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Phage Phenomics: Physiological Approaches to Characterize Novel Viral Proteins
Published on: June 11, 2015
The genome of bacteriophage phiKZ of Pseudomonas aeruginosa
Vadim V Mesyanzhinov1, Johan Robben, Barbara Grymonprez
1Laboratory of Gene Technology, Katholieke Universiteit Leuven, Kardinaal Mercierlaan 92, B-3001 Leuven, Belgium. vvm@bch.ru
Abstract:
Bacteriophage phiKZ is a giant virus that efficiently infects Pseudomonas aeruginosa strains pathogenic to human and, therefore, it is attractive for phage therapy. We present here the complete phiKZ genome sequence and a preliminary analysis of its genome structure. The 280,334 bp genome is a linear, circularly permutated and terminally redundant, A+T-rich double-stranded DNA molecule. The phiKZ DNA has no detectable sequence homology to other viruses and microorganisms, and it does not contain NotI, PstI, SacI, SmaI, XhoI, and XmaIII endonuclease restriction sites. The genome has 306 open reading frames (ORFs) varying in size from 50 to 2237 amino acid residues. According to the orientation of transcription, ORFs are apparently organized into clusters and most have a clockwise direction. The phiKZ genome also encodes six tRNAs specific for Met (AUG), Asn (AAC), Asp (GAC), Leu (TTA), Thr (ACA), and Pro (CCA). A putative promoter sequence containing a TATATTAC block was identified. Most potential stem-loop transcription terminators contain the tetranucleotide UUCG loops. Some genes may be assigned as phage-encoded RNA polymerase subunits. Only 59 phiKZ gene products exhibit similarity to proteins of known function from a diversity of organisms. Most of these conserved gene products, such as dihydrofolate reductase, ribonucleoside diphosphate reductase, thymidylate synthase, thymidylate kinase, and deoxycytidine triphosphate deaminase are involved in nucleotide metabolism. However, no virus-encoded DNA polymerase, DNA replication-associated proteins, or single-stranded DNA-binding protein were found based on amino acid homology, and they may therefore be strongly divergent from known homologous proteins. Fifteen phiKZ gene products show homology to proteins of pathogenic organisms, including Mycobacterium tuberculosis, Haemophilus influenzae, Listeria sp., Rickettsia prowazakeri, and Vibrio cholerae that must be considered before using this phage as a therapeutic agent. The phiKZ coat contains at least 40 polypeptides, and several proteins are cleaved during virus assembly in a way similar to phage T4. Eleven phiKZ-encoded polypeptides are related to proteins of other bacteriphages that infect a variety of hosts. Among these are four gene products that contain a putative intron-encoded endonuclease harboring the H-N-H motif common to many double-stranded DNA phages. These observations provide evidence that phages infecting diverse hosts have had access to a common genetic pool. However, limited homology on the DNA and protein levels indicates that bacteriophage phiKZ represents an evolutionary distinctive branch of the Myoviridae family.
Insights
Bacteriophage phiKZ, a giant virus infecting Pseudomonas aeruginosa, has a unique genome with no homology to other organisms. Its genetic makeup reveals potential therapeutic applications and evolutionary distinctiveness within the Myoviridae family.
Area of Science:
- Microbiology
- Virology
- Genomics
Background:
- Pseudomonas aeruginosa is a significant human pathogen.
- Bacteriophage phiKZ is a giant virus with efficient infectivity against Pseudomonas aeruginosa.
- The phage is a potential candidate for phage therapy.
Purpose of the Study:
- To present the complete genome sequence of bacteriophage phiKZ.
- To conduct a preliminary analysis of its genome structure.
- To identify genes with potential functions and evolutionary significance.
Main Methods:
- Whole-genome sequencing of bacteriophage phiKZ.
- Bioinformatic analysis of the genome sequence.
- Comparative genomics to identify homologous genes and proteins.
Main Results:
- The bacteriophage phiKZ genome is a 280,334 bp linear, circularly permutated, and terminally redundant double-stranded DNA molecule.
- It contains 306 open reading frames (ORFs) with limited homology to known proteins, suggesting unique functions.
- Genes involved in nucleotide metabolism were identified, but key DNA replication proteins appear divergent.
- Homology to proteins from pathogenic organisms was noted, requiring consideration for therapeutic use.
- The phage coat comprises at least 40 polypeptides, with assembly similarities to phage T4.
Conclusions:
- Bacteriophage phiKZ possesses a distinctive genome, representing an evolutionarily unique branch of the Myoviridae family.
- Its genetic makeup offers insights into viral evolution and potential therapeutic strategies against Pseudomonas aeruginosa infections.
- Further investigation into its unique genes and proteins is warranted for phage therapy development.
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