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논문 기본 정보

자료유형
학술저널
저자정보
Hae-Jin Sohn (Graduate School of Ajou University) Heekyoung Kang (Graduate School of Ajou University) Ga-Eun Seo (Graduate School of Ajou University) Jong-Hyun Kim (Gyeongsang National University) Suk-Yul Jung (Namseoul University) Ho-Joon Shin (Graduate School of Ajou University)
저널정보
대한기생충학열대의학회 Parasites, Hosts and Diseases The Korean Journal of Parasitology Vol.55 No.3
발행연도
2017.6
수록면
233 - 238 (6page)

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초록· 키워드

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Pathogenic Naegleria fowleri, Acanthamoeba castellanii, and Acanthamoeba polyphaga, are distributed world¬wide. They are causative agents of primary amoebic meningoencephalitis or acanthamoebic keratitis in humans, respec¬tively. Trophozoites encyst in unfavorable environments, such as exhausted food supply and desiccation. Until recently, the method of N. fowleri encystation used solid non-nutrient agar medium supplemented with heat-inactivated Esche¬richia coli; however, for the amoebic encystment of Acanthamoeba spp., a defined, slightly modified liquid media is used. In this study, in order to generate pure N. fowleri cysts, a liquid encystment medium (buffer 1) modified from Page’s amoeba saline was applied for encystation of N. fowleri. N. fowleri cysts were well induced after 24 hr with the above de¬fined liquid encystment medium (buffer 1). This was confirmed by observation of a high expression of differential mRNA of nfa1 and actin genes in trophozoites. Thus, this liquid medium can replace the earlier non-nutrient agar medium for ob¬taining pure N. fowleri cysts. In addition, for cyst formation of Acanthamoeba spp., buffer 2 (adjusted to pH 9.0) was the more efficient medium. To summarize, these liquid encystment media may be useful for further studies which require axenic and pure amoebic cysts.

목차

Abstract
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
ACKNOWLEDGMENT
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2018-513-001176815