Lappasi Mohanram VenkataKrishna, Boopathi Balasubramaniam, T. J. Sushmitha, V. Ravichandiran and Krishnaswamy Balamurugan
{"title":"阪崎克罗诺杆菌感染涉及秀丽隐杆线虫的多方面神经免疫调节途径。","authors":"Lappasi Mohanram VenkataKrishna, Boopathi Balasubramaniam, T. J. Sushmitha, V. Ravichandiran and Krishnaswamy Balamurugan","doi":"10.1039/D3MO00167A","DOIUrl":null,"url":null,"abstract":"<p >The neural pathways of <em>Caenorhabditis elegans</em> play a crucial role in regulating host immunity and inflammation during pathogenic infections. To understand the major neuro-immune signaling pathways, this study aimed to identify the key regulatory proteins in the host <em>C. elegans</em> during <em>C. sakazakii</em> infection. We used high-throughput label-free quantitative proteomics and identified 69 differentially expressed proteins. KEGG analysis revealed that <em>C. sakazakii</em> elicited host immune signaling cascades primarily including mTOR signaling, axon regeneration, metabolic pathways (<em>let-363</em> and <em>acox-1.4</em>), calcium signaling <em>(mlck-1)</em>, and longevity regulating pathways (<em>ddl-2</em>), respectively. The abrogation in functional loss of mTOR-associated players deciphered that <em>C. sakazakii</em> infection negatively regulated the lifespan of mutant worms (<em>akt-1</em>, <em>let-363</em> and <em>dlk-1</em>), including physiological aberrations, such as reduced pharyngeal pumping and egg production. Additionally, the candidate pathway proteins were validated by transcriptional profiling of their corresponding genes. Furthermore, immunoblotting showed the downregulation of mTORC2/SGK-1 during the later hours of pathogen exposure. Overall, our findings profoundly provide an understanding of the specificity of proteome imbalance in affecting neuro-immune regulations during <em>C. sakazakii</em> infection.</p>","PeriodicalId":19065,"journal":{"name":"Molecular omics","volume":" 1","pages":" 48-63"},"PeriodicalIF":3.0000,"publicationDate":"2023-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cronobacter sakazakii infection implicates multifaceted neuro-immune regulatory pathways of Caenorhabditis elegans†\",\"authors\":\"Lappasi Mohanram VenkataKrishna, Boopathi Balasubramaniam, T. J. Sushmitha, V. Ravichandiran and Krishnaswamy Balamurugan\",\"doi\":\"10.1039/D3MO00167A\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The neural pathways of <em>Caenorhabditis elegans</em> play a crucial role in regulating host immunity and inflammation during pathogenic infections. To understand the major neuro-immune signaling pathways, this study aimed to identify the key regulatory proteins in the host <em>C. elegans</em> during <em>C. sakazakii</em> infection. We used high-throughput label-free quantitative proteomics and identified 69 differentially expressed proteins. KEGG analysis revealed that <em>C. sakazakii</em> elicited host immune signaling cascades primarily including mTOR signaling, axon regeneration, metabolic pathways (<em>let-363</em> and <em>acox-1.4</em>), calcium signaling <em>(mlck-1)</em>, and longevity regulating pathways (<em>ddl-2</em>), respectively. The abrogation in functional loss of mTOR-associated players deciphered that <em>C. sakazakii</em> infection negatively regulated the lifespan of mutant worms (<em>akt-1</em>, <em>let-363</em> and <em>dlk-1</em>), including physiological aberrations, such as reduced pharyngeal pumping and egg production. Additionally, the candidate pathway proteins were validated by transcriptional profiling of their corresponding genes. Furthermore, immunoblotting showed the downregulation of mTORC2/SGK-1 during the later hours of pathogen exposure. Overall, our findings profoundly provide an understanding of the specificity of proteome imbalance in affecting neuro-immune regulations during <em>C. sakazakii</em> infection.</p>\",\"PeriodicalId\":19065,\"journal\":{\"name\":\"Molecular omics\",\"volume\":\" 1\",\"pages\":\" 48-63\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2023-09-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular omics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/mo/d3mo00167a\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular omics","FirstCategoryId":"99","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/mo/d3mo00167a","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
The neural pathways of Caenorhabditis elegans play a crucial role in regulating host immunity and inflammation during pathogenic infections. To understand the major neuro-immune signaling pathways, this study aimed to identify the key regulatory proteins in the host C. elegans during C. sakazakii infection. We used high-throughput label-free quantitative proteomics and identified 69 differentially expressed proteins. KEGG analysis revealed that C. sakazakii elicited host immune signaling cascades primarily including mTOR signaling, axon regeneration, metabolic pathways (let-363 and acox-1.4), calcium signaling (mlck-1), and longevity regulating pathways (ddl-2), respectively. The abrogation in functional loss of mTOR-associated players deciphered that C. sakazakii infection negatively regulated the lifespan of mutant worms (akt-1, let-363 and dlk-1), including physiological aberrations, such as reduced pharyngeal pumping and egg production. Additionally, the candidate pathway proteins were validated by transcriptional profiling of their corresponding genes. Furthermore, immunoblotting showed the downregulation of mTORC2/SGK-1 during the later hours of pathogen exposure. Overall, our findings profoundly provide an understanding of the specificity of proteome imbalance in affecting neuro-immune regulations during C. sakazakii infection.
Molecular omicsBiochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
5.40
自引率
3.40%
发文量
91
期刊介绍:
Molecular Omics publishes high-quality research from across the -omics sciences.
Topics include, but are not limited to:
-omics studies to gain mechanistic insight into biological processes – for example, determining the mode of action of a drug or the basis of a particular phenotype, such as drought tolerance
-omics studies for clinical applications with validation, such as finding biomarkers for diagnostics or potential new drug targets
-omics studies looking at the sub-cellular make-up of cells – for example, the subcellular localisation of certain proteins or post-translational modifications or new imaging techniques
-studies presenting new methods and tools to support omics studies, including new spectroscopic/chromatographic techniques, chip-based/array technologies and new classification/data analysis techniques. New methods should be proven and demonstrate an advance in the field.
Molecular Omics only accepts articles of high importance and interest that provide significant new insight into important chemical or biological problems. This could be fundamental research that significantly increases understanding or research that demonstrates clear functional benefits.
Papers reporting new results that could be routinely predicted, do not show a significant improvement over known research, or are of interest only to the specialist in the area are not suitable for publication in Molecular Omics.