Passage and Adaptation of Maaji Virus in Hamster

Maaji Virus의 Hamster 계대 및 적응

  • Kim, Yun-Cheol (Central Research Institute, Boryung Parmaceutical Co., Ltd.) ;
  • Paik, Woo-Hyun (Central Research Institute, Boryung Parmaceutical Co., Ltd.) ;
  • Lee, Pyung-Woo (Department of Microbiology College of Medicine, Institute for Viral Diseases, Korea University)
  • 김윤철 (보령종합연구소 생명공학연구센터) ;
  • 백우현 (보령종합연구소 생명공학연구센터) ;
  • 이평우 (고려대학교 의과대학 미생물학교실, 고려대학교 바이러스병연구소)
  • Published : 1996.06.30

Abstract

The methods that make Hantavirus grow consist of inoculation into the experimental animals and cultured cells. The cultured cells, such as Vero-E6 and A549 cells, have been usually used for isolation of the virus and the animals, such as mice and rats, are used for large scale preparation of the virus so far. Furthermore, the cell can be used to maintain the virus and assay the infectivity and the animals can be used for the experiment of viral pathogenicity and challenge for assessment of vaccine. Apodemus mice, the own natural host of the virus, has been used for challenge test of Hantaan virus. However it has been pointed out to difficult handling and breeding the animal in laboratory. Therefore, we attempted to establish a new animal model for challenge test at the time of isolation of Maaji virus which is a new hantavirus similar but distinct to Hantaan virus. In suckling hamster, the titer of Maaji virus and the lethality to mice of the virus were increased gradually in the titer and lethality through passage by intracerebral (IC) inoculation. We tried to re-adapt this brain virus to lung of weanling hamster. The brain passaged virus was inoculated into weanling hamster intramuscularly. Again, the titer of the virus in lung was also increased by continuous passage of this virus. This facts could regarded as adaptation to new environment in which the virus proliferates. To identity the virus passaged in hamster with Maaji virus, both of the virus passaged in hamster brain and lung were compared with Maaji virus (MAA-I) and Hantaan virus (HTN 76-118) by means of restriction fragment length polymorphism (RFLP) and slingle strand conformation polymophism (SSCP). As a result, we conclude that Maaji virus could be adapted successfully to weanling hamster through this passage strategy. Utilizing this adapted Maaji virus strain, hamster model is able to be used for challenge test in hantaviral vaccinology and further experiments utilizing hamster system as a rather available and convenient lab animal are expected.

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