Articles

In vitro response of host cell to Chlamydia pneumoniae infection, an ultra structure investigation

Abstract

Background and objectives: Chlamydiae are obligate intracellular bacterial pathogens that share a unique developmental cycle. The cycle alternates between infectious extracellular elementary bodies (EBs) and metabolically active reticulate bodies (RBs), which multiply within intracellular vacuoles known as inclusions. Recent evidence has demonstrated that C. pneumoniae is present and persistent at active sites of infection and thus contributes to coronary artery and respiratory diseases, the leading causes of death in the developed world. To understand the process of Chlamydia infection, it is important to investigate the morphology of both normal and infected Hep-2 cells.
Materials and Methods: Hep-2 cell lines (ATCC CCL23 ) were obtained from the Virology Laboratory, King Abdulaziz University Hospital, Jeddah, Saudi Arabia. Cells were grown on cover-slip in shell vial at 37oC in 5% CO2 humidified atmosphere. Later C. pneumoniae were inoculated in the cell lines. The infected cells were scanned using transmission electron microscopy (TEM).
Results: TEM showed round shaped cells with a smooth surface. Some holdings were observed on the edges which are believed to be due to the fluidity of the cytoplasm membrane. The TEM micrograph revealed smooth membrane and typical eukaryotic undisturbed organelles. The morphology of C. pneumoniae, the reticulate bodies (RBs), the elementary bodies (EBs), and their diameter with loug axis were determined.
Conclusion: Despite the presence of inclusion bodies within the cytoplasm of the majority of the infected cells, an alternating period of host cell destruction and host cell proliferation was observed. We termed this phenomenon as unsuccessful infection (USI).

Philips JI, and Shor A. Association between Chlamydiae pneumonia and atherosclerotic lesions. Cardiovasc J S Afr 2001; 12: 42-46.

Grayston JT. Background and current knowledge of Chlamydia pneumoniae and atherosclerosis. J Infect Dis 2000;181 Suppl 3:S402-410.

Casadevall A. and Pirofski LA. Host-pathogen interaction: basic concepts of microbial commensalisms, colonization, infection and disease. Infect Immun 2000; 68,6511-6518.

Theegarten D, Anhenn O, Hotzel H, Wagner M, Marra A, Stamatis G, Mogilevski G, Sachse K. A comparative ultrastructural and molecular biological study on Chlamydia psittaci infection in alpha-1 antitrypsin deficiency and non- alpha-1 antitrypsin deficiency emphysema versus lung tissue of patients with hamartochondroma. BMC Infect Dis 2004 21;4:38.

Mueller M, Postius S, Thimm JG, Gueinzius K, Muehldorfer I, Hermann C. Toll-like receptors 2 and 4 do not contribute to clearance of Chlamydophila pneumoniae in mice, but are necessary for the release of monokines. Immunobiology 2004;209:599-608.

Wolf K, Fischer E, Hackstadt T. Ultrastructural analysis of developmental events in Chlamydia pneumoniae-infected cells. Infect Immun. 2000 Apr; 68 (4) : 2379-2385.

Torquato EF, de Miranda Neto MH, Brancalhão RM, Franco VS. Nucleopolyhedrovirus: scanning electron microscopy technique. Neotrop Entomol 2006;35:787-90.

Kutlin A, Flegg C, Stenzel D, Reznik T, Roblin PM, Mathews S, Timms P, Hammerschlag MR. Ultrastructural study of Chlamydia pneumoniae in a continuous-infection model. J Clin Microbiol 2001; 39:3721-3723.

Cherian SM, Arumugam SB, Bobryshev Y, Nayar S, Jagannath BR. Is Chlamydia pneumoniae associated with calcification in coronary atherosclerosis? Ind J Thorac Cardivasc Surg, 2006; 22: 126-131.

Carlson JH, Porcella SF, McClarty G, and Caldwell HD. Comparative genomic analysis of Chlamydia trachomatis oculotropic and genitotropic strains. Infect Immun 2005; 73(10): 6407–6418.

Files
IssueVol 1 No 1 (2009) QRcode
SectionArticles
Keywords
Chlamydia pneumoniae infection Ultra-structure

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
1.
Al- ssum R, Marie M. In vitro response of host cell to Chlamydia pneumoniae infection, an ultra structure investigation. Iran J Microbiol. 1;1(1):31-36.