罗氏沼虾克雷伯菌mr-1S全基因组测序及功能分析

IF 1.9 4区 农林科学 Q2 FISHERIES
Yang Xu, Ying Zhao, Haihua Cheng, Fei Peng, Qiang Gao
{"title":"罗氏沼虾克雷伯菌mr-1S全基因组测序及功能分析","authors":"Yang Xu,&nbsp;Ying Zhao,&nbsp;Haihua Cheng,&nbsp;Fei Peng,&nbsp;Qiang Gao","doi":"10.1155/are/3407093","DOIUrl":null,"url":null,"abstract":"<div>\n <p><b>Background:</b><i>Klebsiella</i> mr-1S, a newly emerging pathogen that poses a substantial threat to public health by inducing severe infectious diseases, has been detected in <i>Macrobrachium rosenbergii</i> for the first time in our prior investigation. Given its potential for environmental adaptation and genomic evolution, this study aims to delve into these aspects to better understand its pathogenicity and evolutionary trajectory.</p>\n <p><b>Methods:</b> In this study, the <i>Klebsiella</i> isolates were subjected to routine cultivation in a tryptic soya broth (TSB) medium. Subsequently, the genomic DNA of each isolate was individually extracted and analyzed. Prior to genomic sequencing, the integrity and concentration of the DNA samples were meticulously evaluated to ensure the accuracy and reliability of the subsequent sequencing process.</p>\n <p><b>Results:</b> The genomic sequence of <i>Klebsiella</i> mr-1S was deciphered, revealing a length of 5,143,806 base pairs with a GC content of 54.97%. Remarkably, the genome encompasses a multitude of putative mobile genetic elements (MGEs), including 43 genomic islands (GIs) and 2 prophages. These elements confer upon the bacterium crucial adaptive attributes such as resistance, virulence, and metabolic capabilities. Notably, the identification of prophage-associated clusters originating from the genus Pseudomonas suggests a potential horizontal gene transfer (HGT) mechanism mediated by phages within Pseudomonas, highlighting the complex genetic interactions between different bacterial species.</p>\n <p><b>Conclusion:</b> In addition, the presence of two genes encoding CRISPR-Cas proteins within the <i>Klebsiella</i> mr-1S genome indicates the existence of a functional CRISPR-Cas system in this bacterium. This finding implies that during its evolutionary history, Klebsiella mr-1S may have developed mechanisms to evade host immune recognition, thereby facilitating efficient HGT and enhancing its adaptability and survival capabilities in diverse environments. Overall, this study provides novel insights into the environmental adaptability and genomic plasticity of <i>Klebsiella</i> from <i>Macrobrachium rosenbergii</i>, underscoring its potential as an emerging pathogen in aquatic ecosystems and paving the way for future research on its pathogenic mechanisms and potential control strategies.</p>\n </div>","PeriodicalId":8104,"journal":{"name":"Aquaculture Research","volume":"2025 1","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/are/3407093","citationCount":"0","resultStr":"{\"title\":\"Whole-Genome Sequencing and Functional Analysis of Klebsiella Strain mr-1S Originating From Macrobrachium rosenbergii\",\"authors\":\"Yang Xu,&nbsp;Ying Zhao,&nbsp;Haihua Cheng,&nbsp;Fei Peng,&nbsp;Qiang Gao\",\"doi\":\"10.1155/are/3407093\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n <p><b>Background:</b><i>Klebsiella</i> mr-1S, a newly emerging pathogen that poses a substantial threat to public health by inducing severe infectious diseases, has been detected in <i>Macrobrachium rosenbergii</i> for the first time in our prior investigation. Given its potential for environmental adaptation and genomic evolution, this study aims to delve into these aspects to better understand its pathogenicity and evolutionary trajectory.</p>\\n <p><b>Methods:</b> In this study, the <i>Klebsiella</i> isolates were subjected to routine cultivation in a tryptic soya broth (TSB) medium. Subsequently, the genomic DNA of each isolate was individually extracted and analyzed. Prior to genomic sequencing, the integrity and concentration of the DNA samples were meticulously evaluated to ensure the accuracy and reliability of the subsequent sequencing process.</p>\\n <p><b>Results:</b> The genomic sequence of <i>Klebsiella</i> mr-1S was deciphered, revealing a length of 5,143,806 base pairs with a GC content of 54.97%. Remarkably, the genome encompasses a multitude of putative mobile genetic elements (MGEs), including 43 genomic islands (GIs) and 2 prophages. These elements confer upon the bacterium crucial adaptive attributes such as resistance, virulence, and metabolic capabilities. Notably, the identification of prophage-associated clusters originating from the genus Pseudomonas suggests a potential horizontal gene transfer (HGT) mechanism mediated by phages within Pseudomonas, highlighting the complex genetic interactions between different bacterial species.</p>\\n <p><b>Conclusion:</b> In addition, the presence of two genes encoding CRISPR-Cas proteins within the <i>Klebsiella</i> mr-1S genome indicates the existence of a functional CRISPR-Cas system in this bacterium. This finding implies that during its evolutionary history, Klebsiella mr-1S may have developed mechanisms to evade host immune recognition, thereby facilitating efficient HGT and enhancing its adaptability and survival capabilities in diverse environments. Overall, this study provides novel insights into the environmental adaptability and genomic plasticity of <i>Klebsiella</i> from <i>Macrobrachium rosenbergii</i>, underscoring its potential as an emerging pathogen in aquatic ecosystems and paving the way for future research on its pathogenic mechanisms and potential control strategies.</p>\\n </div>\",\"PeriodicalId\":8104,\"journal\":{\"name\":\"Aquaculture Research\",\"volume\":\"2025 1\",\"pages\":\"\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2025-04-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1155/are/3407093\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Aquaculture Research\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1155/are/3407093\",\"RegionNum\":4,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"FISHERIES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aquaculture Research","FirstCategoryId":"97","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1155/are/3407093","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0

摘要

背景:本文首次在罗氏沼虾(Macrobrachium rosenbergii)中检出克雷伯氏菌(Klebsiella mr-1S),这是一种通过诱导严重传染病对公众健康构成重大威胁的新型病原体。鉴于其在环境适应和基因组进化方面的潜力,本研究旨在深入研究这些方面,以更好地了解其致病性和进化轨迹。方法:在本研究中,克雷伯菌分离株在胰蛋白酶豆汤(TSB)培养基中进行常规培养。随后,每个分离物的基因组DNA被单独提取和分析。在基因组测序之前,对DNA样本的完整性和浓度进行了细致的评估,以确保后续测序过程的准确性和可靠性。结果:获得克雷伯菌mr-1S基因组序列,全长5143,806个碱基对,GC含量为54.97%。值得注意的是,基因组包含大量假定的可移动遗传元件(MGEs),包括43个基因组岛(gi)和2个噬菌体。这些因素赋予细菌至关重要的适应性属性,如抵抗力、毒力和代谢能力。值得注意的是,来自假单胞菌属的噬菌体相关簇的鉴定表明假单胞菌内噬菌体介导的潜在水平基因转移(HGT)机制,突出了不同细菌物种之间复杂的遗传相互作用。结论:此外,克雷伯氏菌mr-1S基因组中存在两个编码CRISPR-Cas蛋白的基因,表明该细菌存在功能性CRISPR-Cas系统。这一发现表明,克雷伯菌mr-1S在其进化史中可能已经形成了逃避宿主免疫识别的机制,从而促进了高效的HGT,增强了其在不同环境中的适应性和生存能力。总之,本研究对罗氏沼虾克雷伯氏菌的环境适应性和基因组可塑性提供了新的见解,强调了其作为水生生态系统中新兴病原体的潜力,为进一步研究其致病机制和潜在的控制策略铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Whole-Genome Sequencing and Functional Analysis of Klebsiella Strain mr-1S Originating From Macrobrachium rosenbergii

Whole-Genome Sequencing and Functional Analysis of Klebsiella Strain mr-1S Originating From Macrobrachium rosenbergii

Background:Klebsiella mr-1S, a newly emerging pathogen that poses a substantial threat to public health by inducing severe infectious diseases, has been detected in Macrobrachium rosenbergii for the first time in our prior investigation. Given its potential for environmental adaptation and genomic evolution, this study aims to delve into these aspects to better understand its pathogenicity and evolutionary trajectory.

Methods: In this study, the Klebsiella isolates were subjected to routine cultivation in a tryptic soya broth (TSB) medium. Subsequently, the genomic DNA of each isolate was individually extracted and analyzed. Prior to genomic sequencing, the integrity and concentration of the DNA samples were meticulously evaluated to ensure the accuracy and reliability of the subsequent sequencing process.

Results: The genomic sequence of Klebsiella mr-1S was deciphered, revealing a length of 5,143,806 base pairs with a GC content of 54.97%. Remarkably, the genome encompasses a multitude of putative mobile genetic elements (MGEs), including 43 genomic islands (GIs) and 2 prophages. These elements confer upon the bacterium crucial adaptive attributes such as resistance, virulence, and metabolic capabilities. Notably, the identification of prophage-associated clusters originating from the genus Pseudomonas suggests a potential horizontal gene transfer (HGT) mechanism mediated by phages within Pseudomonas, highlighting the complex genetic interactions between different bacterial species.

Conclusion: In addition, the presence of two genes encoding CRISPR-Cas proteins within the Klebsiella mr-1S genome indicates the existence of a functional CRISPR-Cas system in this bacterium. This finding implies that during its evolutionary history, Klebsiella mr-1S may have developed mechanisms to evade host immune recognition, thereby facilitating efficient HGT and enhancing its adaptability and survival capabilities in diverse environments. Overall, this study provides novel insights into the environmental adaptability and genomic plasticity of Klebsiella from Macrobrachium rosenbergii, underscoring its potential as an emerging pathogen in aquatic ecosystems and paving the way for future research on its pathogenic mechanisms and potential control strategies.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Aquaculture Research
Aquaculture Research 农林科学-渔业
CiteScore
4.60
自引率
5.00%
发文量
464
审稿时长
5.3 months
期刊介绍: International in perspective, Aquaculture Research is published 12 times a year and specifically addresses research and reference needs of all working and studying within the many varied areas of aquaculture. The Journal regularly publishes papers on applied or scientific research relevant to freshwater, brackish, and marine aquaculture. It covers all aquatic organisms, floristic and faunistic, related directly or indirectly to human consumption. The journal also includes review articles, short communications and technical papers. Young scientists are particularly encouraged to submit short communications based on their own research.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信