四环素诱导 wsp 操作子的表达,促进假单胞菌生物膜的形成。

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Applied and Environmental Microbiology Pub Date : 2025-01-31 Epub Date: 2024-11-26 DOI:10.1128/aem.01071-24
Kexin Mu, Meina He, Haozhe Chen, Tong Liu, Ying Fan, Yongxin Tao, Haoqi Feng, Qiaoyun Huang, Yujie Xiao, Wenli Chen
{"title":"四环素诱导 wsp 操作子的表达,促进假单胞菌生物膜的形成。","authors":"Kexin Mu, Meina He, Haozhe Chen, Tong Liu, Ying Fan, Yongxin Tao, Haoqi Feng, Qiaoyun Huang, Yujie Xiao, Wenli Chen","doi":"10.1128/aem.01071-24","DOIUrl":null,"url":null,"abstract":"<p><p>The overuse and wanton discharge of antibiotics produces a threat to bacteria in the environment, which, in turn, stimulates the more rapid emergence of antibiotic-resistant bacteria. <i>Pseudomonas putida</i> actively forms biofilms to protect the population under tetracycline stress, but the molecular mechanism remains unclear. This study found that tetracycline at sub-minimal inhibitory concentrations increased cyclic diguanylate (c-di-GMP), a second messenger that positively regulates biofilm formation. Four c-di-GMP-metabolizing proteins were found to be involved in the tetracycline-mediated biofilm promotion, including DibA, WspR, PP_3242, and PP_3319. Among them, the diguanylate cyclase WspR displayed the most significant effect on c-di-GMP level and biofilm formation. <i>WspR</i> belongs to the <i>wsp</i> operon comprising seven genes (<i>wspA-wspF</i> and <i>wspR</i>). The <i>wsp</i> operon contained six promoters, including one major start promoter (P<i><sub>wspA</sub></i>) and five internal promoters (P<i><sub>wspB</sub></i>, P<i><sub>wspC</sub></i>, P<i><sub>wspD</sub></i>, P<i><sub>wspF</sub></i>, and P<i><sub>wspR</sub></i>), and tetracycline promoted the activity of P<i><sub>wspA</sub></i>. The stress-response sigma factor RpoS directly bound to P<i><sub>wspA</sub></i> and positively regulated its activity under tetracycline stress. Moreover, RpoS was required for tetracycline to induce P<i><sub>wspA</sub></i> activity and promote biofilm formation. Our results enrich the transcriptional regulation of the <i>wsp</i> operon and reveal the mechanism by which tetracycline promotes biofilm formation in <i>P. putida</i>.IMPORTANCEThe overuse and wanton discharge of antibiotics produces a threat to bacteria in the environment, which, in turn, stimulates the more rapid emergence of antibiotic-resistant bacteria. The <i>Pseudomonas putida</i> actively forms biofilm against antibiotic threats, but the mechanism remains unclear. Here, our results showed that tetracycline treatment at sub-minimal inhibitory concentrations could induce the expression of the Wsp system via the sigma factor RpoS in <i>P. putida</i>, resulting in elevated c-di-GMP levels, which leads to increased biofilm formation. The <i>wsp</i> operon contains one major promoter and five internal promoters, and RpoS directly binds to the major promoter to promote its activity.</p>","PeriodicalId":8002,"journal":{"name":"Applied and Environmental Microbiology","volume":" ","pages":"e0107124"},"PeriodicalIF":3.9000,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11784136/pdf/","citationCount":"0","resultStr":"{\"title\":\"Tetracycline induces <i>wsp</i> operon expression to promote biofilm formation in <i>Pseudomonas putida</i>.\",\"authors\":\"Kexin Mu, Meina He, Haozhe Chen, Tong Liu, Ying Fan, Yongxin Tao, Haoqi Feng, Qiaoyun Huang, Yujie Xiao, Wenli Chen\",\"doi\":\"10.1128/aem.01071-24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The overuse and wanton discharge of antibiotics produces a threat to bacteria in the environment, which, in turn, stimulates the more rapid emergence of antibiotic-resistant bacteria. <i>Pseudomonas putida</i> actively forms biofilms to protect the population under tetracycline stress, but the molecular mechanism remains unclear. This study found that tetracycline at sub-minimal inhibitory concentrations increased cyclic diguanylate (c-di-GMP), a second messenger that positively regulates biofilm formation. Four c-di-GMP-metabolizing proteins were found to be involved in the tetracycline-mediated biofilm promotion, including DibA, WspR, PP_3242, and PP_3319. Among them, the diguanylate cyclase WspR displayed the most significant effect on c-di-GMP level and biofilm formation. <i>WspR</i> belongs to the <i>wsp</i> operon comprising seven genes (<i>wspA-wspF</i> and <i>wspR</i>). The <i>wsp</i> operon contained six promoters, including one major start promoter (P<i><sub>wspA</sub></i>) and five internal promoters (P<i><sub>wspB</sub></i>, P<i><sub>wspC</sub></i>, P<i><sub>wspD</sub></i>, P<i><sub>wspF</sub></i>, and P<i><sub>wspR</sub></i>), and tetracycline promoted the activity of P<i><sub>wspA</sub></i>. The stress-response sigma factor RpoS directly bound to P<i><sub>wspA</sub></i> and positively regulated its activity under tetracycline stress. Moreover, RpoS was required for tetracycline to induce P<i><sub>wspA</sub></i> activity and promote biofilm formation. Our results enrich the transcriptional regulation of the <i>wsp</i> operon and reveal the mechanism by which tetracycline promotes biofilm formation in <i>P. putida</i>.IMPORTANCEThe overuse and wanton discharge of antibiotics produces a threat to bacteria in the environment, which, in turn, stimulates the more rapid emergence of antibiotic-resistant bacteria. The <i>Pseudomonas putida</i> actively forms biofilm against antibiotic threats, but the mechanism remains unclear. Here, our results showed that tetracycline treatment at sub-minimal inhibitory concentrations could induce the expression of the Wsp system via the sigma factor RpoS in <i>P. putida</i>, resulting in elevated c-di-GMP levels, which leads to increased biofilm formation. The <i>wsp</i> operon contains one major promoter and five internal promoters, and RpoS directly binds to the major promoter to promote its activity.</p>\",\"PeriodicalId\":8002,\"journal\":{\"name\":\"Applied and Environmental Microbiology\",\"volume\":\" \",\"pages\":\"e0107124\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-01-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11784136/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied and Environmental Microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1128/aem.01071-24\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/26 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied and Environmental Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/aem.01071-24","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/26 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

抗生素的过度使用和肆意排放对环境中的细菌造成了威胁,反过来又刺激了抗生素耐药菌的更快出现。普氏假单胞菌在四环素压力下会积极形成生物膜以保护种群,但其分子机制仍不清楚。本研究发现,抑制浓度处于次低水平的四环素会增加环二甘氨酸(c-di-GMP),这是一种能积极调节生物膜形成的第二信使。研究发现,四种 c-di-GMP 代谢蛋白参与了四环素介导的生物膜促进作用,包括 DibA、WspR、PP_3242 和 PP_3319。其中,二聚体环化酶 WspR 对 c-di-GMP 水平和生物膜形成的影响最为显著。WspR 属于 wsp 操作子,由七个基因(wspA-wspF 和 wspR)组成。wsp 操作子包含六个启动子,包括一个主要启动子(PwspA)和五个内部启动子(PwspB、PwspC、PwspD、PwspF 和 PwspR),四环素可促进 PwspA 的活性。在四环素胁迫下,胁迫反应σ因子 RpoS 直接与 PwspA 结合并正向调节其活性。此外,RpoS是四环素诱导PwspA活性并促进生物膜形成所必需的。我们的研究结果丰富了 wsp 操作子的转录调控,揭示了四环素促进假单胞菌生物膜形成的机制。重要意义抗生素的过度使用和肆意排放对环境中的细菌造成了威胁,反过来又刺激了耐抗生素细菌的快速出现。普氏假单胞菌会积极形成生物膜来抵御抗生素的威胁,但其机制仍不清楚。在此,我们的研究结果表明,在次低抑制浓度下处理四环素可通过普氏假单胞菌中的标志因子 RpoS 诱导 Wsp 系统的表达,导致 c-di-GMP 水平升高,从而增加生物膜的形成。wsp 操作子包含一个主启动子和五个内部启动子,RpoS 直接与主启动子结合以促进其活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Tetracycline induces wsp operon expression to promote biofilm formation in Pseudomonas putida.

The overuse and wanton discharge of antibiotics produces a threat to bacteria in the environment, which, in turn, stimulates the more rapid emergence of antibiotic-resistant bacteria. Pseudomonas putida actively forms biofilms to protect the population under tetracycline stress, but the molecular mechanism remains unclear. This study found that tetracycline at sub-minimal inhibitory concentrations increased cyclic diguanylate (c-di-GMP), a second messenger that positively regulates biofilm formation. Four c-di-GMP-metabolizing proteins were found to be involved in the tetracycline-mediated biofilm promotion, including DibA, WspR, PP_3242, and PP_3319. Among them, the diguanylate cyclase WspR displayed the most significant effect on c-di-GMP level and biofilm formation. WspR belongs to the wsp operon comprising seven genes (wspA-wspF and wspR). The wsp operon contained six promoters, including one major start promoter (PwspA) and five internal promoters (PwspB, PwspC, PwspD, PwspF, and PwspR), and tetracycline promoted the activity of PwspA. The stress-response sigma factor RpoS directly bound to PwspA and positively regulated its activity under tetracycline stress. Moreover, RpoS was required for tetracycline to induce PwspA activity and promote biofilm formation. Our results enrich the transcriptional regulation of the wsp operon and reveal the mechanism by which tetracycline promotes biofilm formation in P. putida.IMPORTANCEThe overuse and wanton discharge of antibiotics produces a threat to bacteria in the environment, which, in turn, stimulates the more rapid emergence of antibiotic-resistant bacteria. The Pseudomonas putida actively forms biofilm against antibiotic threats, but the mechanism remains unclear. Here, our results showed that tetracycline treatment at sub-minimal inhibitory concentrations could induce the expression of the Wsp system via the sigma factor RpoS in P. putida, resulting in elevated c-di-GMP levels, which leads to increased biofilm formation. The wsp operon contains one major promoter and five internal promoters, and RpoS directly binds to the major promoter to promote its activity.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
期刊最新文献
Inactivation of deposited bioaerosols on food contact surfaces with UV-C light emitting diode devices. Variability in cadmium tolerance of closely related Listeria monocytogenes isolates originating from dairy processing environments. Postdocs should receive relocation benefits from the universities that hire them. Systematic analysis of the glucose-PTS in Streptococcus sanguinis highlighted its importance in central metabolism and bacterial fitness. Papain expression in the Escherichia coli cytoplasm by T7-promoter engineering and co-expression with human protein disulfide isomerase (PDI) and thiol peroxidase (GPx7) genes.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1