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Determination of the optimal inactivation time of FMD virus Type "A" using BEI inactivator during the outbreak 2006 in Egypt and its effect on the antigenicity of the virus [electronic resource].

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Omar, A. A

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Language: English Summary language: Arabic Description: p.1-5Other title:

تأثير المحفز المناعي مستخلص البروبيونوباكتريم والليبوبولي سكاريد لميكروب الإيشريشياكولاي (إنميونير 17.5) علي الإستجابة المناعية للأرانب المحصنة بلقاح النزف الدموى الفيروسي الأرنبي [Added title page title]

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Beni-Suef veterinary medical journal, 2007 v. 17, Special issue [electronic resource]:

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In: Beni-Suef Veterinary Medical Journal. Beni-Suef Vetrinary Medicen Journal November 2007, 5th Scientific conference 2007.v.17(Special issue)Summary: FMD virus type A/1/ Egypt 2006 was inactivated with 0.1 M of BEI (Binary ethylene imine) formed by cyclization of 2- Bromoethyl-amine hydrobromide (BEA) in 0.2 N NaOH at 37 °C with pH 8.0 for 24 h. The virus was complete inactivated after 15 h. post inactivation. No residual virus particles was detected when inoculated in tissue culture. The inactivation rates are linear with a regular loss of titer ranged from 0.5- 1.0 log10 / hour. Control sample of virus at 37 °C without BEI showed only a loss of 1.0 log from the original infectivity titer after 24 h. The sample of virus which kept at -20 °C ,without BEI , showed loss 0.3 log10 from its original infectivity titer after 24 h. There is no change in the complement fixing antigen before and after inactivation process with BEI inactivator and in the CFT ⅛ dilution of antigen was stable (fixed) pre and post inactivation of virus. Also it was found that the inactivation rate of BEI was higher than the inactivation with pure ethylenimine (EI) and formaline.

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FMD virus type A/1/ Egypt 2006 was inactivated with 0.1 M of BEI (Binary ethylene imine) formed by cyclization of 2- Bromoethyl-amine hydrobromide (BEA) in 0.2 N NaOH at 37 °C with pH 8.0 for 24 h. The virus was complete inactivated after 15 h. post inactivation. No residual virus particles was detected when inoculated in tissue culture. The inactivation rates are linear with a regular loss of titer ranged from 0.5- 1.0 log10 / hour. Control sample of virus at 37 °C without BEI showed only a loss of 1.0 log from the original infectivity titer after 24 h. The sample of virus which kept at -20 °C ,without BEI , showed loss 0.3 log10 from its original infectivity titer after 24 h. There is no change in the complement fixing antigen before and after inactivation process with BEI inactivator and in the CFT ⅛ dilution of antigen was stable (fixed) pre and post inactivation of virus. Also it was found that the inactivation rate of BEI was higher than the inactivation with pure ethylenimine (EI) and formaline.

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