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. 1961 Nov 1;11(2):441–447. doi: 10.1083/jcb.11.2.441

LIGHT AND ELECTRON MICROSCOPE STUDIES OF MYCOBACTERIUM—MYCOBACTERIOPHAGE INTERACTIONS

III. Further Studies on the Ultrathin Sections

Kenji Takeya 1, Masaatsu Koike 1, Ryoichi Mori 1, Tadao Toda 1
PMCID: PMC2225159  PMID: 13919270

Abstract

The process of multiplication of mycobacteriophage B-1 in its host cell was studied by means of an improved technic of ultrathin sectioning. The appearance of the nuclear apparatus was not altered throughout the latent period. Phage-shaped dense particles appeared about 30 minutes after infection in less dense areas neighboring the nuclear apparatus and occasionally at the margin of the nuclear apparatus. The less dense areas, which may correspond to the phage multiplication foci according to the authors' interpretation, were not filled with such arrays of fine-stranded fibrils as are seen in the nuclear apparatus. Empty phage heads could frequently be seen within and outside the lysed cells, along with the mature phage particles, at the end of the latent period. Moreover, it was indicated that empty head membranes may possibly exist within the cells during the latent period

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. FUKAI K., SELLERS M. I. A morphologic study of mycobacteria infected with D32 phage. Am Rev Respir Dis. 1960 Jan;81:52–59. doi: 10.1164/arrd.1960.81.1P1.52. [DOI] [PubMed] [Google Scholar]
  2. GLAUERT A. M., GLAUERT R. H. Araldite as an embedding medium for electron microscopy. J Biophys Biochem Cytol. 1958 Mar 25;4(2):191–194. doi: 10.1083/jcb.4.2.191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. KELLENBERGER E., SECHAUD J., RYTER A. Electron microscopical studies of phage multiplication. IV. The establishment of the DNA pool of vegetative phage and the maturation of phage particles. Virology. 1959 Aug;8:478–498. doi: 10.1016/0042-6822(59)90050-9. [DOI] [PubMed] [Google Scholar]
  4. KOIKE M., TAKEYA K. Fine structures of intracytoplasmic organelles of mycobacteria. J Biophys Biochem Cytol. 1961 Mar;9:597–608. doi: 10.1083/jcb.9.3.597. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. RYTER A., KELLENBERGER E., BIRCHANDERSEN A., MAALOE O. Etude au microscope électronique de plasmas contenant de l'acide désoxyribonucliéique. I. Les nucléoides des bactéries en croissance active. Z Naturforsch B. 1958 Sep;13B(9):597–605. [PubMed] [Google Scholar]
  6. SECHAUD J., RYTER A., KELLENBERGER E. Considérations quantitatives sur des coupes ultraminces de bactéries infectées par un bactériophage. J Biophys Biochem Cytol. 1959 May 25;5(3):469–478. [PMC free article] [PubMed] [Google Scholar]
  7. TAKEYA K., KOIKE M., MORI R., YUDA Y., TODA T. Light and electron microscope studies of Mycobacterium-mycobacteriophage interactions. II. Electron microscope studies. J Bacteriol. 1959 Sep;78:313–319. doi: 10.1128/jb.78.3.313-319.1959. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. TAKEYA K., MORI R., NAKASHIMA N., KOIKE M., TODA T. Light and electron microscope studies of Mycobacterium-mycobacteriophage interactions. I. Light microscope studies. J Bacteriol. 1959 Sep;78:307–312. doi: 10.1128/jb.78.3.307-312.1959. [DOI] [PMC free article] [PubMed] [Google Scholar]

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