Effusions and Peritoneal Washings

2018 ◽  
pp. 71-71
Author(s):  
Fang Fan
Keyword(s):  
2006 ◽  
Vol 102 (2) ◽  
pp. 315-318 ◽  
Author(s):  
Ram Eitan ◽  
Robert Soslow ◽  
Oscar Lin ◽  
Noah D. Kauff ◽  
Lisa Liu ◽  
...  

1985 ◽  
Vol 18 (4) ◽  
pp. 251-255 ◽  
Author(s):  
A. L. Melo ◽  
L.H. Pereira

To study the cercaria-schistosomulum transformation in vivo, underthe influence of an antischistosomal compound (oxamniquine), a model using cercarial infections into the abdominal cavity of mice was chosen. This procedure provided easy and reproducible recoveries of larvae from peritoneal washings with appropriate solutions for a long time (30 to 180 min) after inoculation. The results show that high doses of oxamniquine (given intramuscularly one hour before the infection) produce a marked delay in the kinetics of the cercaria-schistosomulum transformation. Cercariae, tail-less cercarial bodies and schistosomula were recovered from the peritoneal cavity ofdrug treated mice in numbers significantly different from those recovered from untreated mice.


1941 ◽  
Vol 73 (5) ◽  
pp. 669-680
Author(s):  
P. Y. Liu ◽  
John C. Snyder ◽  
John F. Enders

A fatal infection of irradiated white mice with the Breinl strain of European typhus has been established and passed serially for 22 passages by the intra-abdominal route. Rickettsiae were abundant and easily demonstrable in the moribund or dead mice. The mortality of irradiated mice infected with passage material (peritoneal washings or blood) was nearly 100 per cent as contrasted to no mortality in the control mice given the same dose of x-ray (450 R) and the same volume of fluid intra-abdominally. (The observation period of control mice was arbitrarily limited to 14 days.) After eighteen passages in irradiated mice no increase in virulence for non-irradiated adult mice was detected. After passage in guinea pigs, the rickettsial infection deriving from the mouse passage material was identical with the Breinl strain as judged by fever, cross immunity tests, and brain lesions in sections.


1912 ◽  
Vol 16 (5) ◽  
pp. 644-664 ◽  
Author(s):  
Rufus Cole

1. The filtered blood serum of rabbits infected with pneumococci is not toxic. 2. Extracts of pneumococci prepared by keeping emulsions of the bacteria in salt solution at 37° C. for varying periods of time may be toxic, and when injected intravenously into guinea pigs, may produce a train of symptoms followed by acute death resembling that seen in acute anaphylaxis. Such extracts, however, are not uniformly toxic and it has been impossible to discover the exact conditions under which such extracts become toxic. 3. When the centrifugalized peritoneal washings of guinea pigs infected with pneumococci are injected into the circulation of normal guinea pigs, these animals very frequently exhibit symptoms like those seen in acute anaphylaxis, and a considerable proportion of the animals die acutely. 4. When pneumococci are dissolved in dilute solutions of bile salts and the solution resulting is injected intravenously into rabbits and guinea pigs, these animals show with great constancy the same symptoms that are seen in acute anaphylaxis. The solution of pneumococci in bile may occur in ten minutes at 37° C. or in half an hour on ice. This is considered evidence that the toxicity of the solution does not result from digestion of the bacterial protein, but is due to substances preformed in the bacterial cells and set free on their solution. The toxicity of the solution is diminished or destroyed by heating to 55° C. or over.


1953 ◽  
Vol 98 (5) ◽  
pp. 433-440 ◽  
Author(s):  
John B. Nelson

The mortality rate for 80 Swiss weanlings infected with mouse hepatitis was 2.5 per cent in comparison with 98 per cent for 140 Princeton weanlings. In Swiss weanlings discrete lesions, which generally failed to progress, were observed in the liver from the 3rd through the 10th day after intraperitoneal injection. The causal virus was demonstrable in peritoneal washings through the 21st day and less regularly in the liver through the 14th day. It was also detectable in both loci after subcutaneous injection. Infant Swiss mice were susceptible through the 10th day of life, intraperitoneal injection being commonly followed by death. The pathogenicity and titer of the virus were significantly increased by successive passage in Swiss weanlings. The virus was detected in the blood of Swiss weanlings on subcutaneous injection only after it had been modified by passage.


1989 ◽  
Vol 30 (1) ◽  
pp. 80-80
Author(s):  
PE Schwartz ◽  
SK Chambers ◽  
JT Chambers ◽  
K Tilton ◽  
R Foemmel

1935 ◽  
Vol 35 (1) ◽  
pp. 23-37 ◽  
Author(s):  
F. Griffith

The characters of the Aronson Streptococcus from Prof. Neufeld's laboratory at the “Robert Koch” Institute in Berlin have been described. This coccus resembles the pneumococcus in many respects, viz. the appearance of the colonies on the surface of horse blood agar, its virulence and capsule production in mice and rabbits, the production of a specific precipitable substance in the peritoneal washings of infected mice, the formation of firm clumps and masses when mixed with homologous antiserum, the ease of production of active and passive immunity in mice and rabbits by intraperitoneal and intravenous inoculation, the alteration in the morphology of colonies, i.e. the appearance of R forms, associated with attenuation of virulence. It differs from the pneumococcus in the following features: the round shape of the cocci, bile-insolubility and the absence of autolysis in surface colonies, the beta haemolysis of deep colonies in horse blood agar, the production of a soluble haemolysin in broth cultures, the difficulty of producing active immunity in mice by the subcutaneous injection of heat-killed vaccines.I have obtained the Aronson Streptococcus (Neufeld type), which Lance-field places in a group containing chiefly streptococci of bovine origin, from human throats, but there was no evidence in any instance that it was producing disease, and it seems probable that it is not pathogenic for man.The results of my investigation of this strain are in agreement with those of Yoshioka (1923), Killian (1924) and Lancefield (1933, 1934).There are in existence other laboratory strains designated Aronson Streptococcus. These have been found to exhibit specific characters identifying them with the Str. pyogenes. It is proposed that the name Streptococcus Aronson should be confined to strains possessing the characters of Aronson N above described.


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