{"title":"The adaptive growth and mechanisms of <i>Klebsiella pneumoniae</i> under sucrose and glucose exposure.","authors":"Yunhui He, Fangfang Liu, Congcong Li, Jiayan Wu, Kewei Fan, Zewen Wen, Duoyun Li, Zhijian Yu, Tieying Hou","doi":"10.1128/spectrum.01603-25","DOIUrl":null,"url":null,"abstract":"<p><p><i>Klebsiella pneumoniae</i> commonly colonizes the gastrointestinal (GI) mucosa of animals and healthy humans. Successful GI colonization by <i>K. pneumoniae</i> requires overcoming the colonization resistance (CR) exerted by the gut microbiota. Although previous studies have demonstrated the role of microbial carbohydrate metabolism in <i>K. pneumoniae</i> colonization, the specific effects of individual carbohydrates, such as glucose and sucrose, particularly across concentration gradients or under sustained induction on the adaptive growth of <i>K. pneumoniae</i> remain unknown. Herein, we demonstrate that 4% or 8% glucose and sucrose are favorable for promoting adaptive growth of sugar-induced strains. Additionally, the growth response to glucose exhibited strain-specific variability. Sustained sugar induction did not significantly alter the hypermucoviscosity (HMV) phenotype but did affect antibiotic resistance of <i>K. pneumoniae</i>. Knockout of the <i>scrA</i> and <i>scrY</i> genes impaired the adaptive growth under sucrose and glucose conditions, yet did not significantly influence antimicrobial susceptibility or the HMV phenotype. These findings provide insights into the metabolic regulation of <i>K. pneumoniae</i> colonization and offer potential guidance for clinical treatment strategies targeting <i>K. pneumoniae</i>-associated infections.</p><p><strong>Importance: </strong>This work elucidates the impact of single-carbon source gradients and sustained sugar induction on the adaptive growth and drug resistance of <i>Klebsiella pneumoniae</i> and preliminarily reveals the roles of <i>scrA</i> and <i>scrY</i> in carbohydrate metabolism, suggesting a possible mechanism by which sucrose and glucose affect the adaptive growth of <i>K. pneumoniae</i>. These findings contribute to the theoretical understanding of CCR and provide insights that may inform clinical management of <i>K. pneumoniae</i>-related infections.</p>","PeriodicalId":18670,"journal":{"name":"Microbiology spectrum","volume":" ","pages":"e0160325"},"PeriodicalIF":3.8000,"publicationDate":"2025-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiology spectrum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/spectrum.01603-25","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
Klebsiella pneumoniae commonly colonizes the gastrointestinal (GI) mucosa of animals and healthy humans. Successful GI colonization by K. pneumoniae requires overcoming the colonization resistance (CR) exerted by the gut microbiota. Although previous studies have demonstrated the role of microbial carbohydrate metabolism in K. pneumoniae colonization, the specific effects of individual carbohydrates, such as glucose and sucrose, particularly across concentration gradients or under sustained induction on the adaptive growth of K. pneumoniae remain unknown. Herein, we demonstrate that 4% or 8% glucose and sucrose are favorable for promoting adaptive growth of sugar-induced strains. Additionally, the growth response to glucose exhibited strain-specific variability. Sustained sugar induction did not significantly alter the hypermucoviscosity (HMV) phenotype but did affect antibiotic resistance of K. pneumoniae. Knockout of the scrA and scrY genes impaired the adaptive growth under sucrose and glucose conditions, yet did not significantly influence antimicrobial susceptibility or the HMV phenotype. These findings provide insights into the metabolic regulation of K. pneumoniae colonization and offer potential guidance for clinical treatment strategies targeting K. pneumoniae-associated infections.
Importance: This work elucidates the impact of single-carbon source gradients and sustained sugar induction on the adaptive growth and drug resistance of Klebsiella pneumoniae and preliminarily reveals the roles of scrA and scrY in carbohydrate metabolism, suggesting a possible mechanism by which sucrose and glucose affect the adaptive growth of K. pneumoniae. These findings contribute to the theoretical understanding of CCR and provide insights that may inform clinical management of K. pneumoniae-related infections.
期刊介绍:
Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.