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Persiste Enfekte Buzağıların İnaktive Edilmiş Serumlarından Bovine Viral Diyare Virusu İzolasyonu

Bovine Viral Diarrhea Virus Propagates in Cell Culture after Inoculation of Inactivated Sera from Persistently Infected Calves

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Abstract (2. Language): 
During routine diagnostic investigations on submitted serum and swab samples from three (n:3) cal-ves in our laboratory for detecting BVDV antibody titers and antigen we noticed that successful virus propaga-tion can occur from heat inactivated (in a water bath at 56° C for 30 min) 2 serum samples. For further confirma-tion of virus propagation in heat inactivated serum samples, 11 sera which were previously detected positive for BVDV were also investigated. As a result, from a total of 14 heat inactivated-field originated sera samples virus propagation was confirmed in 4 (28.5%) samples. This result suggests that heat inactivation of the serum is not eliminating the risk of pestivirus contamination, thus interfere the results of virus isolation and serological diag-nostic methods including serum neutralization. Moreover relative resistance of BVDV to heat inactivation may lead to failure in complete inactivation of the virus in fetal calf sera which is an important contaminant for biolo-gicals like cell cultures and attenuated live vaccines.
Abstract (Original Language): 
Rutin laboratuvar çalışmaları doğrultusunda BVDV antikor ve antijen taraması istenen üç adet (n:3) buza-ğıya ait serum ve svab örneklerinin incelenmesi sırasında serum örnekleri su banyosunda 56° C’de 30 dakika süresince ısı inaktivasyonu tabi tutulmuş ancak 2 adet serum örneğinde virus çoğalmasının gerçekleştiği görül-müştür. Serumların ısı ile inaktive edilmelerine rağmen hücre kültüründe virus üremesinin gerçekleşmesini araş-tırmak amacıyla daha önceden BVDV pozitif olduğu bilinen 11 adet serum örneği de incelemeye alınmıştır. Sonuç olarak ısı inaktivasyonuna tabi tutulmuş saha menşeli 14 adet serum örneğinin 4 adedinde (%28,5) virus çoğalması tespit edilmiştir. Elde edilen bu veri serum inaktivasyon prosedürünün pestivirus kontaminasyonunu elimine etmede yetersiz kaldığını göstermiştir. Bu durum virus izolasyonu ve serolojik teşhis yöntemlerinin sonuçlarını olumsuz etkileyebilir. Ayrıca BVD virusunun ısı inaktivasyonuna karşı direnci, fötal dana serumla-rında bulunabilen virusun tamamen inaktive olmasını engelleyebilmektedir. Buna bağlı olarak BVDV, hücre kültürü ve atenüe canlı aşı gibi biyolojik maddeler için ciddi risk haline gelmektedir.
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