Volume 14, Number 4—April 2008
Rickettsia felis in Fleas, France
To the Editor: Rickettsia felis belongs to the spotted fever group of rickettsia. The pathogenic role of this intracellular Proteobacteria in humans has been reported in patients from the United States (Texas) (1), Mexico (2), Germany (3), Brazil, and France (4). R. felis is widely distributed, is associated with blood-sucking arthropods, and has been isolated from fleas in several countries (5).
To obtain new information about the distribution of R. felis in France and potential vectors/ reservoirs of this emerging pathogen, 550 fleas were collected from 82 dogs and 91 cats in 7 widely distributed locations in France (Bordeaux, Toulouse, Cosnes-Cours sur Loire, Dijon, Moulins, Limoges, and Aix-en-Provence). Specimens were collected by combing, recorded, and stored at –20°C. Samples were shipped on dry ice to the entomologic laboratory of the Institute of Comparative Tropical Medicine and Parasitology in Munich, Germany, and species identification was performed by using light microscopy and following the determination key of Hopkins and Rothschild (6). Because infestation levels varied (1–150 fleas/animal), we randomly analyzed 1–8 fleas (mean 3.4) from each host animal.
We homogenized fleas individually in 80 μL of phosphate-buffered saline by using 5-mm steel beads in a RETSCH Tissue Lyser Mixer Mill 300 (QIAGEN, Hilden, Germany). A total of 100 μL of ATL buffer and 20 μL of proteinase K (QIAGEN) were added, and the homogenate was incubated at 56°C in a thermomixer (Eppendorf, Hamburg, Germany) until the tissues were lysed. DNA was extracted from each flea by using a QIAamp DNA Mini Kit (QIAGEN) according to the manufacturer’s instructions (tissue protocol) and stored at –20°C until used in a PCR.
PCR amplification of rickettsial DNA was performed by using previously described oligonucleotide primer pairs Rp CS.877p/Rp CS.1258n targeting the citrate synthase (gltA) gene and, for the positive samples, Rr 190.70p/Rr 190.602n targeting the outer membrane protein A (ompA) gene (7). Amplification was conducted in 50-μL volumes that contained 5 μL of DNA, 30 μL of distilled water, 10 μL of 5× Taq buffer (Roche, Mannheim, Germany), 3 μL of 25 mmol/L MgCl2 (Roche), 1 μL of 10 mmol/L deoxyncleotide triphosphates (Roche), 0.25 μL of each primer (100 μM), and 0.5 μL (5 U/mL) of Taq polymerase (Roche). Conditions for the gltA and ompA PCRs were as described by Bertolotti et al. (8). Negative and positive controls were included in all PCRs. All PCR products were separated by electrophoresis on 1.5% agarose gels at 100 V for 60 min and examined under UV light. For both genes, positive samples were purified by using the QIAquick PCR Purification Kit (QIAGEN) and sent for sequencing to the MWG Biotech Company (Martinried, Germany). Sequences were compared with those of previously characterized rickettsia in GenBank by using basic local alignment search tool (BLAST) (www.ncbi.nlm.nih.gov) analysis.
Five species of fleas were identified: Ctenocephalides felis (500, 224 from dogs and 276 from cats), C. canis (37 from dogs), Pulex irritans (11 from dogs), Spilopsyllus cuniculi (1 from a cat), and Archaeopsylla erinacei (1 from a cat). Five dogs had mixed populations of fleas; 3 of these had P. irritans and C. felis, and 2 had C. felis and C. canis. One cat had P. irritans and C. felis, and another cat had S. cuniculi and C. felis. A total of 52 (19%) of the 272 fleas from dogs and 44 (16%) of the 278 fleas from cats were positive for both the gltA and ompA genes. Positive samples were obtained from all locations. Prevalence ranged from 6% (Dijon) to 43% (Toulouse) for dogs and from 3% (Moulins) to 37% (Bordeaux) for cats (Table). Of 550 fleas, 96 were positive for both genes (gltA and ompA) and 3 of 5 species of fleas were infected: 10 with C. canis, 85 with C. felis, and 1 with A. erinacei. All sequences matched gltA and ompA genes from R. felis (similarity 99%–100%).
Our investigation provides new information about distribution of R. felis and widespread flea infection with R. felis in France. A total of 88% of infected fleas were C. felis, but we found infected C. canis in Bordeaux and Toulouse and infected A. erinacei in Limoges. We report the presence in France of R. felis in C. canis and A. erinacei in France. R. felis in dog fleas in Uruguay and in hedgehog fleas in Algeria has been reported (9,10). Our findings indicate that these 2 flea species may be vectors of human R. felis rickettsiosis in France.
This study was supported by Merial (Lyon, France).
- Schriefer ME, Sacci JB Jr, Dumler JS, Bullen MG, Azad AF. Identification of a novel rickettsial infection in a patient diagnosed with murine typhus. J Clin Microbiol. 1994;32:949–54.PubMedGoogle Scholar
- Zavala Velázquez JE, Ruiz-Sosa JA, Sanchez-Elias RA, Becerra-Carmona G, Walker DH. Rickettsia felis in Yucatan. Lancet. 2000;356:1079–80. DOIPubMedGoogle Scholar
- Richter J, Fournier P, Petridou J, Haussinger D, Raoult D. Rickettsia felis infection acquired in Europe and documented by polymerase chain reaction. Emerg Infect Dis. 2002;8:207–8.PubMedGoogle Scholar
- Rolain J-M, Franc M, Davoust B, Raoult D. Molecular detection of Bartonella quintana, B. koehlerae, B. henselae, B. clarridgeiae, Rickettsia felis, and Wolbachia pipientis in cat fleas, France. Emerg Infect Dis. 2003;9:338–42.PubMedGoogle Scholar
- Jiang J, Soeatmadji DW, Henry KM, Ratiwayanto S, Bangs MJ, Richards AL. Rickettsia felis in Xenopsylla cheopis, Java, Indonesia. Emerg Infect Dis. 2006;12:1281–3.PubMedGoogle Scholar
- Hopkins GH, Rothschild M. An illustrated catalogue 1 of the Rothschild collection of fleas (Siphonaptera) in the British Museum (Natural History). With keys and short descriptions for the identification of families, genera, species and subspecies of the order. Vol. IV, Ctenophthalmidae, Dino-psyllidae, Doratopsyllidae and Listropsyllidae. London: British Museum (Natural History); 1966.
- Regnery RL, Spruill CL, Plikaytis BD. Genotypic identification of rickettsiae and estimation of intraspecies sequence divergence for portions of two rickettsial genes. J Bacteriol. 1991;173:1576–89.PubMedGoogle Scholar
- Bertolotti L, Tomassone L, Tramuta C, Greco E, Amore G, Ambrogi C, Borrelia lusitaniae and spotted fever group rickettsia in Ixodes ricinus (Acari: Ixodidae) in Tuscany, central Italy. J Med Entomol. 2006;43:159–65. DOIPubMedGoogle Scholar
- Venzal JM, Perez-Martinez L, Félix ML, Portillo A, Blanco JR, Oteo JA. Prevalence of Rickettsia felis in Ctenocephalides felis and Ctenocephalides canis from Uruguay. Ann N Y Acad Sci. 2006;1078:305–8. DOIPubMedGoogle Scholar
- Bitam I, Parola P, de la Cruz KD, Matsumoto K, Baziz B, Rolain JM, First molecular detection of Rickettsia felis in fleas from Algeria. Am J Trop Med Hyg. 2006;74:532–5.PubMedGoogle Scholar
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Table of Contents – Volume 14, Number 4—April 2008
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Please use the form below to submit correspondence to the authors or contact them at the following address:
Jeremie Gilles, Department of Entomology, University of Kentucky, S225 Agricultural Science Center North, Lexington, KY 40506, USA;