Tobi E Nagel, Ivy J Mutai, Theodore Josephs, Martha R J Clokie
{"title":"A Brief History of Phage Research and Teaching in Africa.","authors":"Tobi E Nagel, Ivy J Mutai, Theodore Josephs, Martha R J Clokie","doi":"10.1089/phage.2022.29037.inp","DOIUrl":"10.1089/phage.2022.29037.inp","url":null,"abstract":"","PeriodicalId":74428,"journal":{"name":"PHAGE (New Rochelle, N.Y.)","volume":"3 4","pages":"184-193"},"PeriodicalIF":0.0,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917308/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10728438","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Deyvid Amgarten, Bruno Koshin Vázquez Iha, Carlos Morais Piroupo, Aline Maria da Silva, João Carlos Setubal
{"title":"vHULK, a New Tool for Bacteriophage Host Prediction Based on Annotated Genomic Features and Neural Networks.","authors":"Deyvid Amgarten, Bruno Koshin Vázquez Iha, Carlos Morais Piroupo, Aline Maria da Silva, João Carlos Setubal","doi":"10.1089/phage.2021.0016","DOIUrl":"10.1089/phage.2021.0016","url":null,"abstract":"<p><strong>Background: </strong>The experimental determination of a bacteriophage host is a laborious procedure. Thus, there is a pressing need for reliable computational predictions of bacteriophage hosts.</p><p><strong>Materials and methods: </strong>We developed the program vHULK for phage host prediction based on 9504 phage genome features, which consider alignment significance scores between predicted proteins and a curated database of viral protein families. The features were fed to a neural network, and two models were trained to predict 77 host genera and 118 host species.</p><p><strong>Results: </strong>In controlled random test sets with 90% redundancy reduction in terms of protein similarity, vHULK obtained on average 83% precision and 79% recall at the genus level, and 71% precision and 67% recall at the species level. The performance of vHULK was compared against three other tools on a test data set with 2153 phage genomes. On this data set, vHULK achieved better performance at both the genus and the species levels than the other tools.</p><p><strong>Conclusions: </strong>Our results suggest that vHULK represents an advance on the state of art in phage host prediction.</p>","PeriodicalId":74428,"journal":{"name":"PHAGE (New Rochelle, N.Y.)","volume":"3 4","pages":"204-212"},"PeriodicalIF":0.0,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917316/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10728437","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Emmanuel W Bumunang, Tim A McAllister, Rodrigo Ortega Polo, Collins N Ateba, Kim Stanford, Jared Schlechte, Matthew Walker, Kellie MacLean, Yan D Niu
{"title":"Genomic Profiling of Non-O157 Shiga Toxigenic <i>Escherichia coli</i>-Infecting Bacteriophages from South Africa.","authors":"Emmanuel W Bumunang, Tim A McAllister, Rodrigo Ortega Polo, Collins N Ateba, Kim Stanford, Jared Schlechte, Matthew Walker, Kellie MacLean, Yan D Niu","doi":"10.1089/phage.2022.0003","DOIUrl":"10.1089/phage.2022.0003","url":null,"abstract":"<p><strong>Background: </strong>Non-O157 Shiga toxigenic <i>Escherichia coli</i> (STEC) are one of the most important food and waterborne pathogens worldwide. Although bacteriophages (phages) have been used for the biocontrol of these pathogens, a comprehensive understanding of the genetic characteristics and lifestyle of potentially effective candidate phages is lacking.</p><p><strong>Materials and methods: </strong>In this study, 10 non-O157-infecting phages previously isolated from feedlot cattle and dairy farms in the North-West province of South Africa were sequenced, and their genomes were analyzed.</p><p><strong>Results: </strong>Comparative genomics and proteomics revealed that the phages were closely related to other <i>E. coli</i>-infecting <i>Tunaviruses</i>, <i>Seuratviruses</i>, <i>Carltongylesviruses</i>, <i>Tequatroviruses</i>, and <i>Mosigviruses</i> from the National Center for Biotechnology Information GenBank database. Phages lacked integrases associated with a lysogenic cycle and genes associated with antibiotic resistance and Shiga toxins.</p><p><strong>Conclusions: </strong>Comparative genomic analysis identified a diversity of unique non-O157-infecting phages, which could be used to mitigate the abundance of various non-O157 STEC serogroups without safety concerns.</p>","PeriodicalId":74428,"journal":{"name":"PHAGE (New Rochelle, N.Y.)","volume":"3 4","pages":"221-230"},"PeriodicalIF":0.0,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917312/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10739646","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Purification of Functional Gene Transfer Agents Using Two-Step Preparative Monolithic Chromatography.","authors":"Evan Langille, Christina S Bottaro, Andrew S Lang","doi":"10.1089/phage.2022.0035","DOIUrl":"10.1089/phage.2022.0035","url":null,"abstract":"<p><strong>Background: </strong>Gene transfer agents (GTAs) are phage-like particles that transfer cellular genomic DNA between cells. A hurdle faced in studying GTA function and interactions with cells is the difficulty in obtaining pure and functional GTAs from cultures.</p><p><strong>Materials and methods: </strong>We used a novel two-step method for purification of GTAs from <i>R. capsulatus</i> by monolithic chromatography.</p><p><strong>Results: </strong>Our efficient and simple process had advantages compared to previous approaches. The purified GTAs retained gene transfer activity and the packaged DNA could be used for further studies.</p><p><strong>Conclusions: </strong>This method is applicable to GTAs produced by other species and small phages, and could be useful for therapeutic applications.</p>","PeriodicalId":74428,"journal":{"name":"PHAGE (New Rochelle, N.Y.)","volume":"3 4","pages":"194-203"},"PeriodicalIF":0.0,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917305/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10728440","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
PHAGE (New Rochelle, N.Y.)Pub Date : 2022-12-01Epub Date: 2022-12-19DOI: 10.1089/phage.2022.29038.editorial
Martha Clokie, Thomas Sicheritz-Pontén
{"title":"Reflections on 2022: A Progressive Year for Phage Therapy.","authors":"Martha Clokie, Thomas Sicheritz-Pontén","doi":"10.1089/phage.2022.29038.editorial","DOIUrl":"10.1089/phage.2022.29038.editorial","url":null,"abstract":"","PeriodicalId":74428,"journal":{"name":"PHAGE (New Rochelle, N.Y.)","volume":"3 4","pages":"181-182"},"PeriodicalIF":0.0,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917313/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9297203","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ivan Vuong, Catherine M Mageeney, Kelly P Williams
{"title":"BigDNA: Primer Design Software for Overlap-Based Assembly of Phage Genomes and Larger DNAs.","authors":"Ivan Vuong, Catherine M Mageeney, Kelly P Williams","doi":"10.1089/phage.2022.0033","DOIUrl":"10.1089/phage.2022.0033","url":null,"abstract":"<p><strong>Background: </strong>Gibson assembly and assembly-in-yeast are strategies to create long synthetic DNAs from diverse fragments, for example, when engineering bacteriophage genomes. Design for these methods requires terminal sequence overlaps in the fragments, determining the order of assembly. Design to rebuild a genomic fragment that is too long for a single PCR presents a puzzle since some candidate joint regions cannot yield satisfactory primers for the overlap. No existing overlap assembly design software is open-source, and none explicitly supports rebuilding.</p><p><strong>Methods: </strong>We describe here bigDNA software that solves the rebuilding puzzle by recursive backtracking, with options to remove or introduce genes; it also tests for mispriming on the template DNA. BigDNA was tested with 3082 prophages and other genomic islands (GIs), from 20 to 100 kb, and the synthetic <i>Mycoplasma genitalium</i> genome.</p><p><strong>Results: </strong>Rebuilding assembly design succeeded for all but ∼1% of GIs.</p><p><strong>Conclusion: </strong>BigDNA will speed and standardize assembly design.</p>","PeriodicalId":74428,"journal":{"name":"PHAGE (New Rochelle, N.Y.)","volume":"3 4","pages":"213-220"},"PeriodicalIF":0.0,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917320/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10728439","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Special Issue on Phage/Host Combat: Phage Strategies for Taking Over the Host and Host Strategies for Defenses.","authors":"Martha R J Clokie, Deborah M Hinton","doi":"10.1089/phage.2022.29034.editorial","DOIUrl":"https://doi.org/10.1089/phage.2022.29034.editorial","url":null,"abstract":"","PeriodicalId":74428,"journal":{"name":"PHAGE (New Rochelle, N.Y.)","volume":"3 3","pages":"125-126"},"PeriodicalIF":0.0,"publicationDate":"2022-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917307/pdf/phage.2022.29034.editorial.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10190528","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"<i>Enterobacteria</i> Phage Ac3's Genome Annotation and Host Range Analysis Against the ECOR Reference Library.","authors":"Emma L Farquharson, Sam R Nugen","doi":"10.1089/phage.2022.0008","DOIUrl":"https://doi.org/10.1089/phage.2022.0008","url":null,"abstract":"<p><p>Host range analyses and genome sequencing/annotation of bacteriophage isolates allow more effective development of tools for applications in medicine, agriculture, and the environment and expand our understanding of phage biology. Here we present the complete sequence of phage Ac3's assembled and annotated genome (accession OK040907). Originally referred to simply as \"3,\" Ac3 has previously been described as a T4-like bacteriophage belonging to the <i>Myoviridae</i> family in the <i>Caudovirales</i> order of tailed bacteriophages. Using a combination of spot tests and full plate plaque assays, Ac3's permissive and adsorptive host range were evaluated against the ECOR Reference Library; a panel of 72 <i>Escherichia coli</i> isolates meant to represent the diversity of <i>E. coli</i>. Spot assays revealed that Ac3 could adsorb to 43 of the 72 strains (59.7%), whereas plaque assays demonstrated Ac3's ability to complete replication within 27 of the 72 strains (37.5%). By overlaying spot test and plaque assay results, 16 of the 45 nonpermissive ECOR strains (35.5%) were highlighted as being able to support Ac3's adsorption and tail contraction, but not its replication. Further characterization of Ac3 is still needed, however, the study presented here provides a solid starting point for future research.</p>","PeriodicalId":74428,"journal":{"name":"PHAGE (New Rochelle, N.Y.)","volume":"3 3","pages":"165-170"},"PeriodicalIF":0.0,"publicationDate":"2022-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527048/pdf/phage.2022.0008.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10136377","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Study of Ren, RexA, and RexB Functions Provides Insight Into the Complex Interaction Between Bacteriophage λ and Its Host, <i>Escherichia coli</i>.","authors":"Lynn C Thomason, Donald L Court","doi":"10.1089/phage.2022.0020","DOIUrl":"https://doi.org/10.1089/phage.2022.0020","url":null,"abstract":"<p><p>The phage λ <i>rexA</i> and <i>rexB</i> genes are expressed from the <i>P</i> <sub>RM</sub> promoter in λ lysogens along with the <i>c</i>I repressor gene. <i>RexB</i> is also expressed from a second promoter, <i>P</i> <sub>LIT</sub>, embedded in <i>rexA</i>. The combined expression of <i>rexA</i> and <i>rexB</i> causes <i>Escherichia coli</i> to be more ultraviolet (UV) sensitive. Sensitivity is further increased when RexB levels are reduced by a defect in the <i>P</i> <sub>LIT</sub> promoter, thus the degree of sensitivity can be modulated by the ratio of RexA/RexB. Expression of the phage λ <i>ren</i> gene rescues this host UV sensitive phenotype; Ren also rescues an aberrant lysis phenotype caused by RexA and RexB. We screened an <i>E. coli</i> two-hybrid library to identify bacterial proteins with which each of these phage proteins physically interact. The results extend previous observations concerning λ Rex exclusion and show the importance of <i>E. coli</i> electron transport and sulfur assimilation pathways for the phage.</p>","PeriodicalId":74428,"journal":{"name":"PHAGE (New Rochelle, N.Y.)","volume":"3 3","pages":"153-164"},"PeriodicalIF":0.0,"publicationDate":"2022-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529316/pdf/phage.2022.0020.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10130913","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}