Structure of the Capsid Size-Determining Scaffold Of
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CHAPTER 1 Viruses and Their Importance CHAPTER 1 AT A GLANCE Viruses infect: • Humans • Other vertebrates • Invertebrates Smallpox1 Bluetongue virus-infected sheep2 Tipula sp. larvae (leatherjackets) infected with invertebrate iridescent virus 1 • Plants • Fungi • Bacteria COPYRIGHTED MATERIAL Escherichia coli Delayed emergence of Damaged potato Mushroom virus X4 cell potato caused by tobacco (spraing) caused by with phage T4 attached5 rattle virus infection3 tobacco rattle virus infection3 1 cc01.indd01.indd 1 118/01/138/01/13 88:14:14 PPMM 2 CHAPTER 1 VIRUSES AND THEIR IMPORTANCE CHAPTER 1 AT A GLANCE (continued) Some viruses are useful: • Phage typing of bacteria • Sources of enzymes • Pesticides • Anti-bacterial agents • Anti-cancer agents • Gene vectors Viruses are parasites; they depend on cells for molecular building blocks, machinery, and energy. Virus particles are small; dimensions range approx. from 20–400 nm. A virus genome is composed of one of the following: double-stranded single-stranded double-stranded single-stranded DNA DNA RNA RNA Photographs reproduced with permission of 1 World Health Organization. 2 From Umeshappa et al . (2011) Veterinary Immunology and Immunopathology , 141, 230. Reproduced by permission of Elsevier and the authors. 3 MacFarlane and Robinson (2004) Chapter 11, Microbe-Vector Interactions in Vector-Borne Diseases , 63rd Symposium of the Society for General Microbiology, Cambridge University Press. Reprinted with permission. 4 University of Warwick. 5 Cornell Integrated Microscopy Center. The presence of viruses is obvious in host organ- 1.1 VIRUSES ARE UBIQUITOUS ON EARTH isms showing signs of disease. Many healthy organisms, however, are hosts of non-pathogenic virus infections, Viruses infect all cellular life forms: eukaryotes (ver- some of which are active, while some are quiescent. -
Abstract 9 10 Bacteriophages (Phages) Are Bacterial Parasites That Can Themselves Be Parasitized by Phage 11 Satellites
bioRxiv preprint doi: https://doi.org/10.1101/2021.03.30.437493; this version posted March 30, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 To catch a hijacker: abundance, evolution and genetic diversity of 2 P4-like bacteriophage satellites 3 Jorge A. Moura de Sousa1,*& Eduardo P.C. Rocha1,* 4 5 1Microbial Evolutionary Genomics, Institut Pasteur, CNRS, UMR3525, Paris 75015, France 6 * corresponding authors: [email protected], [email protected] 7 8 Abstract 9 10 Bacteriophages (phages) are bacterial parasites that can themselves be parasitized by phage 11 satellites. The molecular mechanisms used by satellites to hijack phages are sometimes 12 understood in great detail, but the origins, abundance, distribution, and composition of these 13 elements are poorly known. Here, we show that P4-like elements are present in more than 14 10% of the genomes of Enterobacterales, and in almost half of those of Escherichia coli, 15 sometimes in multiple distinct copies. We identified over 1000 P4-like elements with very 16 conserved genetic organization of the core genome and a few hotspots with highly variable 17 genes. These elements are never found in plasmids and have very little homology to known 18 phages, suggesting an independent evolutionary origin. Instead, they are scattered across 19 chromosomes, possibly because their integrases are often exchanged with other elements. 20 The rooted phylogenies of hijacking functions are correlated and suggest longstanding co- 21 evolution. -
United States Patent ( 10 ) Patent No.: US 10,676,721 B2 Collins Et Al
US010676721B2 United States Patent ( 10 ) Patent No.: US 10,676,721 B2 Collins et al. (45 ) Date of Patent : Jun . 9 , 2020 ( 54 ) BACTERIOPHAGES EXPRESSING 6,699,701 B1 3/2004 Sulakvelidze et al . ANTIMICROBIAL PEPTIDES AND USES 6,759,229 B2 * 7/2004 Schaak 435 /235.1 7,211,426 B2 5/2007 Bruessow et al. THEREOF 8,153,119 B2 4/2012 Collins et al. 8,182,804 B1 5/2012 Collins et al. ( 75 ) Inventors : James J. Collins, Newton , MA (US ) ; 2001/0026795 A1 10/2001 Merril et al . Michael Koeris , Natick , MA (US ) ; 2002/0013671 Al 1/2002 Ananthaiyer et al. 2004/0161141 A1 8/2004 Dewaele Timothy Kuan - Ta Lu , Charlestown, 2005/0004030 A1 1/2005 Fischetti et al . MA (US ) ; Tanguy My Chau , Palo 2007/0020240 A1 1/2007 Jayasheela et al. Alto , CA ( US ) ; Gregory 2007/0134207 Al 6/2007 Bruessow et al . Stephanopoulos , Winchester , MA (US ) ; 2007/0207209 A1 * 9/2007 Murphy A61K 9/06 Christopher Jongsoo Yoon , Seoul 424/484 (KR ) 2007/0248724 Al 10/2007 Sulakvelidze et al. 2008/0194000 Al 8/2008 Pasternack et al. ( 73 ) Assignees : Trustees of Boston University , Boston , 2008/0247997 Al 10/2008 Reber et al . MA (US ) ; Massachusetts Institute of 2008/0311643 A1 12/2008 Sulakvelidze et al. Technology , Cambridge, MA (US ) 2008/0318867 A1 12/2008 Loessner et al. FOREIGN PATENT DOCUMENTS ( * ) Notice: Subject to any disclaimer , the term of this patent is extended or adjusted under 35 EP 0403458 A1 12/1990 CO7K 7/10 WO 2002/034892 Al 5/2002 U.S.C. -
Article Differential Codon Adaptation
Differential Codon Adaptation between dsDNA and ssDNA Phages in Escherichia coli Shivapriya Chithambaram,1 Ramanandan Prabhakaran,1 and Xuhua Xia*,1 1Department of Biology and Center for Advanced Research in Environmental Genomics, University of Ottawa, Ottawa, Ontario, Canada *Corresponding author: E-mail: [email protected]. Associate editor: Helen Piontkivska Abstract Because phages use their host translation machinery, their codon usage should evolve toward that of highly expressed host genes. We used two indices to measure codon adaptation of phages to their host, rRSCU (thecorrelationinrelative synonymous codon usage [RSCU] between phages and their host) and Codon Adaptation Index (CAI) computed with highly expressed host genes as the reference set (because phage translation depends on host translation machinery). These indices used for this purpose are appropriate only when hosts exhibit little mutation bias, so only phages para- Downloaded from sitizing Escherichia coli were included in the analysis. For double-stranded DNA (dsDNA) phages, both rRSCU and CAI decrease with increasing number of transfer RNA genes encoded by the phage genome. rRSCU is greater for dsDNA phages than for single-stranded DNA (ssDNA) phages, and the low rRSCU values are mainly due to poor concordance in RSCU values for Y-ending codons between ssDNA phages and the E. coli host, consistent with the predicted effect of C!T mutation bias in the ssDNA phages. Strong C!T mutation bias would improve codon adaptation in codon families (e.g., Gly) where U-ending codons are favored over C-ending codons (“U-friendly” codon families) by highly expressed host http://mbe.oxfordjournals.org/ genes but decrease codon adaptation in other codon families where highly expressed host genes favor C-ending codons against U-ending codons (“U-hostile” codon families). -
Analysis of Virulence Potential of Escherichia Coli O145 Isolated from Cattle Feces and Hide Samples Based on Whole Genome Sequencing
RESEARCH ARTICLE Analysis of virulence potential of Escherichia coli O145 isolated from cattle feces and hide samples based on whole genome sequencing Pragathi B. Shridhar1, Jay N. Worley2, Xin Gao2, Xun Yang2, Lance W. Noll3, Xiaorong Shi1, 3 2 1 Jianfa Bai , Jianghong Meng , T. G. NagarajaID * 1 Department of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, Kansas, United States of America, 2 Joint Institute for Food Safety and Applied Nutrition and Department of Nutrition and Food Science, University of Maryland, College Park, Maryland, United States of America, 3 Veterinary a1111111111 Diagnostic Laboratory, Kansas State University, Manhattan, Kansas, United States of America a1111111111 a1111111111 * [email protected] a1111111111 a1111111111 Abstract Escherichia coli O145 serogroup is one of the big six non-O157 Shiga toxin producing E. coli (STEC) that causes foodborne illnesses in the United States and other countries. Cattle OPEN ACCESS are a major reservoir of STEC, which harbor them in their hindgut and shed in the feces. Cat- Citation: Shridhar PB, Worley JN, Gao X, Yang X, Noll LW, Shi X, et al. (2019) Analysis of virulence tle feces is the main source of hide and subsequent carcass contaminations during harvest potential of Escherichia coli O145 isolated from leading to foodborne illnesses in humans. The objective of our study was to determine the cattle feces and hide samples based on whole virulence potential of STEC O145 strains isolated from cattle feces and hide samples. A genome sequencing. PLoS ONE 14(11): e0225057. total of 71 STEC O145 strains isolated from cattle feces (n = 16), hide (n = 53), and human https://doi.org/10.1371/journal.pone.0225057 clinical samples (n = 2) were used in the study. -
Chapter 20974
Genome Replication of Bacterial and Archaeal Viruses Česlovas Venclovas, Vilnius University, Vilnius, Lithuania r 2019 Elsevier Inc. All rights reserved. Glossary RNA-primed DNA replication Conventional DNA Negative sense ( À ) strand A negative-sense DNA or RNA replication used by all cellular organisms whereby a strand has a nucleotide sequence complementary to the primase synthesizes a short RNA primer with a free 3′-OH messenger RNA and cannot be directly translated into protein. group which is subsequently elongated by a DNA Positive sense (+) strand A positive sense DNA or RNA polymerase. strand has a nucleotide sequence, which is the same as that Rolling-circle DNA replication DNA replication whereby of the messenger RNA, and the RNA version of this sequence the replication initiation protein creates a nick in the circular is directly translatable into protein. double-stranded DNA and becomes covalently attached to Protein-primed DNA replication DNA replication whereby the 5′ end of the nicked strand. The free 3′-OH group at the a DNA polymerase uses the 3′-OH group provided by the nick site is then used by the DNA polymerase to synthesize specialized protein as a primer to synthesize a new DNA strand. the new strand. Genomes of Prokaryotic Viruses At present, all identified archaeal viruses have either double-stranded (ds) or single-stranded (ss) DNA genomes. Although metagenomic analyzes suggested the existence of archaeal viruses with RNA genomes, this finding remains to be substantiated. Bacterial viruses, also refered to as bacteriophages or phages for short, have either DNA or RNA genomes, including circular ssDNA, circular or linear dsDNA, linear positive-sense (+)ssRNA or segmented dsRNA (Table 1). -
The P2 Phage Old Gene: Sequence, Transcription and Translational Control
Gene, 85 (1989) 25-33 25 Elsevier GENE 03284 The P2 phage old gene: sequence, transcription and translational control (Bacte~ophage; codon usage; plasmid; promoter; r~ornb~~t DNA; tRNA) Elisabeth Hagglrd-Ljungquist”, Virginia Barreiro=, Richard Calendar b, David M. Kumit c and Hans Cheng b a Department of Microbiai Genetics. Karolinska Institute&S-10401 Stockholm 60 (Sweden);’ Department ofMolecular and Cell Biology, Wendell M. Stanley Hall, University of Cal~ornia, Berkeley, CA 94720 (U.S.A.) Tel. (413)642-5951 and c Howard Hughes medical r~ti~te, ~niversi~ of ~ich~an, Ann Arbor, MI 48109 (U.S.A.) Tel. f313)?4?-474? Received by Y. Sakaki: 18 April 1989 Revised: 15 June 1989 Accepted: 17 July 1989 SUMMARY The old (overcoming lysogenization defect) gene product of bacteriophage P2 kills Escherichia coli recB and reccmutants and interferes with phage I growth [ Sironi et al., Virology 46 (1971) 387-396; Lindahl et al., Proc. Natl. Acad. Sci. USA 66 (1970) 587-5941. Specialized transducing f phages, which lack the recombination region, can be selected by plating 11stocks on E. coli that carry the old gene on a prophage or plasmid [ Finkel et al., Gene 46 (1986) 65-691. Deletion and sequence analyses indicate that the old-encoded protein has an M, of 65 373 and that its ~~sc~ption is leftward. Primer extension analyses locate the transcription start point near the right end of the virion DNA. A bacterial mutant, named pin3 and able to suppress the effects of the old gene, has been isolated [Ghisotti et al., J. Virol. -
Virus and Potential Host Microbes from Viral-Enriched Metagenomic Characterization in the High-Altitude Wetland, Salar De Huasco, Chile
microorganisms Communication Virus and Potential Host Microbes from Viral-Enriched Metagenomic Characterization in the High-Altitude Wetland, Salar de Huasco, Chile Yoanna Eissler 1,* , Cristina Dorador 2,3 , Brandon Kieft 4 , Verónica Molina 5,6 and Martha Hengst 3,7 1 Instituto de Química y Bioquímica, Facultad de Ciencias, Universidad de Valparaíso, Gran Bretaña 1111, Playa Ancha, Valparaíso 2360102, Chile 2 Laboratorio de Complejidad Microbiana y Ecología Funcional, Instituto de Antofagasta & Departamento de Biotecnología, Facultad de Ciencias del Mar y Recursos Biológicos, Universidad de Antofagasta, Avenida Universidad de Antofagasta s/n, Antofagasta 1240000, Chile; [email protected] 3 Centre for Biotechnology and Bioengineering, Universidad de Chile, Beaucheff 851 (Piso 7), Santiago 8320000, Chile; [email protected] 4 Lab of Dr. Steven Hallam, University of British Columbia, Vancouver, BC V6T 1Z4, Canada; [email protected] 5 Departamento de Biología, Observatorio de Ecología Microbiana, Facultad de Ciencias Naturales y Exactas, Universidad de Playa Ancha, Avenida Leopoldo Carvallo 270, Playa Ancha, Valparaíso 2340000, Chile; [email protected] 6 HUB Ambiental UPLA, Universidad de Playa Ancha, Avenida Leopoldo Carvallo 200, Playa Ancha, Valparaíso 2340000, Chile 7 Departamento de Ciencias Farmacéuticas, Facultad de Ciencias, Universidad Católica del Norte, Av Angamos 0610, Antofagasta 1270709, Chile * Correspondence: [email protected]; Tel.: +56-32-250-8063 Received: 24 June 2020; Accepted: 3 July 2020; Published: 20 July 2020 Abstract: Salar de Huasco is a wetland in the Andes mountains, located 3800 m above sea level at the Chilean Altiplano. Here we present a study aimed at characterizing the viral fraction and the microbial communities through metagenomic analysis. -
Regulation of Bacteriophage P2 Late-Gene Expression: the Ogr Gene (DNA Sequence/Cloning/Overproduction/RNA Polymerase/Transcriptional Control Factor) GAIL E
Proc. Nati. Acad. Sci. USA Vol. 83, pp. 3238-3242, May 1986 Biochemistry Regulation of bacteriophage P2 late-gene expression: The ogr gene (DNA sequence/cloning/overproduction/RNA polymerase/transcriptional control factor) GAIL E. CHRISTIE*t, ELISABETH HAGGARD-IUUNGQUISTt, ROBERT FEIWELL*, AND RICHARD CALENDAR* *Department of Molecular Biology, University of California, Berkeley, CA 94720; tDepartment of Microbiology and Immunology, Virginia Commonwealth University, Box 678 MCV Station, Richmond, VA 23235; and WDepartment of Microbial Genetics, Karolinska Institute, S-10401 Stockholm, Sweden Communicated by Howard K. Schachman, January 14, 1986 ABSTRACT The ogr gene product of bacteriophage P2 is mutation. E. coli K-12 strain RR1 (15) carrying the plasmid a positive regulatory factor required for P2 late-gene transcrip- pRK248cIts (16) was used as the host for derivatives of the tion. We have determined the nucleotide sequence of the ogr plasmid pRC23 (17). P2 virl carries a point mutation that gene, which encodes a basic polypeptide of 72 amino acids. P2 blocks lysogeny (18, 19). P2 vir22 has a 5% deletion that growth is blocked by a host mutation, rpoA09, in the a subunit removes the P2 attachment site and carries a 0.5% insertion of DNA-dependent RNA polymerase. The ogr52 mutation, at the site of this deletion (20, 21). P2 vir22 ogrS2 is a mutant which allows P2 to grow in an rpoAl09 strain, was shown to be derived from P2 vir22 by B. Sauer (E. I. DuPont de Nemours, a single nucleotide change, in the codon for residue 42, that Wilmington, DE). It carries a mutation that permits growth in changes tyrosine to cysteine. -
(12) Patent Application Publication (10) Pub. No.: US 2010/0322903A1 Collins Et Al
US 20100322903A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2010/0322903A1 Collins et al. (43) Pub. Date: Dec. 23, 2010 (54) ENGINEERED BACTERIOPHAGES AS Related U.S. Application Data ADUVANTS FOR ANTIMICROBAL AGENTS AND COMPOSITIONS AND METHODS OF (60) Provisional application No. 61/020,197, filed on Jan. USE THEREOF 10, 2008. Publication Classification (75) Inventors: James J Collins, Newton, MA (US); Timothy Kuan-Ta Lu, (51) Int. Cl. Boston, MA (US) A6II 35/76 (2006.01) CI2N 7/01 (2006.01) Correspondence Address: A6IP3L/04 (2006.01) RONALDI. EISENSTEIN (52) U.S. Cl. ..................................... 424/93.2:435/235.1 100 SUMMER STREET, NIXON PEABODY LLP (57) ABSTRACT BOSTON, MA 02110 (US) The present invention relates to the treatment and prevention (73) Assignees: TRUSTEES OF BOSTON of bacteria and bacterial infections. In particular, the present UNIVERSITY, Boston, MA (US); invention relates to engineered bacteriophages used in com MASSACHUSETTS INSTITUTE bination with antimicrobial agents to potentiate the antimi OF TECHNOLOGY, Cambridge, crobial effect and bacterial killing by the antimicrobial agent. MA (US) The present invention generally relates to methods and com positions comprising engineered bacteriophages and antimi (21) Appl. No.: 12/812,212 crobial agents for the treatment of bacteria, and more particu larly to bacteriophages comprising agents that inhibit (22) PCT Filed: Jan. 12, 2009 antibiotic resistance genes and/or cell Survival genes, and/or bacteriophages comprising repressors of SOS response genes (86). PCT No.: PCT/USO9/30755 or inhibitors of antimicrobial defense genes and/or express ing an agent which increases the sensitivity of bacteria to an S371 (c)(1), antimicrobial agent in combination with at least one antimi (2), (4) Date: Aug. -
Analysis of a Novel Bacteriophage Vb Achrs Achv4 Highlights the Diversity of Achromobacter Viruses
viruses Article Analysis of a Novel Bacteriophage vB_AchrS_AchV4 Highlights the Diversity of Achromobacter Viruses Laura Kaliniene 1,* , Algirdas Noreika 1, Algirdas Kaupinis 2, Mindaugas Valius 2 , Edvinas Jurgelaitis 1, Justas Lazutka 3, Rita Meškiene˙ 1 and Rolandas Meškys 1 1 Department of Molecular Microbiology and Biotechnology, Institute of Biochemistry, Life Sciences Center, Vilnius University, Sauletekio˙ av. 7, LT-10257 Vilnius, Lithuania; [email protected] (A.N.); [email protected] (E.J.); [email protected] (R.M.); [email protected] (R.M.) 2 Proteomics Centre, Institute of Biochemistry, Life Sciences Centre, Vilnius University, Sauletekio˙ av. 7, LT-10257 Vilnius, Lithuania; [email protected] (A.K.); [email protected] (M.V.) 3 Department of Eukaryote Gene Engineering, Institute of Biotechnology, Life Sciences Center, Vilnius University, Sauletekio˙ av. 7, LT-10257 Vilnius, Lithuania; [email protected] * Correspondence: [email protected]; Tel.: +370-5-2234384 Abstract: Achromobacter spp. are ubiquitous in nature and are increasingly being recognized as emerging nosocomial pathogens. Nevertheless, to date, only 30 complete genome sequences of Achromobacter phages are available in GenBank, and nearly all of those phages were isolated on Achromobacter xylosoxidans. Here, we report the isolation and characterization of bacteriophage vB_AchrS_AchV4. To the best of our knowledge, vB_AchrS_AchV4 is the first virus isolated from Achromobacter spanius. Both vB_AchrS_AchV4 and its host, Achromobacter spanius RL_4, were isolated in Lithuania. VB_AchrS_AchV4 is a siphovirus, since it has an isometric head (64 ± 3.2 nm in diameter) and a non-contractile flexible tail (232 ± 5.4). -
Regulation of Expression and Activity of the Late Gene Activator, B, Of
UNI I ìo J RnCUT,ATION OF EXPRESSION AND ACTIVITY OF THE LATE çENE ACTIVATOR, B, On BACTERIOPHAGE 186. A thesis submitted in fulfilment of the requirements for the degree of Doctor of Philosophy in the School of Molecular and Biomedical Sciences (Biochemistry Discipline) at the University of Adelaide' Rachel Ann Schubert, B. Sc. (Hons) March,2005 TABLE OF CONTENTS THESIS SUMMARY VI DECLARATION vII ACKNOWLEDGEMENTS VIII ABBREVIATIONS Ix lft CHAPTER 1: INTRODUCTION lô 1.A. BACTERIOPHAGE DEVELOPMENT tt 1.4. 1. A GENERAL INTRODUCTION TO BAC"TERIOPFIAGES.,,,..,,.....,.. 1l I.4.2. DEVELOPMENTALLIFECYCLES OFDOUBLE-STRANDED DNA PHAGES ......,,I2 I.4.3. CONTROL OF MORPHOGENETIC PTIAGE GENE EXPRESSION. l3 t4 1.B. I. I 86 BELONGS TO A LARGE FAMILY OF P2_LKE PHAGES t4 1.8,2, THE GENOMIC ORGANIZATION OF 186 AND P2....,.... t4 I.B,3. 186 GENE EXPRESSION DIJRING DEVELOPMENT...,,... 15 1.8.3.1. 186 lytic development. l5 I .8.3.2. 1 86 lyso genic development. 17 1.C. MECHANISM OF LATE GENE ACTIVATION IN 186. 1.C. 1. B BELONGS TO A LARGE FAMILY OF ZINC-FINGER PROTEINS t9 1.C,2. CHARACTERIZED B HOMOLOGUES ARE FUNCTIONALLY INTERCHANGEABLE TRANSCRIPTIONAL 20 I.C.3. NATIVE PRoMOTER TARGETS ASTIVATED BY 186 B PROTEIN AND ITS HOMOLOGUES.,,..,,..,.....,, 2l 1.C.3.1. Promoters actívated by P2 Ogr and other B homologues 21 1.C.3.2. B-activated promoters of phage 186. 22 1.C,4. DNA BINDING BY 186 B AND B-HOMOLOGOUS PROTEINS. .23 1.C.4.1. Activated promoters are bound by the B homologues .23 1.C.4.2.