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Published on: August 9, 2013
A novel vibriophage exhibits inhibitory activity against host protein synthesis machinery
Khrongkhwan Thammatinna1, MacKennon E Egan2, Htut Htut Htoo3
1Center of Excellence for Molecular Biology and Genomics of Shrimp, Department of Biochemistry, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand.
Abstract:
Since the emergence of deadly pathogens and multidrug-resistant bacteria at an alarmingly increased rate, bacteriophages have been developed as a controlling bioagent to prevent the spread of pathogenic bacteria. One of these pathogens, disease-causing Vibrio parahaemolyticus (VPAHPND) which induces acute hepatopancreatic necrosis, is considered one of the deadliest shrimp pathogens, and has recently become resistant to various classes of antibiotics. Here, we discovered a novel vibriophage that specifically targets the vibrio host, VPAHPND. The vibriophage, designated Seahorse, was classified in the family Siphoviridae because of its icosahedral capsid surrounded by head fibers and a non-contractile long tail. Phage Seahorse was able to infect the host in a broad range of pH and temperatures, and it had a relatively short latent period (nearly 30 minutes) in which it produced progeny at 72 particles per cell at the end of its lytic cycle. Upon phage infection, the host nucleoid condensed and became toroidal, similar to the bacterial DNA morphology seen during tetracycline treatment, suggesting that phage Seahorse hijacked host biosynthesis pathways through protein translation. As phage Seahorse genome encodes 48 open reading frames with many hypothetical proteins, this genome could be a potential untapped resource for the discovery of phage-derived therapeutic proteins.
Insights
Researchers discovered Seahorse, a novel bacteriophage targeting Vibrio parahaemolyticus (VPAHPND), a deadly shrimp pathogen. This phage shows potential for controlling antibiotic-resistant bacteria and discovering new therapeutic proteins.
Area of Science:
- Microbiology
- Virology
- Aquaculture
Background:
- Emergence of multidrug-resistant bacteria and deadly pathogens necessitates novel control strategies.
- Vibrioparahaemolyticus (VPAHPND) is a significant shrimp pathogen causing acute hepatopancreatic necrosis, exhibiting increasing antibiotic resistance.
Purpose of the Study:
- To discover and characterize a novel bacteriophage targeting the shrimp pathogen Vibrio parahaemolyticus (VPAHPND).
- To evaluate the potential of this bacteriophage as a bioagent for controlling bacterial infections and as a source of therapeutic proteins.
Main Methods:
- Isolation and classification of a novel vibriophage, Seahorse, belonging to the Siphoviridae family.
- Assessment of Seahorse's infectivity across various pH and temperature conditions.
- Analysis of the phage's lytic cycle, including latent period and progeny production.
- Investigation of host cell morphological changes post-infection and genome sequencing.
Main Results:
- Seahorse bacteriophage specifically targets and infects VPAHPND.
- The phage exhibits stability over a broad pH and temperature range, with a short latent period of approximately 30 minutes and high progeny yield (72 particles/cell).
- Phage infection induces significant changes in host nucleoid morphology, suggesting hijacking of host biosynthesis pathways.
- The Seahorse genome contains 48 open reading frames, including hypothetical proteins with therapeutic potential.
Conclusions:
- Seahorse is a promising bacteriophage for controlling VPAHPND, offering a potential alternative to antibiotics in aquaculture.
- The characterized phage demonstrates robust infectivity and a rapid lytic cycle.
- The Seahorse genome represents a valuable resource for discovering novel phage-derived therapeutic proteins for combating bacterial infections.
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