Abstract
Guinea pig inclusion conjunctivitis, a naturally occurring chlamydial disease of guinea pigs, resolves spontaneously after 3 to 4 weeks. The factors responsible for curbing the infection have not yet been specifically defined. Since Iwata (Invest. Ophthalmol. 15:297-301, 1976) reported cytochemical activity for peroxidase in the conjunctival epithelium of the normal rat, we undertook these studies to determine whether a similar activity exists in the guinea pig, and if so, whether it functions in the elimination of this Chlamydia psittaci infection. Tarsal conjunctivas of 14 normal guinea pigs, 34 infected ones, and 7 control guinea pigs (inoculated with yolk sac only) were excised and tested for peroxidase by the Graham and Karnovsky method (J. Histochem. Cytochem. 14:291-302, 1966). We found that peroxidase activity, virtually absent in normal animals, was intensely stimulated by the infection. This enzymatic activity appeared 2 days after inoculation of the conjunctiva with chlamydia and persisted for 6 to 7 weeks. The enzyme was localized in the rough endoplasmic reticulum and perinuclear cisternae of all layers of the conjunctival epithelium from the external surface to the basal lamina, including cells with no apparent inclusions as well as those heavily parasitized. Reaction in the Golgi complex was variable. No reaction, however, was ever evident in the chlamydial vacuoles or lysosomes, and the organisms continued to grow and multiply during peak enzymatic activity. We therefore concluded that the stimulated enzyme is apparently not directly responsible for the waning of the infection, but instead reflects an alteration of host metabolism that occurs as a consequence of the infection.
Full text
PDF









Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Ackerman G. A., Clark M. A. Ultrastructural localization of peroxidase activity in normal human bone marrow cells. Z Zellforsch Mikrosk Anat. 1971;117(4):463–475. doi: 10.1007/BF00330708. [DOI] [PubMed] [Google Scholar]
- Bainton D. F., Farquhar M. G. Segregation and packaging of granule enzymes in eosinophilic leukocytes. J Cell Biol. 1970 Apr;45(1):54–73. doi: 10.1083/jcb.45.1.54. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bainton D. F., Ullyot J. L., Farquhar M. G. The development of neutrophilic polymorphonuclear leukocytes in human bone marrow. J Exp Med. 1971 Oct 1;134(4):907–934. doi: 10.1084/jem.134.4.907. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bodel P. T., Nichols B. A., Bainton D. F. Appearance of peroxidase reactivity within the rough endoplasmic reticulum of blood monocytes after surface adherence. J Exp Med. 1977 Feb 1;145(2):264–274. doi: 10.1084/jem.145.2.264. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bodel P. T., Nichols B. A., Bainton D. F. Differences in peroxidase localization of rabbit peritoneal macrophages after surface adherence. Am J Pathol. 1978 Apr;91(1):107–117. [PMC free article] [PubMed] [Google Scholar]
- Brökelmann J., Fawcett D. W. The localization of endogenous peroxidase in the rat uterus and its induction by estradiol. Biol Reprod. 1969 Apr;1(1):59–71. doi: 10.1095/biolreprod1.1.59. [DOI] [PubMed] [Google Scholar]
- Churg A., Anderson W. A. Induction of endometrial peroxidase synthesis and secretion by estrogen and estrogen antagonist. J Cell Biol. 1974 Aug;62(2):449–459. doi: 10.1083/jcb.62.2.449. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cotran R. S., Litt M. Ultrastructural localization of horseradish peroxidase and endogenous peroxidase activity in guinea pig peritoneal macrophages. J Immunol. 1970 Dec;105(6):1536–1546. [PubMed] [Google Scholar]
- Daems W. T., Poelman R. E., Brederoo P., van Lohuzen E. J. Peroxidatic activity in resident peritoneal macrophages and exudate monocytes of the guinea pig after ingestion of latex particles. J Histochem Cytochem. 1973 Jan;21(1):93–95. doi: 10.1177/21.1.93. [DOI] [PubMed] [Google Scholar]
- Essner E. Localization of endogenous peroxidase in rat exorbital lacrimal gland. J Histochem Cytochem. 1971 Apr;19(4):216–225. doi: 10.1177/19.4.216. [DOI] [PubMed] [Google Scholar]
- Friis R. R. Interaction of L cells and Chlamydia psittaci: entry of the parasite and host responses to its development. J Bacteriol. 1972 May;110(2):706–721. doi: 10.1128/jb.110.2.706-721.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GORDON F. B., QUAN A. L. OCCURENCE OF GLYCOGEN IN INCLUSIONS OF THE PSITTACOSIS-LYMPHOGRANULOMA VENEREUM-TRACHOMA AGENTS. J Infect Dis. 1965 Apr;115:186–196. doi: 10.1093/infdis/115.2.186. [DOI] [PubMed] [Google Scholar]
- Graham R. C., Jr, Karnovsky M. J. The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique. J Histochem Cytochem. 1966 Apr;14(4):291–302. doi: 10.1177/14.4.291. [DOI] [PubMed] [Google Scholar]
- Herzog V., Fahimi H. D. Intracellular distinction between peroxidase and catalase in exocrine cells of rat lacrimal gland: a biochemical and cytochemical study. Histochemistry. 1976 Mar 31;46(4):273–286. doi: 10.1007/BF02464417. [DOI] [PubMed] [Google Scholar]
- Herzog V., Miller F. Endogenous peroxidase in the lacrimal gland of the rat and its differentiation against injected catalase and horseradish-peroxidase. Histochemie. 1972;30(3):235–246. doi: 10.1007/BF00277594. [DOI] [PubMed] [Google Scholar]
- Iwata T. Cytochemical studies on endogenous peroxidase in conjunctival and corneal epithelial cells. Invest Ophthalmol. 1976 Apr;15(4):297–301. [PubMed] [Google Scholar]
- Kazdan J. J., Schachter J., Okumoto M. Inclusion conjunctivitis in the guinea pig. Am J Ophthalmol. 1967 Jul;64(1):116–124. doi: 10.1016/0002-9394(67)93351-x. [DOI] [PubMed] [Google Scholar]
- Klebanoff S. J., Hamon C. B. Role of myeloperoxidase-mediated antimicrobial systems in intact leukocytes. J Reticuloendothel Soc. 1972 Aug;12(2):170–196. [PubMed] [Google Scholar]
- Lazarow P. B., de Duve C. The synthesis and turnover of rat liver peroxisomes. V. Intracellular pathway of catalase synthesis. J Cell Biol. 1973 Nov;59(2 Pt 1):507–524. doi: 10.1083/jcb.59.2.507. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MURRAY E. S. GUINEA PIG INCLUSION CONJUNCTIVITIS VIRUS. I. ISOLATION AND IDENTIFICATION AS A MEMBER OF THE PSITTACOSIS-LYMPHOGRANULOMA-TRACHOMA GROUP. J Infect Dis. 1964 Feb;114:1–12. doi: 10.1093/infdis/114.1.1. [DOI] [PubMed] [Google Scholar]
- Nichols B. A., Bainton D. F. Differentiation of human monocytes in bone marrow and blood. Sequential formation of two granule populations. Lab Invest. 1973 Jul;29(1):27–40. [PubMed] [Google Scholar]
- Nichols B. A., Bainton D. F., Farquhar M. G. Differentiation of monocytes. Origin, nature, and fate of their azurophil granules. J Cell Biol. 1971 Aug;50(2):498–515. doi: 10.1083/jcb.50.2.498. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Roels F., Wisse E., De Prest B., van der Meulen J. Cytochemical discrimination between catalases and peroxidases using diaminobenzidine. Histochemistry. 1975;41(4):281–312. doi: 10.1007/BF00490073. [DOI] [PubMed] [Google Scholar]
- Schachter J. Chlamydial infections (third of three parts). N Engl J Med. 1978 Mar 9;298(10):540–549. doi: 10.1056/NEJM197803092981005. [DOI] [PubMed] [Google Scholar]
- Strum J. M., Karnovsky M. J. Cytochemical localization of endogenous peroxidase in thyroid follicular cells. J Cell Biol. 1970 Mar;44(3):655–666. doi: 10.1083/jcb.44.3.655. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stöhr G., Deimann W., Fahimi H. D. Peroxidase-positive endothelial cells in sinusoids of the mouse liver. J Histochem Cytochem. 1978 May;26(5):409–411. doi: 10.1177/26.5.659841. [DOI] [PubMed] [Google Scholar]
- Todd W. J., Storz J. Ultrastructural cytochemical evidence for the activation of lysosomes in the cytocidal effect of Chlamydia psittaci. Infect Immun. 1975 Sep;12(3):638–646. doi: 10.1128/iai.12.3.638-646.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]






