Helicobacter hepaticus ATCC51449

A Microbial Biorealm page on the genus Helicobacter hepaticus ATCC51449

Helicobacter hepaticus

Classification

Higher order taxa

Cellular Organisms; Bacteria; Proteobacteria; Delta/Epsilon Subdivisions; Epsilonproteobacteria; Campylobacterales; Helicobacteraceae; Helicobacter; Helicobacter hepaticus ATCC51449

Species

Helicobacter hepaticus

NCBI: Taxonomy Genome: H. hepaticus ATCC51449

Description and significance

Helicobacter hepaticus ATCC514459 is a Gram-negative, spiral (anywhere from one to seven spirals) shaped bacteria. It is usually between 0.2 to 0.3 µm in diameter and 1.5 to 5.0 µm long. It is a microaerophilic organism since it requires oxygen to live, but can live at environments that contain less oxygen than atmospheric levels. Like other species of Helicobacter, Helicobacter hepaticus, can be found in the mucosal layer of the gastrointestinal tract or in liver tissue. In mice, it has been found to cause chronic hepatitis, liver cancer, and inflammatory bowel disease. Its importance in humans is not fully understood yet. (EMBL-EBI)

Helicobacter hepaticus was first isolated from hepatic tissue by when a spiral bacteria was able to be cultivated on blood agar plates incubated at 37ºC under anaerobic or microaerobic conditions. Ultrastructural morphologic examination, biochemical characteristics examination, and 16S rRNA gene sequencing were all used to characterize Helicobacter hepaticus. (Rice 129-30)

Genome structure

Helicobacter hepaticus has a circular genome consisting of 1,799,146 base pairs, which are thought to encode for 1,875 proteins. It has a 35.9% GC content and 938 of its proteins have orthologs with Helicobacter pylori, 953 are orthologous with Campylobacter jejuni, and 821 are orthologous with both H. pylori and C. jejuni. The genome also contains a 71 kb genomic island HHGI1. The genomic island encodes three components of a type IV secretion system. A type IV secretion system is a conjugation system that allows for the transporting of DNA or proteins. Five other strains of Helicobacter hepaticus that are known to cause liver disease lacked anywhere from 85 to 229 genes, including large parts of the genomic island HHGI1. (Suerbaum S)

Cell structure and metabolism

Helicobacter hepaticus has bipolar sheathed flagella for motility. However, unlike other Helicobacter species, Helicobacter hepaticus does not have the periplasmic fibers that envelope the bacterial cell.

For metabolism, Helicobacter hepaticus has a strong urease activity. Urease is an enzyme that catalyzes the hyrdolysis of urea into bicarbonate and ammonia, both of which neutralize gastric acid and therefore allows the bacteria to colonize the acidic environment that the gastrointestinal tract can be. Helicobacter hepaticus tests positive in both oxidase and catalase tests. The oxidase test shows the presence of cytochrome c oxidases which show that a cell would be capable of using oxygen to produce energy via an Electon Transport Chain. The catalase test further proves this ability since catalase is an enzyme that decomposes hydrogen peroxide (a Reactive Oxygen Species) into water and oxygen. Helicobacter hepaticus can also gain energy anaerobically by reducing different compounds. It can reduce sulfur and produce hydrogen sulfide (H2S) and it can also reduce nitrate to nitrite. Helicobacter hepaticus is sensitive to the antibiotic metronidazole which kills anaaerobic bacterias. It is resistant to the antibiotics nalidixic acid and cephalothin. (Rice 129-31)

Ecology

Helicobacter hepaticus is an enterohepatic bacteria that can "infect the intestinal tracts and biliary trees of various mammals, including mice and humans, and are associated with chronic inflammatory diseases of the intestine, gallstone formation, and malignant transformation." (Sterzenbach) It is becoming and increasing concern in the biomedical research field where a recent study discovered that out of a sample of 79 mice from 34 sources, 62 of 79 mice had a Helicobacter infection and the, "Mice from 20 of the 34 institutions (59%) were most commonly colonized with H. hepaticus alone or in combination with other Helicobacter [species]." The potential of the impact the Helicobacter infections have on biomedical research experiments in vivo is therefore an important issue and under research. (Taylor)

Pathology

As stated above, the HHGI1 genomic island encodes three basic components of a type IV secretion system which is a system of conjugation for DNA and protein transport. However, Helicobacter hepaticus lacks orthologs of H. pylori virulence factors such as adhesins, VacA cytotoxin, and almost all cag pathogenicity island proteins. It does have orthologs of Campylobacter jejuni adhesin PEB1 and the the cytolethal distending toxin (CDT). These factors are what contribute to Helicobacter hepaticus' ability to infect organisms. (Suerbaum)

In addition, Helicobacter suppresses and evades the immune system in order to cause chronic inflammatory diseases. Helicobacter hepaticus produces soluble bacterial factors that reduce the ability of the Toll-like receptors TLR-4 (which binds to LPS) and TLR-5 (which binds to flagellin) to produce immune responses. The lysate of Helicobacter hepaticus and its soluble LPS also inhibited development of endotoxin tolerance to Escherichia coli LPS. Thus supression of immune responses by Helicobacter hepaticus may have wider effects over the entire intestinal flora, its homeostasis, and its inflammatory conditions. (Sterzenbach)

Current Research

Enter summaries of the most recent research here--at least three required

References

Rice, Jerry M. "Helicobacter hepaticus, a Recently Recognized Bacterial Pathogen, Associated with Chronic Hepatitis and Hepatocellular Neoplasia in Laboratory Mice." Emerging Infectious Diseases. 1995. Volume 1, No. 4. p. 129-31. ftp://ftp.cdc.gov/pub/EID/vol1no4/adobe/rice.pdf

Sterzenbach T, Lee SK, Brenneke B, von Goetz F, Schauer DB, Fox JG, Suerbaum S, Josenhans C. “Inhibitory Effect of Enterohepatic Helicobacter hepaticus on Innate Immune Responses of Mouse Intestinal Epithelial Cells.” Infection and Immunity. 2007 Jun;75(6):2717-28. Epub 2007 Mar 19. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=17371851&query_hl=15&itool=pubmed_DocSum

Suerbaum S, Josenhans C, Sterzenbach T, Drescher B, Brandt P, Bell M, Droge M, Fartmann B, Fischer HP, Ge Z, Horster A, Holland R, Klein K, Konig J, Macko L, Mendz GL, Nyakatura G, Schauer DB, Shen Z, Weber J, Frosch M, Fox JG. "The complete genome sequence of the carcinogenic bacterium Helicobacter hepaticus.", Proc Natl Acad Sci U S A, 2003 Jun 24;100(13):7901-6 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12810954&dopt=Abstract

Taylor NS, Xu S, Nambiar P, Dewhirst FE, Fox JG. “Enterohepatic Helicobacter species are Prevalent in Mice Obtained from Commercial and Academic Institutions in Asia, Europe, and North America.” Journal of Clinical Microbiology. 2007 May 16. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=17507523&query_hl=15&itool=pubmed_DocSum

Edited by Arpan Patel, a student of Rachel Larsen