Effect of Subcutaneous Injection of Ginseng on Cows with Subclinical Staphylococcus aureus Mastitis

2008 ◽  
Vol 48 (7) ◽  
pp. 519-528 ◽  
Author(s):  
S. Hu ◽  
C. Concha ◽  
A. Johannisson ◽  
G. Meglia ◽  
K. P. Waller
2001 ◽  
Vol 48 (7) ◽  
pp. 519-528 ◽  
Author(s):  
S. Hu ◽  
C. Concha ◽  
A. Johannisson ◽  
G. Meglia ◽  
K. P. Waller

Thorax ◽  
2013 ◽  
Vol 68 (Suppl 3) ◽  
pp. A140.2-A140
Author(s):  
AAR Thompson ◽  
HM Marriott ◽  
L Williams ◽  
G Shaw ◽  
A Hameed ◽  
...  

1928 ◽  
Vol 47 (5) ◽  
pp. 663-675 ◽  
Author(s):  
S. O. Freedlander ◽  
J. A. Toomey

1. Plain broth is just as effective as specific broth filtrate if used as a skin compress for the protection of guinea pigs against a subcutaneous injection of Staphylococcus aureus. 2. Plain broth compresses applied for 48 hours previous to bacterial injection sometimes prevent the death of the animal and practically always alter the inflammatory reactions. 3. This protection is not specific and is localized to the area "compressed." 4. The protection lasts at least 24 hours after removal of the compress. 5. Broth compresses applied to the abdominal wall of a guinea pig for 48 hours produced definite histological changes, especially in the subcutis, i.e., edema, proliferation of clasmatocytes, thickening of the epidermis together with a moderate exudation of polymorphonuclears and small mononuclear cells. 6. The histological response to the subcutaneous injection of staphylococci was different in the control and the broth-prepared animal. 7. In the broth-prepared animal, there was an increase in clasmatocytes and fibroblasts with a dense exudation of polymorphonuclears, which latter, in the main, did not degenerate. The clasmatocytes phagocyted bacteria early and later engulfed the polymorphonuclears, while the fibroblasts rapidly walled off the lesion. The result was a localized abscess which either came to the surface and ruptured or was absorbed and organized.


1991 ◽  
Vol 106 (2) ◽  
pp. 311-317 ◽  
Author(s):  
G. R. Smith ◽  
S. A. Barton ◽  
L. M. Wallace

SUMMARYThe isolation of Fusobacterium necrophorum present in small numbers in heavily contaminated material such as faeces or soil is hampered by the lack of an efficient selective medium and by the high minimum infective dose of the organism. A sensitive method for the detection and isolation of faecal strains of F. necrophorum type A was based on the subcutaneous injection of faeces, suspended (5% w/v) in broth culture of Actinomyces (Corynebacterium) pyogenes or Staphylococcus aureus to increase fusobacterial infectivity, into mice pretreated with clostridial antitoxins. When necrobacillosis developed F. necrophorum was identified microscopically in tissue from the advancing edge of the lesion and isolated on a partly selective medium.The enhancement of fusobacterial infectivity produced by A. pyogenes and by S. aureus was high, but the latter was slightly the more efficient, enabling as few as 80 F. necrophorum organisms/g of faeces to be detected.Use of the method showed that 3 of 16 wallabies had F. necrophorum in their faeces at the time of examination. Numerous epidemiological applications are suggested.


Author(s):  
Masaatsu Koike ◽  
Koichi Nakashima ◽  
Kyoko Iida

Penicillin exerts the activity to inhibit the peptide cross linkage between each polysaccharide backbone at the final stage of wall-peptidoglycan biosynthesis of bacteria. Morphologically, alterations of the septal wall and mesosome in gram-positive bacteria, which were occurred in early time after treatment with penicillin, have been observed. In this experiment, these alterations were cytochemically investigated by means of silver-methenamine staining after periodate oxidation, which is applied for detection of localization of wall mucopolysaccharide.Staphylococcus aureus strain 209P treated with 100 u/ml of penicillin G was divided into two aliquotes. One was fixed by Kellenberger-Ryter's OSO4 fixative at 30, 60 and 120 min after addition of the antibiotic, dehydrated through alcohol series, and embedded in Epon 812 (Specimen A). The other was fixed by 21 glutaraldehyde, dehydrated through glycolmethacrylate series and embedded in glycolmethacrylate mixture, according to Bernhard's method (Specimen B).


Author(s):  
Margaret Hukee

Gold labeling of two antigens (double labeling) is often done on two section surfaces separated by section thickness. Whether labeling is done on both sides of the same section or on two parallel surfaces separated by section thickness (PSSST), comparable results are dependent on an equal number of epitopes being exposed at each surface. We propose a method to study protein labeling within the same field of proteins, by examining two directly adjacent surfaces that were split during sectioning. The number of labeling sites on adjacent surfaces (AS) were compared to sites on PSSST surfaces in individual bacteria.Since each bacteria needed to be recognizable in all three section surfaces, one-hole grids were used for labeling. One-hole grids require a supporting membrane and excessive handling during labeling often ruptures the membrane. To minimize handling, a labeling chamber was designed that is inexpensive, disposable, minimizes contamination, and uses a minimal amount of solution.


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