Abstract
Rickettsia typhi and Rickettsia conorii, the etiologic agents of, respectively, murine typhus and Mediterranean spotted fever, are recognized as frequent causes of fever of intermediate duration in southern Spain; in addition, in recent years Rickettsia felis has been detected in potential vectors in this area. Nevertheless, limited data exist regarding the actual prevalence of past infection due to these three pathogens. In the present study, the prevalence of past infection due to R. felis, R. typhi, and R. conorii was determined in a representative population of southern Spain during 2002. In addition, the possible risk factors associated with exposure to these pathogens were investigated. An epidemiological survey was completed by all subjects included in the study. Serum samples were tested by indirect immunofluorescence assay. The prevalence of past infection due to R. felis, R. typhi, and R. conorii among the 504 total subjects was 6.5, 3.8 and 8.7%, respectively. In multivariate analysis, infection due to R. felis was independently associated with a high-risk occupation (one that required working outdoors in nature, close contact with domestic animals, or potential contact with rodents) (OR=5.8; 95%CI 2.1–15.6), while infection due to R. typhi was associated with older age (factor of 1.04 [95%CI 1.008–1.068]) and frequent insect bites (OR=10.3; 95%CI 2.3–45.5). Two factors were associated with infection due to R. conorii: a high-risk occupation (OR=9.3; 95%CI 3.7–23.2), and participation in outdoor activities (OR=7.2; 95%CI 1.4–38.5). The results confirm the widespread prevalence of past infection due to R. felis, R. typhi, and R. conorii in the population of southern Spain.
Similar content being viewed by others
References
Anton E, Font B, Munoz T, Sanfeliu I, Segura F (2003) Clinical and laboratory characteristics of 144 patients with Mediterranean spotted fever. Eur J Clin Microbiol Infect Dis 22:126–128
Font-Creus B, Bella-Cueto F, Espejo-Arenas E et al (1985) Mediterranean spotted fever: a cooperative study of 227 cases. Rev Infect Dis 7:635–642
Bernabeu-Wittel M, Pachon J, Alarcon A et al (1999) Murine typhus as a common cause of fever of intermediate duration: a 17-year study in the south of Spain. Arch Intern Med 159:872–876
Ruiz-Beltrán R, Herrero-Herrero JI, Martín-Sánchez A, Martín-González JA (1990) Prevalence of antibodies to Rickettsia conorii, Coxiella burnetii and Rickettsia typhi in Salamanca province (Spain). Serosurvey in the human population. Eur J Epidemiol 6:293–299
Lledo L, Gegundez MI, Saz JV, Beltran M (2001) Prevalence of antibodies to Rickettsia typhi in an area of the center of Spain. Eur J Epidemiol 17:927–928
Cardeñosa N, Sanfeliu I, Segura F, Diestre G, Muñoz T, Font B (1999) Seroepidemiological survey of Rickettsia typhi infection in Catalonia, Spain. In: Program and abstracts of the International Conference on Rickettsiae and Rickettsial Disease & American Society for Rickettsiology. 14th Sesquiannual Joint Meeting, Marseille, France, 13–16 June 1999
Higgins JA, Radulovic S, Schriefer ME, Azad AF (1996) Rickettsia felis: a new species of pathogenic rickettsia isolated from cat fleas. J Clin Microbiol 34:671–674
Bouyer DH, Stenos J, Crocquet-Valdes P et al (2001) Rickettsia felis: molecular characterization of a new member of the spotted fever group. Int J Syst Evol Microbiol 51:339–347
Azad AF, Radulovic S, Higgins JA, Noden BH, Troyer JM (1997) Flea-borne rickettsioses: ecologic considerations. Emerg Infect Dis 3:319–327
Boostrom A, Beier MS, Macaluso JA et al (2002) Geographic association of Rickettsia felis-infected opossums with human murine typhus, Texas. Emerg Infect Dis 8:549–554
Oliveira RP, Galvao MA, Mafra CL et al (2002) Rickettsia felis in Ctenocephalides spp. fleas, Brazil. Emerg Infect Dis 8:317–319
Shriefer ME, Sacci JB Jr, Dumler JR, Bullen MG, Azad AF (1994) Identification of a novel rickettsial infection in a patient diagnosed with murine typhus. J Clin Microbiol 32:949–954
Richter J, Fournier PE, Petridou J, Haussinger D, Raoult D (2002) Rickettsia felis infection acquired in Europe and documented by polymerase chain reaction. Emerg Infect Dis 8:207–208
Zavala-Velazquez JE, Ruiz-Sosa JA, Sanchez-Elias RA, Becerra-Carmona G, Walker DH (2000) Rickettsia felis rickettsiosis in Yucatan. Lancet 356:1079–1080
Marquez FJ, Muniain MA, Perez JM, Pachon J (2002) Presence of Rickettsia felis in the cat flea from southwestern Europe. Emerg Infect Dis 8:89–91
Instituto de Estadística de Andalucía (Institute of Statistics of Andalusia) (2003) Anuario Estadístico de Andalucía 2003. Cited November 2003 (http://www.juntadeandalucia.es/institutodeestadistica/anuario/anuario03/index.htm)
Daniel SA, Manika K, Arvanmdou M, Antoniadis A (2002) Prevalence of Rickettsia conorii and Rickettsia typhi infections in the population of northern Greece. Am J Trop Med Hyg 66:76–79
Meskini M, Beati L, Benslimane A, Raoult D (1995) Seroepidemiology of rickettsial infections in Morocco. Eur J Epidemiol 11:655–660
Dupont HT, Brouqui P, Faugere B, Raoult D (1995) Prevalence of antibodies to Coxiella burnetti, Rickettsia conorii, and Rickettsia typhi in seven African countries. Clin Infect Dis 21:1126–1133
Okabayashi T, Hasebe F, Samui KL et al (1999) Short report: prevalence of antibodies against spotted fever, murine typhus, and Q fever rickettsiae in humans living in Zambia. Am J Trop Med Hyg 61:70–72
Lledo L, Gegundez I, Ruiz E, Rodriguez L, Bacellar F, Saz JV (2003) Rickettsia typhi infection in wild rodents from central Spain. Ann Trop Med Parasitol 97:411–414
Lledo L, Gegundez MI, Serrano JL, Saz JV, Beltran M (2003) A sero-epidemiological study of Rickettsia typhi infection in dogs from Soria province, central Spain. Ann Trop Med Parasitol 97:861–864
Azad AF, Beard CB (1998) Rickettsial pathogens and their arthropod vectors. Emerg Infect Dis 4:179–186
Boostrom A, Beier MS, Macaluso JA et al (2002) Geographic association of Rickettsia felis-infected opossums with human murine typhus, Texas. Emerg Infect Dis 8:549–554
Zavala-Velazquez JE, Zavala-Castro JE, Vado-Solis I et al (2002) Identification of Ctenocephalides felis fleas as a host of Rickettsia felis, the agent of a spotted fever rickettsiosis in Yucatán, Mexico. Vector Borne Zoonotic Dis 2:69–75
Kelly PJ, Meads N, Theobald A, Fournier PE, Raoult D (2004) Rickettsia felis, Bartonella henselae, and B. clarridgeiae, New Zealand. Emerg Infect Dis 10:967–968
Shaw SE, Kenny MJ, Tasker S, Birtles RJ (2004) Pathogen carriage by the cat flea Ctenocephalides felis in the United Kingdom. Vet Microbiol 102:183–188
Raoult D, Roux V (1997) Rickettsioses as paradigms of new or emerging infectious diseases. Clin Microbiol Rev 10:694–719
Acknowledgements
This study has been financially supported by the Consejería de Salud, Junta de Andalucía, Spain. We are grateful to Dr. Didier Raoult and all professionals of the Unité de Rickettsies, Marseille, France, for their technical assistance.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Bernabeu-Wittel, M., del Toro, M.D., Nogueras, M.M. et al. Seroepidemiological study of Rickettsia felis, Rickettsia typhi, and Rickettsia conorii infection among the population of southern Spain. Eur J Clin Microbiol Infect Dis 25, 375–381 (2006). https://doi.org/10.1007/s10096-006-0147-6
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10096-006-0147-6