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other Chlamydiae

Chlamydophila abortus strains colonize the placenta and are primarily associated with cases of abortion and weak neonates, particularly in sheep and goats. The agent is endemic among ruminants (goats, sheep, cattle) world­wide and has also been associated with cases of abortion in a horse, a rabbit, guinea pigs, mice and swine.

Chlamy- dophila abortus is a zoonotic pathogen and may cause abortion in women. Recently, C. abortus has been associ­ated with gammopathy in the protein electrophoresis pattern in Spanish common (F tinnunculus) and lesser kestrel (7? naumanni) nestlings. A concurrent Chlamydo- phila outbreak among sheep led to the suggestion of cross-infection between livestock, insects and a kestrel in the same area(20). Chlamydophila abortus was also detected in pulmonary lymph nodes, uterus and placenta of free- ranging wild boar in Germany1-7). High prevalence of anti­bodies against C. abortus and Chlamydiaceae was shown in wild ungulates from Spain, including wild boar, red deer (Cervus elaphus), roe deer (Capreolus capreolus), fallow deer (Dama dama), mouflon ( Ovis aries musimon), Barbary sheep (Ammotragus lervia), southern chamois (Rupicapra pyrenaica) and Iberian ibex (Capra pyrena- ica)(18). A case of abortion caused by C. abortus in a springbok (Antidorcas marsupialis) has been reported from Paris Zoo(21). Infections due to C. abortus in ruminants may result in fever as high as 41°C on day 1 or 2, which may last for 3—5 days. In sheep, abortions usually occur during the last month of gestation. In cattle, abortions occur in the last trimester and are usually sporadic. Abor­tion rates may vary between 1 and 5% in chronic infected herds and 30% in flocks with recently introduced C. abortus. Infection occurs via inhalation or ingestion and first affects the tonsil, from which it spreads via the bloodstream to other body sites.
Placental infections establish between days 60 and 90 of gestation, with path­ological lesions first seen after 90 days, and include loss of chorionic epithelial cells, fibrino-purulent arteritis, necrosis and sloughing of the endometrial epithelium. Infection of the fetus occurs secondary to placentitis, but the mechanism by which C. abortus migrates from the maternal side of the placenta to the fetus is still uncertain. Inflammation and necrotic foci are found in most fetal organs and tissues. Infected fetuses usually reveal enlarged popliteal and mesenteric lymph nodes having a demar­cated cortex with follicles and germinal centres(22). The commercially available IDEXX Chlamydiosis Total Ab Test is an indirect ELISA for the detection of antibodies against C. abortus in serum and plasma of ruminants. The guidelines for the diagnosis of enzootic abortion in ewes are given in the OIE Manual of Diagnostic Tests and Vac­cines for Terrestrial Animals1-15,23).

Chlamydophila pecorum strains are serologically and pathogenically diverse. Isolation is from mammals only: ruminants, koalas and swine. In koalas, reproductive disease, infertility, and urinary tract disease have been described. In other mammals, the agent causes abortion, conjunctivitis, encephalomyelitis, enteritis, pneumonia and polyarthritis(1). Chlamydophila pecorum may produce diarrhoea in ruminants after oral infection. Polyarthritis/ polyserositis due to C. pecorum is characterized by subcu­taneous oedema and fluid-filled synovial sacs. Swollen joints contain a greyish-yellow turbid synovial fluid. His­topathological lesions are primarily inflammatory changes in the synovium, tendon sheaths and subsynovial tissues. Syndromes associated with chlamydial infections in the koala include keratoconjunctivitis with serous ocular dis­charge and mild blepharospasm, cystitis, increased fre­quency of urination and dysuria, and infertility1-13).

Chlamydophila pneumoniae infects humans, koalas and horses, primarily causing respiratory disease.

Koala isolates are most often recovered from ocular and urogeni­tal sites, where they appear less pathogenic1-1). Chlamy- diosis in the koala is the most intensively studied chlamydial infection of wild mammals worldwide, and the koala biovar of C. pneumoniae has been found in all Aus­tralian free-ranging koala populations that have been investigated.

Chlamydophila felis is endemic among domestic cats worldwide. The infection is characterized by severe con­junctivitis, blepharospasm, hyperaemia, chemosis and serous to mucopurulent ocular discharge, often concurrent with mild respiratory signs, slight nasal discharge and sneezing. Chlamydophila felis may also colonize the gas­trointestinal and reproductive tract. Transmission of C. felis is by direct contact with infected secretions and droplet infection. Clinical signs develop within 4 days and gradually subside after 30 days post- infection, but long­term persistency has been suggested. Zoonotic infection of humans has been described(1).

Chlamydophila caviae primarily infects the mucosal epi­thelium, is non- invasive and is markedly species- specific for guinea pigs ( Cavia cobaya)(1). The natural site of infec­tion is the conjunctiva, but C. caviae also infects the genital tract of guinea pigs.

Chlamydia suis strains have only been isolated from swine. In experimental studies C. suis caused subclinical intestinal infections in young weanling pigs, with intes­tinal lesions but without diarrhoea. Chlamydia suis has also been associated with conjunctivitis, pneumonia and a high proportion of apparently subclinical infections1-1). Chlamydia suis was detected in lung and pulmonary lymph nodes of free- ranging wild boar in Germany(7).

Chlamydia muridarum has been isolated from mice and hamsters. The strain from hamsters is not known to cause disease, but pneumonia has been seen in mice(1).The two latter species were recently detected by PCR in blood samples from Spanish common and lesser kestrels nestlings but have never been recorded in birds before(20).

REFERENCES

1. Evereττ, K.D.E. Chlamydia and Chlamydiales: more than meets the eye. Veterinary Microbiology. 2000;75:109-26.

2. Harkinezhad, T., Geens, T. & Vanrompay, D. Chlamydophila psittaci infections in birds: a review with emphasis on zoonotic consequences. Veterinary Microbiology. 2009;135:68-77.

3. Magnino, S., Haag-Wackernagel, D., Geigenfeind, I. et al. Chlamydial infections in feral pigeons in Europe: review of data and focus on public health implications. Veterinary Microbiology. 2009;135:54-67.

4. Bracewell, C.D. & Bevan, B.J. Chlamydiosis in birds in Great Britain. 1. Serological reactions to chlamydia in birds sampled between 1974 and 1983. Journal of Hygiene (London). 1986;96:447-51.

5. Pennycott, T.W, Dagleish, M.P, Wood, A.M. & Garcia, C. Chlamy- dophila psittaci in wild birds in the UK. Veterinary Record. 2009;164: 157-8.

6. Schettler, E., Fickel, J., Hotzel, H. et al. Newcastle disease virus and Chlamydia psittaci in free-living raptors from Eastern Germany Journal of Wildlife Diseases. 2003;39:57-63.

7. Hotzel, H., Berndt, A., Melzer, F. & Sachse, K. Occurrence of Chlamy- diaceae spp. in a wild boar (Sus scrofa L.) population in Thuringia (Germany). Veterinary Microbiology. 2004;103:121-6.

8. Giacometti, M., Tolari, F., Mannelli, A. & Lanfranchi, P. Seroepide- miologic investigations in the Alpine ibex ( Capra i. ibex) of Piz Albris in the canton of Grigioni (Switzerland). Schweizer Archiv fur Tierheilkunde. 1995;137:537^2.

9. Shewen, P. Chlamydial infection in animals: a Review. Canadian Vet­erinary Journal. 1980;21:2-11.

10. Pinard, C.L., Brightman, A.H., Yeary, TJ. et al. Normal conjunctival flora in the North American opossum (Didelphis virginiand) and raccoon (Procyon loto r). Journal of Wildlife Diseases. 2002;38:851-5.

11. Schettler, E., Langgemach, T., Sommer, P. Streich, J. & Frolich, K. Seroepizootiology of selected infectious disease agents in free- living birds of prey in Germany.

Journal of Wildlife Diseases. 2001;37: 145-52.

12. Andersen, A.A. & Franson, J.C. Avian Chlamydiosis. In: Thomas, N.J., Hunter, D.B. & Atkinson, C.T., (eds). Infectious Diseases of Wild Birds. Ames, Iowa, USA: Blackwell Publishing; 2007; pp. 306-9.

13. Whittington, R. Chlamydiosis of koalas. In: Williams, E.S. & Barker, I.K. (eds). Infectious Diseases of Wild Mammals, 3rd edn. Ames, Iowa, USA: Blackwell Publishing; 2001; pp. 423-34.

14. WQR. Wildlife Quarterly Reports (WQR) 2003-2010, Duff, J.P & Barlow, A.M. (eds) Available online at: http://www.defra.gov.uk/vla/ reports/rep_surv_wildlife.htm [accessed 23 March 2012].

15. OIE. Diseases of Wildlife in the UK Reports 2000-2003, Duff, J. P. (ed.) Available online at: http://www.defra.gov.uk/vla/reports/rep_ wildlife.htm [accessed 23 March 2012].

16. Sharples, E. & Baines, S.J. Prevalence of Chlamydophilapsittac∕-positive cloacal PCR tests in wild avian casualties in the UK. Veterinary Record. 2009;164:16-7.

17. OIE. Manual of Diagnostic Tests and Vaccines for Terrestrial Animals 2011. Office International des Epizooties. Available online at: http:// www.oie.int/international-standard-setting/terrestrial-manual/access- online [accessed 26 March 2012].

18. Salinas, J., Caro, M.R., Vicente, J. et al. High prevalence of antibodies against Chlamydiaceae and Chlamydophila abortus in wild ungulates using two ‘in house' blocking-ELISA tests. Veterinary Microbiology. 2009;135:46-53.

19. Simpson, V.R. & Bevan, R. Chlamydia psittaci infection in robins. Veterinary Record. 1989;125:537.

20. Lemus, J.A., Fargallo, J.A., Vergara, P, Parejo, D. & Banda, E. Natural cross chlamydial infection between livestock and free-living bird species. PloS One. 2010;19:e13512.

21. Berri, M., Bernard, F., Lecu, A., Ollivet-Courtois, F. & Radolakis, A. Molecular characterisation and ovine live vaccine 1B evaluation toward a Chlamydophila abortus strain isolated from springbok antelope abor­tion. Veterinary Microbiology. 2004;103:231^0.

22. Andersen, A.A. Chlamydia. In: Gyles, C.L., Prescott, J.F., Songer, J.G. & Thoen, C.O. (eds). Pathogenesis of Bacterial Infections in Animals, 3rd edn. Ames, Iowa, USA: Blackwell Publishing; 2004; pp. 415-24.

23. OIE. Enzootic abortion of ewes (ovine chlamydiosis). Manual of Diag­nostic Tests and Vaccines for Terrestrial Animals. Paris: OIE; 2008; pp. 1013-20.

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Source: Gavier-Widen D., Meredith A., Duff Paul J. (eds.). Infectious Diseases of Wild Mammals and Birds in Europe. London: Wiley-Blackwell,2012. — 568 p.. 2012
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