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Published on: October 23, 2013
Host range of chlamydiaphages phiCPAR39 and Chp3
J S Everson1, S A Garner, P R Lambden
1Molecular Microbiology and Infection, University Medical School, Southampton General Hospital, Southampton, SO16 6YD, United Kingdom.
Abstract:
The host range of phiCPAR39 is limited to four Chlamydophila species: C. abortus, C. caviae, C. pecorum, and C. pneumoniae. Chp3 (a newly discovered bacteriophage isolated from C. pecorum) shares three of these hosts (C. abortus, C. caviae, and C. pecorum) but can additionally infect Chlamydophila felis. The ability to support replication was directly correlated with the binding properties of the respective bacteriophages with their host species. Binding studies also show that phiCPAR39 and Chp3 use different host receptors to infect the same host cells: cell binding is sensitive to proteinase K treatment, confirming that the chlamydiaphage receptors are proteinaceous in nature.
Insights
Two bacteriophages, phiCPAR39 and Chp3, infect Chlamydophila species. Their differing host ranges are determined by specific protein receptors on the host cell surface, influencing bacteriophage binding and replication.
Area of Science:
- Microbiology
- Virology
- Bacteriology
Background:
- Chlamydophila species are important animal and human pathogens.
- Bacteriophages are viruses that infect bacteria and can be specific to certain hosts.
- Understanding bacteriophage-host interactions is crucial for developing phage-based therapies.
Purpose of the Study:
- To compare the host range and binding characteristics of two Chlamydophila-infecting bacteriophages: phiCPAR39 and Chp3.
- To investigate the nature of the host receptors utilized by these bacteriophages.
Main Methods:
- Infection assays to determine the host range of phiCPAR39 and Chp3 against various Chlamydophila species.
- Binding studies to quantify the interaction between bacteriophages and host cells.
- Proteinase K treatment to assess the proteinaceous nature of host receptors.
Main Results:
- phiCPAR39 infects Chlamydophila abortus, C. caviae, C. pecorum, and C. pneumoniae.
- Chp3 infects C. abortus, C. caviae, C. pecorum, and additionally Chlamydophila felis.
- Bacteriophage replication ability correlated with host binding efficiency.
- Binding studies revealed that phiCPAR39 and Chp3 utilize distinct proteinaceous receptors on host cells.
Conclusions:
- The host specificity of phiCPAR39 and Chp3 is determined by their differential binding to specific protein receptors on Chlamydophila species.
- These findings contribute to understanding bacteriophage-host interactions and have implications for phage therapy development against Chlamydophila infections.
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