Inactivation of Hepatitis a Virus by Heat and Formaldehyde

1985 ◽  
Vol 17 (10) ◽  
pp. 43-45 ◽  
Author(s):  
B. Flehmig ◽  
A. Billing ◽  
A. Vallbracht ◽  
K. Botzenhart

The GBM strain of hepatitis A virus adapted to a fetal rhesus monkey kidney cell line (Frhk-4/R) was treated and inactivated at several different temperatures and with several different formaldehyde concentrations. Heat inactivation showed that no inactivation occurred after treatment for 60 minutes at 37°C. Treatment for 60 minutes at 50°C reduced infectivity by 1 log 10 step ; treatment for 60 minutes at 60°C, by 4 log 10 steps. Treatment for 30 minutes at 70°C resulted in complete inactivation of HAV. Complete inactivation by formaldehyde treatment was achieved only with a 0.35% concentration. Treatment with lower concentrations resulted in incomplete HAV inactivation.

2011 ◽  
Vol 3 (1) ◽  
pp. 31-34 ◽  
Author(s):  
Jennifer Harlow ◽  
Denise Oudit ◽  
Ashton Hughes ◽  
Kirsten Mattison

1987 ◽  
Vol 98 (3) ◽  
pp. 397-414 ◽  
Author(s):  
Judith Millard ◽  
Hazel Appleton ◽  
J. V. Parry

SUMMARYThe consumption of bi-valve mollusean shellfish has been associated with outbreaks of viral gastroenteritis and hepatitis A. Investigations were undertaken to determine the heat inactivation conditions necessary to render shellfish such as cockles safe for the consumer. Conditions for the laboratory maintenance of live cockles are described. In preliminary experiments either poliovirus (106TCID50/ml seawater) or hepatitis A virus (HAV) (approx. 104RFU/ml seawater) was introduced into the shellfish tank. Following 48 h filter feeding, virus was recovered from cockles using an adsorption-elution extraction procedure. Titres of virus recovered ranged from 104to 105TCID50/ml of shellfish extract for poliovirus and from 103to 105RFU/ml of shellfish extract for HAV. Active ingestion of the virus from the seawater was demonstrated by recovering virus from within cockle guts. To quantify recovered HAV, end-point dilutions and an adaptation of a radioimmunofocus assay (RIFA) were compared. The tests were of similar sensitivity but the RIFA has the advantage of being relatively rapid, shortening the time taken to complete an experiment by as much as 4 weeks.


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