Difference between revisions of "Lawsonia intracellularis"

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==Classification==
 
==Classification==

Revision as of 19:20, 23 May 2007

A Microbial Biorealm page on the genus Lawsonia intracellularis

Classification

Gram-negative

Higher order taxa

Phylum: Bacteria

Bacteria; Proteobacteria; Deltaproteobacteria; Desulfovibrionales; Desulfovibrionaceae; Lawsonia.

Strain: PHE/MN1-00.

(there may be additional subcategories included as well. You can just copy this information from the NCBI taxonomy page)


Genus

Genus species: Lawsonia intracellularis


Description and significance

Lawsonia Intracellularis is a bacterial pathogen which causes disease in a wide range of animals, mainly pigs. The bacterial pathogen invades the intestinal epithelial cells which causes hyperplasia of the infected cells which leads to the process of disease pathogenesis. Lawsonia intracelluaris is an intracellular enterophathogen that is the cause of intestinal hyperplasia which include proliferative enteropathy, intestinal adenomatosis, and ileitis. Lawsonia intracellularis though primarily recognized in pigs, is spreading to a wide range of mammals. With a 16SrRNA gene sequence, Lawsonia intracellularis is related to Desulfovibio, a sulfate-reducing bacteria and Bilophila wadsworthia.


Genome structure

Lawsonia intracellularis is made up of a circular chromosome and the length is 1,457,619 nucleotides. The genomic content includes 1,719,014 nucleotides. It had 1, 337 protein genes and 49 RNA genes.


Cell structure and metabolism

The structure of Lawsonia intracellularis reveals non-spore-forming curved rods. It contains gram-negative cells that are able to retain carbol-fushsin when stained using the Ziehl-Neelsen method. It is nonpifmented and nonflagellated. Through the Ziehl-Neelsen method the cell wall of a gram-negative is shown as well as the protoplasmic structure of a prokaryote. The cells replicate within the cytplasm and are not enclosed by membrane-bound vacuoles. This occurs in epitheilial cells of pigs.


Ecology

Natural infection has not been detected in either wild or laboratory mice however, the former represent a potential reservoir, therefore studies have further implications for the ecology and epidemiology of PE, particularly in pigs. The environment is more likely to be cohabited by rodents. Though the major animal that is most susceptible are pigs, it is becoming more apparent that Lawsonia intracellularis has a broad host range which is wider than currently known. Though there is evidence of infection in primates, there is currently no direct evidence that Lawsonia intracellularis can infect humans, although one report has suggested a link with human disease.


Pathology

Lawsonia intracellularis is an intracellular bacterial pathogen which cause intestinal hyperplasia in a wide range of mammalian and avian species.


Application to Biotechnology

Does this organism produce any useful compounds or enzymes? What are they and how are they used?

Current Research

"Single-chain antibodies (scFv) exhibiting specific binding to Lawsonia intracellularis were isolated from a phagemid library expressing scFvs molecules on the surface of filamentous bacteriophages. For scFv selection whole bacterial cells were used and individual clones were tested in ELISA test. The total of seven unique clones with different fingerprint profiles was isolated. All clones were able to bind specifically in immunofluorescence assay. This is the first report of species specific recombinant antibodies against L. intracellularis".

"An in situ hybridization (ISH) procedure with a digoxigenin-labeled oligonucleotide probe for detection of Lawsonia intracellularis in paraffin-embedded tissue is described. This technique recognized 71% of PCR-positive cases and was thus superior to Warthin-Starry silver stain, which only detected 41%. The presented ISH is of comparable sensitivity to previously published immunohistochemical assays and is recommended for laboratories wishing to diagnose L. intracellularis infections in tissue sections but without access to antibodies".

References

http://www.pubmedcentral.nih.gov/botrender.fcgi?blobtype=html&artid=97774 http://www.genome.jp/kegg-bin/show_organism?org=lip http://ijs.sgmjournals.org/cgi/reprint/45/4/820.pdf http://rice.tigr.org/tigr-scripts/CMR2/GenomePage3.spl?database=ntli04