A Microbial Biorealm page on the genus Rickettsia felis
Higher order taxa
cellular organisms; Bacteria; Proteobacteria; Alphaproteobacteria; Rickettsiales; Rickettsiaceae; Rickettsieae; Rickettsia; spotted fever group1
Description and significance
“Rickettsia felis” is an obligate intracellular parasite that was first isolated from cat fleas. It is a gram-negative bacteria that was that differs from Rickettsia typhi by only 32 nucleotide differences3. It was identified in patients clinically diagnosed with murine typhus4. It was originally thought to be a member of the typhus group of rickettsiae, but upon sequencing was found to be closer to the spotted fever group of rickettsiae5.
The genome of R. felis consists of a 1,485,148 bp circular chromosome and two circular plasmids, pRF (62,829 bp) and pRδ (39,263 bp). This results in 1,512 open reading frames that encode proteins2. This genome is much larger than any other Rickettsial organism with the next largest genome being the 1,111,523 bp genome of R. prowazekii2. The two plasmids have identical nucleotide sequences except for a 23,566 bp segment present only in pRF2.
R. felis has multiple genes encoding toxin-antitoxin systems that are rare in obligate intracellular bacteria. These systems may help ensure propagation of bacteria in a eukaryotic host2. R. felis also has genes whose analogs in other bacteria encode conjugative pili proteins, suggesting that some of the R. felis genome may have been acquired by lateral transmission5. It appears that R. felis is the first obligate intracellular parasite to have a conjugative plasmid2. It also has genes homologous to genes encoding streptomycin and penicillin resistance2.
Cell structure and metabolism
R. felis has two types of pili on its cell surface. The first is used to establish contact between two bacterial cells and are most likely specialized for conjugation6. The other type are short, hair-like projections that are most likely involved in attachment to other cells and may be involved in the virulence of R. felis6.
R. felis is thought to generate ATP through the TCA cycle because two enzymes that generate ATP during the cycle and four subunits of the pyruvate dehydrogenase complex that initiate the TCA cycle were identified6. Also, four subunits of ATP synthase and several components of two ABC transporters have been identified6.
R. felis is maintained transovarially in fleas and as such is transferred from parent to offspring in the flea eggs. It appears to have no detrimental effect on the flea life cycle. It infects humans bitten by infected fleas and the organism is deposited near the bite site in flea feces8. Infections are rare but appear in areas prone to flea infestations such as certain parts of Texas and Los Angeles and Orange County in California. R. felis infections have also appeared in France, Germany, Brazil and the first Asian case was documented in Thailand. Since fleas can bite multiple human hosts the infection can be readily spread in flea-infested areas8.
This organism is an obligate intracellular parasite found in cat fleas, C. felis. It is maintained transovarially in fleas has no effect on the fleas it infects. When a flea bites an animal or human, R. felis is deposited in the flea feces at the bite site8. R. felis infection causes a disease very similar to (and often mistaken for) murine typhus caused by its close relative R. typhi. The only way to differentiate between the two diseases is to use PCR to amplify a portion of a Rickettsia antigen gene7. The main symptom is fever of an unknown origin. Other symptoms include headache, rash, vomiting, and stupor7.
Application to Biotechnology
No applications to biotechnology were found for this organism.
Didier Raoult et al analyzed the proteome of R. felis and were able to identify the genes and the proteins they encoded for virulence factors, metabolic activities, and ribosomal proteins. They found that the proteome of R. felis to be typical of intracellular bacteria as the vast majority of its proteins are used in translation while relatively few are used in metabolic activities. They also identified two adhesins as virulence factors that R. felis utilizes in the initial steps of host-cell interaction6.
Joseph Gillespie et al used phylogeny estimation to determine the mode of inheritance of a conjugative plasmid among Rickettsia bacteria. The existence of the pRF genes on the plasmid indicated that Rickettsia felis doesn’t completely fall into the spotted fever group or the typhus group completely. Rather, the plasmid indicates that R. felis has undergone some horizontal gene transfer with ancient group rickettsiae and may indeed be basis for a fourth group of rickettsiae bacteria called the transitional group that have characteristics of both typhus group and spotted fever group rickettsiae. This plasmid may have been incorporated into the chromosomes of other rickettsial bacteria, explaining why R. felis is the only rickettsial bacteria with a sequenced genome to have a plasmid5.
A research study conducted by Jennifer Hawley et al sampled 92 pairs of cat blood and their corresponding flea extracts and used polymerase chain reaction (PCR) to amplify DNA from R. felis. Of the samples examined, 67.4% of the flea extracts and none of the cat blood samples were positive for R. felis DNA. This was the first study using PCR to examine the prevalence of R. felis in the United States in client-owned cats from Maryland, Alabama, and Texas. The high prevalence of R. felis has health implications as cats are becoming more popular pets and humans are susceptible to R. felis infection9.
2. Ogata H, Resto P, Audic S, Robert C, Blang G, etal. (2005) The genome sequence of Rickettsia felis identifies the first putative conjugative plasmid in an obligate intracellular parasite. PLoS Biol 3(8): e248
3. Azad, Abdu et al. “Rickettsia felis: a New Species of Pathogenic Rickettsia Isolated from Cat Fleas.” Journal of Clinical Microbiology. Vol. 34 No 3 (1996): 671-674
4. Azad, Abdu F et al. “Identification of a Novel Rickettsial Infection in a Patient Diagnosed with Murine Typhus.” Journal of Clinical Microbiology. Vol. 32, No. 4 (1994): 949-954
5. Gillespie JJ, Bier MS, Rahman MS, Ammerman NC, Shallom JM, et al. (2007) Plasmids and Rickettsial Evolution: Insight from Rickettsia felis. PLoS ONE 2(3): e266. Doi:10.1371/journal.pone.0000266
6. Raoult, Didier et al. “Proteome analysis of Rickettsia felis highlights the expression profile of intracellular bacteria,” Proteomics 7 (2007): 1232-1248
7. Raoult, Didier et al. “A Flea-Associated Rickettsia Pathogenic for Humans.” Emerging Infectious Diseases. Vol. 7, No. 1 (2001): 73-81
8. Azad, Abdu and Charles Beard. “Rickettsial Pathogens and their Arthropod Vectors.” Emerging Infectious Diseases. Vol. 4, No. 2 (1998): 179-186
9. Hawley, Jennifer R et al. Prevalence of Rickettsia felis DNA in the blood of cats and their fleas in the United States, J Feline Med Surg (2007), doi:10.1016/j.jfms.2006.12.005
Edited by Kristen Whetsell, a student of Rachel Larsen and Kit Pogliano