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논문 기본 정보

자료유형
학술저널
저자정보
A Tai Truong (Kyonggi University) Jung Min Kim (Kyonggi University) Su Jin Lim (Kyonggi University) Mi Sun Yoo (Animal and Plant Quarantine Agency) Yun Sang Cho (Animal and Plant Quarantine Agency) Byoung Su Yoon (Kyonggi University)
저널정보
한국양봉학회 Journal of Apiculture Journal of Apiculture Vol.33 No.2
발행연도
2018.6
수록면
83 - 98 (16page)
DOI
10.17519/apiculture.2018.06.33.2.83

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초록· 키워드

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Sacbrood virus (SBV) is one of the main honeybee pathogens. It has been detected worldwide. Five genotypes of SBV were proposed based on the analysis of coding DNA sequences (CDSs) and deduced amino acids. However, a reliable tool to examine each SBV-genotype has not been developed yet. To establish a PCR system for SBV-genotyping, designation of specific primer-pairs and construction of standard DNAs for 5 genotypes were carried out. The detection system for SBVgenotypes was optimized using each standard DNA and specific primer-pairs. Then PCR system for SBV-genotyping was applied with SBV-infected honeybee samples. Interestingly, in some of SBVinfected Apis mellifera, 2134D51 genotype (kSBV) and 2100D0 genotype (wSBV) were both detected, however, 2100D0 was existed dominantly. Whereas, 2100D0 was not detected from SBVinfected samples of Apis cerana, only 2134D51 was identified as solo pathogen in this species. PCR system for SBV-genotyping might be helpful to understand SBV-distribution and spreading.

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Abstract
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
LITERATURE CITED

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UCI(KEPA) : I410-ECN-0101-2018-527-003142853