests that each inoculum cell contained one or only a few phage replicons. The data are compatible with the idea that the carrier state in media without antisera is maintained entirely by reinfection and without replication of phage in the latent state. Alternative models which involve replication of latent phage are not ruled out, however.

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Year:  1968        PMID: 4967775      PMCID: PMC252215          DOI: 10.1128/jb.95.5.1804-1812.1968

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  11 in total

1.  RELEASE OF MALE-SPECIFIC BACTERIOPHAGES FROM SURVIVING HOST BACTERIA.

Authors:  H HOFFMANN BERLING; R MAZE
Journal:  Virology       Date:  1964-03       Impact factor: 3.616

2.  THE CARRIER STATE OF BACILLUS SUBTILIS INFECTED WITH THE TRANSDUCING BACTERIOPHAGE SP10.

Authors:  K BOTT; B STRAUSS
Journal:  Virology       Date:  1965-02       Impact factor: 3.616

3.  Phenotypic alterations associated with the bacteriophage carrier state of Shigella dysenteriae.

Authors:  K LI; L BARKSDALE; L GARMISE
Journal:  J Gen Microbiol       Date:  1961-03

4.  Lysogenization, transduction and genetic recombination in bacteria.

Authors:  S E LURIA; D K FRASER; J N ADAMS; J W BURROUS
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1958

5.  Lysogenization and superinfection immunity in Salmonella.

Authors:  N D ZINDER
Journal:  Virology       Date:  1958-04       Impact factor: 3.616

6.  Retention of episomes during protoplasting and during propagation in the L state.

Authors:  M Kawakami; O E Landman
Journal:  J Bacteriol       Date:  1966-08       Impact factor: 3.490

7.  Comparison of ultraviolet sensitivity of Bacillus subtilis bacteriophage SPO2 and its infectious DNA.

Authors:  S Okubo; W R Romig
Journal:  J Mol Biol       Date:  1965-11       Impact factor: 5.469

8.  INCORPORATION OF BACTERIOPHAGE GENOME BY SPORES OF BACILLUS SUBTILIS.

Authors:  I TAKAHASHI
Journal:  J Bacteriol       Date:  1964-06       Impact factor: 3.490

9.  Transduction in Bacillus subtilis.

Authors:  C B THORNE
Journal:  J Bacteriol       Date:  1962-01       Impact factor: 3.490

10.  Isolation and preliminary characterization of bacteriophages for Bacillus subtilis.

Authors:  W R ROMIG; A M BRODETSKY
Journal:  J Bacteriol       Date:  1961-07       Impact factor: 3.490

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  7 in total

1.  Production of bacteriophage by temperature-sensitive sporulation mutants of Bacillus cereus T.

Authors:  G N Stelma; H L Sadoff
Journal:  J Bacteriol       Date:  1973-11       Impact factor: 3.490

2.  Infectivity of Bacillus subtilis bacteriophage deoxyribonucleic acids extracted from mature particles and from lysogenic hosts.

Authors:  W R Romig
Journal:  Bacteriol Rev       Date:  1968-12

Review 3.  Bacteriophages of Bacillus subtilis.

Authors:  H E Hemphill; H R Whiteley
Journal:  Bacteriol Rev       Date:  1975-09

4.  Bacteriophages of Bacillus subtilis: comparison of different isolation techniques and possible use for classification of Bacillus subtilis strains.

Authors:  B K Rima; H Y Steensma
Journal:  Antonie Van Leeuwenhoek       Date:  1971       Impact factor: 2.271

5.  Penetration of a bacteriophage into Bacillus subtilis: blockage of infection by deoxyribonuclease.

Authors:  R M Zsigray; A L Miss; O E Landman
Journal:  J Virol       Date:  1973-01       Impact factor: 5.103

6.  Growth of male-specific bacteriophage in Pasteurella harboring F-genotes derived from Escherichia coli.

Authors:  D M Molnar; W D Lawton
Journal:  J Virol       Date:  1971-01       Impact factor: 5.103

7.  Transduction in Bacillus subtilis by bacteriophage SPP1.

Authors:  R E Yasbin; F E Young
Journal:  J Virol       Date:  1974-12       Impact factor: 5.103

  7 in total

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