| ID | 69756 |
| FullText URL | |
| Author |
Ohara, Sakiko
Department of Oral Microbiology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Sheng, Yijuan
Department of Oral Microbiology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Nishiya, Yuki
Department of Oral Microbiology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Tosa, Ikue
Department of Oral Microbiology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Takebe, Katsuki
Department of Dental Pharmacology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Arimura, Yuki
Department of Oral and Maxillofacial Reconstructive Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Mese, Hiroshi
Department of Dentistry and Oral Surgery, Fukuyama City Hospital
Ohara, Naoko
Department of Operative Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Ohara, Naoya
Department of Oral Microbiology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Kaken ID
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| Abstract | Objectives: Genetic manipulation tools are essential for elucidating the pathogenic mechanisms of microorganisms. Several species of Actinomyces, including A. israelii, are present in the oral cavity and they are the causative agents of actinomycosis. However, efficient gene-editing tools for these species have not yet been developed. In this study, the aim was to evaluate the introduction of foreign genes into Actinomyces using plasmids derived from Mycobacterium, which belong to the same class as Actinomycetes.
Methods: A truncated derivative of pYT923, pYT923S, which contains the replication origin of the M. scrofulaceum plasmid pMSC262 was constructed and introduced into A. israelii by electrotransformation. Results: pYT923S was successfully introduced into A. israelii. The transformation efficiency of A. israelii was approximately 7–66 CFU/μg of DNA, and all transformed colonies harbored pYT923S. The plasmid recovered from A. israelii replicated in Escherichia coli. Conclusions: pYT923S was introduced into and maintained within A. israelii. Therefore, the pYT923S vector represents a useful genetic tool for Actinomyces and it is expected to facilitate future studies on the biology and pathogenicity of Actinomyces. |
| Keywords | Actinomyces
Plasmid
Shuttle vector
Transformation
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| Published Date | 2026-02
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| Publication Title |
Journal of Oral Biosciences
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| Volume | volume68
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| Issue | issue1
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| Publisher | Elsevier BV
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| Start Page | 100718
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| ISSN | 1349-0079
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| NCID | AA11896386
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| Content Type |
Journal Article
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| language |
English
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| OAI-PMH Set |
岡山大学
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| Copyright Holders | © 2025 Japanese Association for Oral Biology.
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| File Version | publisher
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| DOI | |
| Related Url | isVersionOf https://doi.org/10.1016/j.job.2025.100718
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| License | http://creativecommons.org/licenses/by-nc-nd/4.0/
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| 助成情報 |
23K09459:
細菌の酵素反応を基盤とした根面う蝕管理法の開発 研究課題
( 独立行政法人日本学術振興会 / Japan Society for the Promotion of Science )
24K02614:
歯周病細菌主要病原因子ジンジパインの宿主直接作用と必須新奇オペロンの解明
( 独立行政法人日本学術振興会 / Japan Society for the Promotion of Science )
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