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Cell-to-cell natural transformation in Bacillus subtilis facilitates large scale of genomic exchanges and the transfer of long continuous DNA regions

Natural transformation is one of the major mechanisms of horizontal gene transfer. Although it is usually studied using purified DNA in the laboratory, recent studies showed that many naturally competent bacteria acquired exogenous DNA from neighboring donor cells. Our previous work indicates that c...

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Autores principales: Deng, Liping, Wang, Chao, Zhang, Xiaoming, Yang, Wenjie, Tang, Hao, Chen, Xinru, Du, Shishen, Chen, Xiangdong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10164588/
https://www.ncbi.nlm.nih.gov/pubmed/36912090
http://dx.doi.org/10.1093/nar/gkad138
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author Deng, Liping
Wang, Chao
Zhang, Xiaoming
Yang, Wenjie
Tang, Hao
Chen, Xinru
Du, Shishen
Chen, Xiangdong
author_facet Deng, Liping
Wang, Chao
Zhang, Xiaoming
Yang, Wenjie
Tang, Hao
Chen, Xinru
Du, Shishen
Chen, Xiangdong
author_sort Deng, Liping
collection PubMed
description Natural transformation is one of the major mechanisms of horizontal gene transfer. Although it is usually studied using purified DNA in the laboratory, recent studies showed that many naturally competent bacteria acquired exogenous DNA from neighboring donor cells. Our previous work indicates that cell-to-cell natural transformation (CTCNT) using two different Bacillus subtilis strains is a highly efficient process; however, the mechanism is unclear. In this study, we further characterized CTCNT and mapped the transferred DNA in the recombinants using whole genome sequencing. We found that a recombinant strain generated by CTCNT received up to 66 transferred DNA segments; the average length of acquired continuous DNA stretches was approximately 27 kb with a maximum length of 347 kb. Moreover, up to 1.54 Mb genomic DNA (37% of the chromosome) was transferred from the donors into one recipient cell. These results suggest that B. subtilis CTCNT facilitates horizontal gene transfer by increasing the transfer of DNA segments and fostering the exchange of large continuous genomic regions. This indicates that the potency of bacterial natural transformation is underestimated using traditional approaches and reveals that DNA donor cells may play an important role in the transformation process in natural environments.
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spelling pubmed-101645882023-05-08 Cell-to-cell natural transformation in Bacillus subtilis facilitates large scale of genomic exchanges and the transfer of long continuous DNA regions Deng, Liping Wang, Chao Zhang, Xiaoming Yang, Wenjie Tang, Hao Chen, Xinru Du, Shishen Chen, Xiangdong Nucleic Acids Res Molecular Biology Natural transformation is one of the major mechanisms of horizontal gene transfer. Although it is usually studied using purified DNA in the laboratory, recent studies showed that many naturally competent bacteria acquired exogenous DNA from neighboring donor cells. Our previous work indicates that cell-to-cell natural transformation (CTCNT) using two different Bacillus subtilis strains is a highly efficient process; however, the mechanism is unclear. In this study, we further characterized CTCNT and mapped the transferred DNA in the recombinants using whole genome sequencing. We found that a recombinant strain generated by CTCNT received up to 66 transferred DNA segments; the average length of acquired continuous DNA stretches was approximately 27 kb with a maximum length of 347 kb. Moreover, up to 1.54 Mb genomic DNA (37% of the chromosome) was transferred from the donors into one recipient cell. These results suggest that B. subtilis CTCNT facilitates horizontal gene transfer by increasing the transfer of DNA segments and fostering the exchange of large continuous genomic regions. This indicates that the potency of bacterial natural transformation is underestimated using traditional approaches and reveals that DNA donor cells may play an important role in the transformation process in natural environments. Oxford University Press 2023-03-13 /pmc/articles/PMC10164588/ /pubmed/36912090 http://dx.doi.org/10.1093/nar/gkad138 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Deng, Liping
Wang, Chao
Zhang, Xiaoming
Yang, Wenjie
Tang, Hao
Chen, Xinru
Du, Shishen
Chen, Xiangdong
Cell-to-cell natural transformation in Bacillus subtilis facilitates large scale of genomic exchanges and the transfer of long continuous DNA regions
title Cell-to-cell natural transformation in Bacillus subtilis facilitates large scale of genomic exchanges and the transfer of long continuous DNA regions
title_full Cell-to-cell natural transformation in Bacillus subtilis facilitates large scale of genomic exchanges and the transfer of long continuous DNA regions
title_fullStr Cell-to-cell natural transformation in Bacillus subtilis facilitates large scale of genomic exchanges and the transfer of long continuous DNA regions
title_full_unstemmed Cell-to-cell natural transformation in Bacillus subtilis facilitates large scale of genomic exchanges and the transfer of long continuous DNA regions
title_short Cell-to-cell natural transformation in Bacillus subtilis facilitates large scale of genomic exchanges and the transfer of long continuous DNA regions
title_sort cell-to-cell natural transformation in bacillus subtilis facilitates large scale of genomic exchanges and the transfer of long continuous dna regions
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10164588/
https://www.ncbi.nlm.nih.gov/pubmed/36912090
http://dx.doi.org/10.1093/nar/gkad138
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