Literature DB >> 24699949

Complete Genome Sequence of an F8-Like Lytic Myovirus ({varphi}SPM-1) That Infects Metallo-β-Lactamase-Producing Pseudomonas aeruginosa.

Patrícia R Neves1, Louise T Cerdeira, Miguel Mitne-Neto, Théo G M Oliveira, John A McCulloch, Jorge L M Sampaio, Elsa M Mamizuka, Carlos E Levy, Maria I Z Sato, Nilton Lincopan.   

Abstract

Pseudomonas aeruginosa is an important cause of infection, especially in immunocompromised patients. In this regard, strains producing carbapenemases, mainly metallo-β-lactamases (MBLs), have become a significant public health concern. Here, we present the complete annotated genome sequence (65.7 kb) of an F8-related lytic myovirus (Pbunalikevirus genus) that infects MBL-producing P. aeruginosa strains.

Entities:  

Year:  2014        PMID: 24699949      PMCID: PMC3974931          DOI: 10.1128/genomeA.00061-14

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Metallo-β-lactamase (MBL)-producing Pseudomonas aeruginosa strains have become a significant public health problem (1). Here, we report the sequencing and annotation of a lytic myovirus infecting MBL-producing P. aeruginosa. A lytic myovirus, called φSPM-1, was recovered from a collection of environmental isolates (from surface water samples from rivers in southeastern Brazil) and oldest-typing-set phages (2); it was propagated in an environmental SPM-1-producing P. aeruginosa host strain (3) and then was characterized by transmission electron microscopy and complete-genome sequencing. This phage was able to lyse clonally unrelated MBL-producing P. aeruginosa strains (4), including the Brazilian endemic clone harboring the blaSPM-1 MBL gene, sequence type 277 (ST277) (5). The phage had an elongated icosahedral head with an approximately 50-nm diameter and a tail near 70 nm in length, showing that it belongs to the Myoviridae family of the order Caudovirales (6). The bacteriophage genome was sequenced by Ion Torrent PGM (Life Technologies) using the Ion Xpress Plus fragment library kit, with size selection by electrophoresis before emulsion PCR on an Ion OneTouch apparatus, using the Ion PGM sequencing 400 and Ion PGM template OT2 400 kits. A total of 82,540 reads (~200× coverage), with a mean length of 159 bp, were obtained after sequencing, and de novo assembly of next-generation sequencing (NGS) reads (CLC bio Genomics Workbench version 6.5) yielded 19 contigs (7). The whole-genome sequence (WGS) of the myophage was assembled using crossmatch alignment (40-bp minimum overlap), and the prediction of protein-coding sequences (CDSs) was obtained using phage annotation tools and methods (PhAnToMe) (http://www.phantome.org). Manual curation of opening reading frames (ORFs) was carried out by comparative genomics using BLASTp (http://www.ncbi.nlm.nih.gov/blast/Blast.cgi) analysis of proteins against the GenBank NR database. The WGS of φSPM-1 comprises 65,729 bp, with a G+C content of 54.97%, 92 ORFs, and no tRNAs, harboring genetic information needed for replication of nucleic acid and synthesis of protein coats (i.e., genes coding for DNA replication, capsid, tail, packaging, and lytic enzymes). Moreover, the φSPM-1 genome is 95.6% identical to that of the P. aeruginosa F8 phage (GenBank accession no. NC_007810.1). In this regard, a 237-bp region, which is absent in φSPM-1 and present in the F8 phage, partially encodes a hypothetical protein of unknown function in the F8 phage genome. The start point of the F8 genome sequence was positioned at a locus that possesses a CDS that is predicted to code for a tail-length tape-measure protein (locus tag PPGF8SP_0065). We have therefore marked the genome sequence as circular. In this respect, the linear supercontig was extended by adding 100 ambiguous “N” bases on either side. Alignment of the reads to this supercontig was then carried out using CLC Genomics Workbench, and their extension was possible in regions that had a read coverage of >10× and that spanned the supercontig ends and the ambiguous “N” bases added; this yielded a 40-bp overlap of the extension, circularizing the sequence. Finally, the φSPM-1 phage genome has high identities to other P. aeruginosa phages belonging to the Pbunalikevirus genus (8) (i.e., PB1 [93.3%], LBL3 [89.9%], LMA2 [87%], 14-1 [86.9%], and SN [87%] phages), as analyzed using Geneious software (Biomatters Ltd.).

Nucleotide sequence accession number.

The complete genome sequence of F8-like lytic myovirus φSPM-1 (Pbunalikevirus genus) was deposited in GenBank with the accession no. KF981875.
  8 in total

Review 1.  Bacteriophages of Pseudomonas.

Authors:  Pieter-Jan Ceyssens; Rob Lavigne
Journal:  Future Microbiol       Date:  2010-07       Impact factor: 3.165

Review 2.  Metallo-β-lactamases: a last frontier for β-lactams?

Authors:  Giuseppe Cornaglia; Helen Giamarellou; Gian Maria Rossolini
Journal:  Lancet Infect Dis       Date:  2011-05       Impact factor: 25.071

3.  Isolation of Pseudomonas aeruginosa coproducing metallo-β-lactamase SPM-1 and 16S rRNA methylase RmtD1 in an urban river.

Authors:  Lívia C Fontes; Patrícia R Neves; Silvane Oliveira; Ketrin C Silva; Elayse M Hachich; Maria I Z Sato; Nilton Lincopan
Journal:  Antimicrob Agents Chemother       Date:  2011-04-04       Impact factor: 5.191

Review 4.  Ultrastructure of bacteriophage and bacteriocins.

Authors:  D E Bradley
Journal:  Bacteriol Rev       Date:  1967-12

5.  Phage typing of Pseudomonas aeruginosa: clinical and epidemiologic considerations.

Authors:  R B Lindberg; R L Latta
Journal:  J Infect Dis       Date:  1974-11       Impact factor: 5.226

6.  Rapid hybrid de novo assembly of a microbial genome using only short reads: Corynebacterium pseudotuberculosis I19 as a case study.

Authors:  Louise Teixeira Cerdeira; Adriana Ribeiro Carneiro; Rommel Thiago Jucá Ramos; Sintia Silva de Almeida; Vivian D'Afonseca; Maria Paula Cruz Schneider; Jan Baumbach; Andreas Tauch; John Anthony McCulloch; Vasco Ariston Carvalho Azevedo; Artur Silva
Journal:  J Microbiol Methods       Date:  2011-05-18       Impact factor: 2.363

7.  SPM-1-producing Pseudomonas aeruginosa: analysis of the ancestor relationship using multilocus sequence typing, pulsed-field gel electrophoresis, and automated ribotyping.

Authors:  Fernanda M Silva; Mirian S Carmo; Suzane Silbert; Ana C Gales
Journal:  Microb Drug Resist       Date:  2011-02-19       Impact factor: 3.431

8.  Dissemination in distinct Brazilian regions of an epidemic carbapenem-resistant Pseudomonas aeruginosa producing SPM metallo-beta-lactamase.

Authors:  Ana C Gales; Liana C Menezes; Suzane Silbert; Hélio S Sader
Journal:  J Antimicrob Chemother       Date:  2003-09-01       Impact factor: 5.790

  8 in total
  1 in total

1.  Pseudomonas PB1-Like Phages: Whole Genomes from Metagenomes Offer Insight into an Abundant Group of Bacteriophages.

Authors:  Siobhan C Watkins; Emily Sible; Catherine Putonti
Journal:  Viruses       Date:  2018-06-16       Impact factor: 5.048

  1 in total

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