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Rickettsia felis and changing paradigms about pathogenic Rickettsiae.

To the Editor: Mediannikov et al. recently reported several features common to the epidemiology of Rickettsia felis infection and malaria in Africa (1). Similar to the findings of several other recent studies in Africa (2,3), the authors diagnosed R. felis infection in febrile--and to a lesser extent in afebrile--persons by detecting R. felis DNA in human blood samples processed by highly sensitive real-time PCR. These results challenge some paradigms in rickettsiology that need to be more critically evaluated.

Because R. felis DNA was detected in circulating blood of asymptomatic persons (albeit more frequently in patients with mild febrile illness), Mediannikov et al. proposed that humans could be a natural reservoir of R. felis, as they are for malaria parasites. R. felis antibodies failed to develop in nearly all patients in whom R. felis DNA was detected, even after repeated detection of R. felis DNA. In 2 other studies, the same researchers proposed that patients might have several episodes of R. felis infection (relapse or reinfection) to explain why DNA of the agent was detected in the blood at multiple times (2,3). They also proposed that the absence of an antibody response would explain why the disease relapses in some persons (3).

These changing paradigms in rickettsiology require thorough evaluation. Once inside a vertebrate host, pathogenic rickettsiae have been believed to multiply primarily within endothelial cells in the patient's organs. As far as we know, rickettsiae do not multiply within circulating blood cells (4). In contrast, the agents of malaria (Plasmodium spp.) are typically parasites of erythrocytes. Therefore, a blood sample from a person with malaria is an excellent source for PCR diagnostic testing. The sensitivity of PCR for rickettsiae in human blood samples is very low because the sensitivity depends on the magnitude of the vasculitic lesions, i.e., the number of endothelial cells destroyed or detached by rickettsial growth, resulting in circulating rickettsiae. R. conorii (5) and R. rickettsii (6) were detected by highly sensitive PCR in 100% of fatal cases and in only very few nonfatal cases.

In addition to never having been isolated from humans, R. felis has many characteristics of a symbiotic organism. It possesses a mosaic structure genome (size 1.48 Mb) with a high coding capacity (83%) that is typical of symbiotic bacteria (7). Merhej et al. have proposed that within a given bacterial genus (including Rickettsia), pathogenic species have smaller genomes than nonpathogenic species (8). In the genus Rickettsia, the pathogens R. rickettsii, R. prowazekii, R. sibirica, R. typhi, R. parkeri, and R. conorii have genomes of -1.2-1.3 Mb, whereas the apparently nonpathogenic R. bellii has a 1.5-Mb genome, similar to that of R. felis. In contrast to the well-known pathogenic Rickettsia species, R. felis has been reported in a variety of invertebrate hosts, including hematophagous (fleas, ticks, flies, mosquitoes) and non-hematophagous (book lice) arthropods (9). Behar et al. have suggested that R. felis is responsible for inducing parthenogenesis in book lice, similar to the manner of Wolbachia organisms in various invertebrate hosts (9). Furthermore, R. felis forms mycetomes in book lice, a growth feature typical of bacterial endosymbionts (10).

The current view in rickettsiology has a strong anthropocentric bias because the studies have concentrated on parasitic arthropods that feed on humans rather than on free-living arthropods. In fact, the number of Rickettsia species associated with non-hematophagous hosts might be much greater than the ones of medical importance (9). Thus, considering R. felis as an important pathogen in Africa (and in the world) might be premature. Several questions need to be answered before such a conclusion. In asymptomatic persons in whom endothelial cells are likely to be intact, where does R. felis grow to be released at detectable levels in the circulating blood? Considering that all classical spotted fever agents induce an antibody response (4), why do R. felis antibodies fail to develop in humans after a clinical illness attributed to R. felis? In addition, repeated reports that the main vector of R. felis is the cat flea, Ctenocephalides felis, need to be proven by experimental demonstration of its vector capacity.

Given the numerous questions about R. felis, we would add another: could R. felis be a symbiont of a human parasite, such as a protozoon or a helminth? Obviously, the answer is unknown. However, had we not known that Wolbachia organisms are typically endosymbiotic bacteria of both human and animal filarial nematodes, what would we conclude if we detected Wolbachia DNA in blood of either asymptomatic or ill patients?

Marcelo B. Labruna and David H. Walker

Author affiliations: University of Sao Paulo, Sao Paulo, Brazil (M.B. Labruna); and University of Texas Medical Branch, Galveston, Texas, USA (D.H. Walker)



(1.) Mediannikov O, Socolovschi C, Eduoard S, Fenollar F, Mouffok N, Bassene H, et al. Common epidemiology of Rickettsia felis infection and malaria, Africa. Emerg Infect Dis. 2013;19:1775-83.

(2.) Mediannikov O, Fenollar F, Bassene H, Tall A, Sokhna C, Trape JF, et al. Description of "yaaf', the vesicular fever caused by acute Rickettsia felis infection in Senegal. J Infect. 2013;66:536-40. http://

(3.) Socolovschi C, Mediannikov O, Sokhna C, Tall A, Diatta G, Bassene H, et al. Rickettsia felis-associated uneruptive fever, Senegal. Emerg Infect Dis. 2010;16:1140-2.

(4.) Yu XJ, Walker DH. Genus Rickettsia da Rocha-Lima 1916. In: Brenner DJ, Krieg NR, Staley JR, editors. Bergey's manual of systematic bacteriology. Vol. 2, part C. 2nd ed. New York: Springer; 2005, p, 96-106.

(5.) Leitner M, Yitzhaki S, Rzotkiewicz S, Keysary A. Polymerase chain reaction-based diagnosis of Mediterranean spotted fever in serum and tissue samples. Am J Trop Med Hyg. 2002;67:166-9.

(6.) Santos FCP, Brasil RA, Nascimento EMM, Angerami RN, Colombo S, Pinter A, et al. Evaluacion de la PCR en tiempo real para el diagnostico de la Fiebre Manchada Brasilena. Acta Med Costarric. 2013;55(supp):77.

(7.) Merhej V, Raoult D. Rickettsial evolution in the light of comparative genomics. Biol Rev Camb Philos Soc. 2011;86:379-405. 2010.00151.x

(8.) Merhej V, Georgiades K, Raoult D. Post-genomic analysis of bacterial pathogens repertoire reveals genome reduction rather than virulence factors. Brief Funct Genomics. 2013;12:291-304. http://dx.

(9.) Behar A, McCormick LJ, Perlman SJ. Rickettsia felis infection in a common household insect pest, Liposcelis bostrychophila (Psocoptera: Liposcelidae). Appl Environ Microbiol. 2010;76:2280-5.

(10.) Thepparit C, Sunyakumthorn P, Guillotte ML, Popov VL, Foil LD, Macaluso KR. Isolation of a rickettsial pathogen from a non-hematophagous arthropod. PLoS ONE. 2011;6:e16396. http://

Address for correspondence: David H. Walker, University of Texas Medical Branch--Galveston, 301 University Blvd, Galveston, TX 77555-0609, USA; email:
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Title Annotation:LETTERS
Author:Labruna, Marcelo B.; Walker, David H.
Publication:Emerging Infectious Diseases
Article Type:Letter to the editor
Date:Oct 1, 2014
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