{"title":"Functional Characterization of Transcriptional Regulator Rem in <i>Candidatus</i> Liberibacter asiaticus.","authors":"Wenting Wang, Jin Xu, Nian Wang","doi":"10.1094/PHYTO-10-24-0339-R","DOIUrl":null,"url":null,"abstract":"<p><p>Citrus HLB, caused by <i>Candidatus</i> Liberibacter asiaticus (CLas), is the most devastating citrus disease worldwide. Usually 10% of total genes in bacteria are regulatory genes, but only 2% of CLas genes encode transcriptional factors. Here, 20 transcriptional regulators were predicted including eight genes (<i>lsrB, ldtR, rem, visR, visN, ctrA, mucR, pelD,</i> and <i>atoC</i>) directly or indirectly involved in regulating motility, and five genes (i.e., <i>rpoH, prbP, phrR, rirA,</i> and <i>lsrB</i>) involved in oxidative stress response. We demonstrated that <i>rem, lsrB,</i> and <i>visNR</i> of CLas can complement the corresponding mutants of <i>S. meliloti</i> in their reduced motility. We further investigated traits controlled by Rem in <i>S. meliloti</i> and CLas using RNA-seq analyses of <i>rem</i> mutant vs. complementation strains with <i>rem<sub>Smc</sub></i> or <i>rem<sub>Las</sub></i>. Transcriptomic analysis showed Rem<sub>Las</sub> significantly regulates the expression of genes in <i>S. meliloti</i>, which was used to infer its regulation of CLas genes by identification of homologous genes. We found Rem is involved in regulating motility, chemotaxis, transporters, and oxidative phosphorylation in <i>S. meliloti</i> and regulating flagellar and transporter genes in CLas. Among the 39 putative Rem<sub>Las</sub>-regulated genes in CLas, 16 contain Rem binding motif, including 10 genes involved in flagellar assembly. Taken together, this study offers valuable insights regarding regulatory genes of CLas with many of them involved in regulating motility and oxidative stress response. The regulation of flagellar genes by Rem in CLas unravels critical information regarding motility in CLas infection of hosts.</p>","PeriodicalId":20410,"journal":{"name":"Phytopathology","volume":" ","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytopathology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1094/PHYTO-10-24-0339-R","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Citrus HLB, caused by Candidatus Liberibacter asiaticus (CLas), is the most devastating citrus disease worldwide. Usually 10% of total genes in bacteria are regulatory genes, but only 2% of CLas genes encode transcriptional factors. Here, 20 transcriptional regulators were predicted including eight genes (lsrB, ldtR, rem, visR, visN, ctrA, mucR, pelD, and atoC) directly or indirectly involved in regulating motility, and five genes (i.e., rpoH, prbP, phrR, rirA, and lsrB) involved in oxidative stress response. We demonstrated that rem, lsrB, and visNR of CLas can complement the corresponding mutants of S. meliloti in their reduced motility. We further investigated traits controlled by Rem in S. meliloti and CLas using RNA-seq analyses of rem mutant vs. complementation strains with remSmc or remLas. Transcriptomic analysis showed RemLas significantly regulates the expression of genes in S. meliloti, which was used to infer its regulation of CLas genes by identification of homologous genes. We found Rem is involved in regulating motility, chemotaxis, transporters, and oxidative phosphorylation in S. meliloti and regulating flagellar and transporter genes in CLas. Among the 39 putative RemLas-regulated genes in CLas, 16 contain Rem binding motif, including 10 genes involved in flagellar assembly. Taken together, this study offers valuable insights regarding regulatory genes of CLas with many of them involved in regulating motility and oxidative stress response. The regulation of flagellar genes by Rem in CLas unravels critical information regarding motility in CLas infection of hosts.
期刊介绍:
Phytopathology publishes articles on fundamental research that advances understanding of the nature of plant diseases, the agents that cause them, their spread, the losses they cause, and measures that can be used to control them. Phytopathology considers manuscripts covering all aspects of plant diseases including bacteriology, host-parasite biochemistry and cell biology, biological control, disease control and pest management, description of new pathogen species description of new pathogen species, ecology and population biology, epidemiology, disease etiology, host genetics and resistance, mycology, nematology, plant stress and abiotic disorders, postharvest pathology and mycotoxins, and virology. Papers dealing mainly with taxonomy, such as descriptions of new plant pathogen taxa are acceptable if they include plant disease research results such as pathogenicity, host range, etc. Taxonomic papers that focus on classification, identification, and nomenclature below the subspecies level may also be submitted to Phytopathology.