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Journal of Bacteriology, November 2003, p. 6490-6492, Vol. 185, No. 21
0021-9193/03/$08.00+0 DOI: 10.1128/JB.185.21.6490-6492.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
CPAR39 and Chp3
Molecular Microbiology and Infection, University Medical School, Southampton General Hospital, Southampton, SO16 6YD, United Kingdom,1 Department of Veterinary Science and Microbiology, The University of Arizona, Tucson, Arizona 85721-00902
Received 19 June 2003/ Accepted 3 August 2003
The host range of
CPAR39 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
CPAR39 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.
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