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Diadenosine tetraphosphate modulated quorum sensing in bacteria treated with kanamycin

BACKGROUND: The dinucleotide alarmone diadenosine tetraphosphate (Ap4A), which is found in cells, has been shown to affect the survival of bacteria under stress. RESULTS: Here, we labeled Ap4A with biotin and incubated the labeled Ap4A with the total proteins extracted from kanamycin-treated Escheri...

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Autores principales: Ji, Xia, Yu, Ruojing, Zhu, Meilian, Zhang, Cuilin, Zhou, Libin, Cai, Tianshu, Li, Weiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657157/
https://www.ncbi.nlm.nih.gov/pubmed/37978430
http://dx.doi.org/10.1186/s12866-023-03113-3
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author Ji, Xia
Yu, Ruojing
Zhu, Meilian
Zhang, Cuilin
Zhou, Libin
Cai, Tianshu
Li, Weiwei
author_facet Ji, Xia
Yu, Ruojing
Zhu, Meilian
Zhang, Cuilin
Zhou, Libin
Cai, Tianshu
Li, Weiwei
author_sort Ji, Xia
collection PubMed
description BACKGROUND: The dinucleotide alarmone diadenosine tetraphosphate (Ap4A), which is found in cells, has been shown to affect the survival of bacteria under stress. RESULTS: Here, we labeled Ap4A with biotin and incubated the labeled Ap4A with the total proteins extracted from kanamycin-treated Escherichia coli to identify the Ap4A binding protein in bacteria treated with kanamycin. Liquid chromatography‒mass spectrometry (LCMS) and bioinformatics were used to identify novel proteins that Ap4A interacts with that are involved in biofilm formation, quorum sensing, and lipopolysaccharide biosynthesis pathways. Then, we used the apaH knockout strain of E. coli K12-MG1655, which had increased intracellular Ap4A, to demonstrate that Ap4A affected the expression of genes in these three pathways. We also found that the swarming motility of the apaH mutant strain was reduced compared with that of the wild-type strain, and under kanamycin treatment, the biofilm formation of the mutant strain decreased. CONCLUSIONS: These results showed that Ap4A can reduce the survival rate of bacteria treated with kanamycin by regulating quorum sensing (QS). These effects can expand the application of kanamycin combinations in the treatment of multidrug-resistant bacteria. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-023-03113-3.
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spelling pubmed-106571572023-11-17 Diadenosine tetraphosphate modulated quorum sensing in bacteria treated with kanamycin Ji, Xia Yu, Ruojing Zhu, Meilian Zhang, Cuilin Zhou, Libin Cai, Tianshu Li, Weiwei BMC Microbiol Research BACKGROUND: The dinucleotide alarmone diadenosine tetraphosphate (Ap4A), which is found in cells, has been shown to affect the survival of bacteria under stress. RESULTS: Here, we labeled Ap4A with biotin and incubated the labeled Ap4A with the total proteins extracted from kanamycin-treated Escherichia coli to identify the Ap4A binding protein in bacteria treated with kanamycin. Liquid chromatography‒mass spectrometry (LCMS) and bioinformatics were used to identify novel proteins that Ap4A interacts with that are involved in biofilm formation, quorum sensing, and lipopolysaccharide biosynthesis pathways. Then, we used the apaH knockout strain of E. coli K12-MG1655, which had increased intracellular Ap4A, to demonstrate that Ap4A affected the expression of genes in these three pathways. We also found that the swarming motility of the apaH mutant strain was reduced compared with that of the wild-type strain, and under kanamycin treatment, the biofilm formation of the mutant strain decreased. CONCLUSIONS: These results showed that Ap4A can reduce the survival rate of bacteria treated with kanamycin by regulating quorum sensing (QS). These effects can expand the application of kanamycin combinations in the treatment of multidrug-resistant bacteria. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-023-03113-3. BioMed Central 2023-11-17 /pmc/articles/PMC10657157/ /pubmed/37978430 http://dx.doi.org/10.1186/s12866-023-03113-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ji, Xia
Yu, Ruojing
Zhu, Meilian
Zhang, Cuilin
Zhou, Libin
Cai, Tianshu
Li, Weiwei
Diadenosine tetraphosphate modulated quorum sensing in bacteria treated with kanamycin
title Diadenosine tetraphosphate modulated quorum sensing in bacteria treated with kanamycin
title_full Diadenosine tetraphosphate modulated quorum sensing in bacteria treated with kanamycin
title_fullStr Diadenosine tetraphosphate modulated quorum sensing in bacteria treated with kanamycin
title_full_unstemmed Diadenosine tetraphosphate modulated quorum sensing in bacteria treated with kanamycin
title_short Diadenosine tetraphosphate modulated quorum sensing in bacteria treated with kanamycin
title_sort diadenosine tetraphosphate modulated quorum sensing in bacteria treated with kanamycin
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657157/
https://www.ncbi.nlm.nih.gov/pubmed/37978430
http://dx.doi.org/10.1186/s12866-023-03113-3
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