Factors Influencing Host-Virus Interactions. II. Alteration of Coxsackie Virus Infection in Adult Mice by Cold.

1956 ◽  
Vol 93 (2) ◽  
pp. 273-277 ◽  
Author(s):  
W. D. Boring ◽  
G. M. Z. Rhein ◽  
D. L. Walker
1955 ◽  
Vol 102 (6) ◽  
pp. 753-766 ◽  
Author(s):  
William D. Boring ◽  
D. Murray Angevine ◽  
Duard L. Walker

A study was made of the pathogenesis of infection due to the Conn.-5 strain of Coxsackie virus in 4 to 5 day old infant mice, untreated adult mice, and adult mice treated with cortisone. The quantitative distribution of virus and the evolution of lesions in different tissues were followed for the first 7 days of the infection. Virus dissemination was prompt and widespread via the blood in all groups. In 4 to 5 day old infant mice viral multiplication and cellular injury occurred in many organs and tissues, while in untreated adult mice these processes were largely limited to the pancreas, even though infecting virus appeared to be equally available to other tissues from the blood. Treatment of adult mice with a single injection of 2.5 mg. cortisone resulted in viral multiplication and tissue damage in several sites in addition to the pancreas, the most marked occurring in the liver and heart. In a consideration of possible mechanisms involved, it was thought unlikely that the differences in the course of the disease in the three groups could be attributed solely to differences in the specific immune response. It is suggested that developmental changes in cells and tissues, perhaps related to cellular metabolism and alterable by cortisone administration, are the major factors determining the location and extent of viral multiplication and tissue injury in this infection in mice.


1951 ◽  
Vol 93 (3) ◽  
pp. 247-266 ◽  
Author(s):  
Joseph L. Melnick ◽  
Gabriel C. Godman

The quantitative distribution of the Conn.-5 strain of Coxsackie virus in different tissues was determined by serial titration at intervals after inoculation of 4 to 5 day old mice. High titers were reached by the 2nd day in blood, heart, liver, muscle, intestine, and its contents, and these were maintained through the 8th day, except for the blood, in which the virus level fell earlier. In paralyzed mice, muscle and brain attained the highest titers and it was in these tissues alone that virus persisted through the 9th day of illness. The pathology of the infection has been briefly described. In particular, the evolution of morbid changes in striated muscle was correlated with the concentrations of virus in muscle. Acute muscle necrosis first occurred when there was a peak viral concentration (4th day), and reached maximal intensity on the 8th day. Scattered acute lesions continued to appear while the virus titer remained above 10–4, from the 9th to 12th day. With the decrease in the myositis, there was a concomitant decrease in the incidence of perceptible disease. Inflammation was found to follow upon the development of necrosis, and subsided slowly. Regeneration began very early, became exuberant, and led finally to restitution of the muscle.


Thorax ◽  
1970 ◽  
Vol 25 (5) ◽  
pp. 624-626 ◽  
Author(s):  
J. D. Matthews ◽  
S. J. Cameron ◽  
M. George

1954 ◽  
Vol 99 (1) ◽  
pp. 21-27 ◽  
Author(s):  
Gilbert Dalldorf ◽  
Rebecca Gifford

Gravid mice become progressively more susceptible to infection with the pancreatic line of Group B-1 Coxsackie virus during the last week of pregnancy. A Group A-8 strain did not have such an effect. The young that survive despite the fact that their mothers are infected with a B-1 strain appear to be normal in the gross and microscopically, to grow at the usual rate, to be free of demonstrable virus, and to be susceptible on challenge with a homologous strain.


2016 ◽  
Vol 11 (5) ◽  
pp. 1871-1874
Author(s):  
XUEJING ZHU ◽  
HONG LIU ◽  
SHUGUANG YUAN ◽  
XIANGQING XU ◽  
ZHEN DONG ◽  
...  

2008 ◽  
Vol 197 (11) ◽  
pp. 1558-1566 ◽  
Author(s):  
M. Danta ◽  
N. Semmo ◽  
P. Fabris ◽  
D. Brown ◽  
O. G. Pybus ◽  
...  

2001 ◽  
Vol 98 (6) ◽  
pp. 1019-1026 ◽  
Author(s):  
Elizabeth Euscher ◽  
Jonathan Davis ◽  
Ian Holzman ◽  
Gerard J. Nuovo

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