Tissue culture storage of potato germplasm. 1. Minimal growth storage

1981 ◽  
Vol 24 (3) ◽  
pp. 331-342 ◽  
Author(s):  
R. J. Westcott
Nematology ◽  
2019 ◽  
Vol 21 (6) ◽  
pp. 613-623 ◽  
Author(s):  
James M. Mwangi ◽  
Björn Niere ◽  
Matthias Daub ◽  
Maria R. Finckh ◽  
Sebastian Kiewnick

Summary Globodera pallida infestation on potato is responsible for huge yield losses globally. Screening of potato germplasm for resistance to the nematode at the early stages of a breeding programme can significantly enhance resistance-based management. This study assessed the suitability of tissue culture (TC)-derived potato plants as screening material for resistance to G. pallida. Reproduction of the nematode on TC plants was similar to the reproduction on tuber- and eye-plug-derived plants. The pot volume, inoculum density and inoculation time had a significant effect on the reproduction. A positive correlation was found between the mean number of white females on the root surface and the final number of nematode cysts after extraction. Resistance ranking using TC plants and the tubers yielded comparable results, thus justifying the use of TC in the screening process. Tissue culture plants have the potential of speeding up the screening process and reducing resource requirements, thus lowering breeding cost.


1981 ◽  
Vol 24 (3) ◽  
pp. 343-352 ◽  
Author(s):  
R. J. Westcott

1977 ◽  
Vol 9 (4) ◽  
pp. 309-315 ◽  
Author(s):  
Roger J Westcott ◽  
Graham G Henshaw ◽  
William M Roca

PEDIATRICS ◽  
1967 ◽  
Vol 39 (3) ◽  
pp. 425-432
Author(s):  
S. H. Waxman ◽  
D. T. Arakaki ◽  
J. B. Smith

Eighty-five specimens (56%) of 149 samples of spontaneous fetal abortions grew initially in tissue culture. Sixty were cultivated with only minimal growth and were subsequently lost in attempted chromosomal preparations. Of the remaining 25 cultures, 10 had abnormal karyotypes. These consisted of one monosomy-3, three trisomy-16, one mosaic trisomy-16, one trisomy-F (19-20), an XO, two polyploid, and an unusually long unidentified translocation chromosome karotypes. The remaining 15 cultures had normal karyotypes. The sex ratio as determined by sex chromatin was: males, 13 and females, 15. Eleven were confirmed chromosomally to be XY males and 13 to be XX females. Two of the trisomy-16, the mosiac trisomy, and the polyploid fetuses were males; the other four fetuses with abnormal karyotypes were females. The sex of the XO specimen could not be ascertained.


Author(s):  
Adrian F. van Dellen

The morphologic pathologist may require information on the ultrastructure of a non-specific lesion seen under the light microscope before he can make a specific determination. Such lesions, when caused by infectious disease agents, may be sparsely distributed in any organ system. Tissue culture systems, too, may only have widely dispersed foci suitable for ultrastructural study. In these situations, when only a few, small foci in large tissue areas are useful for electron microscopy, it is advantageous to employ a methodology which rapidly selects a single tissue focus that is expected to yield beneficial ultrastructural data from amongst the surrounding tissue. This is in essence what "LIFTING" accomplishes. We have developed LIFTING to a high degree of accuracy and repeatability utilizing the Microlift (Fig 1), and have successfully applied it to tissue culture monolayers, histologic paraffin sections, and tissue blocks with large surface areas that had been initially fixed for either light or electron microscopy.


Author(s):  
L. Z. de Tkaczevski ◽  
E. de Harven ◽  
C. Friend

Despite extensive studies, the correlation between the morphology and pathogenicity of murine leukemia viruses (MLV) has not yet been clarified. The virus particles found in the plasma of leukemic mice belong to 2 distinct groups, 1 or 2% of them being enveloped A particles and the vast majority being of type C. It is generally believed that these 2 types of particles represent different phases in the development of the same virus. Particles of type A have been thought to be an earlier form of type C particles. One of the tissue culture lines established from Friend leukemia solid tumors has provided the material for the present study. The supernatant fluid of the line designated C-1A contains an almost pure population of A particles as illustrated in Figure 1. The ratio is, therefore, the reverse of what is unvariably observed in the plasma of leukemic mice where C particles predominate.


Author(s):  
A. M. Watrach

During a study of the development of infectious laryngotracheitis (LT) virus in tissue culture cells, unusual tubular formations were found in the cytoplasm of a small proportion of the affected cells. It is the purpose of this report to describe the morphologic characteristics of the tubules and to discuss their possible association with the development of virus.The source and maintenance of the strain of LT virus have been described. Prior to this study, the virus was passed several times in chicken embryo kidney (CEK) tissue culture cells.


Author(s):  
Lee F. Ellis ◽  
Richard M. Van Frank ◽  
Walter J. Kleinschmidt

The extract from Penicillum stoliniferum, known as statolon, has been purified by density gradient centrifugation. These centrifuge fractions contained virus particles that are an interferon inducer in mice or in tissue culture. Highly purified preparations of these particles are difficult to enumerate by electron microscopy because of aggregation. Therefore a study of staining methods was undertaken.


Author(s):  
R. Stephens ◽  
G. Schidlovsky ◽  
S. Kuzmic ◽  
P. Gaudreau

The usual method of scraping or trypsinization to detach tissue culture cell sheets from their glass substrate for further pelletization and processing for electron microscopy introduces objectionable morphological alterations. It is also impossible under these conditions to study a particular area or individual cell which have been preselected by light microscopy in the living state.Several schemes which obviate centrifugation and allow the embedding of nondetached tissue culture cells have been proposed. However, they all preserve only a small part of the cell sheet and make use of inverted gelatin capsules which are in this case difficult to handle.We have evolved and used over a period of several years a technique which allows the embedding of a complete cell sheet growing at the inner surface of a tissue culture roller tube. Observation of the same cell by light microscopy in the living and embedded states followed by electron microscopy is performed conveniently.


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