scholarly journals THE REACTIONS BETWEEN BACTERIA AND ANIMAL TISSUES UNDER CONDITIONS OF ARTIFICIAL CULTIVATION

1915 ◽  
Vol 21 (2) ◽  
pp. 103-112 ◽  
Author(s):  
Henry Field Smyth

This report gives an outline of the results of observations on over 1,100 tissue cultures made during the fall, winter, and spring of 1913 to 1914. The work has been resumed in the fall of 1914 and will be continued along the same and allied lines, confirming the above results with other strains of the same organisms and with other bacteria and bacterial products. Tests should be made with tissue and plasma from other animals, and the known pathogenicity of the organism for the animal and tissue used should always be borne in mind. We hope to be able to grow on these cultures some of the more strictly parasitic bacteria not developing on ordinary media, as other strict parasites have been grown by other workers, viz., poliomyelitis virus by Levaditi (4), vaccinia by Steinhardt, Israeli, and Lambert (5), and rabies by Moon (6). By comparative studies with various types of cells and various natural and artificial media, clearer ideas as to the exact part of cell plasma in antibody production, by elaborating on the methods of Carrel and Ingebrigtsen (7), Lüdke (8), Przygode (9), and others, should be possible. After this work was begun a reference was found to the use of some pathogenic bacteria in tissue cultures by Pheiler and Lentz (10), but no publication of the results of these observations has been observed. The results here reported may be summarized as follows: Bactericidal Action of Chicken Plasma.—On Bacillus typhosus, very strong—never grows in plasma alone; on Bacillus prodigiosus, very strong—never grows in plasma alone; on Bacterium pseudodiphtheriticum, strong—slight growth in cover-glass preparations; on Bacterium diphtheriticum, moderately strong; on Bacillus coli verus, slight; on Micrococcus aureus, very slight or none. A few pseudodiphtheria bacilli and more diphtheria bacilli survived in plasma stored in the cold for four days. The presence of growing tissue overcomes the bactericidal influence of plasma on diphtheria bacilli and in some instances on pseudodiphtheria bacilli. Bacterium diphtheriticum grows in plasma without tissue only if inoculations are very heavy; and very heavy inoculations of all organisms will probably overcome the bactericidal action of plasma, as it is undoubtedly a quantitative reaction. The bactericidal influence of plasma is overcome by exposure to incubator temperature for twenty-four to forty-eight hours. Bacterium diphtheriticum in light or moderate inoculations grows in tissue cultures only in clusters around the tissue fragments, and never in plasma away from tissue. The growth of this organism has a decided inhibitory influence on tissue activity and growth, especially marked with nervous tissue, but this action may be overcome by the addition of antitoxin to the plasma. Cultures inhibited by diphtheria growth have a tendency to resume growth later, probably due to antitoxin production. Bacterium pseudodiphtheriticum is distinctly less active in tissue cultures than is Bacterium diphtheriticum and never develops in plasma without tissue. The presence of diphtheria toxin in tissue cultures causes this organism to behave as does Bacterium diphtheriticum. Without toxin it has little or no direct influence on tissue growth except in massive doses. Bacillus prodigiosus fails to develop, as a rule, in tissue cultures except where inoculated from hypertonic media, and then it has no decided influence on tissue growth. Micrococcus aureus grows freely in these cultures with or without tissue, and inhibits tissue growth markedly, except as noted with splenic tissue. Bacillus coli verus always grows freely with or without tissue fragments and is uninfluenced by splenic tissue growth. In heavy inoculations it lessens tissue growth. Bacillus typhosus, except with extremely heavy inoculations, fails absolutely to grow in these cultures with or without plasma, unless the bactericidal action of the plasma has been destroyed by incubation. When this is the case it develops freely with especial affinity for the tissue cells either for support or nourishment. It appears to have no toxic action on the tissue cells. Note the sharp differentiation between typhoid and coli verus organisms. Diphtheria toxin has a quantitatively inhibiting action on all tissue growth and on heart tissue pulsations, the action being greatest on nervous tissue and least on heart tissue growth. Tissues affected by toxin tend to recovery if not killed. Antitoxin counteracts the action of toxin. Splenic tissue has little or no effect on the growth of Bacillus coli verus, but has a decided bactericidal action on Bacterium diphtheriticum and Micrococcus aureus, probably due to lymphatic cells and cell products, as seen by the area of cell migration coinciding with the bacteria-free area, by the similar action of splenic extract on cultures, and by the failure of such action in cultures of very early splenic tissue showing no lymphatic cells.

1916 ◽  
Vol 23 (3) ◽  
pp. 265-274 ◽  
Author(s):  
Henry Field Smyth

The results here reported confirm those of the former papers and strengthen the conclusions drawn therefrom. They may be summarized as follows: Chicken plasma has a marked bactericidal action on Bacillus typhosus, which may be in some slight degree overcome by the presence of growing tissue, especially splenic tissue, in the cultures. On Bacillus dysenteriœ this bactericidal action of chicken plasma is present, but much less marked, and the same counteracting action of tissue, especially splenic tissue, is evident. On Bacillus coli verus chicken plasma has little or no bactericidal action. On Bacterium diphtheriticum chicken plasma has a very strong bactericidal action which may be strongly counteracted by the presence of growing tissue in the cultures. In all cases the bactericidal action of the plasma is decidedly diminished by dilution, as shown by the comparative results of these and the cultures formerly reported. The migrating white cells from splenic cultures, or substances closely associated with these cells, have a distinctly bactericidal influence on all organisms tested except Bacillus coli verus. Murphy states that lymphocytes first appear in the general circulation of the chick embryo on the 18th to 20th day, but in my cultures of splenic tissue cells resembling lymphocytes in morphology and behavior begin to appear in cultures of 11 or 12 day spleen and are abundant in cultures of spleen from 14 day or older embryos.


1916 ◽  
Vol 23 (3) ◽  
pp. 283-291 ◽  
Author(s):  
Henry Field Smyth

In plasma cultures, with or without tissue, tubercle bacilli form characteristic streptothrix-like colonies of loosely twisted skeins of threads. In plasma tissue cultures embryonal connective tissue and epithelial cells phagocytyze tubercle bacilli freely. Splenic tissue cultures from fourteen day or older embryos if inoculated with isolated bacilli will phagocytyze and prevent the development of all or nearly all bacilli present. If heavy inoculations of tubercle bacilli with many bacillary clumps are made in splenic cultures the bacilli develop more freely than in similar connective tissue cultures from heart tissue in spite of marked phagocytosis. In such cultures the first change seen is a clustering of small round cells, interpreted as lymphocytes, around bacillary clumps and colonies followed by a similar clustering of larger parenchymatous polygonal cells with one or several nuclei, interpreted as epithelioid cells, which phagocytyze any bacilli with which they may come in contact. The larger cells containing bacilli then fuse to form larger multinuclear cells and these by further fusion form typical giant cells with quiescent nuclei in characteristic groupings and bacilli in degenerated protoplasm away from the nuclear groups. Cells which have phagocytyzed bacilli may digest them or may be unable to do so, in which case the bacilli develop within the cells and eventually cause complete cell degeneration.


1945 ◽  
Vol 23e (3) ◽  
pp. 80-84 ◽  
Author(s):  
Reta Anderson ◽  
J. H. Orr ◽  
G. B. Reed

The toxicity of several sulphonamides for tissue cells has been tested by adding the compounds to tissue cultures of fibroblasts (guinea pig heart tissue in guinea pig serum). Supersaturated solutions of sulphadiazine or sulphapyrazine, in serum, have no influence on the growth of fibroblasts. Sulphathiazole, N1-benzoyl-sulphanilamide, or sulphanilamide in similar concentrations inhibit fibroblast growth. The above-mentioned five sulphonamides in concentrations up to 100 mgm. per 100 ml. have no apparent influence on fibroblast growth. In contrast, azochloramide in concentrations of 5 to 10 mgm. per 100 ml. inhibit growth.


Nature ◽  
1968 ◽  
Vol 220 (5171) ◽  
pp. 1004-1004
Author(s):  
DAVID R. GARDNER
Keyword(s):  

1972 ◽  
Vol 30 (6) ◽  
pp. 628-633 ◽  
Author(s):  
T. D. CHANG ◽  
G. R. CUMMING

1916 ◽  
Vol 24 (6) ◽  
pp. 683-688 ◽  
Author(s):  
Robert A. Lambert

The comparative resistance of bacteria and human tissue cells to antiseptics and other chemicals may be easily tested by tissue cultures under conditions which approximate those found in the living body. A comparative study shows that while human cells (connective tissue and wandering cells) are highly resistant to many antiseptics, they are in general more easily killed than bacteria (Staphylococcus aureus). Of the antiseptics tested, which include mercuric chloride, iodine, potassium mercuric iodide, phenol, tricresol, hydrogen peroxide, hypochlorites (Dakin's solution), argyrol, and alcohol, the one which approaches most closely the ideal disinfectant is iodine, which kills bacteria in strengths that do not seriously injure connective tissue cells or wandering cells.


1991 ◽  
Vol 72 (4) ◽  
pp. 809-815 ◽  
Author(s):  
V. E. C. J. Schijns ◽  
R. Van der Neut ◽  
B. L. Haagmans ◽  
D. R. Bar ◽  
H. Schellekens ◽  
...  

Weed Science ◽  
1978 ◽  
Vol 26 (6) ◽  
pp. 527-530 ◽  
Author(s):  
J. B. Huffman ◽  
N. D. Camper

Tobacco(Nicotiana tabacumL. ‘X-73’) callus tissue cultures were used in a bioassay system for determining the effect of the following substituted 2,6-dinitroaniline herbicides on growth: trifluralin (α,α,α-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine); oryzalin (3,5-dinitro-N4,N4-dipropylsulfanilamide); benefin(N-butyl-N-ethyl-α,α,α-trifluoro-2,6-dinitro-p-toluidine); AC 92390(N-sec-butyl-2,6-dinitro-3,4-xylidine); penoxalin [N-(1-ethylpropyl)-2,6-dinitro-3,4-xylidine]; GS-38946(N-ethyl-N-tetrahydrofurfuryl-4-trifluoromethyl-2,6-dinitroaniline); chlornidine [N,N-di(2-chloroethyl)-4-methyl-2,6-dinitroaniline]; nitralin [4-(methylsulfonyl)2,6-dinitro-N,N-dipropylaniline]; dinitramine(N4,N4-diethyl-α,α,α-trifluoro-3,5-dinitrotoluene-2,4-diamine); isopropalin (2,6-dinitro-N,N-dipropylcumidine), and profluralin [N(cyclopropylmethyl)-α,α,α-trifluoro-2,6-dinitro-N-propyl-p-toluidine]. The molar concentration required to inhibit fresh weight gain by 50% (I50) was determined by using linear regression analysis on data from a range of five concentrations of each chemical. I50values did not correlate with structural variations or available physical constants. Herbicides listed in order of increasing activity are AC 92390< GD-38946<profluralin = isopropalin<benefin = chlornidine = trifluralin = nitralin<oryzalin = penoxalin < dinitramine. Exogenously applied D-α-tocopherol acetate at 100 times the I50concentrations decreased the inhibition of tissue growth by the herbicides.


1960 ◽  
Vol 6 (6) ◽  
pp. 605-609 ◽  
Author(s):  
Paul Fenje

A strain of fixed rabies virus adapted to hamster kidney tissue cells has produced culture fluids of high infectivity for rabbits and mice. These culture fluids were rendered non-infective by treatment with formaldehyde at a concentration of 8 m M. Rabbits immunized with this material produced autirabies antibody to a high titer and were subsequently proved to be resistant to intramuscular inoculation of rabies virus from the salivary glands of a naturally infected fox.


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