scholarly journals OBSERVATIONS ON MIXTURES OF ELEMENTARY BODIES OF VACCINIA AND COATED COLLODION PARTICLES BY MEANS OF ULTRACENTRIFUGATION AND ELECTROPHORESIS

1940 ◽  
Vol 72 (5) ◽  
pp. 523-529 ◽  
Author(s):  
J. E. Smadel ◽  
E. G. Pickels ◽  
T. Shedlovsky ◽  
T. M. Rivers

It has been shown experimentally that mixtures of two types of particles, namely, elementary bodies of vaccinia and collodion particles coated with protein, sediment with a single boundary in the analytical centrifuge. Such mixtures have been shown to develop one or two boundaries on electrophoresis in the Tiselius apparatus, depending on the type of coating on the surface of the collodion particles. When covered with the heat-stable soluble antigen of vaccinia, collodion particles migrate in the electrical field at the same rate as elementary bodies. On the other hand, if they are coated with a component of normal rabbit serum, they migrate at a different rate. The estimation of purity of preparations of virus by means of data obtained by ultracentrifugation and electrophoresis is discussed.

1940 ◽  
Vol 72 (4) ◽  
pp. 389-405 ◽  
Author(s):  
J. E. Smadel ◽  
M. J. Wall

Anti-soluble substance antibodies and neutralizing substances, which develop following infection with the virus of lymphocytic choriomeningitis, appear to be separate entities. The times of appearance and regression of the two antibodies are different in both man and the guinea pig; the antisoluble substance antibodies appear earlier and remain a shorter time. Moreover, mice develop them but no demonstrable neutralizing substances. Injection of formalin-treated, virus-free extracts containing considerable amounts of soluble antigen fails to elicit anti-soluble substance antibodies and to induce immunity in normal guinea pigs; administration of such preparations to immune pigs, however, is followed by a marked increase in the titer of anti-soluble substance antibodies in their serum. On the other hand, suspensions of formolized washed virus are effective in normal guinea pigs in stimulating both anti-soluble substance antibodies and protective substances, and in inducing immunity to infection.


1914 ◽  
Vol 14 (2) ◽  
pp. 215-241 ◽  
Author(s):  
William Jas. Penfold

(1) If B. coli be subcultured into another sample of the same medium when growing at full pace, it will continue to grow at the same pace.(2) If the maximum rate of growth be interrupted by a short application of cold, growth will recommence without lag on the temperature being raised. If the cold be long continued, lag will tend to reappear.(3) Differences in the size of inoculum have practically no effect on lag in the case of large inoculums, in the case of small ones, on the other hand, diminution of the seeding has the effect of lengthening lag, and this lengthening effect is more marked the smaller the seedings become.(4) Lowering the temperature lengthens the lag. The effect is very similar to the effect on growth.(5) The older a parent culture (within limits) the longer the lag.(6) The length of lag varies with the medium even if adaptation has been arranged for beforehand.(7) Heat-stable products in B. coli cultures on peptone water have, in the case of overnight cultures, but little effect on lag.(8) After washing the bacteria for two hours with saline in order to remove possible inhibiting agents, it was found that the lag, on subculture, still occurred and was indeed slightly longer.(9) If a peptone water culture of B. coli be centrifuged, it is found that the few bacteria remaining in the supernatant commence to grow again at a quick rate but not without a period of lag.


1940 ◽  
Vol 71 (1) ◽  
pp. 43-53 ◽  
Author(s):  
J. E. Smadel ◽  
M. J. Wall ◽  
R. D. Baird

The soluble antigen of lymphocytic choriomeningitis which is readily separable from the virus is a relatively stable substance and appears to be of a protein nature. A specific precipitin reaction can be demonstrated when immune serum is added to solutions of antigen which have been freed of certain serologically inactive substances. The complement-fixation and precipitation reactions which occur in the presence of immune serum and non-infectious extracts of splenic tissue obtained from guinea pigs moribund with lymphocytic choriomeningitis seem to be manifestations of union of the same soluble antigen and its antibody. On the other hand, the antisoluble substance antibodies and neutralizing substances appear to be different entities.


1962 ◽  
Vol 115 (3) ◽  
pp. 453-466 ◽  
Author(s):  
Stephen Boyden

An in vitro technique is described for assessing the chemotactic activity of soluble substances on motile cells. Antibody-antigen mixtures when incubated (37°C) in medium containing fresh (i.e. non-inactivated) normal rabbit serum exert a strong chemotactic effect on rabbit polymorphonuclear leucocytes. Results are described which indicate that, when antibody-antigen complexes are incubated (37°C) in fresh serum, a heat-stable (56°C) substance (or substances) is produced which acts directly as a chemotactic stimulus on the polymorphs. This heat-stable chemotactic substance is not produced when antibody-antigen complexes are incubated in serum which has been heated at 56°C for 30 minutes.


1940 ◽  
Vol 72 (5) ◽  
pp. 511-521 ◽  
Author(s):  
Theodore Shedlovsky ◽  
Joseph E. Smadel

Electrophoretic studies were made on vaccine virus, collodion particles, and glass particles suspended in 0.01 molar buffer solutions at pH 7.9, in which the moving boundary method was used. In some experiments, uncoated particles were used; in others, particles were coated with proteins and then resuspended in the buffer solution after a washing; in still others, an excess of protein which had been used to coat the particles was included in the buffer medium. Streaming boundaries were obtained with all dilute suspensions of particles in solutions containing no soluble protein instead of the flat ones usually observed with the Tiselius moving boundary technique. This boundary artifact was suppressed by maintaining a density gradient of sufficient magnitude in association with the moving boundary to counteract the tendency of endosmotic flow. This was done partially by increasing the concentration of the particles in the suspensions, and almost completely by retaining an excess of soluble-coating substance in the solutions containing the particles. The mobility of elementary bodies of vaccinia corresponds to that found for the heat-stable (S) antigen. This value was not altered by drying, heating, ether extraction, or simple washing, but was materially increased by treatment with the surface active detergent (duponol) which presumably altered the nature of the surface of the virus particles. Collodion particles coated with the heat-stable antigen of vaccinia had the same mobility as elementary bodies under comparable conditions. Glass particles coated with normal rabbit serum moved at the rate of albumin, the fastest serum component in the buffer solutions used. However, both collodion particles and vaccine virus moved at a somewhat slower rate when they were similarly coated and measured in the presence of an excess of serum in the solutions. This was probably due to adsorption of a small amount of one of the slower components (globulin) of rabbit serum on the surface of the particles. Simple washing after treatment seemed to remove the coating of serum proteins, at least in part, from both collodion particles and elementary bodies of vaccinia.


1973 ◽  
Vol 137 (2) ◽  
pp. 359-368 ◽  
Author(s):  
Phyllis R. Strauss ◽  
Richard D. Berlin

The effects of normal rabbit serum (NRS) on two transport systems in rabbit lung macrophages have been examined. A 20 min preincubation with serum was required for the effects, which were retained for at least 40 min after serum was removed. No serum was present during the transport studies. (a) Preincubation with 0.5 or 1.0% NRS resulted in depression of lysine transport to 59 ± 2.6% (SE, 31 observations) of control levels. The activity was heat stable to 100°C for 30 min and lost after dialysis. Pretreatment with serum did not alter the intracellular concentration of lysine attained when cells were then incubated with 10 mM lysine for 30 min. The relative depression of lysine transport by serum was unaltered by preloading with such high concentrations of lysine. (b) Preincubation with 5% NRS resulted in enhancement of adenosine transport by 35 ± 2.3% (SE, 60 observations). Activity was stable to heating at 65°C for 40 min but lost at 100°C for 20 min. It was nondialyzable. Total radioactivity accumulated after 30 min incubation with 1 mM adenosine was unaffected by serum pretreatment. The two activities were separable by passage over Sephadex G25.


1967 ◽  
Vol 126 (5) ◽  
pp. 795-818 ◽  
Author(s):  
Richard B. Roberts

The interaction in vitro between group B meningococci and rabbit polymorphonuclear leukocytes has been described. Phagocytosis did not occur in the presence of normal rabbit serum. Antiserum collected 12–21 days following one subcutaneous inoculation of living log phase meningococci exhibited opsonic activity with type specificity; this opsonic action depended on both heat-labile and heat-stable factors. Following ingestion by granulocytes, meningococci were rapidly killed. These studies suggest that group B meningococcal strains contain specific antiphagocytic surface factors of an as yet unknown chemical nature. Antisera obtained 4 or more wk after immunization showed bactericidal activity with the same type specificity as opsonic activity. This bactericidal activity was also lost after heating and restored by the addition of normal serum. Further studies on opsonins and bactericidins for meningococci may shed light on virulence factors in these microorganisms, and may prove useful for a more precise classification of meningococci according to type rather than group specificity.


1973 ◽  
Vol 59 (1) ◽  
pp. 1-9 ◽  
Author(s):  
Carlo D. Baroni ◽  
Roberto Scelsi ◽  
Laura Peronace ◽  
Stefania Uccini ◽  
Anna Cavallero

The present paper describes the effects of repeated administration of rabbit anti-mouse lymphocyte serum (ALS) or normal rabbit serum (NRS) on tumors induced in Charles–River mice by 7,12-dimethylbenz (a) anthracene (DMBA) given at birth. ALS or NRS were given at the same time of DMBA administration and subsequently at weekly intervals for the first 10 weeks of life or at daily intervals for 7 days during the first, second, third or fourth week of life. Incidence, latency, diffusion and histology of the tumors were studied. It was found that either chronic administration of ALS or treatment of very young mice with the serum, greatly reduced the mean survival time of mice, markedly increased the number of tumor bearing mice and the incidence of all histological types of tumors, and decreased their latency period. Administration of ALS in the other experimental groups gave results essentially similar to those observed in DMBA control and NRS treated mice.


1923 ◽  
Vol 37 (3) ◽  
pp. 383-394
Author(s):  
Hideyo Noguchi

From the results of the experiments presented it is evident that in guinea pigs an early administration of immune rabbit serum will suppress the infection; that is, if it is given within the period of incubation, the effect being proportionately greater the earlier the serum is administered. Almost no beneficial effect is observed when the serum is given after the onset of the disease. In the animals inoculated with 10 to 100 M.L.D. the incubation period is shorter than when 1 M.L.D. is injected; nevertheless 1 cc. of the immune serum saved the animals as late as 96 hours from the time of the introduction of the virus into the system. When administered within 24 hours in the case of 100 M.L.D. and within 48 hours in the case of 10 M.L.D., the serum completely neutralized the virus, and the animals escaped infection altogether. On the other hand, the same quantity of the serum only modified the infection into a non-fatal one when given a day or two later. In the animals which were inoculated with 1 M.L.D. the incubation period was a day or two longer, and the neutralizing effect of the serum was much more powerful. Here animals were saved as late as 5, 6, and 7 days and with a much smaller quantity of the serum (0.1 cc.). As to the usefulness of such an immune serum in human cases, the relative susceptibility of man and the guinea pig must first be considered. In a large number of experimental infections carried out with guinea pigs in the past 6 years almost never has a naturally refractory animal been encountered. The mortality is nearly 80 per cent with most strains, although as low as 50 per cent with some. The strain used in the present study caused death in nearly 80 per cent of the animals. Hence the susceptibility of guinea pigs is at least as great as that of man, in whom the mortality in the Bitter Root Valley is estimated to be about 70 per cent. The relative length of the incubation period in guinea pig and in man is another point which requires analysis. In guinea pigs it varies somewhat according to the number of passages, being as short as 3 days when 100 M.L.D. or more of an adapted virus are inoculated. On the other hand, when the infection is the result of 1 M.L.D. or the bite of an infected tick, the incubation period is much longer, being 5, 6, or 7 days in the former and 7 to 8½ days in the latter instance, as with the present strain. In man the infection is brought on by the bite of an infected tick, and the period of incubation varies from 3 to 10 days but is usually 7 days; i.e., it is about the same as in guinea pigs infected with 1 M.L.D. Hence we may regard the susceptibility of man and the guinea pig as nearly equal. The final point to be considered is the quantity of the immune serum that may be recommended for use in human cases. To prevent the infection in a guinea pig weighing 500 gm., 0.1 cc. of the serum was sufficient. This quantity protected the animal against 1 M.L.D. even as late as 5, 6, or 7 days. Calculated on this basis, 16 cc. of the serum would be required for a man weighing 80 kilos (about 160 pounds); that is, 16 cc. of an immune rabbit serum, administered before onset of the disease, should theoretically be sufficient to save a man of average weight against an infection brought about by the bite of an infected tick or by a laboratory accident. It would probably be best to administer the serum intravenously. The titer of the immune serum should be previously determined in guinea pigs, and 1 cc. should neutralize 100 M.L.D. completely and 0.1 and 0.01 cc. render the infection non-fatal. Such a serum is easily produced in rabbits (a rabbit weighing 2,500 gm. will yield 50 to 60 cc. of the serum) and probably will remain active a year or longer when kept at refrigerator temperature.


1917 ◽  
Vol 25 (6) ◽  
pp. 765-788 ◽  
Author(s):  
Hideyo Noguchi ◽  
Seinai Akatsu

Experiments were carried out for the study of culture spirochetes in their relation to various immunity reactions in vitro. Several strains of Treponema pallidum and one each of Treponema calligyrum, Spirochata refringens, Treponema microdentium, and Treponema mucosum were used. Tests were made of immune substances responsible for agglutination, complement fixation, spirocheticidosis, and opsonization. In cases of agglutination and complement fixation, cross titrations were made. 1. In the sera derived from rabbits immunized with various spirochetes agglutinins were demonstrated in varying quantities for the homologous antigens. The amounts of agglutinins developed were considerably higher in the pallidum immune sera than in the other groups. There was no parallelism between the amounts of antigens injected and the amounts of agglutinins developed. 2. Cross titrations among different pallidum strains revealed that the agglutiantion is not necessarily strongest when homologous antigens and immune sera are brought together. 3. On the other hand, the reactions between the immune sera and antigens belonging to different species were sufficiently specific to justify the grouping. 4. Certain degrees of group reactions were observed between the pallidum immune sera and the calligyrum, and occasionally very faintly also between the pallidum and the refringes antigens and vice versa. There was a much more pronounced group reaction between the calligyrum and refringes. The immune serum and antigen of the microdentium showed a slight affinity for the mucosum but none for the pallidum, calligyrum, or refringes, while the mucosum immune serum caused a slight agglutination with many members of the other groups. Hence, it appears that the pallidum is more or less related to the calligyrum, while the affinity between the calligyrum and refringes, and possibly also between the calligyrum and mucosum in a much smaller degree, seems close. The microdentium showed the least relation to any other spirochetes. 5. Titration of agglutinins in the sera obtained 3 months after the cessation of immunization revealed that the agglutinin contents were already greatly reduced, having fallen roughly to 0.01 of the original strenght. The rates of disappearance were irregular in different animals and bore no direct relation to the initial titers. Titration made of the immune sera which had been preserved aseptically in a refrigerator (6°C.) during the same period (3 months) indicated that the original strength of these sera was reduced to about one-tenth. The agglutinins for spirochetes disappear from the rabbit's body much more rapidly than they are reduced in the separated sera by deterioration on standing at 6°C. 6. Titration of the immune sera for complement fixation power showed with a few exceptions, in which there was only slight complement binding, that the titers were high enough to indicate the presence of this principle. The anti-pallidum sera possessed higher average titers than the other immune sera tested with correspondingly homologous antigens. The least active were the anti-refrigens sera. 7. Cross titration of anti-pallidum immune sera for complement fixation showed that a given serum with a high titer for its own strain of antigen was also strong with most of the other strains of the pallidum. Instances occurred also in which the titers with heterologous pallidum antigens fell far below those of the homologous. Group reactions between the different spirochetes) such as the pallidum and the calligyrum, the calligyrum and the refringens, and the microdentium and the mucosum, were also indicated. The mucosum and the pallidum showed a slight degree of group reaction. No anti-pallidum serum fixed complement with the microdentium. 8. The immune sera were tested for their spirochetiddal properties in vitro against the correspondingly specific and heterologous varieties with and without the addition of complement. Many of the anti-pallidum sera killed their own strains. Normal rabbit serum exhibited only a slight degree of inhibition. Without complement, the immune sera caused a considerable reduction in the number or density of colonies, but not a complete suppression of growth. Complement alone had no injurious effect upon the pallidum strains. The antisera for the calligyrum, refringens, and mucosum showed feeble spirocheticidal action, while the antisera for microdentium was stronger. A syphilitic rabbit serum tested against a strain of culture pallidum gave a feeble inhibitory effect. 9. Under the influence of immune sera and complement, the spirochetes undergo within a few hours complete disintegration or granular degeneration. Without complement, they are more powerfully agglutinated, but no disintegration occurs, even after 20 hours, and complement alone has no effect. 10. In the presence of homologous immune serum and complement, the culture pallidum may be ingested by the leukocytes, but phagocytosis is slight, possibly on account of the filamentous nature of the organisms. The spirochetes in such a mixture disintegrate within a few hours, disintegration being especially rapid when the immune leukocytes are used. In the absence of immune serum, phagocytosis is not noticeable, while without complement but in the presence of immune serum and leukocytes, some phagocytosis, without subsequent lysis, occurs. A virulent strain of pallidum, obtained from syphilitic orchitis in a rabbit, exposed to agglutination, lysis, and phagocytosis by an immune serum prepared by means of culture pallidum strains, showed only slight agglutination and phagocytosis but rapid immobilization without disintegration in the presence of complement.


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