scholarly journals In vitro virucidal efficacy of a dry steam disinfection system against Human Coronavirus, Human Influenza Virus and Echovirus

Author(s):  
Isabella Marchesi ◽  
Arianna Sala ◽  
Giuseppina Frezza ◽  
Stefania Paduano ◽  
Sara Turchi ◽  
...  
2020 ◽  
Vol 30 (2) ◽  
pp. 172-177 ◽  
Author(s):  
Minjee Kim ◽  
Dinh-Van Nguyen ◽  
Yoonki Heo ◽  
Ki Hoon Park ◽  
Hyun-Dong Paik ◽  
...  

1937 ◽  
Vol 65 (6) ◽  
pp. 861-872 ◽  
Author(s):  
T. P. Magill ◽  
Thomas Francis

Studies have been conducted on the effect of immune serum upon a strain of human influenza virus (PR8) grown in chick embryo tissue culture medium. The results have demonstrated (a) that when cells are exposed to the action of immune serum of high titer and subsequently washed freely, these cells support the growth of virus as well as cells treated with normal serum; (b) that, in agreement with the results of other workers, when virus is added to cell suspensions before the addition of immune serum of low titer, virus survives in the cells; (c) that when mixtures of immune serum of low titer and virus are added to cells, there is little evidence of survival or multiplication of the virus. Furthermore, when immune serum of high titer is used the virus is inactivated regardless of whether the cells are first exposed to virus or immune serum. Finally, virus mixed with a strong immune serum is inactivated in the absence of cells, as shown by the fact that centrifugation at high speeds of such serum-virus mixtures yields no active virus, whereas normal serum-virus mixtures yield fully active virus.


2005 ◽  
Vol 79 (13) ◽  
pp. 8431-8439 ◽  
Author(s):  
Michelle Quinlivan ◽  
Dmitriy Zamarin ◽  
Adolfo García-Sastre ◽  
Ann Cullinane ◽  
Thomas Chambers ◽  
...  

ABSTRACT Equine influenza is a common disease of the horse, causing significant morbidity worldwide. Here we describe the establishment of a plasmid-based reverse genetics system for equine influenza virus. Utilizing this system, we generated three mutant viruses encoding carboxy-terminally truncated NS1 proteins. We have previously shown that a recombinant human influenza virus lacking the NS1 gene (delNS1) could only replicate in interferon (IFN)-incompetent systems, suggesting that the NS1 protein is responsible for IFN antagonist activity. Contrary to previous findings with human influenza virus, we found that in the case of equine influenza virus, the length of the NS1 protein did not correlate with the level of attenuation of that virus. With equine influenza virus, the mutant virus with the shortest NS1 protein turned out to be the least attenuated. We speculate that the basis for attenuation of the equine NS1 mutant viruses generated is related to their level of NS1 protein expression. Our findings show that the recombinant mutant viruses are impaired in their ability to inhibit IFN production in vitro and they do not replicate as efficiently as the parental recombinant strain in embryonated hen eggs, in MDCK cells, or in vivo in a mouse model. Therefore, these attenuated mutant NS1 viruses may have potential as candidates for a live equine influenza vaccine.


2011 ◽  
Vol 44 (13) ◽  
pp. S351
Author(s):  
Mohammad Derakhshan ◽  
Saeed Niazmand ◽  
Ali Sadeghian ◽  
Rahim Rezaee ◽  
Mehrangiz Khajakaramodin ◽  
...  

1936 ◽  
Vol 63 (6) ◽  
pp. 803-811 ◽  
Author(s):  
T. P. Magill ◽  
Thomas Francis

The in vitro cultivation of strains of human influenza virus has been successfully conducted through a prolonged series of successive transfers. The cultivated virus has retained the antigenic and immunological properties which characterized the animal passage virus from which it was derived. The culture virus is still virulent for mice and ferrets; it is capable of inducing an active state of immunity in animals vaccinated subcutaneously or intraperitoneally; it elicits specific neutralizing antibodies in the serum of infected or vaccinated animals. The virus has been successfully cultivated to date only in the presence of oxygen; when conditions of reduced oxygenation are imposed by the use of vaseline seal, with or without the addition of cystein, multiplication of the virus is not supported. On the other hand, it has been possible to cultivate the virus in the medium of Li and Rivers in ordinary test tubes. This affords a greatly simplified procedure, since the interval between transfers may be prolonged. The results of neutralization tests with various sera and the culture virus are presented and discussed.


1970 ◽  
Vol 32 (2-3) ◽  
pp. 286-290 ◽  
Author(s):  
K. F. Shortridge ◽  
G. Belyavin ◽  
D. E. Bidwell

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