scholarly journals Experimental Feeding of Fusarium Moniliforme Culture Material Containing Fumonisin B1 to Channel Catfish, Ictalurus Punctatus

1994 ◽  
Vol 6 (1) ◽  
pp. 123-124 ◽  
Author(s):  
David W. Brown ◽  
C. Pat McCoy ◽  
George E. Rottinghaus
2008 ◽  
Vol 51 (2) ◽  
pp. 333-344 ◽  
Author(s):  
Rejane Maria Cirra Scaff ◽  
Vildes Maria Scussel

The histopathological effects of fumonisin B1 (FB1) injected intraperitoneally (IP), was evaluated in catfish (Ictalurus punctatus). Fishes were divided into four Groups. Groups II, III and IV were treated IP with FB1 injections of 1; 5 and 10 mg/kg bw/day, respectively, during 21 days. At the 7th, 14th and 21st day, fishes were sacrificed. The livers were hystologicaly analysed by the light and transmission electronic microscopy. Livers from the 7th day showed organelles alterations, particularly in the granular endoplasmatic reticle, mitochondria, nucleus and nucleolus mediated by FB1 doses. The occurrence of processes involved in the necrosis and apoptosis was detected. At the highest FB1 dose,the livers presented an intense response with an accentuate tissue disorganization, absence of cell limits and intense cytoplasm vacuolization. The image analysis showed the occurrence of necrosis in some areas, characterized by fully broken or swollen cells. The apoptosis was observed as the cytoplasm contraction and the chromatin formed masses concentrated in the edge of the nucleus. There was strong evidence that the numerous hepatocytes in the liver from the fishes under the toxic dose of FBs were selectively removed by the apoptosis process.


1995 ◽  
Vol 74 (2) ◽  
pp. 306-313 ◽  
Author(s):  
L.F. KUBENA ◽  
T.S. EDRINGTON ◽  
C. KAMPS-HOLTZAPPLE ◽  
R.B. HARVEY ◽  
M.H. ELISSALDE ◽  
...  

1993 ◽  
Vol 72 (3) ◽  
pp. 456-466 ◽  
Author(s):  
T.S. WEIBKING ◽  
D.R. LEDOUX ◽  
A.J. BERMUDEZ ◽  
J.R. TURK ◽  
G.E. ROTTINGHAUS ◽  
...  

1997 ◽  
Vol 76 (2) ◽  
pp. 256-264 ◽  
Author(s):  
LF Kubena ◽  
TS Edrington ◽  
RB Harvey ◽  
TD Phillips ◽  
AB Sarr ◽  
...  

1994 ◽  
Vol 77 (2) ◽  
pp. 522-525 ◽  
Author(s):  
Paul E Nelson ◽  
Jean H Juba ◽  
P Frank Ross ◽  
Larry G Rice

Abstract Fumonisins were produced by strains of Fusarium moniliforme and F. proliferatum on a medium consisting of 500 g yellow corn kernels and 500 mL distilled water added to a 30.5 × 61 cm autoclavable polyethylene bag. The corn was inoculated by drawing a suspension from a lyophilized culture into a sterile 5 mL syringe fitted with a 19 gauge needle and injecting 1 mL through the side of each polyethylene culture bag. Bags of inoculated com were incubated in the dark at 20° to 22°C for 4 weeks. Seven to 8 days after inoculation, holes were punched near the tops of the bags to promote aeration. After a 4 week incubation, cultures were soaked in chloroform–acetone (50 + 50, v/v) in 4 L flasks overnight to kill fungus and to remove water. Next, the culture media was filtered through 2 mm nylon mesh screens and air dried from 24 to 48 h. Fumonisin concentrations were determined by liquid chromatography/o-phthalaldialdehyde fluorescence. Confirmation was by gas chromatography/mass spectrometry. We observed that the 3 most important factors in the production of fumonisins in bulk corn cultures were temperature control, moisture, and aeration. Extraction by acetonitrile–water (50 + 50, v/v) for 30 min produced the highest yields of fumonisins. Measurable concentrations were reduced by as much as 50% when culture material was heated at 50°C overnight. Fusarium moniliforme strains consistently produced fumonisin B1 as the major component, but some strains of F. proliferatum produced fumonisin B2 and/or fumonisin B3 at higher concentrations than fumonisin B1. Results were calculated on the basis of dried culture material.


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