S. Hari Krishna Kumar , Ragothaman Prathiviraj , Muregesan Sobanaa , George Seghal Kiran , Joseph Selvin
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Identification of functional annotation revealed 17 antimicrobial resistance (AMR) genes, including three copies of the <em>adeF</em> gene, which encapsulates a resistance-nodulation-division (RND) efflux system that provides resistance to tetracyclines and fluoroquinolones. At the same time, related genes were also associated with resistance to β-lactams, aminoglycosides, macrolides, glycopeptides, and disinfectants, suggesting that this strain may have multidrug resistance potential. Further secondary metabolite prediction revealed biosynthetic gene clusters for ririwpeptide, a cyclic lipopetide with membrane-disrupting antibacterial and anticancer activity, and prodigiosin, which has gained notoriety for its antimicrobial, anticancer, and immunosuppressant activities as a red-colored pigment. Genome-based evidence clearly indicates that <em>S. marcescens</em> CAB03 is a contributor to coral health degradation through the proliferation of AMR bacteria and also a potential repository of bioactive compounds for pharmaceutical purposes. We used whole-genome sequencing here to address a long-standing knowledge gap regarding AMR bacteria associated with coral from Indian reefs. This study illustrates the need for genomic surveillance and conservation for AMR bacteria, ideally and more generally advances the study of microbial metabolites for drug discovery. 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Coral-associated microbial diversity is crucial for reef resilience; however, there is a limited understanding of opportunistic pathogens from Indian reefs. Here, we report the identification of <em>Serratia marcescens</em> CAB03, which may be associated with coral disease, isolated from <em>Acropora cythera</em> of Palk Bay coral reef, India. Whole genome sequencing of <em>S. marcescens</em> CAB03 produced 24 contigs (total G + C 59.7 %) and 4713 predicted genes. Identification of functional annotation revealed 17 antimicrobial resistance (AMR) genes, including three copies of the <em>adeF</em> gene, which encapsulates a resistance-nodulation-division (RND) efflux system that provides resistance to tetracyclines and fluoroquinolones. At the same time, related genes were also associated with resistance to β-lactams, aminoglycosides, macrolides, glycopeptides, and disinfectants, suggesting that this strain may have multidrug resistance potential. 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引用次数: 0
摘要
人们对耐抗生素病原体了解甚少,并对珊瑚礁生态系统构成新威胁。与珊瑚相关的微生物多样性对珊瑚礁的恢复力至关重要;然而,人们对来自印度珊瑚礁的机会性病原体的了解有限。本文报道了从印度Palk Bay珊瑚礁的Acropora cythera中分离到的可能与珊瑚病有关的粘质沙雷氏菌CAB03。S. marcescens CAB03全基因组测序得到24个contigs(总G + C 59.7%)和4713个预测基因。功能注释鉴定揭示了17个抗微生物药物耐药性(AMR)基因,其中包括3个拷贝的adeF基因,该基因封装了一个耐药-结核-分裂(RND)外排系统,提供对四环素和氟喹诺酮类药物的耐药性。同时,相关基因还与β-内酰胺类、氨基糖苷类、大环内酯类、糖肽类和消毒剂耐药有关,提示该菌株可能具有多药耐药潜力。进一步的次生代谢物预测揭示了ririwpeptide(一种具有破坏膜的抗菌和抗癌活性的环状脂肽)和prodigiosin(作为一种红色色素,因其抗菌、抗癌和免疫抑制活性而闻名)的生物合成基因簇。基于基因组的证据清楚地表明,S. marcescens CAB03是通过AMR细菌的增殖导致珊瑚健康退化的一个贡献者,也是用于制药目的的生物活性化合物的潜在储存库。我们在这里使用全基因组测序来解决长期以来关于与印度珊瑚礁珊瑚相关的AMR细菌的知识差距。这项研究说明了AMR细菌基因组监测和保护的必要性,理想地和更广泛地推进了药物发现的微生物代谢物研究。将病原体基因组图谱与珊瑚礁健康和应用生物技术的进展联系起来,揭示了保护珊瑚礁的新理由,并为潜在的药物开发提供了新的数据来源。
Antimicrobial resistance and bioactive metabolites of Serratia marcescens CAB03 from a Palk Bay coral reef
Antimicrobial-resistant pathogens are poorly understood and pose emerging threats to coral reef ecosystems. Coral-associated microbial diversity is crucial for reef resilience; however, there is a limited understanding of opportunistic pathogens from Indian reefs. Here, we report the identification of Serratia marcescens CAB03, which may be associated with coral disease, isolated from Acropora cythera of Palk Bay coral reef, India. Whole genome sequencing of S. marcescens CAB03 produced 24 contigs (total G + C 59.7 %) and 4713 predicted genes. Identification of functional annotation revealed 17 antimicrobial resistance (AMR) genes, including three copies of the adeF gene, which encapsulates a resistance-nodulation-division (RND) efflux system that provides resistance to tetracyclines and fluoroquinolones. At the same time, related genes were also associated with resistance to β-lactams, aminoglycosides, macrolides, glycopeptides, and disinfectants, suggesting that this strain may have multidrug resistance potential. Further secondary metabolite prediction revealed biosynthetic gene clusters for ririwpeptide, a cyclic lipopetide with membrane-disrupting antibacterial and anticancer activity, and prodigiosin, which has gained notoriety for its antimicrobial, anticancer, and immunosuppressant activities as a red-colored pigment. Genome-based evidence clearly indicates that S. marcescens CAB03 is a contributor to coral health degradation through the proliferation of AMR bacteria and also a potential repository of bioactive compounds for pharmaceutical purposes. We used whole-genome sequencing here to address a long-standing knowledge gap regarding AMR bacteria associated with coral from Indian reefs. This study illustrates the need for genomic surveillance and conservation for AMR bacteria, ideally and more generally advances the study of microbial metabolites for drug discovery. Linking pathogen genomic profiles to reef health and advances in applied biotechnology reveal new reasons for coral reef conservation and provide new sources of data for potential drug development.
Gene ReportsBiochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍:
Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.