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TP114 型 Incl conjugative 质粒能够在小鼠肠道微生物群中实现高效的基因转移。

Highly efficient gene transfer in the mouse gut microbiota is enabled by the Incl conjugative plasmid TP114.

机构信息

Département de biologie, Université de Sherbrooke, Sherbrooke, QC, J1K 2R1, Canada.

出版信息

Commun Biol. 2020 Sep 22;3(1):523. doi: 10.1038/s42003-020-01253-0.

DOI:10.1038/s42003-020-01253-0
PMID:32963323
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7508951/
Abstract

The gut microbiota is a suspected hotspot for bacterial conjugation due to its high density and diversity of microorganisms. However, the contribution of different conjugative plasmid families to horizontal gene transfer in this environment remains poorly characterized. Here, we systematically quantified the transfer rates in the mouse intestinal tract for 13 conjugative plasmids encompassing 10 major incompatibility groups. The vast majority of these plasmids were unable to perform conjugation in situ or only reached relatively low transfer rates. Surprisingly, IncI conjugative plasmid TP114 was identified as a proficient DNA delivery system in this environment, with the ability to transfer to virtually 100% of the probed recipient bacteria. We also show that a type IV pilus present in I-complex conjugative plasmids plays a crucial role for the transfer of TP114 in the mouse intestinal microbiota, most likely by contributing to mating pair stabilization. These results provide new insights on the mobility of genes in the gut microbiota and highlights TP114 as a very efficient DNA delivery system of interest for microbiome editing tools.

摘要

肠道微生物群是细菌接合的一个可疑热点,因为其微生物的密度和多样性都很高。然而,不同的可移动性基因盒家族在这种环境中对水平基因转移的贡献仍未得到充分描述。在这里,我们系统地定量了 13 种包含 10 种主要不相容群的可移动性基因盒在小鼠肠道中的转移率。这些质粒中的绝大多数不能在原位进行接合,或者只能达到相对较低的转移率。令人惊讶的是,IncI 可移动性基因盒 TP114 被鉴定为该环境中一种有效的 DNA 输送系统,能够几乎 100%地将供体细菌转移到受体内。我们还表明,I 型复杂可移动性基因盒中的一种 IV 型菌毛在 TP114 在小鼠肠道微生物群中的转移中起着至关重要的作用,很可能是通过促进交配对的稳定。这些结果为肠道微生物群中基因的移动性提供了新的见解,并强调了 TP114 作为一种非常有效的 DNA 输送系统,是微生物组编辑工具的研究重点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81fd/7508951/a66189d27dbe/42003_2020_1253_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81fd/7508951/d3fe5bd72567/42003_2020_1253_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81fd/7508951/68b762b670c7/42003_2020_1253_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81fd/7508951/59f2b83c61b9/42003_2020_1253_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81fd/7508951/a66189d27dbe/42003_2020_1253_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81fd/7508951/d3fe5bd72567/42003_2020_1253_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81fd/7508951/68b762b670c7/42003_2020_1253_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81fd/7508951/59f2b83c61b9/42003_2020_1253_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81fd/7508951/a66189d27dbe/42003_2020_1253_Fig4_HTML.jpg

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Nature. 2019 Sep;573(7773):276-280. doi: 10.1038/s41586-019-1521-8. Epub 2019 Sep 4.
2
Assembly of large mobilizable genetic cargo by double recombinase operated insertion of DNA (DROID).通过双重组酶操作插入 DNA(DROID)实现大型可移动遗传载体的组装。
Plasmid. 2019 Jul;104:102419. doi: 10.1016/j.plasmid.2019.102419. Epub 2019 Jun 25.
3
Engineered toxin-intein antimicrobials can selectively target and kill antibiotic-resistant bacteria in mixed populations.
BMC Vet Res. 2025 May 15;21(1):343. doi: 10.1186/s12917-025-04808-7.
4
Information storage across a microbial community using universal RNA barcoding.使用通用RNA条形码在微生物群落中进行信息存储。
Nat Biotechnol. 2025 Mar 18. doi: 10.1038/s41587-025-02593-0.
5
Genomic diversity of mcr-carrying plasmids and the role of type IV secretion systems in IncI2 plasmids conjugation.携带mcr的质粒的基因组多样性以及IV型分泌系统在IncI2质粒接合中的作用。
Commun Biol. 2025 Mar 1;8(1):342. doi: 10.1038/s42003-025-07748-y.
6
Dynamic Spread of Antibiotic Resistance Determinants by Conjugation to a Human-Derived Gut Microbiota in a Transplanted Mouse Model.在移植小鼠模型中,抗生素抗性决定因子通过接合作用向人源肠道微生物群的动态传播
Antibiotics (Basel). 2025 Feb 4;14(2):152. doi: 10.3390/antibiotics14020152.
7
Encounter rates and engagement times limit the transmission of conjugative plasmids.相遇率和接合时间限制了接合质粒的传播。
PLoS Genet. 2025 Feb 7;21(2):e1011560. doi: 10.1371/journal.pgen.1011560. eCollection 2025 Feb.
8
CRISPR-Cas Systems in the Fight Against Antimicrobial Resistance: Current Status, Potentials, and Future Directions.对抗抗菌药物耐药性中的CRISPR-Cas系统:现状、潜力及未来方向
Infect Drug Resist. 2024 Nov 26;17:5229-5245. doi: 10.2147/IDR.S494327. eCollection 2024.
9
Design, potential and limitations of conjugation-based antibacterial strategies.基于缀合的抗菌策略的设计、潜力和局限性。
Microb Biotechnol. 2024 Nov;17(11):e70050. doi: 10.1111/1751-7915.70050.
10
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Appl Environ Microbiol. 2024 Oct 23;90(10):e0081124. doi: 10.1128/aem.00811-24. Epub 2024 Sep 10.
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4
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Nat Methods. 2019 Feb;16(2):167-170. doi: 10.1038/s41592-018-0301-y. Epub 2019 Jan 14.
5
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J Antimicrob Chemother. 2018 May 1;73(5):1121-1137. doi: 10.1093/jac/dkx488.
6
Microbial Ecology along the Gastrointestinal Tract.胃肠道中的微生物生态学
Microbes Environ. 2017 Dec 27;32(4):300-313. doi: 10.1264/jsme2.ME17017. Epub 2017 Nov 10.
7
A comprehensive guide to pilus biogenesis in Gram-negative bacteria.革兰氏阴性菌菌毛生物发生的综合指南。
Nat Rev Microbiol. 2017 May 12;15(6):365-379. doi: 10.1038/nrmicro.2017.40.
8
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9
Horizontal gene transfer: building the web of life.水平基因转移:构建生命之网。
Nat Rev Genet. 2015 Aug;16(8):472-82. doi: 10.1038/nrg3962.
10
Escherichia coli EDL933 requires gluconeogenic nutrients to successfully colonize the intestines of streptomycin-treated mice precolonized with E. coli Nissle 1917.大肠杆菌EDL933需要糖异生营养物质才能成功定殖于预先定殖了大肠杆菌Nissle 1917的经链霉素处理的小鼠肠道中。
Infect Immun. 2015 May;83(5):1983-91. doi: 10.1128/IAI.02943-14. Epub 2015 Mar 2.