Chlamydophila abortus

A Microbial Biorealm page on the genus Chlamydophila abortus

Classification

Higher order taxa

Kingdom: Bacteria

Phylum: Chlamydiae

Class: Chlamydiae(class)

Order: Chlamydiales

Family: Chlamydiaceae

Genus: Chlamydophila

Species: Chlamydiae

Species

Chlamydophila abortus Description and significance This gram-negative bacteria is an obligate intracellular pathogen of eukaryotic cells. Chlamydophila abortus is found in cows, goats, sheep, and pigs where it causes abortion during the later period of pregnancy by colonizing in the placenta. This bacteria is enzootic where its infection is specific to animals; or it can be zoonotic where an animal disease spreads and infects a human. The enzootic abortion in sheep is called ovine enzootic abortion (OEA). This pathogen when zoonotic will cause abortion or serious health problems in women, by invading the placenta and causing infection and irritation. It is important to know the genome sequence due to its pathogenic affects on humans. The infection of C.abortus kills many livestock and causes economic burden to agricultural industries worldwide.(2 and 3) The first report of C. abortus was in 1936 in Scotland by J.R. Grieg who decribed an unexpected abortion in a sheep. Grieg believed the abortion was due to a dietary deficiency; years later in 1950 Stamp and his associates discovered the abortion was due to an infection caused by an organism. This organism was later named C. abortus and sequence S26/3 was isolated years later in 1979 in Scotland.(3) C. abortus is derived from the group Chlamydiales, which is divided into four families including Chlamydiaceae, Simkaniaceae, Parachlamydiaceae, and Waddliaceae. The Chlamydiaceae family is divided into two genera including Chlamydophila or Chlamydia. Chlamydia include those microbes the are responsible for STDS. Chlamydophila abortus once went by Chlamydophila psittaci, is responsible for weak newborn bovine animals or abortions. Genome structure This bacteria contains 1,144,377 base pairs within its genome, with a guanine-cytosine pairing taking up 39.9% of the base pairs. C. abortus contains 961 genes which are all arranged in a circular manner. 842 of the genes are conserved with Chlamydophila caviae and chlamydophila pneumoniae. The genome contains single copies of 23S, 16S, and 5S rRNA genes which is different from Chlamydia. Through its genome sequence it is apparent that the pathogen has many varible proteins along it membrane that account for its varible contents. (3 and 7) Cell structure and metabolism This bacteria has two membranes and no flagella. It contains four specific proteins on its outer membrane, coded by the genes POMP 90A/B, and 91A/B. These genes are believed to be glycosylated which may be the reason for their heterogeneity. This pathogen lacks any toxin genes and lacks genes involved in tryptophan metabolism and nucleotide salvaging. Since C. abortus is a pathogen, this organism depends on its host for its proper nutrients and energy. Ecology C. abortus lives and infects the placenta of pregnant livestock such as sheep, cows, and pigs. It has also been found in humans. Bacteria has been found in milk of cattle and also in bulls. If released to the environment through vaginal emission the bacteria is easily spread, and infects other organisms. Pathology The class Chlamydiaceae have a very interesting developmental characteristic where they undergo a biphasic process of being infectious but metabolically inactive known as the elementary body, and then switching to a noninfectious but metabolically active cell called the reticulate body. Chlamydophila abortus cause infection by the elementary body binding to a host cell and becoming metabolically active, it then multiplies within the cells inclusion bodies. The inclusion bodies evade lysosomes and avoid the endocytic pathway and intercepts the exocytic pathway. They become secretory vacuoles to the host. The reticulate body are changed back to elementary bodies, then the inclusion bodies then are lysed off or exocytosis occurs, completing the infection. The metabolically active form can be spread through ingestion, aerosols, or physical contact with the infected organism. The bacteria is easily contracted if one infected animal excretes uterine fluid in the environment and another animal comes into contact with it. In humans the symptoms are severe pain in the abdomen area, along with inflamation, influenza-like symptoms, and respiratory problems. An interesting characteristic of C. abortus is its immune response in mice. A study was done on mice and how their T cells respond to infection of C. abortus. Mice were depleted of CD8+ and CD4+ through monoclonal antibody injections and infected with C. abortus, the results of this experiment shows that the mice depleted from the CD8+ all died. This shows that CD8+ may be needed to stop infection of C. abortus. the absence of CD8+ caused Chlamydail burden on the liver and more apoptotic cells in the inflammatory foci. The CD4+ mice had a lower morbidity than all the other samples, this may show that CD4+ has a play into the activation of C. abortus. (9) Chlamydophila abortus may cause infertility in bovine animals. C. abortus was used to infect bovine oviduct cells. After infection, inclusion bodies and vacuoles formed in the cells; the cells appeared to be damaged and the microvilli were congregated and stuck together, this causes infertility within the animals. (10) Application to Biotechnology This organism is not known to produce any useful compunds or enzymes. C. abortus is mostly known to infect its host and cause health problems. Due to its problematic and pathogenic nature there have been many studies to try to prevent or fight off this pathogen. There is an experimental vaccine against this pathogen that includes the inactivated C. abortus and C. pecorum elementary bodies. This vaccine was injected in cattle and seemed to prevent bovine mastitis and increase the antibody level against Chlamydophila. (4) Current Research C. abortus has become a major problem all around the world infecting livestock, and causing them to abort their babies. A study done in 2006, looked at the abortion rate of a group of sheep and goats in Hungary. The study took place over a seven and a half year period. They found that 63% of all the abortions were due to Chlamydophila abortus. As this study shows, C. abortus is very common and it has become more important to study to try to prevent the death of so many livestock. Recent research was done on cows who often suffer from bovine mastitis which is characterized by the inflammation of the bovine mammary gland. The presence of C. abortus and the lack of antibodies where associated with the presence of bovine mastitis. A vaccine against Chlamydophila reduced milk somatic cell numbers and reduced the presence of bovine mastitis, as well as increased the amount of antibodies. The vaccine lasted 14 weeks then C. abortus became present again in the milk produced by the cow. The presence of C. abortus increased after the vaccination. This study shows the presence of C. abortus causes bovine mastitis. This first attempt with the vaccine can lead to many more experiments and studies of the disease, and soon a solution will be found to rid C. abortus from milk ensuring the safety of the dairy cows and the humans that drink the milk. In April 2007 a study was done on endangered Hawaiian monk seals. Samples were collected from these monk seals from 1997 to 2001. The samples were tested for bacteria and parasites that are known to cause morbidity or mortality in other marine animals; the seals were also tested for antibodies against viruses. Antibodies for phocine herpesvirus-1, Leptospira bratislava, L. hardjo, L. icterohaemorrhagiae, L. Pomona, and Brucella spp. were found in the samples along with antibodies for Clamydophila abortus. The amount of antibody for C. abortus increased as the monk seal aged. The constant observation of these bacteria, pathogens, and antibodies are important to the survival of this species of seals. (11) References 1) http://www.genome.org/cgi/content/full/15/5/629 2) http://www.sanger.ac.uk/Projects/C_abortus/ 3) http://expasy.org/sprot/hamap/CHLAB.html 4) Biesenkamp-Uhe, C., Li, Y., Hehnen, HR., Sachse, K., Kaltenboeck, B., "Therapeutic Chlamydophila abortua and C. pecorum vaccination transiently reduces bovine mastitis associated with Chlamydophila infection". Infect Immun. 2007 Feb. 5) Entrican, G., BSc PhD, Buxton, D., BVM&S PhD, Longbottom, D., "Chlamydial infection in sheep: immune control versus fetal pathology". The Royal Society of Medicine 2001. June. 94(6): 273-277. 6) Szeredi, L., Janosi, S., Tenk, M., Tekes, L., Bozso, M., Deim, Z., Molnar, T. "Epidemiological and pathological study on the causes of abortion in sheep and goats in Hungary". Acta Vet Hung. 2006. Dec. 54(4): 503-15. 7) Thompson, N.,Yeats, C., Bell, K., Holden, M.,Bentley, S.,Livingstone, M., Cerdeno-Tarraga, A., Harris, B., Doggett, J., Ormund, D., Mungall, K., Clarke, K., Feltwell, T., Hance, Z., Sanders, M., Quail, M., Price, C., Barrell, B., Parkhill, J., Longbottom, D. "The Chlamydophila abortus sequence reveals an array of variable proteins that contribute to interspecies variation." Published online April 18, 2005. 8) Vretou1, E., Giannikopoulou1, P., Psarrou1, E. "Polymorphic outer-membrane proteins of Chlamydophila abortus are glycosylated". Microbiology. 2001. 9) Martinez, C., Buendia, A., Sanchez, j., Ortega, N., Caro, M., Gallego, M., Navarro, J., Cuallo, F., Salinas, J. "Relative importance of CD4+ and CD8+ T cells in resolution of Chlamydophila abortus primary infection in mice." Journal of comparative pathology. 2006. 10) Appino S, Pregel P, Manuali E, Vincenti L, Rota A, Carnieletto P, Tiberi C, Bollo E. "Infection of Bovine Oviduct cell cultures with Chlamydophila abortus." Animal Reproductive Science. 2007. Apr. 98(3-4):350-6. 11) Aguirre, A., Keefe, T., Reif, J., Kashinsky, L., Yochem, P., Saliki, J., Stott, J., Goldstein, T., Dubey. J., Braun. R., Antonelis, G. "Infectious disease monitoring of the endangered hawaiian monk seal." Journal of wildlife diseases. 2007. Apr. 43(2):229-41. Edited by Kylee Lim, student of Rachel Larsen and Kit Pogliano