Pavlovian-Type Learning in Environmental Bacteria: Regulation of Herbicide Resistance by Arsenic in Pseudomonas putida

IF 4.3 2区 生物学 Q2 MICROBIOLOGY Environmental microbiology Pub Date : 2024-12-12 DOI:10.1111/1462-2920.70012
David Paez-Espino, Gonzalo Durante-Rodríguez, Elena Alonso Fernandes, Manuel Carmona, Victor de Lorenzo
{"title":"Pavlovian-Type Learning in Environmental Bacteria: Regulation of Herbicide Resistance by Arsenic in Pseudomonas putida","authors":"David Paez-Espino,&nbsp;Gonzalo Durante-Rodríguez,&nbsp;Elena Alonso Fernandes,&nbsp;Manuel Carmona,&nbsp;Victor de Lorenzo","doi":"10.1111/1462-2920.70012","DOIUrl":null,"url":null,"abstract":"<p>The canonical <i>arsRBC</i> genes of the <i>ars1</i> operon in <i>Pseudomonas putida</i> KT2440, which confer tolerance to arsenate and arsenite, are followed by a series of additional ORFs culminating in <i>phoN1</i>. The phoN1 gene encodes an acetyltransferase that imparts resistance to the glutamine synthetase inhibitor herbicide phosphinothricin (PPT). The co-expression of <i>phoN1</i> and <i>ars</i> genes in response to environmental arsenic, along with the physiological effects, was analysed through transcriptomics of cells exposed to the oxyanion and phenotypic characterization of <i>P. putida</i> strains deficient in different components of the bifan motif governing arsenic resistance in this bacterium. Genetic separation of <i>arsRBC</i> and <i>phoN1</i> revealed that their associated phenotypes operate independently, indicating that their natural co-regulation is not functionally required for simultaneous response to the same signal. The data suggest a scenario of associative evolution, akin to Pavlovian conditioning, where two unrelated but frequently co-occurring signals result in one regulating the other's response – even if there is no functional link between the signal and the response. Such surrogate regulatory events may provide an efficient solution to complex regulatory challenges and serve as a genetic patch to address transient gaps in evolving regulatory networks.</p>","PeriodicalId":11898,"journal":{"name":"Environmental microbiology","volume":"26 12","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/1462-2920.70012","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental microbiology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/1462-2920.70012","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The canonical arsRBC genes of the ars1 operon in Pseudomonas putida KT2440, which confer tolerance to arsenate and arsenite, are followed by a series of additional ORFs culminating in phoN1. The phoN1 gene encodes an acetyltransferase that imparts resistance to the glutamine synthetase inhibitor herbicide phosphinothricin (PPT). The co-expression of phoN1 and ars genes in response to environmental arsenic, along with the physiological effects, was analysed through transcriptomics of cells exposed to the oxyanion and phenotypic characterization of P. putida strains deficient in different components of the bifan motif governing arsenic resistance in this bacterium. Genetic separation of arsRBC and phoN1 revealed that their associated phenotypes operate independently, indicating that their natural co-regulation is not functionally required for simultaneous response to the same signal. The data suggest a scenario of associative evolution, akin to Pavlovian conditioning, where two unrelated but frequently co-occurring signals result in one regulating the other's response – even if there is no functional link between the signal and the response. Such surrogate regulatory events may provide an efficient solution to complex regulatory challenges and serve as a genetic patch to address transient gaps in evolving regulatory networks.

Abstract Image

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
环境细菌的巴甫洛夫学习:砷对恶臭假单胞菌除草剂抗性的调节
普氏假单胞菌(Pseudomonas putida)KT2440 的 ars1 操作子的典型 arsRBC 基因可赋予其对砷酸盐和亚砷酸盐的耐受性,其后还有一系列额外的 ORF,最终形成 phoN1 基因。phoN1 基因编码一种乙酰基转移酶,它能使假单胞菌耐受谷氨酰胺合成酶抑制剂除草剂膦菊酯(PPT)。通过对暴露于氧阴离子的细胞进行转录组学分析,以及对缺乏支配该细菌砷抗性的 bifan 基序不同成分的 P. putida 菌株进行表型鉴定,分析了 phoN1 和 ars 基因在应对环境砷时的共同表达及其生理效应。对 arsRBC 和 phoN1 进行遗传分离后发现,它们的相关表型是独立运行的,这表明它们的自然共同调控在功能上并不需要同时对同一信号做出反应。这些数据提出了一种类似于巴甫洛夫条件反射的关联进化情景,在这种情景中,两个不相关但经常同时出现的信号会导致一个信号调节另一个信号的反应--即使信号和反应之间没有功能上的联系。这种代用调控事件可能为复杂的调控挑战提供了有效的解决方案,并可作为基因补丁来解决不断演化的调控网络中的短暂缺口。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Environmental microbiology
Environmental microbiology 环境科学-微生物学
CiteScore
9.90
自引率
3.90%
发文量
427
审稿时长
2.3 months
期刊介绍: Environmental Microbiology provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens
期刊最新文献
Contrasting Methane, Sulfide and Nitrogen-Loading Regimes in Bioreactors Shape Microbial Communities Originating From Methane-Rich Coastal Sediment of the Stockholm Archipelago Thermodynamics Underpinning the Microbial Community-Level Nitrogen Energy Metabolism Phylogenetic and Functional Diversity of Soluble Di-Iron Monooxygenases Highly Dynamic Archaeal and Bacterial Communities From the Surface to the Deep in the Atlantic Ocean Insects as Natural Hosts, Vectors and Reservoirs of Botulinum Neurotoxin-Producing Clostridia and Their Non-Toxinogenic Counterparts: Preliminary Evidence
×
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