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Journal of Clinical Microbiology logoLink to Journal of Clinical Microbiology
. 1997 Nov;35(11):2883–2885. doi: 10.1128/jcm.35.11.2883-2885.1997

Seroprevalence of Bartonella henselae infection and correlation with disease status in cats in Switzerland.

T Glaus 1, R Hofmann-Lehmann 1, C Greene 1, B Glaus 1, C Wolfensberger 1, H Lutz 1
PMCID: PMC230080  PMID: 9350752

Abstract

The prevalence of infection with Bartonella henselae was investigated in cats from different areas of Switzerland. Serum samples of 728 cats were examined for antibodies to B. henselae by immunofluorescent antibody testing, and the results were analyzed with a view to a possible correlation between a positive titer and signalment, clinical signs, infection with feline leukemia virus (FeLV), feline immunodeficiency virus (FIV), feline coronavirus (FCoV), or feline spumavirus (FeSFV), and the living environments of the cats. The seroprevalence in all cats was 8.3%. No significantly different prevalence was found in sick versus healthy cats (9.2 versus 7.2%); however, in sick cats seropositive for B. henselae, there was an increased frequency of stomatitis and a variety of diseases of the kidneys and the urinary tract. There was an increased prevalence of B. henselae in cats positive for FCoV (P = 0.0185) or FeSFV (P = 0.0235) and no statistically significant increased prevalence in cats infected with FeLV or FIV. There was no correlation between a positive titer and sex or breed. The same prevalence of B. henselae antibodies was found in cats with and without access to the outdoors and in cats from single- and multicat households. The seroprevalence was increased in cats living south of the Alps (12.1%); however, this difference was not significant (P = 0.0616).

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Selected References

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  1. Childs J. E., Olson J. G., Wolf A., Cohen N., Fakile Y., Rooney J. A., Bacellar F., Regnery R. L. Prevalence of antibodies to Rochalimaea species (cat-scratch disease agent) in cats. Vet Rec. 1995 May 20;136(20):519–520. doi: 10.1136/vr.136.20.519. [DOI] [PubMed] [Google Scholar]
  2. Chomel B. B., Abbott R. C., Kasten R. W., Floyd-Hawkins K. A., Kass P. H., Glaser C. A., Pedersen N. C., Koehler J. E. Bartonella henselae prevalence in domestic cats in California: risk factors and association between bacteremia and antibody titers. J Clin Microbiol. 1995 Sep;33(9):2445–2450. doi: 10.1128/jcm.33.9.2445-2450.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Chomel B. B., Kasten R. W., Floyd-Hawkins K., Chi B., Yamamoto K., Roberts-Wilson J., Gurfield A. N., Abbott R. C., Pedersen N. C., Koehler J. E. Experimental transmission of Bartonella henselae by the cat flea. J Clin Microbiol. 1996 Aug;34(8):1952–1956. doi: 10.1128/jcm.34.8.1952-1956.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Dolan M. J., Wong M. T., Regnery R. L., Jorgensen J. H., Garcia M., Peters J., Drehner D. Syndrome of Rochalimaea henselae adenitis suggesting cat scratch disease. Ann Intern Med. 1993 Mar 1;118(5):331–336. doi: 10.7326/0003-4819-118-5-199303010-00002. [DOI] [PubMed] [Google Scholar]
  5. Greene C. E., McDermott M., Jameson P. H., Atkins C. L., Marks A. M. Bartonella henselae infection in cats: evaluation during primary infection, treatment, and rechallenge infection. J Clin Microbiol. 1996 Jul;34(7):1682–1685. doi: 10.1128/jcm.34.7.1682-1685.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hadfield T. L., Warren R., Kass M., Brun E., Levy C. Endocarditis caused by Rochalimaea henselae. Hum Pathol. 1993 Oct;24(10):1140–1141. doi: 10.1016/0046-8177(93)90196-n. [DOI] [PubMed] [Google Scholar]
  7. Higgins J. A., Radulovic S., Jaworski D. C., Azad A. F. Acquisition of the cat scratch disease agent Bartonella henselae by cat fleas (Siphonaptera:Pulicidae). J Med Entomol. 1996 May;33(3):490–495. doi: 10.1093/jmedent/33.3.490. [DOI] [PubMed] [Google Scholar]
  8. Hofmann-Lehmann R., Holznagel E., Ossent P., Lutz H. Parameters of disease progression in long-term experimental feline retrovirus (feline immunodeficiency virus and feline leukemia virus) infections: hematology, clinical chemistry, and lymphocyte subsets. Clin Diagn Lab Immunol. 1997 Jan;4(1):33–42. doi: 10.1128/cdli.4.1.33-42.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Jameson P., Greene C., Regnery R., Dryden M., Marks A., Brown J., Cooper J., Glaus B., Greene R. Prevalence of Bartonella henselae antibodies in pet cats throughout regions of North America. J Infect Dis. 1995 Oct;172(4):1145–1149. doi: 10.1093/infdis/172.4.1145. [DOI] [PubMed] [Google Scholar]
  10. Koehler J. E., Glaser C. A., Tappero J. W. Rochalimaea henselae infection. A new zoonosis with the domestic cat as reservoir. JAMA. 1994 Feb 16;271(7):531–535. doi: 10.1001/jama.271.7.531. [DOI] [PubMed] [Google Scholar]
  11. Koehler J. E., Quinn F. D., Berger T. G., LeBoit P. E., Tappero J. W. Isolation of Rochalimaea species from cutaneous and osseous lesions of bacillary angiomatosis. N Engl J Med. 1992 Dec 3;327(23):1625–1631. doi: 10.1056/NEJM199212033272303. [DOI] [PubMed] [Google Scholar]
  12. Lutz H., Arnold P., Hübscher U., Egberink H., Pedersen N., Horzinek M. C. Specificity assessment of feline T-lymphotropic lentivirus serology. Zentralbl Veterinarmed B. 1988 Dec;35(10):773–778. doi: 10.1111/j.1439-0450.1988.tb00559.x. [DOI] [PubMed] [Google Scholar]
  13. Lutz H., Lehmann R., Winkler G., Kottwitz B., Dittmer A., Wolfensberger C., Arnold P. Das Feline Immunschwächevirus in der Schweiz: Klinik und Epidemiologie im Vergleich mit dem leukämie- und dem Coronavirus. Schweiz Arch Tierheilkd. 1990;132(5):217–225. [PubMed] [Google Scholar]
  14. Lutz H., Pedersen N. C., Durbin R., Theilen G. H. Monoclonal antibodies to three epitopic regions of feline leukemia virus p27 and their use in enzyme-linked immunosorbent assay of p27. J Immunol Methods. 1983 Jan 28;56(2):209–220. doi: 10.1016/0022-1759(83)90413-1. [DOI] [PubMed] [Google Scholar]
  15. Pedersen N. C., Boyle J. F., Floyd K. Infection studies in kittens, using feline infectious peritonitis virus propagated in cell culture. Am J Vet Res. 1981 Mar;42(3):363–367. [PubMed] [Google Scholar]
  16. Regnery R. L., Olson J. G., Perkins B. A., Bibb W. Serological response to "Rochalimaea henselae" antigen in suspected cat-scratch disease. Lancet. 1992 Jun 13;339(8807):1443–1445. doi: 10.1016/0140-6736(92)92032-b. [DOI] [PubMed] [Google Scholar]
  17. Regnery R. L., Rooney J. A., Johnson A. M., Nesby S. L., Manzewitsch P., Beaver K., Olson J. G. Experimentally induced Bartonella henselae infections followed by challenge exposure and antimicrobial therapy in cats. Am J Vet Res. 1996 Dec;57(12):1714–1719. [PubMed] [Google Scholar]
  18. Tappero J. W., Mohle-Boetani J., Koehler J. E., Swaminathan B., Berger T. G., LeBoit P. E., Smith L. L., Wenger J. D., Pinner R. W., Kemper C. A. The epidemiology of bacillary angiomatosis and bacillary peliosis. JAMA. 1993 Feb 10;269(6):770–775. [PubMed] [Google Scholar]
  19. Ueno H., Hohdatsu T., Muramatsu Y., Koyama H., Morita C. Does coinfection of Bartonella henselae and FIV induce clinical disorders in cats? Microbiol Immunol. 1996;40(9):617–620. doi: 10.1111/j.1348-0421.1996.tb01118.x. [DOI] [PubMed] [Google Scholar]
  20. Welch D. F., Pickett D. A., Slater L. N., Steigerwalt A. G., Brenner D. J. Rochalimaea henselae sp. nov., a cause of septicemia, bacillary angiomatosis, and parenchymal bacillary peliosis. J Clin Microbiol. 1992 Feb;30(2):275–280. doi: 10.1128/jcm.30.2.275-280.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Zangwill K. M., Hamilton D. H., Perkins B. A., Regnery R. L., Plikaytis B. D., Hadler J. L., Cartter M. L., Wenger J. D. Cat scratch disease in Connecticut. Epidemiology, risk factors, and evaluation of a new diagnostic test. N Engl J Med. 1993 Jul 1;329(1):8–13. doi: 10.1056/NEJM199307013290102. [DOI] [PubMed] [Google Scholar]

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