Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2009 Mar;77(3):1216-21.
doi: 10.1128/IAI.01109-08. Epub 2009 Jan 12.

Effect of Chlamydiaphage phiCPG1 on the course of conjunctival infection with "Chlamydia caviae" in guinea pigs

Affiliations

Effect of Chlamydiaphage phiCPG1 on the course of conjunctival infection with "Chlamydia caviae" in guinea pigs

Roger G Rank et al. Infect Immun. 2009 Mar.

Abstract

Over the last several years, four different phages of chlamydiae, in addition to a phage associated with Chlamydia psittaci isolated from an ornithosis infection in ducks over 25 years ago, have been described and characterized. While these phages and their chlamydial host specificities have been characterized in vitro, there is virtually nothing known about the interaction of the phage with chlamydiae in their natural animal host. phiCPG1 is a lytic phage specific for "Chlamydia caviae," which is a natural parasite of the guinea pig. In this study, guinea pigs were inoculated in the conjunctiva with suspensions of phiCPG1 and C. caviae and the effect on the development of pathology and on the course of chlamydial infection in the conjunctiva was determined. The presence of phage delayed the appearance of the peak level of chlamydiae in the animal and decreased the pathological response. Evidence for replication of the phage in C. caviae in the conjunctival tissue was observed. Modifying the ratio of phage to chlamydiae altered the course of infection and affected phage replication. There was no evidence for the phage increasing the virulence of C. caviae infection.

PubMed Disclaimer

Figures

FIG. 1.
FIG. 1.
Kinetics of C. caviae infection in the guinea pig conjunctiva and the effect of the presence of ϕCPG1 on (A) the gross pathological response in the conjunctiva and (B) the course of C. caviae infection with and without phage. The inoculum was the original C. caviae/phage culture lysate containing 106 IFU of C. caviae and 51.44 μg/ml of VP1 DNA. Each group contains five animals each, and the data points represent the means of each group except for the pathology scores, which are the means of both conjunctivas from each animal. The error bars for the phage DNA represent 1 standard deviation.
FIG. 2.
FIG. 2.
Kinetics of C. caviae infection in the guinea pig conjunctiva and the effect of the presence of ϕCPG1 on (A) the gross pathological response in the conjunctiva and (B) the course of C. caviae infection with and without phage. The inoculum was prepared by adding 106 IFU of C. caviae to purified phage. Each group contains five animals each, and the data points represent the means of each group except for the pathology scores, which are the means of both conjunctivas from each animal. The error bars for the phage DNA represent 1 standard deviation.
FIG. 3.
FIG. 3.
Effect of different ratios of chlamydiae and phage on chlamydial infection in the conjunctiva. (A) C. caviae (106 IFU) and purified phage from the original C. caviae/phage culture lysate or a 1:10 dilution of the purified phage from the lysate were inoculated into the conjunctiva. (B) C. caviae (105 IFU) and purified phage from the original phage stock were inoculated into the conjunctiva. Each group contains five animals each, and the data points represent the means for each group. The error bars for the phage DNA represent 1 standard deviation.

References

    1. Brentlinger, K. L., S. Hafenstein, C. R. Novak, B. A. Fane, R. Borgon, R. McKenna, and M. Agbandje-McKenna. 2002. Microviridae, a family divided: isolation, characterization, and genome sequence of phiMH2K, a bacteriophage of the obligate intracellular parasitic bacterium Bdellovibrio bacteriovorus. J. Bacteriol. 1841089-1094. - PMC - PubMed
    1. Everson, J. S., S. A. Garner, B. Fane, B. L. Liu, P. R. Lambden, and I. N. Clarke. 2002. Biological properties and cell tropism of Chp2, a bacteriophage of the obligate intracellular bacterium Chlamydophila abortus. J. Bacteriol. 1842748-2754. - PMC - PubMed
    1. Garner, S. A., J. S. Everson, P. R. Lambden, B. A. Fane, and I. N. Clarke. 2004. Isolation, molecular characterisation and genome sequence of a bacteriophage (Chp3) from Chlamydophila pecorum. Virus Genes 28207-214. - PubMed
    1. Hayashi, M., A. Aoyama, J. D. L. Richardson, and M. N. Hayashi. 1988. Biology of the bacteriophage phiX174, p. 1-71. In R. Calendar (ed.), The bacteriophages (the viruses). Plenum Press, New York, NY.
    1. Hough, A. J., Jr., and R. G. Rank. 1988. Induction of arthritis in C57Bl/6 mice by chlamydial antigen: effect of prior immunization or infection. Am. J. Pathol. 130163-172. - PMC - PubMed

Publication types