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Varroa mite DNA and RNA libraries were created and sequenced for ethanol preserved samples, 15 and 21 days post-treatment. All DNA sequences mapped to the V. destructor genome at above 95% on average, while RNA sequences mapped to V. destructor, but also sometimes to high levels of the deformed-wing virus and to various organisms. \nConclusions Ethanolic preservation of field-collected mites is inexpensive and simple, and allows them to be shipped and processed successfully in the lab for a wide variety of sequencing applications. 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  1. 学術雑誌論文
  2. ミケェエブユニット

A toolkit for studying Varroa genomics and transcriptomics: preservation, extraction, and sequencing library preparation

https://oist.repo.nii.ac.jp/records/1954
https://oist.repo.nii.ac.jp/records/1954
d43711a5-6606-4944-a904-013159d6c1b8
名前 / ファイル ライセンス アクション
Hasegawa-2021-A Hasegawa-2021-A toolkit for studying Varroa ge (2.4 MB)
Creative Commons Attribution 4.0 International(https://creativecommons.org/licenses/by/4.0/)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2021-03-02
タイトル
言語 en
タイトル A toolkit for studying Varroa genomics and transcriptomics: preservation, extraction, and sequencing library preparation
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者(英) Hasegawa, Nonno

× Hasegawa, Nonno

WEKO 12844

Hasegawa, Nonno

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Techer, Maeva

× Techer, Maeva

WEKO 12845

Techer, Maeva

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Mikheyev, Alexander S.

× Mikheyev, Alexander S.

WEKO 12846

Mikheyev, Alexander S.

Search repository
書誌情報 en : BMC Genomics

巻 22, 号 1, p. 54, 発行日 2021-01-14
抄録
内容記述タイプ Other
内容記述 Background The honey bee parasite, Varroa destructor, is a leading cause of honey bee population declines. In addition to being an obligate ectoparasitic mite, Varroa carries several viruses that infect honey bees and act as the proximal cause of colony collapses. Nevertheless, until recently, studies of Varroa have been limited by the paucity of genomic tools. Lab- and field-based methods exploiting such methods are still nascent. This study developed a set of methods for preserving Varroa DNA and RNA from the field to the lab and processing them into sequencing libraries. We performed preservation experiments in which Varroa mites were immersed in TRIzol, RNAlater, and absolute ethanol for preservation periods up to 21 days post-treatment to assess DNA and RNA integrity.
Results For both DNA and RNA, mites preserved in TRIzol and RNAlater at room temperature degraded within 10 days post-treatment. Mites preserved in ethanol at room temperature and 4 degrees C remained intact through 21 days. Varroa mite DNA and RNA libraries were created and sequenced for ethanol preserved samples, 15 and 21 days post-treatment. All DNA sequences mapped to the V. destructor genome at above 95% on average, while RNA sequences mapped to V. destructor, but also sometimes to high levels of the deformed-wing virus and to various organisms.
Conclusions Ethanolic preservation of field-collected mites is inexpensive and simple, and allows them to be shipped and processed successfully in the lab for a wide variety of sequencing applications. It appears to preserve RNA from both Varroa and at least some of the viruses it vectors.
出版者
出版者 BMC
ISSN
収録物識別子タイプ ISSN
収録物識別子 1471-2164
PubMed番号
関連タイプ isIdenticalTo
識別子タイプ PMID
関連識別子 info:pmid/33446105
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 info:doi/10.1186/s12864-020-07363-7
権利
権利情報 © 2020 The Author(s).
関連サイト
識別子タイプ URI
関連識別子 https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-020-07363-7
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
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