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Autores principales: Kou, Tian-Shun, Shang, Yan-Yan, Zhang, Qi-Chao, Tian, Si-Qi, Li, Juan, Yang, Li-Na, Min, Ling, Peng, Bo
Formato: Artículo científico
Lenguaje:en
Publicado: Virulence 2025
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Acceso en línea:https://pubmed.ncbi.nlm.nih.gov/40773514/
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author Kou, Tian-Shun
Shang, Yan-Yan
Zhang, Qi-Chao
Tian, Si-Qi
Li, Juan
Yang, Li-Na
Min, Ling
Peng, Bo
author_facet Kou, Tian-Shun
Shang, Yan-Yan
Zhang, Qi-Chao
Tian, Si-Qi
Li, Juan
Yang, Li-Na
Min, Ling
Peng, Bo
Kou, Tian-Shun
Shang, Yan-Yan
Zhang, Qi-Chao
Tian, Si-Qi
Li, Juan
Yang, Li-Na
Min, Ling
Peng, Bo
collection PubMed - marine biology
contents Exogenous proline promotes serum killing of . Kou, Tian-Shun Shang, Yan-Yan Zhang, Qi-Chao Tian, Si-Qi Li, Juan Yang, Li-Na Min, Ling Peng, Bo Klebsiella pneumoniae Animals Klebsiella Infections Mice Proline Humans Blood Bactericidal Activity Complement System Proteins Metabolomics Disease Models, Animal Female Metabolic Networks and Pathways , a common pathogen responsible for bloodstream infections, can evade clearance by the complement-dependent killing in serum, known as serum resistance. However, strategy in managing serum resistance is still lacking. In this study, we employed metabolomics to identify the metabolic features of . We found that the pyruvate/TCA cycle and alanine, aspartate, and glutamate metabolic pathways were significantly downregulated. Proline, identified as a key biomarker, effectively increased the serum sensitivity to multiple clinical isolates and restored the bactericidal activity of complement. The synergistic effect of proline was validated in a murine infection model. Furthermore, we demonstrated that proline activates the pyruvate/TCA cycle, increases proton motive force, and enhances complement proteins binding to bacterial surface, forming membrane attack complex to kill serum-resistant . Our findings provide new insights for the development of metabolism-based approach to manage serum resistance and offer potential targets and strategies for host immunity-based anti-infection therapies.
format Artículo científico
id pubmed_40773514
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language en
publishDate 2025
publisher Virulence
record_format pubmed
spellingShingle Exogenous proline promotes serum killing of .
Kou, Tian-Shun
Shang, Yan-Yan
Zhang, Qi-Chao
Tian, Si-Qi
Li, Juan
Yang, Li-Na
Min, Ling
Peng, Bo
Klebsiella pneumoniae
Animals
Klebsiella Infections
Mice
Proline
Humans
Blood Bactericidal Activity
Complement System Proteins
Metabolomics
Disease Models, Animal
Female
Metabolic Networks and Pathways
Exogenous proline promotes serum killing of . Kou, Tian-Shun Shang, Yan-Yan Zhang, Qi-Chao Tian, Si-Qi Li, Juan Yang, Li-Na Min, Ling Peng, Bo Klebsiella pneumoniae Animals Klebsiella Infections Mice Proline Humans Blood Bactericidal Activity Complement System Proteins Metabolomics Disease Models, Animal Female Metabolic Networks and Pathways , a common pathogen responsible for bloodstream infections, can evade clearance by the complement-dependent killing in serum, known as serum resistance. However, strategy in managing serum resistance is still lacking. In this study, we employed metabolomics to identify the metabolic features of . We found that the pyruvate/TCA cycle and alanine, aspartate, and glutamate metabolic pathways were significantly downregulated. Proline, identified as a key biomarker, effectively increased the serum sensitivity to multiple clinical isolates and restored the bactericidal activity of complement. The synergistic effect of proline was validated in a murine infection model. Furthermore, we demonstrated that proline activates the pyruvate/TCA cycle, increases proton motive force, and enhances complement proteins binding to bacterial surface, forming membrane attack complex to kill serum-resistant . Our findings provide new insights for the development of metabolism-based approach to manage serum resistance and offer potential targets and strategies for host immunity-based anti-infection therapies.
title Exogenous proline promotes serum killing of .
topic Klebsiella pneumoniae
Animals
Klebsiella Infections
Mice
Proline
Humans
Blood Bactericidal Activity
Complement System Proteins
Metabolomics
Disease Models, Animal
Female
Metabolic Networks and Pathways
url https://pubmed.ncbi.nlm.nih.gov/40773514/