scholarly journals INTERACTION OF DIPHTHERIA TOXIN WITH CELL CULTURES FROM SUSCEPTIBLE AND RESISTANT ANIMALS

1966 ◽  
Vol 123 (4) ◽  
pp. 723-732 ◽  
Author(s):  
Janis Gabliks ◽  
Marcia Falconer

The cytotoxicity (TD) level of diphtheria toxin for human Chang liver strain was 0.1 guinea pig MLD per ml; for mouse liver NCTC 1469 strain, the TD was 500 MLD per ml. The results of cell culture toxicity correlated well with relative susceptibility of both man and mouse. The initial effects of toxin on the susceptible Chang liver cells were studied at one half the TD level (0.05 MLD per ml). At this low concentration of toxin, the number of cells per culture was reduced slightly below the "0" hr values, whereas the amounts of cell protein, RNA, and DNA were increased. Analysis of the toxin-treated cells indicated an enlargement of the cells. The individual cells contained significantly more protein, RNA, and DNA than the control cells and the cell volume was increased 1.9 times. When purified diphtheria toxin was incubated with the susceptible Chang liver cells and then tested for its biological activity, the results showed an increased diffusion rate in parabiotic culture chambers and definite cytotoxicity to the normally resistant mouse liver cells. The cytotoxicity was neutralizable with antitoxin. The results suggest that the toxin-susceptible cells transform the toxin molecule to a more active derivative which affects the highly resistant mouse liver cell.

2005 ◽  
Vol 79 (5) ◽  
pp. 2950-2955 ◽  
Author(s):  
Dino A. Feigelstock ◽  
Peter Thompson ◽  
Gerardo G. Kaplan

ABSTRACT Hepatitis A virus (HAV) has been adapted to grow efficiently in primate and some nonprimate cell lines but not in cells of murine origin. To understand the inability of the virus to grow in mouse cells, we studied the replication of HAV in immortalized and nontransformed MMH-D3 mouse liver cells, which require growth factors and collagen to maintain their phenotype. HAV grew in MMH-D3 cells transfected with virion RNA but not in those infected with viral particles, indicating a cell entry block for HAV. However, MMH-D3 cells cultured under suboptimal conditions in the absence of growth factors acquired susceptibility to HAV infection. Serial passages of the virus in MMH-D3 cells under suboptimal growth conditions resulted in the selection of HAV variants that grew efficiently in MMH-D3 cells cultured under both optimal and suboptimal conditions. Nucleotide sequence analysis of the MMH-D3 cell-adapted HAV revealed that N1237D and D2132G substitutions were present in the capsid regions of six viral clones. These two mutations are most likely located on the surface of the virion and may play a role in the entry of HAV into the mouse liver cells. Our results demonstrate that mouse hepatocyte-like cells code for all factors required for the efficient growth of HAV in cell culture.


1977 ◽  
Vol 252 (24) ◽  
pp. 8975-8980 ◽  
Author(s):  
G.J. Schroepfer ◽  
E.J. Parish ◽  
H.W. Chen ◽  
A.A. Kandutsch

2001 ◽  
Vol 532 (3) ◽  
pp. 661-672 ◽  
Author(s):  
Robert Wondergem ◽  
Wei Gong ◽  
Scott H. Monen ◽  
Sean N. Dooley ◽  
Joel L. Gonce ◽  
...  

1992 ◽  
Vol 64-65 ◽  
pp. 581-587 ◽  
Author(s):  
Andrew W. Harman ◽  
Gregory M. Adamson ◽  
Scott G. Shaw

1993 ◽  
Vol 14 (7) ◽  
pp. 1457-1463 ◽  
Author(s):  
Yi Sun ◽  
Larry W. Oberley ◽  
Terry D. Oberley ◽  
James H. Elwell ◽  
Elaine Sierra-Rivera

Author(s):  
Håvard Danielsen ◽  
Mette Lier ◽  
Anton Brøgger ◽  
Albrecht Reith

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