Genome Annotation of Novel K1 Subcluster Mycobacteriophage Blizzard

Morgane Brouillard-Galipeau, Bao-An Chau, Jamie Cyr, Rafael Intrevado, Sunu Kim, Cal Koger-Pease, E. Lapshina, A. Mircescu, Daniella Serrador, Michael Slattery, Benjamin Vonniessen, Michael Shamash, J. Chahal
{"title":"Genome Annotation of Novel K1 Subcluster Mycobacteriophage Blizzard","authors":"Morgane Brouillard-Galipeau, Bao-An Chau, Jamie Cyr, Rafael Intrevado, Sunu Kim, Cal Koger-Pease, E. Lapshina, A. Mircescu, Daniella Serrador, Michael Slattery, Benjamin Vonniessen, Michael Shamash, J. Chahal","doi":"10.26443/msurj.v17i1.173","DOIUrl":null,"url":null,"abstract":"The evolution of antimicrobial resistant pathogens constitutes a significant global public health threat. Combined with the lack of incentive for pharmaceutical companies to invest in developing new antibiotics, it is clear alternative treatments are needed. Bacteriophages present one possible avenue as they harness the diversity and specificity of a microorganism that has coevolved with bacteria. However, little is known about these bacterial viruses. The SEA-PHAGES program was designed to identify and characterize novel bacteriophages and their associated gene functions. Herein, we report the genome annotation of one such novel phage: Mycobacteriophage Blizzard (GenBank accession number MW712733). Blizzard’s gene content was functionally annotated using bioinformatic tools including DNA Master, Phamerator, and NCBI BLAST, to call start sites as well as predict gene function. Overall, 96 genes were identified, including a tRNA and a translational frameshift, using highly similar reference phages BEEST, Belladonna, and CREW. From the 96 genes identified, 46 were functionally annotated. The remaining 50 genes have unknown functions due to the lack of significant matches in the databases. Our results demonstrate a novel annotated phage, whose genome serves to expand the understanding of phage biology and potential implications as alternative treatment to antibiotics.","PeriodicalId":91927,"journal":{"name":"McGill Science undergraduate research journal : MSURJ","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"McGill Science undergraduate research journal : MSURJ","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26443/msurj.v17i1.173","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The evolution of antimicrobial resistant pathogens constitutes a significant global public health threat. Combined with the lack of incentive for pharmaceutical companies to invest in developing new antibiotics, it is clear alternative treatments are needed. Bacteriophages present one possible avenue as they harness the diversity and specificity of a microorganism that has coevolved with bacteria. However, little is known about these bacterial viruses. The SEA-PHAGES program was designed to identify and characterize novel bacteriophages and their associated gene functions. Herein, we report the genome annotation of one such novel phage: Mycobacteriophage Blizzard (GenBank accession number MW712733). Blizzard’s gene content was functionally annotated using bioinformatic tools including DNA Master, Phamerator, and NCBI BLAST, to call start sites as well as predict gene function. Overall, 96 genes were identified, including a tRNA and a translational frameshift, using highly similar reference phages BEEST, Belladonna, and CREW. From the 96 genes identified, 46 were functionally annotated. The remaining 50 genes have unknown functions due to the lack of significant matches in the databases. Our results demonstrate a novel annotated phage, whose genome serves to expand the understanding of phage biology and potential implications as alternative treatment to antibiotics.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
新的K1亚簇食管分枝杆菌暴雪的基因组注释
抗微生物药物耐药性病原体的演变构成了重大的全球公共卫生威胁。再加上制药公司投资开发新抗生素的动力不足,显然需要替代疗法。噬菌体提供了一种可能的途径,因为它们利用与细菌共同进化的微生物的多样性和特异性。然而,人们对这些细菌病毒知之甚少。SEA-PHAGES程序旨在鉴定和表征新型噬菌体及其相关基因功能。在此,我们报道了一种这样的新型噬菌体的基因组注释:Mycobacteriophage Blizzard (GenBank登录号MW712733)。使用DNA Master、Phamerator和NCBI BLAST等生物信息学工具对暴雪的基因内容进行功能注释,以调用起始位点并预测基因功能。总共鉴定了96个基因,包括一个tRNA和一个翻译移码,使用高度相似的参考噬菌体BEEST、颠茄和CREW。在鉴定的96个基因中,46个被功能注释。其余50个基因由于在数据库中缺乏显著匹配而功能未知。我们的研究结果展示了一种新的带注释的噬菌体,其基因组有助于扩大对噬菌体生物学的理解和作为抗生素替代治疗的潜在意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Role of Iron in Epidermal Healing and Infection At Once Friends and Foes Enduring Controversial Story in the Human Brain Rho GTPase regulatory proteins contribute to podocyte morphology and function Uncovering the Regulators of CRISPR-Cas Immunity
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1