Don't need the entire report?
Generate a print friendly version containing only the sections you need.Generate report
IdentityTop of page
Preferred Scientific Name
- Chlamydophila abortus
Taxonomic TreeTop of page
- Domain: Eukaryota
- Kingdom: Planctomycetes [kingdom]
- Class: Planctomycetes [class]
- Order: Chlamydiales
- Family: Chlamydiaceae
- Genus: Chlamydophila
- Species: Chlamydophila abortus
Diseases TableTop of page chlamydial infections of livestock and poultry
chlamydophila abortus, enzootic abortion, in ruminants and pigs
enzootic abortion of ewes
Distribution TableTop of page
The distribution in this summary table is based on all the information available. When several references are cited, they may give conflicting information on the status. Further details may be available for individual references in the Distribution Table Details section which can be selected by going to Generate Report.Last updated: 10 Jan 2020
Pathogen CharacteristicsTop of page
The Chlamydiales, thought to be viruses for a long time, are obligate intracellular bacterial pathogens of higher cells. The chlamydial elementary body (EB) is near the limit of light microscopic visibility with approximately 0.3 µm in diameter, round or occasionally pear-shaped, and contains electron-dense structures. It is the infectious stage of the chlamydial developmental cycle, and functions as a tough ‘spore-like’ body whose purpose is to permit chlamydial survival in the non-supportive environment outside the host cell. The ultrastructure of EB has been extensively studied (Eb et al., 1976; Louis et al., 1980; Matsumoto, 1982; 1988; Rockey et al., 2000; Solof et al., 1982).
The chlamydial reticulate body (RB) is the chlamydial developmental stage during intracellular replication, and it is non-infectious. Typically, the RB has a diameter of approximately 1 µm. The RB is metabolically active, the cytoplasm is rich in ribosomes, which are required for protein synthesis. As the RB begins to differentiate into an EB, sites of re-condensation of nucleic acid appear in its cytoplasm. In the maturing inclusion, chlamydial particles appear to be packed tightly in the inclusion membrane. Development of chlamydiae is highly dependent on nutrient supply and metabolic status of host cells. Nutrient deficiencies such as low glucose levels lead to delayed development and to a few, aberrant chlamydial organisms within the inclusions.
Chlamydial agents, classically have been propagated in the yolk sacs of chicken embryos (Storz, 1971). Cultivation in cell culture is now preferred, and the use of appropriate techniques is important for high-yield culture (Li, et al., 2005). Buffalo Green Monkey Kidney (BGMK) cells support chlamydial replication effectively, particularly when cultivated in Iscove’s Modified Dulbecco’s Medium. EBs are purified by sedimentation, separated from cellular nuclei by low-speed centrifugation, and separated from cell debris by step-gradient centrifugation in a 30% RenoCal-76 50% sucrose step-gradient. Extensive sonication increases yield and infectivity of chlamydial EBs.
Disease(s) associated with this pathogen is/are on the list of diseases notifiable to the World Organisation for Animal Health (OIE). The distribution section contains data from OIE's Handistatus database on disease occurrence. Please see the AHPC library for further information from OIE, including the International Animal Health Code and the Manual of Standards for Diagnostic Tests and Vaccines. Also see the website: www.oie.int.
Host AnimalsTop of page
ReferencesTop of page
Eb F; Orfila J; Lefebvre JF, 1976. Ultrastructural study of the development of the agent of ewe’s abortion. Journal of Ultrastructure Research, 56:177-185.
Li D; Vaglenov A; Kim T; Wang C; Gao D; Kaltenboeck B, 2005. High-yield culture and purification of Chlamydiaceae bacteria. Journal of Microbiological Methods, 61(1):17-24.
Louis C; Nicolas G; Eb F; Lefebvre JF; Orfila J, 1980. Modifications of the envelope of Chlamydia psittaci during its developmental cycle: freeze-fracture study of complementary replicas. Journal of Bacteriology, 141:868-875.
Matsumoto A, 1982. Surface projections of Chlamydia psittaci elementary bodies as revealed by freeze-deep-etching. Journal of Bacteriology, 151:1040-1042.
Matsumoto A, 1988. Structural characteristics of chlamydial bodies. In: Baron AL, ed. Microbiology of Chlamydia. Boca Raton, Fl., USA: CRC Press, 21-45.
OIE Handistatus, 2002. World Animal Health Publication and Handistatus II (dataset for 2001). Paris, France: Office International des Epizooties.
OIE Handistatus, 2003. World Animal Health Publication and Handistatus II (dataset for 2002). Paris, France: Office International des Epizooties.
OIE Handistatus, 2004. World Animal Health Publication and Handistatus II (data set for 2003). Paris, France: Office International des Epizooties.
OIE Handistatus, 2005. World Animal Health Publication and Handistatus II (data set for 2004). Paris, France: Office International des Epizooties.
Rockey DD; Matsumoto A, 2000. The chlamydial developmental cycle. In: Brun YV, Shimkets LJ, eds. Prokaryotic Development. Washington DC, USA: ASM Press, 403-425.
Soloff B; Rank RG; Barron AL, 1982. Ultrastructural studies of chlamydial infection in guinea-pig urogenital tract. Journal of Comparative Pathology, 92:547.
Storz J, 1971. Chlamydia and Chlamydia-Induced Diseases. Springfield, IL, USA: Charles C. Thomas, Publisher.
OIE Handistatus, 2005. World Animal Health Publication and Handistatus II (dataset for 2004)., Paris, France: Office International des Epizooties.
Distribution MapsTop of page
Unsupported Web Browser:
One or more of the features that are needed to show you the maps functionality are not available in the web browser that you are using.
Please consider upgrading your browser to the latest version or installing a new browser.
More information about modern web browsers can be found at http://browsehappy.com/